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You searched for subject:(myopathies). Showing records 1 – 30 of 35 total matches.

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University of Debrecen

1. Bercovici, Einav. Treatment of idiopathic Inflammatory myopathies .

Degree: DE – Általános Orvostudományi Kar, 2014, University of Debrecen

 Idiopathic inflammatory myopathies are a group of rare, disorders with the primary features of muscle weakness and inflammatory lesions identified in skeletal muscle specimens. The… (more)

Subjects/Keywords: myopathies; Inflammatory myopathies

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Bercovici, E. (2014). Treatment of idiopathic Inflammatory myopathies . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/194935

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Bercovici, Einav. “Treatment of idiopathic Inflammatory myopathies .” 2014. Thesis, University of Debrecen. Accessed April 23, 2019. http://hdl.handle.net/2437/194935.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Bercovici, Einav. “Treatment of idiopathic Inflammatory myopathies .” 2014. Web. 23 Apr 2019.

Vancouver:

Bercovici E. Treatment of idiopathic Inflammatory myopathies . [Internet] [Thesis]. University of Debrecen; 2014. [cited 2019 Apr 23]. Available from: http://hdl.handle.net/2437/194935.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Bercovici E. Treatment of idiopathic Inflammatory myopathies . [Thesis]. University of Debrecen; 2014. Available from: http://hdl.handle.net/2437/194935

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Université de Bordeaux I

2. Belbachir, Karima. Etude de l’organisation des collagènes dans les myopathies par spéctro-imagerie IRTF : Deterministic and stochastic optimization techniques for hard problems in cryptology.

Degree: Docteur es, Sciences Chimiques. Chimie-Organique, 2010, Université de Bordeaux I

Les myopathies sont une maladie rare qui entraine une déficience musculaire. Il apparait que la plupart des myopathies présentent une modification dans la biodistribution et… (more)

Subjects/Keywords: Spectro-imagerie IRTF; Myopathies; Collagènes; Spectro-imaging IRTF; Myopathies; Collagens

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APA (6th Edition):

Belbachir, K. (2010). Etude de l’organisation des collagènes dans les myopathies par spéctro-imagerie IRTF : Deterministic and stochastic optimization techniques for hard problems in cryptology. (Doctoral Dissertation). Université de Bordeaux I. Retrieved from http://www.theses.fr/2010BOR14215

Chicago Manual of Style (16th Edition):

Belbachir, Karima. “Etude de l’organisation des collagènes dans les myopathies par spéctro-imagerie IRTF : Deterministic and stochastic optimization techniques for hard problems in cryptology.” 2010. Doctoral Dissertation, Université de Bordeaux I. Accessed April 23, 2019. http://www.theses.fr/2010BOR14215.

MLA Handbook (7th Edition):

Belbachir, Karima. “Etude de l’organisation des collagènes dans les myopathies par spéctro-imagerie IRTF : Deterministic and stochastic optimization techniques for hard problems in cryptology.” 2010. Web. 23 Apr 2019.

Vancouver:

Belbachir K. Etude de l’organisation des collagènes dans les myopathies par spéctro-imagerie IRTF : Deterministic and stochastic optimization techniques for hard problems in cryptology. [Internet] [Doctoral dissertation]. Université de Bordeaux I; 2010. [cited 2019 Apr 23]. Available from: http://www.theses.fr/2010BOR14215.

Council of Science Editors:

Belbachir K. Etude de l’organisation des collagènes dans les myopathies par spéctro-imagerie IRTF : Deterministic and stochastic optimization techniques for hard problems in cryptology. [Doctoral Dissertation]. Université de Bordeaux I; 2010. Available from: http://www.theses.fr/2010BOR14215

3. Schartner, Vanessa. Identification et validation fonctionnelle de nouveaux gènes impliqués dans les myopathies : Identification and functional validation of new genes of myopathy.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2017, Université de Strasbourg

Les myopathies congénitales sont des maladies neuromusculaires dont le diagnostic est établi grâce aux données cliniques, histologiques et génétique. Cependant, le diagnostic génétique est manquant… (more)

Subjects/Keywords: Myopathies congénitales; Séquençage d'exomes; PYROXD1; CACNA1S; Congenital myopathies; Exome sequencing; PYROXD1; CACNA1S; 572.8; 616.748

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APA (6th Edition):

Schartner, V. (2017). Identification et validation fonctionnelle de nouveaux gènes impliqués dans les myopathies : Identification and functional validation of new genes of myopathy. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2017STRAJ026

Chicago Manual of Style (16th Edition):

Schartner, Vanessa. “Identification et validation fonctionnelle de nouveaux gènes impliqués dans les myopathies : Identification and functional validation of new genes of myopathy.” 2017. Doctoral Dissertation, Université de Strasbourg. Accessed April 23, 2019. http://www.theses.fr/2017STRAJ026.

MLA Handbook (7th Edition):

Schartner, Vanessa. “Identification et validation fonctionnelle de nouveaux gènes impliqués dans les myopathies : Identification and functional validation of new genes of myopathy.” 2017. Web. 23 Apr 2019.

Vancouver:

Schartner V. Identification et validation fonctionnelle de nouveaux gènes impliqués dans les myopathies : Identification and functional validation of new genes of myopathy. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2017. [cited 2019 Apr 23]. Available from: http://www.theses.fr/2017STRAJ026.

Council of Science Editors:

Schartner V. Identification et validation fonctionnelle de nouveaux gènes impliqués dans les myopathies : Identification and functional validation of new genes of myopathy. [Doctoral Dissertation]. Université de Strasbourg; 2017. Available from: http://www.theses.fr/2017STRAJ026

4. Saclier, Marielle. Functional phenotyping of macrophage subsets during skeletal muscle regeneration and in degenerative myopathies : Phénotypes fonctionnels des sous populations de macrophages au cours de la régénération musculaire et lors des myopathies dégénératives.

Degree: Docteur es, Biologie cellulaire, 2014, Université Paris Descartes – Paris V

 Le muscle squelettique a la capacité de se régénérer suite à une lésion grâce aux cellules satellites qui sont les cellules souches du muscle. Après… (more)

Subjects/Keywords: Macrophages; Régénération musculaire; Myopathies; Fibroblastes; Inflammation; Inflammation chronique; Interactions cellulaires; Macrophages; Muscle regeneration; Myopathies; Fibroblasts; Inflammation; Chronic inflammation; Cellular interactions; 616.74

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APA (6th Edition):

Saclier, M. (2014). Functional phenotyping of macrophage subsets during skeletal muscle regeneration and in degenerative myopathies : Phénotypes fonctionnels des sous populations de macrophages au cours de la régénération musculaire et lors des myopathies dégénératives. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2014PA05T004

Chicago Manual of Style (16th Edition):

Saclier, Marielle. “Functional phenotyping of macrophage subsets during skeletal muscle regeneration and in degenerative myopathies : Phénotypes fonctionnels des sous populations de macrophages au cours de la régénération musculaire et lors des myopathies dégénératives.” 2014. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed April 23, 2019. http://www.theses.fr/2014PA05T004.

MLA Handbook (7th Edition):

Saclier, Marielle. “Functional phenotyping of macrophage subsets during skeletal muscle regeneration and in degenerative myopathies : Phénotypes fonctionnels des sous populations de macrophages au cours de la régénération musculaire et lors des myopathies dégénératives.” 2014. Web. 23 Apr 2019.

Vancouver:

Saclier M. Functional phenotyping of macrophage subsets during skeletal muscle regeneration and in degenerative myopathies : Phénotypes fonctionnels des sous populations de macrophages au cours de la régénération musculaire et lors des myopathies dégénératives. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2014. [cited 2019 Apr 23]. Available from: http://www.theses.fr/2014PA05T004.

Council of Science Editors:

Saclier M. Functional phenotyping of macrophage subsets during skeletal muscle regeneration and in degenerative myopathies : Phénotypes fonctionnels des sous populations de macrophages au cours de la régénération musculaire et lors des myopathies dégénératives. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2014. Available from: http://www.theses.fr/2014PA05T004

5. Bourdenet, Gwladys. Étude physiopathologique de la myopathie auto-immune des souris NOD invalidées pour la voie de costimulation ICOS/ICOSL. : Physiopathological study of autoimmune myopathy in disabled NOD mice for the ICOS/ICOSL costimulation pathway.

Degree: Docteur es, Aspects moleculaires et cellulaires de la biologie, 2017, Normandie

Les myopathies inflammatoires (MI) représentent un groupe hétérogène de maladies caractérisépar une faiblesse musculaire chronique et symétrique associée à une augmentation du taux sérique decréatine… (more)

Subjects/Keywords: Myopathies inflammatoires; Physiopathologie; Auto-anticorps; Biomarqueurs; Costimulation; ICOS/ICOSL; IRM musculaire; Inflammatory Myopathies (IM); Muscle weakness; Creatine phosphokinase (CPK); 616.74

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APA (6th Edition):

Bourdenet, G. (2017). Étude physiopathologique de la myopathie auto-immune des souris NOD invalidées pour la voie de costimulation ICOS/ICOSL. : Physiopathological study of autoimmune myopathy in disabled NOD mice for the ICOS/ICOSL costimulation pathway. (Doctoral Dissertation). Normandie. Retrieved from http://www.theses.fr/2017NORMR062

Chicago Manual of Style (16th Edition):

Bourdenet, Gwladys. “Étude physiopathologique de la myopathie auto-immune des souris NOD invalidées pour la voie de costimulation ICOS/ICOSL. : Physiopathological study of autoimmune myopathy in disabled NOD mice for the ICOS/ICOSL costimulation pathway.” 2017. Doctoral Dissertation, Normandie. Accessed April 23, 2019. http://www.theses.fr/2017NORMR062.

MLA Handbook (7th Edition):

Bourdenet, Gwladys. “Étude physiopathologique de la myopathie auto-immune des souris NOD invalidées pour la voie de costimulation ICOS/ICOSL. : Physiopathological study of autoimmune myopathy in disabled NOD mice for the ICOS/ICOSL costimulation pathway.” 2017. Web. 23 Apr 2019.

Vancouver:

Bourdenet G. Étude physiopathologique de la myopathie auto-immune des souris NOD invalidées pour la voie de costimulation ICOS/ICOSL. : Physiopathological study of autoimmune myopathy in disabled NOD mice for the ICOS/ICOSL costimulation pathway. [Internet] [Doctoral dissertation]. Normandie; 2017. [cited 2019 Apr 23]. Available from: http://www.theses.fr/2017NORMR062.

Council of Science Editors:

Bourdenet G. Étude physiopathologique de la myopathie auto-immune des souris NOD invalidées pour la voie de costimulation ICOS/ICOSL. : Physiopathological study of autoimmune myopathy in disabled NOD mice for the ICOS/ICOSL costimulation pathway. [Doctoral Dissertation]. Normandie; 2017. Available from: http://www.theses.fr/2017NORMR062

6. Bergua, Cecile. Pathogénicité des auto-anticorps anti-SRP et anti-HMGCR au cours des myopathies nécrosantes auto-immunes : Pathogenicity of autoantibodies anti-SRP and anti-HMGCR in autoimmune necrotizing myopathies.

Degree: Docteur es, Aspects moleculaires et cellulaires de la biologie, 2017, Normandie

Les myopathies auto-immunes (MAI), classiquement appelées myosites ou myopathies inflammatoires idiopathiques, représentent un groupe de maladies définies par des caractéristiques cliniques, histopathologiques et biologiques. Une… (more)

Subjects/Keywords: Myosite; Myopathie nécrosante auto-immune; Auto-anticorps; SRP; Modèle murin; Autoimmune myopathies; Myositis; Idiopathic inflammatory myopathies; 616.74; WE 559

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APA (6th Edition):

Bergua, C. (2017). Pathogénicité des auto-anticorps anti-SRP et anti-HMGCR au cours des myopathies nécrosantes auto-immunes : Pathogenicity of autoantibodies anti-SRP and anti-HMGCR in autoimmune necrotizing myopathies. (Doctoral Dissertation). Normandie. Retrieved from http://www.theses.fr/2017NORMR067

Chicago Manual of Style (16th Edition):

Bergua, Cecile. “Pathogénicité des auto-anticorps anti-SRP et anti-HMGCR au cours des myopathies nécrosantes auto-immunes : Pathogenicity of autoantibodies anti-SRP and anti-HMGCR in autoimmune necrotizing myopathies.” 2017. Doctoral Dissertation, Normandie. Accessed April 23, 2019. http://www.theses.fr/2017NORMR067.

MLA Handbook (7th Edition):

Bergua, Cecile. “Pathogénicité des auto-anticorps anti-SRP et anti-HMGCR au cours des myopathies nécrosantes auto-immunes : Pathogenicity of autoantibodies anti-SRP and anti-HMGCR in autoimmune necrotizing myopathies.” 2017. Web. 23 Apr 2019.

Vancouver:

Bergua C. Pathogénicité des auto-anticorps anti-SRP et anti-HMGCR au cours des myopathies nécrosantes auto-immunes : Pathogenicity of autoantibodies anti-SRP and anti-HMGCR in autoimmune necrotizing myopathies. [Internet] [Doctoral dissertation]. Normandie; 2017. [cited 2019 Apr 23]. Available from: http://www.theses.fr/2017NORMR067.

Council of Science Editors:

Bergua C. Pathogénicité des auto-anticorps anti-SRP et anti-HMGCR au cours des myopathies nécrosantes auto-immunes : Pathogenicity of autoantibodies anti-SRP and anti-HMGCR in autoimmune necrotizing myopathies. [Doctoral Dissertation]. Normandie; 2017. Available from: http://www.theses.fr/2017NORMR067

7. Roman, William. Positioning nuclei at the periphery of skeletal muscle cells : Positionnement des noyaux à la périphérie des cellules musculaires.

Degree: Docteur es, Complexité du Vivant, 2016, Université Pierre et Marie Curie – Paris VI

Les mouvements nucléaires sont importants pour une multitude de fonctions cellulaires et sont induits par des forces produites par des protéines moteurs et le cytosquelette.… (more)

Subjects/Keywords: Biologie cellulaire; Mouvement nucléaire; Myologie; Cytosquelette; Myopathies Centro-Nucléés; Triades; Cytoskeleton; Nuclear movement; Centronuclear myopathies; 571.6

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APA (6th Edition):

Roman, W. (2016). Positioning nuclei at the periphery of skeletal muscle cells : Positionnement des noyaux à la périphérie des cellules musculaires. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2016PA066408

Chicago Manual of Style (16th Edition):

Roman, William. “Positioning nuclei at the periphery of skeletal muscle cells : Positionnement des noyaux à la périphérie des cellules musculaires.” 2016. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed April 23, 2019. http://www.theses.fr/2016PA066408.

MLA Handbook (7th Edition):

Roman, William. “Positioning nuclei at the periphery of skeletal muscle cells : Positionnement des noyaux à la périphérie des cellules musculaires.” 2016. Web. 23 Apr 2019.

Vancouver:

Roman W. Positioning nuclei at the periphery of skeletal muscle cells : Positionnement des noyaux à la périphérie des cellules musculaires. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. [cited 2019 Apr 23]. Available from: http://www.theses.fr/2016PA066408.

Council of Science Editors:

Roman W. Positioning nuclei at the periphery of skeletal muscle cells : Positionnement des noyaux à la périphérie des cellules musculaires. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. Available from: http://www.theses.fr/2016PA066408

8. Poursaeed, Nasim. Genetic diagnosis and identification of novel genes in neuromuscular disorders using next generation sequencing : Diagnostic génétique et identification de nouveau gènes impliqués dans les maladies neuromusculaires par séquençage haut débit.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2012, Université de Strasbourg

Les maladies neuromusculaires sont des maladies souvent très sévères et très handicapantes, et un fardeau pour les patients, leurs familles, ainsi que pour le système… (more)

Subjects/Keywords: Maladies neuromusculaires; Myopathies centronucléaires; Séquençage haut débit; Neuromuscular disorders; Centronuclear myopathies; Massively parallel sequencing; 616.7; 660.65; 572.8

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APA (6th Edition):

Poursaeed, N. (2012). Genetic diagnosis and identification of novel genes in neuromuscular disorders using next generation sequencing : Diagnostic génétique et identification de nouveau gènes impliqués dans les maladies neuromusculaires par séquençage haut débit. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2012STRAJ055

Chicago Manual of Style (16th Edition):

Poursaeed, Nasim. “Genetic diagnosis and identification of novel genes in neuromuscular disorders using next generation sequencing : Diagnostic génétique et identification de nouveau gènes impliqués dans les maladies neuromusculaires par séquençage haut débit.” 2012. Doctoral Dissertation, Université de Strasbourg. Accessed April 23, 2019. http://www.theses.fr/2012STRAJ055.

MLA Handbook (7th Edition):

Poursaeed, Nasim. “Genetic diagnosis and identification of novel genes in neuromuscular disorders using next generation sequencing : Diagnostic génétique et identification de nouveau gènes impliqués dans les maladies neuromusculaires par séquençage haut débit.” 2012. Web. 23 Apr 2019.

Vancouver:

Poursaeed N. Genetic diagnosis and identification of novel genes in neuromuscular disorders using next generation sequencing : Diagnostic génétique et identification de nouveau gènes impliqués dans les maladies neuromusculaires par séquençage haut débit. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2012. [cited 2019 Apr 23]. Available from: http://www.theses.fr/2012STRAJ055.

Council of Science Editors:

Poursaeed N. Genetic diagnosis and identification of novel genes in neuromuscular disorders using next generation sequencing : Diagnostic génétique et identification de nouveau gènes impliqués dans les maladies neuromusculaires par séquençage haut débit. [Doctoral Dissertation]. Université de Strasbourg; 2012. Available from: http://www.theses.fr/2012STRAJ055

9. Mias-Lucquin, Dominique. Dynamique et mécanique de complexes dystrophine-actine-lipides membranaires : Dynamics et mecanics of dystrophin complexes with actin and mambrane lipids.

Degree: Docteur es, Biologie moléculaire et structurale, Biochimie, 2018, Rennes 1

La dystrophine est une protéine filamenteuse qui contribue à la structuration des cellules musculaires en créant un lien entre le cytosquelette et le sarcolemme. Avec… (more)

Subjects/Keywords: Dystrophine; Myopathies; Modélisation moléculaire; Interaction protéine-Protéine; Interaction protéine-Lipides; Dystrophin; Myopathies; Molecular modeling; Protein-Protein interaction; Protein-Lipid interaction

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APA (6th Edition):

Mias-Lucquin, D. (2018). Dynamique et mécanique de complexes dystrophine-actine-lipides membranaires : Dynamics et mecanics of dystrophin complexes with actin and mambrane lipids. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2018REN1B024

Chicago Manual of Style (16th Edition):

Mias-Lucquin, Dominique. “Dynamique et mécanique de complexes dystrophine-actine-lipides membranaires : Dynamics et mecanics of dystrophin complexes with actin and mambrane lipids.” 2018. Doctoral Dissertation, Rennes 1. Accessed April 23, 2019. http://www.theses.fr/2018REN1B024.

MLA Handbook (7th Edition):

Mias-Lucquin, Dominique. “Dynamique et mécanique de complexes dystrophine-actine-lipides membranaires : Dynamics et mecanics of dystrophin complexes with actin and mambrane lipids.” 2018. Web. 23 Apr 2019.

Vancouver:

Mias-Lucquin D. Dynamique et mécanique de complexes dystrophine-actine-lipides membranaires : Dynamics et mecanics of dystrophin complexes with actin and mambrane lipids. [Internet] [Doctoral dissertation]. Rennes 1; 2018. [cited 2019 Apr 23]. Available from: http://www.theses.fr/2018REN1B024.

Council of Science Editors:

Mias-Lucquin D. Dynamique et mécanique de complexes dystrophine-actine-lipides membranaires : Dynamics et mecanics of dystrophin complexes with actin and mambrane lipids. [Doctoral Dissertation]. Rennes 1; 2018. Available from: http://www.theses.fr/2018REN1B024


University of Western Australia

10. Ravenscroft, Gianina. A therapeutic approach for the skeletal muscle a-actin based congenital myopathies.

Degree: PhD, 2009, University of Western Australia

 [Truncated abstract] Mutations in the skeletal muscle -actin gene (ACTA1) have been shown to be one cause of a broad group of muscle disorders all… (more)

Subjects/Keywords: Muscles; Muscles; Congenital myopathies; Skeletal muscle alpha-actin; Up-regulation therapy

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APA (6th Edition):

Ravenscroft, G. (2009). A therapeutic approach for the skeletal muscle a-actin based congenital myopathies. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=12788&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Ravenscroft, Gianina. “A therapeutic approach for the skeletal muscle a-actin based congenital myopathies.” 2009. Doctoral Dissertation, University of Western Australia. Accessed April 23, 2019. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=12788&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Ravenscroft, Gianina. “A therapeutic approach for the skeletal muscle a-actin based congenital myopathies.” 2009. Web. 23 Apr 2019.

Vancouver:

Ravenscroft G. A therapeutic approach for the skeletal muscle a-actin based congenital myopathies. [Internet] [Doctoral dissertation]. University of Western Australia; 2009. [cited 2019 Apr 23]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=12788&local_base=GEN01-INS01.

Council of Science Editors:

Ravenscroft G. A therapeutic approach for the skeletal muscle a-actin based congenital myopathies. [Doctoral Dissertation]. University of Western Australia; 2009. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=12788&local_base=GEN01-INS01


University of Texas Southwestern Medical Center

11. Garg, Ankit. Discovery of New Regulatory Proteins and Mechanisms in Muscle Biology and Disease.

Degree: 2014, University of Texas Southwestern Medical Center

 In an effort to discover new regulators of muscle function, we identified a novel muscle-specific protein, Klhl40. Genetic deletion of Klhl40 in mice results in… (more)

Subjects/Keywords: MEF2 Transcription Factors; Microfilament Proteins; Muscle Proteins; Myofibrils; Myopathies, Nemaline

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APA (6th Edition):

Garg, A. (2014). Discovery of New Regulatory Proteins and Mechanisms in Muscle Biology and Disease. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/3340

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Garg, Ankit. “Discovery of New Regulatory Proteins and Mechanisms in Muscle Biology and Disease.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed April 23, 2019. http://hdl.handle.net/2152.5/3340.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Garg, Ankit. “Discovery of New Regulatory Proteins and Mechanisms in Muscle Biology and Disease.” 2014. Web. 23 Apr 2019.

Vancouver:

Garg A. Discovery of New Regulatory Proteins and Mechanisms in Muscle Biology and Disease. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2019 Apr 23]. Available from: http://hdl.handle.net/2152.5/3340.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Garg A. Discovery of New Regulatory Proteins and Mechanisms in Muscle Biology and Disease. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/3340

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Indian Institute of Science

12. Salvi, Sheetal S. Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants.

Degree: 2011, Indian Institute of Science

 Myofibrillogenesis is a complex process, which involves assembly of hundreds of structural proteins in a highly ordered manner to form the contractile structural unit of… (more)

Subjects/Keywords: Myopathy; Myofibrillogenesis; Drosophila Melanogaster; Muscular Diseases; Muscle Diseases; Sacromeric Proteins; Actin Myopathy; Myosin Myopathy; Drosophila Melanogaster - Indirect Flight Muscle System; Myositis; Drosophila Mutants; Human Myopathies; Myopathies; Molecular Biology

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APA (6th Edition):

Salvi, S. S. (2011). Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/2128

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Salvi, Sheetal S. “Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants.” 2011. Thesis, Indian Institute of Science. Accessed April 23, 2019. http://hdl.handle.net/2005/2128.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Salvi, Sheetal S. “Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants.” 2011. Web. 23 Apr 2019.

Vancouver:

Salvi SS. Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants. [Internet] [Thesis]. Indian Institute of Science; 2011. [cited 2019 Apr 23]. Available from: http://hdl.handle.net/2005/2128.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Salvi SS. Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants. [Thesis]. Indian Institute of Science; 2011. Available from: http://hdl.handle.net/2005/2128

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Indian Institute of Science

13. Salvi, Sheetal S. Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants.

Degree: 2011, Indian Institute of Science

 Myofibrillogenesis is a complex process, which involves assembly of hundreds of structural proteins in a highly ordered manner to form the contractile structural unit of… (more)

Subjects/Keywords: Myopathy; Myofibrillogenesis; Drosophila Melanogaster; Muscular Diseases; Muscle Diseases; Sacromeric Proteins; Actin Myopathy; Myosin Myopathy; Drosophila Melanogaster - Indirect Flight Muscle System; Myositis; Drosophila Mutants; Human Myopathies; Myopathies; Molecular Biology

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APA (6th Edition):

Salvi, S. S. (2011). Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants. (Thesis). Indian Institute of Science. Retrieved from http://etd.iisc.ernet.in/handle/2005/2128 ; http://etd.ncsi.iisc.ernet.in/abstracts/2732/G25022-Abs.pdf

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Salvi, Sheetal S. “Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants.” 2011. Thesis, Indian Institute of Science. Accessed April 23, 2019. http://etd.iisc.ernet.in/handle/2005/2128 ; http://etd.ncsi.iisc.ernet.in/abstracts/2732/G25022-Abs.pdf.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Salvi, Sheetal S. “Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants.” 2011. Web. 23 Apr 2019.

Vancouver:

Salvi SS. Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants. [Internet] [Thesis]. Indian Institute of Science; 2011. [cited 2019 Apr 23]. Available from: http://etd.iisc.ernet.in/handle/2005/2128 ; http://etd.ncsi.iisc.ernet.in/abstracts/2732/G25022-Abs.pdf.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Salvi SS. Unravelling The Mechanisms Of Myofibrillogenesis And Human Myopathies Using Drosophila Mutants. [Thesis]. Indian Institute of Science; 2011. Available from: http://etd.iisc.ernet.in/handle/2005/2128 ; http://etd.ncsi.iisc.ernet.in/abstracts/2732/G25022-Abs.pdf

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

14. Tasfaout, Hichem. Physiopathologie et validation préclinique dans les myopathies centronucleaires : Physiopathology and preclinical validation in centronuclear myopathies.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2017, Université de Strasbourg

La myopathie myotubulaire est une maladie musculaire congénitale très sévère. Le laboratoire d’accueil a démontré que les échantillons de muscle de patients atteints de cette… (more)

Subjects/Keywords: Myopathie myotubulaire; Myopathies centronucléaires; Virus adéno-associés; Oligonucleotides antisens; Dynamine2; Myotubularine1; Myotubular myopathy; Centronuclear myopathies; Adeno-associated virus; Antisense oligonucleotides; Dynamin2; Myotubularin1; 572.8; 616.7

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APA (6th Edition):

Tasfaout, H. (2017). Physiopathologie et validation préclinique dans les myopathies centronucleaires : Physiopathology and preclinical validation in centronuclear myopathies. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2017STRAJ066

Chicago Manual of Style (16th Edition):

Tasfaout, Hichem. “Physiopathologie et validation préclinique dans les myopathies centronucleaires : Physiopathology and preclinical validation in centronuclear myopathies.” 2017. Doctoral Dissertation, Université de Strasbourg. Accessed April 23, 2019. http://www.theses.fr/2017STRAJ066.

MLA Handbook (7th Edition):

Tasfaout, Hichem. “Physiopathologie et validation préclinique dans les myopathies centronucleaires : Physiopathology and preclinical validation in centronuclear myopathies.” 2017. Web. 23 Apr 2019.

Vancouver:

Tasfaout H. Physiopathologie et validation préclinique dans les myopathies centronucleaires : Physiopathology and preclinical validation in centronuclear myopathies. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2017. [cited 2019 Apr 23]. Available from: http://www.theses.fr/2017STRAJ066.

Council of Science Editors:

Tasfaout H. Physiopathologie et validation préclinique dans les myopathies centronucleaires : Physiopathology and preclinical validation in centronuclear myopathies. [Doctoral Dissertation]. Université de Strasbourg; 2017. Available from: http://www.theses.fr/2017STRAJ066


Université de Grenoble

15. Dieterich, Klaus. Arthrogryposes multiples congénitales neuromusculaires : Identification d’un nouveau gène, ECEL1, et recherche des mécanismes physiopathologiques liés au complexe de relâchement de calcium : Study of arthrogryposis related syndromes : Identification of novel candidate genes and expression analysis during embryonic and fetal development of calcium release complex proteins in human skeletal muscle.

Degree: Docteur es, Biologie cellulaire, 2013, Université de Grenoble

Les arthrogryposes multiples congénitales (AMC), limitations articulaires multiples survenant au cours du développement et présentes à la naissance, sont un ensemble hétérogène de maladies dont… (more)

Subjects/Keywords: Arthrogrypose; Limitations articulaires congénitales multiples; Complexe de relâchement du calcium; Sarcomère; Myopathies; Arthrogryposis; Multiple congenital joint contractures; Calcium release complex; Sarcomer; Myopathies; 570

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APA (6th Edition):

Dieterich, K. (2013). Arthrogryposes multiples congénitales neuromusculaires : Identification d’un nouveau gène, ECEL1, et recherche des mécanismes physiopathologiques liés au complexe de relâchement de calcium : Study of arthrogryposis related syndromes : Identification of novel candidate genes and expression analysis during embryonic and fetal development of calcium release complex proteins in human skeletal muscle. (Doctoral Dissertation). Université de Grenoble. Retrieved from http://www.theses.fr/2013GRENV082

Chicago Manual of Style (16th Edition):

Dieterich, Klaus. “Arthrogryposes multiples congénitales neuromusculaires : Identification d’un nouveau gène, ECEL1, et recherche des mécanismes physiopathologiques liés au complexe de relâchement de calcium : Study of arthrogryposis related syndromes : Identification of novel candidate genes and expression analysis during embryonic and fetal development of calcium release complex proteins in human skeletal muscle.” 2013. Doctoral Dissertation, Université de Grenoble. Accessed April 23, 2019. http://www.theses.fr/2013GRENV082.

MLA Handbook (7th Edition):

Dieterich, Klaus. “Arthrogryposes multiples congénitales neuromusculaires : Identification d’un nouveau gène, ECEL1, et recherche des mécanismes physiopathologiques liés au complexe de relâchement de calcium : Study of arthrogryposis related syndromes : Identification of novel candidate genes and expression analysis during embryonic and fetal development of calcium release complex proteins in human skeletal muscle.” 2013. Web. 23 Apr 2019.

Vancouver:

Dieterich K. Arthrogryposes multiples congénitales neuromusculaires : Identification d’un nouveau gène, ECEL1, et recherche des mécanismes physiopathologiques liés au complexe de relâchement de calcium : Study of arthrogryposis related syndromes : Identification of novel candidate genes and expression analysis during embryonic and fetal development of calcium release complex proteins in human skeletal muscle. [Internet] [Doctoral dissertation]. Université de Grenoble; 2013. [cited 2019 Apr 23]. Available from: http://www.theses.fr/2013GRENV082.

Council of Science Editors:

Dieterich K. Arthrogryposes multiples congénitales neuromusculaires : Identification d’un nouveau gène, ECEL1, et recherche des mécanismes physiopathologiques liés au complexe de relâchement de calcium : Study of arthrogryposis related syndromes : Identification of novel candidate genes and expression analysis during embryonic and fetal development of calcium release complex proteins in human skeletal muscle. [Doctoral Dissertation]. Université de Grenoble; 2013. Available from: http://www.theses.fr/2013GRENV082


Université de Lorraine

16. Salgado Ruiz, Nallely. Le Téléthon : étude comparée en France et au Mexique : The Telethon : comparative study in France and Mexico.

Degree: Docteur es, Sciences de l'Information et de la Communication, 2014, Université de Lorraine

Le Téléthon est un format adapté avec succès à la télévision française par le binôme Groupe France Télévisions – Association française contre les myopathies depuis… (more)

Subjects/Keywords: Téléthon; Étude comparée; Format de télévision; Association française contre les myopathies; Fundación Teletón; Handicap; Telethon; Comparative study; TV format; Association française contre les myopathies; Fundación Teletón; Handicap

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APA (6th Edition):

Salgado Ruiz, N. (2014). Le Téléthon : étude comparée en France et au Mexique : The Telethon : comparative study in France and Mexico. (Doctoral Dissertation). Université de Lorraine. Retrieved from http://www.theses.fr/2014LORR0160

Chicago Manual of Style (16th Edition):

Salgado Ruiz, Nallely. “Le Téléthon : étude comparée en France et au Mexique : The Telethon : comparative study in France and Mexico.” 2014. Doctoral Dissertation, Université de Lorraine. Accessed April 23, 2019. http://www.theses.fr/2014LORR0160.

MLA Handbook (7th Edition):

Salgado Ruiz, Nallely. “Le Téléthon : étude comparée en France et au Mexique : The Telethon : comparative study in France and Mexico.” 2014. Web. 23 Apr 2019.

Vancouver:

Salgado Ruiz N. Le Téléthon : étude comparée en France et au Mexique : The Telethon : comparative study in France and Mexico. [Internet] [Doctoral dissertation]. Université de Lorraine; 2014. [cited 2019 Apr 23]. Available from: http://www.theses.fr/2014LORR0160.

Council of Science Editors:

Salgado Ruiz N. Le Téléthon : étude comparée en France et au Mexique : The Telethon : comparative study in France and Mexico. [Doctoral Dissertation]. Université de Lorraine; 2014. Available from: http://www.theses.fr/2014LORR0160

17. Rothwell, Simon. Identification of Disease Susceptibility Genes in the Idiopathic Inflammatory Myopathies.

Degree: 2016, University of Manchester

 Background: The idiopathic inflammatory myopathies (IIM) are a heterogeneous group of rare autoimmune diseases comprising of polymyositis (PM), dermatomyositis (DM), and inclusion body myositis (IBM).… (more)

Subjects/Keywords: Genetics; Idiopathic Inflammatory Myopathies; Myositis

…Identification of Disease Susceptibility Genes in the Idiopathic Inflammatory Myopathies, 2015… …Background: The idiopathic inflammatory myopathies (IIM) are a heterogeneous group of… …idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and… …inflammatory myopathies. Curr Opin Rheumatol. 2013 Nov;25(6):735-41. doi: 10.1097/01.bor… …Immunochip Study in the Idiopathic Inflammatory Myopathies Identifies Genetic Differences between… 

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APA (6th Edition):

Rothwell, S. (2016). Identification of Disease Susceptibility Genes in the Idiopathic Inflammatory Myopathies. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:294276

Chicago Manual of Style (16th Edition):

Rothwell, Simon. “Identification of Disease Susceptibility Genes in the Idiopathic Inflammatory Myopathies.” 2016. Doctoral Dissertation, University of Manchester. Accessed April 23, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:294276.

MLA Handbook (7th Edition):

Rothwell, Simon. “Identification of Disease Susceptibility Genes in the Idiopathic Inflammatory Myopathies.” 2016. Web. 23 Apr 2019.

Vancouver:

Rothwell S. Identification of Disease Susceptibility Genes in the Idiopathic Inflammatory Myopathies. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Apr 23]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:294276.

Council of Science Editors:

Rothwell S. Identification of Disease Susceptibility Genes in the Idiopathic Inflammatory Myopathies. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:294276


Universitat Autònoma de Barcelona

18. Alejaldre Monforte, Aída. Uutilidad de los estudios de imagen muscular en el diagnóstico de un grupo de miopatías con debilidad axial.

Degree: Departament de Medicina, 2016, Universitat Autònoma de Barcelona

 Hereditary myopathies are diseases with a complex diagnosis. They may present with different phenotypes of muscle weakness. A relatively new phenotype is the axial phenotype.… (more)

Subjects/Keywords: Miopaties; Miopatías; Myopathies; Axial; Radiologia; Radiología; Radiology; Ciències de la Salut; 616.8

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APA (6th Edition):

Alejaldre Monforte, A. (2016). Uutilidad de los estudios de imagen muscular en el diagnóstico de un grupo de miopatías con debilidad axial. (Thesis). Universitat Autònoma de Barcelona. Retrieved from http://hdl.handle.net/10803/399847

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Alejaldre Monforte, Aída. “Uutilidad de los estudios de imagen muscular en el diagnóstico de un grupo de miopatías con debilidad axial.” 2016. Thesis, Universitat Autònoma de Barcelona. Accessed April 23, 2019. http://hdl.handle.net/10803/399847.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Alejaldre Monforte, Aída. “Uutilidad de los estudios de imagen muscular en el diagnóstico de un grupo de miopatías con debilidad axial.” 2016. Web. 23 Apr 2019.

Vancouver:

Alejaldre Monforte A. Uutilidad de los estudios de imagen muscular en el diagnóstico de un grupo de miopatías con debilidad axial. [Internet] [Thesis]. Universitat Autònoma de Barcelona; 2016. [cited 2019 Apr 23]. Available from: http://hdl.handle.net/10803/399847.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Alejaldre Monforte A. Uutilidad de los estudios de imagen muscular en el diagnóstico de un grupo de miopatías con debilidad axial. [Thesis]. Universitat Autònoma de Barcelona; 2016. Available from: http://hdl.handle.net/10803/399847

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

19. Bach, Aurea Beatriz Martins. Avaliação não invasiva de modelos murinos para doenças musculares genéticas.

Degree: PhD, Biologia (Genética), 2015, University of São Paulo

Novas abordagens terapêuticas vêm sendo introduzidas para doenças musculares genéticas como distrofias musculares e miopatias congênitas, distúrbios que permanecem sem cura até o momento. Estes… (more)

Subjects/Keywords: Congenital myopathies; Distrofia muscular; Miopatias congênitas; MNR-Nuclear Magnetic Resonance; Muscle dystrophy; RMN-Ressonância Magnética Nuclear

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APA (6th Edition):

Bach, A. B. M. (2015). Avaliação não invasiva de modelos murinos para doenças musculares genéticas. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/41/41131/tde-21092015-160628/ ;

Chicago Manual of Style (16th Edition):

Bach, Aurea Beatriz Martins. “Avaliação não invasiva de modelos murinos para doenças musculares genéticas.” 2015. Doctoral Dissertation, University of São Paulo. Accessed April 23, 2019. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-21092015-160628/ ;.

MLA Handbook (7th Edition):

Bach, Aurea Beatriz Martins. “Avaliação não invasiva de modelos murinos para doenças musculares genéticas.” 2015. Web. 23 Apr 2019.

Vancouver:

Bach ABM. Avaliação não invasiva de modelos murinos para doenças musculares genéticas. [Internet] [Doctoral dissertation]. University of São Paulo; 2015. [cited 2019 Apr 23]. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-21092015-160628/ ;.

Council of Science Editors:

Bach ABM. Avaliação não invasiva de modelos murinos para doenças musculares genéticas. [Doctoral Dissertation]. University of São Paulo; 2015. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-21092015-160628/ ;


University of Western Australia

20. Rojana-udomsart, Arada. Clinical, immunological and immunogenetic studies on sporadic inclusion body myositis and other inflammatory myopathies.

Degree: PhD, 2013, University of Western Australia

[Truncated abstract] The pathogenesis of sporadic inclusion body myositis (sIBM), the most common myopathy in individuals over 50 years of age, is still poorly understood.… (more)

Subjects/Keywords: Sporadic inclusion body myositis; Inflammatory myopathies; Necrotising myopathy; HLA-DRB1; HLA-DRB3; Autoantibody in sIBM; Paraspinal myopathy; Sjogren's syndrome

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APA (6th Edition):

Rojana-udomsart, A. (2013). Clinical, immunological and immunogenetic studies on sporadic inclusion body myositis and other inflammatory myopathies. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=40117&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Rojana-udomsart, Arada. “Clinical, immunological and immunogenetic studies on sporadic inclusion body myositis and other inflammatory myopathies.” 2013. Doctoral Dissertation, University of Western Australia. Accessed April 23, 2019. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=40117&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Rojana-udomsart, Arada. “Clinical, immunological and immunogenetic studies on sporadic inclusion body myositis and other inflammatory myopathies.” 2013. Web. 23 Apr 2019.

Vancouver:

Rojana-udomsart A. Clinical, immunological and immunogenetic studies on sporadic inclusion body myositis and other inflammatory myopathies. [Internet] [Doctoral dissertation]. University of Western Australia; 2013. [cited 2019 Apr 23]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=40117&local_base=GEN01-INS01.

Council of Science Editors:

Rojana-udomsart A. Clinical, immunological and immunogenetic studies on sporadic inclusion body myositis and other inflammatory myopathies. [Doctoral Dissertation]. University of Western Australia; 2013. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=40117&local_base=GEN01-INS01


University of Debrecen

21. Saar, Norin. Rituximab Therapy in Idiopathic Inflammatory Myositis .

Degree: DE – Általános Orvostudományi Kar, University of Debrecen

 Idiopathic inflammatory myopathies are chronic group of autoimmune diseases that affects striated muscles tissue. Pathological and serological classifications are recognised. The thesis reviews litrature and… (more)

Subjects/Keywords: Rituximab; Idiopathic inflamatory myopathies; Autoimmune disease; Polymyositis; Dermatomyositis

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APA (6th Edition):

Saar, N. (n.d.). Rituximab Therapy in Idiopathic Inflammatory Myositis . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/242864

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Saar, Norin. “Rituximab Therapy in Idiopathic Inflammatory Myositis .” Thesis, University of Debrecen. Accessed April 23, 2019. http://hdl.handle.net/2437/242864.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Saar, Norin. “Rituximab Therapy in Idiopathic Inflammatory Myositis .” Web. 23 Apr 2019.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Saar N. Rituximab Therapy in Idiopathic Inflammatory Myositis . [Internet] [Thesis]. University of Debrecen; [cited 2019 Apr 23]. Available from: http://hdl.handle.net/2437/242864.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Saar N. Rituximab Therapy in Idiopathic Inflammatory Myositis . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/242864

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

22. Bankolé, Sénakpon Landry Cyrille. Thérapie par l’exercice et dystrophie facio-scapulo-humérale : étude contrôlée randomisée de 6 mois d’entraînement à domicile : précédée d’une étude histologique du potentiel régénératif musculaire dans deux modèles distincts de myopathies : Exercise therapy and facioscapulohumeral muscular dystrophy : a randomized, controlled trial of 6-month home-base : preceded by a histological study of muscle regenerative potential in two distinct models of myopathies.

Degree: Docteur es, Biologie et Physiologie de l'Exercice, 2014, Saint-Etienne

Bien que l’innocuité de la pratique de l’activité physique (AP) ait été acceptée dans les myopathies y compris dans les dystrophies, il existe très peu… (more)

Subjects/Keywords: Myopathies; FSHD; Entraînement mixte adapté à domicile; Capacité aérobie; Fatigue; Myopathy and dystrophy; FSHD; Adapted home-based training; Aerobic capacity; Fatigue

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APA (6th Edition):

Bankolé, S. L. C. (2014). Thérapie par l’exercice et dystrophie facio-scapulo-humérale : étude contrôlée randomisée de 6 mois d’entraînement à domicile : précédée d’une étude histologique du potentiel régénératif musculaire dans deux modèles distincts de myopathies : Exercise therapy and facioscapulohumeral muscular dystrophy : a randomized, controlled trial of 6-month home-base : preceded by a histological study of muscle regenerative potential in two distinct models of myopathies. (Doctoral Dissertation). Saint-Etienne. Retrieved from http://www.theses.fr/2014STET008T

Chicago Manual of Style (16th Edition):

Bankolé, Sénakpon Landry Cyrille. “Thérapie par l’exercice et dystrophie facio-scapulo-humérale : étude contrôlée randomisée de 6 mois d’entraînement à domicile : précédée d’une étude histologique du potentiel régénératif musculaire dans deux modèles distincts de myopathies : Exercise therapy and facioscapulohumeral muscular dystrophy : a randomized, controlled trial of 6-month home-base : preceded by a histological study of muscle regenerative potential in two distinct models of myopathies.” 2014. Doctoral Dissertation, Saint-Etienne. Accessed April 23, 2019. http://www.theses.fr/2014STET008T.

MLA Handbook (7th Edition):

Bankolé, Sénakpon Landry Cyrille. “Thérapie par l’exercice et dystrophie facio-scapulo-humérale : étude contrôlée randomisée de 6 mois d’entraînement à domicile : précédée d’une étude histologique du potentiel régénératif musculaire dans deux modèles distincts de myopathies : Exercise therapy and facioscapulohumeral muscular dystrophy : a randomized, controlled trial of 6-month home-base : preceded by a histological study of muscle regenerative potential in two distinct models of myopathies.” 2014. Web. 23 Apr 2019.

Vancouver:

Bankolé SLC. Thérapie par l’exercice et dystrophie facio-scapulo-humérale : étude contrôlée randomisée de 6 mois d’entraînement à domicile : précédée d’une étude histologique du potentiel régénératif musculaire dans deux modèles distincts de myopathies : Exercise therapy and facioscapulohumeral muscular dystrophy : a randomized, controlled trial of 6-month home-base : preceded by a histological study of muscle regenerative potential in two distinct models of myopathies. [Internet] [Doctoral dissertation]. Saint-Etienne; 2014. [cited 2019 Apr 23]. Available from: http://www.theses.fr/2014STET008T.

Council of Science Editors:

Bankolé SLC. Thérapie par l’exercice et dystrophie facio-scapulo-humérale : étude contrôlée randomisée de 6 mois d’entraînement à domicile : précédée d’une étude histologique du potentiel régénératif musculaire dans deux modèles distincts de myopathies : Exercise therapy and facioscapulohumeral muscular dystrophy : a randomized, controlled trial of 6-month home-base : preceded by a histological study of muscle regenerative potential in two distinct models of myopathies. [Doctoral Dissertation]. Saint-Etienne; 2014. Available from: http://www.theses.fr/2014STET008T

23. Ramanoudjame, Laetitia. Etude du collagène VI dans le développement musculaire chez le poisson zèbre : implications pour les myopathies liées au COLVI : Study of collagen VI during the zebrafish muscle development : implications for COLVI-related myopathies.

Degree: Docteur es, Science de la Vie, 2014, Université Pierre et Marie Curie – Paris VI

 Les muscles sont des structures très organisées qui nous permettent d’effectuer un grand nombre de fonctions. Ils sont constitués de cellules musculaires mais aussi de… (more)

Subjects/Keywords: Collagène VI; Poisson-Zèbre; Matrice extracellulaire; Myopathies liées au COLVI; Dystrophie myotonique; Morpholino; Extracellular matrix; Zebrafish; 570

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APA (6th Edition):

Ramanoudjame, L. (2014). Etude du collagène VI dans le développement musculaire chez le poisson zèbre : implications pour les myopathies liées au COLVI : Study of collagen VI during the zebrafish muscle development : implications for COLVI-related myopathies. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2014PA066416

Chicago Manual of Style (16th Edition):

Ramanoudjame, Laetitia. “Etude du collagène VI dans le développement musculaire chez le poisson zèbre : implications pour les myopathies liées au COLVI : Study of collagen VI during the zebrafish muscle development : implications for COLVI-related myopathies.” 2014. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed April 23, 2019. http://www.theses.fr/2014PA066416.

MLA Handbook (7th Edition):

Ramanoudjame, Laetitia. “Etude du collagène VI dans le développement musculaire chez le poisson zèbre : implications pour les myopathies liées au COLVI : Study of collagen VI during the zebrafish muscle development : implications for COLVI-related myopathies.” 2014. Web. 23 Apr 2019.

Vancouver:

Ramanoudjame L. Etude du collagène VI dans le développement musculaire chez le poisson zèbre : implications pour les myopathies liées au COLVI : Study of collagen VI during the zebrafish muscle development : implications for COLVI-related myopathies. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2014. [cited 2019 Apr 23]. Available from: http://www.theses.fr/2014PA066416.

Council of Science Editors:

Ramanoudjame L. Etude du collagène VI dans le développement musculaire chez le poisson zèbre : implications pour les myopathies liées au COLVI : Study of collagen VI during the zebrafish muscle development : implications for COLVI-related myopathies. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2014. Available from: http://www.theses.fr/2014PA066416

24. Neji, Radhouène. Diffusion Tensor Imaging of the Human Skeletal Muscle : Contributions and Applications : IRM du tenseur de diffusion du muscle squelettique humain : contributions et applications.

Degree: Docteur es, mathématiques appliquées, 2010, Châtenay-Malabry, Ecole centrale de Paris

Cette thèse propose des techniques pour le traitement d'images IRM de diffusion. Les méthodes proposées concernent l'estimation et la régularisation, le groupement et la segmentation… (more)

Subjects/Keywords: IRM de diffusion; Tenseur de diffusion; Fibre; Noyaux; Groupement; Recalage; Débruitage; Muscle squelettique; Myopathies; Diffusion Tensor; DTI; Human Skeletal Muscle

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Neji, R. (2010). Diffusion Tensor Imaging of the Human Skeletal Muscle : Contributions and Applications : IRM du tenseur de diffusion du muscle squelettique humain : contributions et applications. (Doctoral Dissertation). Châtenay-Malabry, Ecole centrale de Paris. Retrieved from http://www.theses.fr/2010ECAPO005

Chicago Manual of Style (16th Edition):

Neji, Radhouène. “Diffusion Tensor Imaging of the Human Skeletal Muscle : Contributions and Applications : IRM du tenseur de diffusion du muscle squelettique humain : contributions et applications.” 2010. Doctoral Dissertation, Châtenay-Malabry, Ecole centrale de Paris. Accessed April 23, 2019. http://www.theses.fr/2010ECAPO005.

MLA Handbook (7th Edition):

Neji, Radhouène. “Diffusion Tensor Imaging of the Human Skeletal Muscle : Contributions and Applications : IRM du tenseur de diffusion du muscle squelettique humain : contributions et applications.” 2010. Web. 23 Apr 2019.

Vancouver:

Neji R. Diffusion Tensor Imaging of the Human Skeletal Muscle : Contributions and Applications : IRM du tenseur de diffusion du muscle squelettique humain : contributions et applications. [Internet] [Doctoral dissertation]. Châtenay-Malabry, Ecole centrale de Paris; 2010. [cited 2019 Apr 23]. Available from: http://www.theses.fr/2010ECAPO005.

Council of Science Editors:

Neji R. Diffusion Tensor Imaging of the Human Skeletal Muscle : Contributions and Applications : IRM du tenseur de diffusion du muscle squelettique humain : contributions et applications. [Doctoral Dissertation]. Châtenay-Malabry, Ecole centrale de Paris; 2010. Available from: http://www.theses.fr/2010ECAPO005

25. Rothwell, Simon. Identification of disease susceptibility genes in the idiopathic inflammatory myopathies.

Degree: PhD, 2016, University of Manchester

 Background: The idiopathic inflammatory myopathies (IIM) are a heterogeneous group of rare autoimmune diseases comprising of polymyositis (PM), dermatomyositis (DM), and inclusion body myositis (IBM).… (more)

Subjects/Keywords: 616.97; Genetics; Idiopathic Inflammatory Myopathies; Myositis

…Identification of Disease Susceptibility Genes in the Idiopathic Inflammatory Myopathies, 2015… …Background: The idiopathic inflammatory myopathies (IIM) are a heterogeneous group of… …idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and… …inflammatory myopathies. Curr Opin Rheumatol. 2013 Nov;25(6):735-41. doi: 10.1097/01.bor… …Immunochip Study in the Idiopathic Inflammatory Myopathies Identifies Genetic Differences between… 

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Rothwell, S. (2016). Identification of disease susceptibility genes in the idiopathic inflammatory myopathies. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/identification-of-disease-susceptibility-genes-in-the-idiopathic-inflammatory-myopathies(8d7ecb91-3ca2-4ed1-b1d0-35bcd41a593d).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680008

Chicago Manual of Style (16th Edition):

Rothwell, Simon. “Identification of disease susceptibility genes in the idiopathic inflammatory myopathies.” 2016. Doctoral Dissertation, University of Manchester. Accessed April 23, 2019. https://www.research.manchester.ac.uk/portal/en/theses/identification-of-disease-susceptibility-genes-in-the-idiopathic-inflammatory-myopathies(8d7ecb91-3ca2-4ed1-b1d0-35bcd41a593d).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680008.

MLA Handbook (7th Edition):

Rothwell, Simon. “Identification of disease susceptibility genes in the idiopathic inflammatory myopathies.” 2016. Web. 23 Apr 2019.

Vancouver:

Rothwell S. Identification of disease susceptibility genes in the idiopathic inflammatory myopathies. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Apr 23]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/identification-of-disease-susceptibility-genes-in-the-idiopathic-inflammatory-myopathies(8d7ecb91-3ca2-4ed1-b1d0-35bcd41a593d).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680008.

Council of Science Editors:

Rothwell S. Identification of disease susceptibility genes in the idiopathic inflammatory myopathies. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/identification-of-disease-susceptibility-genes-in-the-idiopathic-inflammatory-myopathies(8d7ecb91-3ca2-4ed1-b1d0-35bcd41a593d).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680008

26. Παπαδημητρίου, Αλέξανδρος. Μιτοχονδριακές μυοπάθειες: βιοχημική μελέτη 30 περιπτώσεων.

Degree: 1984, Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); National and Kapodistrian University of Athens

Subjects/Keywords: Μιτοχόνδρια; Νοσήματα, Μυϊκά; Καρνιτίνη; Τρανσφεράση ( CPT); Σύνδρομο Fukuhara; Σύνδρομο Kearns - Sayre; Μιτοχονδριακή μυοπάθεια; Μυοπάθειες, Εγκεφαλομιτοχονδριακή; Mitochondrial myopathies; Myopathies; CPT

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APA (6th Edition):

Παπαδημητρίου, . (1984). Μιτοχονδριακές μυοπάθειες: βιοχημική μελέτη 30 περιπτώσεων. (Thesis). Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); National and Kapodistrian University of Athens. Retrieved from http://hdl.handle.net/10442/hedi/23488

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Παπαδημητρίου, Αλέξανδρος. “Μιτοχονδριακές μυοπάθειες: βιοχημική μελέτη 30 περιπτώσεων.” 1984. Thesis, Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); National and Kapodistrian University of Athens. Accessed April 23, 2019. http://hdl.handle.net/10442/hedi/23488.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Παπαδημητρίου, Αλέξανδρος. “Μιτοχονδριακές μυοπάθειες: βιοχημική μελέτη 30 περιπτώσεων.” 1984. Web. 23 Apr 2019.

Vancouver:

Παπαδημητρίου . Μιτοχονδριακές μυοπάθειες: βιοχημική μελέτη 30 περιπτώσεων. [Internet] [Thesis]. Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); National and Kapodistrian University of Athens; 1984. [cited 2019 Apr 23]. Available from: http://hdl.handle.net/10442/hedi/23488.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Παπαδημητρίου . Μιτοχονδριακές μυοπάθειες: βιοχημική μελέτη 30 περιπτώσεων. [Thesis]. Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); National and Kapodistrian University of Athens; 1984. Available from: http://hdl.handle.net/10442/hedi/23488

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

27. Παπαδόπουλος, Κωνσταντίνος. Αυτοάνοσες φλεγμονώδεις μυοπάθειες: ανοσοϊστοχημική μελέτη των παθογενετικών μηχανισμών.

Degree: 2013, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

 IntroductionAutoimmune inflammatory myopathies constitute a heterogeneous group ofdiseases that share in common the inflammation of skeletal muscle and the presenceof muscle weakness. Immune mechanisms are… (more)

Subjects/Keywords: ΦΛΕΓΜΟΝΩΔΕΙΣ ΜΥΟΠΑΘΕΙΕΣ; Δερματομυοσίτις; Πολυμυοσίτις; Ανοσοϊστοχημεία; Παθογένεση; Φλεγμονώδη κύτταρα; Μείζον σύμπλεγμα ιστοσυμβατότητας; Συνδιεγερτικά μόρια; INFLAMMATORY MYOPATHIES; Dermatomyositis; Polymyositis; Immunohistochemic; Pathogenesis; Inflammatory cells; Maior mistocompatibility complex; Co-stilmulatory molecules

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APA (6th Edition):

Παπαδόπουλος, . . (2013). Αυτοάνοσες φλεγμονώδεις μυοπάθειες: ανοσοϊστοχημική μελέτη των παθογενετικών μηχανισμών. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/38423

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Παπαδόπουλος, Κωνσταντίνος. “Αυτοάνοσες φλεγμονώδεις μυοπάθειες: ανοσοϊστοχημική μελέτη των παθογενετικών μηχανισμών.” 2013. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed April 23, 2019. http://hdl.handle.net/10442/hedi/38423.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Παπαδόπουλος, Κωνσταντίνος. “Αυτοάνοσες φλεγμονώδεις μυοπάθειες: ανοσοϊστοχημική μελέτη των παθογενετικών μηχανισμών.” 2013. Web. 23 Apr 2019.

Vancouver:

Παπαδόπουλος . Αυτοάνοσες φλεγμονώδεις μυοπάθειες: ανοσοϊστοχημική μελέτη των παθογενετικών μηχανισμών. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2013. [cited 2019 Apr 23]. Available from: http://hdl.handle.net/10442/hedi/38423.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Παπαδόπουλος . Αυτοάνοσες φλεγμονώδεις μυοπάθειες: ανοσοϊστοχημική μελέτη των παθογενετικών μηχανισμών. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2013. Available from: http://hdl.handle.net/10442/hedi/38423

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Indian Institute of Science

28. Madan, Aditi. Developmental and Functional Roles of Troponin-T Isoforms, and Exploring Genome-Wide Alterations in Drosophila Indirect Flight Muscle Mutants.

Degree: 2015, Indian Institute of Science

 Muscle contraction is a highly fine-tuned process that requires the precise and timely construction of large protein sub-assemblies to form sarcomeres, the individual contractile units.… (more)

Subjects/Keywords: Troponin-T Isoforms; Indirect Flight Muscle Mutants; Drosophila melanogaster Model; Myopathies; GAL4; Troponin T (TnT); Drosophila Indirect Flight Muscles (IFMs); UAS-TnT; Molecular Genetics

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APA (6th Edition):

Madan, A. (2015). Developmental and Functional Roles of Troponin-T Isoforms, and Exploring Genome-Wide Alterations in Drosophila Indirect Flight Muscle Mutants. (Thesis). Indian Institute of Science. Retrieved from http://etd.iisc.ernet.in/2005/3601 ; http://etd.iisc.ernet.in/abstracts/4470/G27158-Abs.pdf

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Madan, Aditi. “Developmental and Functional Roles of Troponin-T Isoforms, and Exploring Genome-Wide Alterations in Drosophila Indirect Flight Muscle Mutants.” 2015. Thesis, Indian Institute of Science. Accessed April 23, 2019. http://etd.iisc.ernet.in/2005/3601 ; http://etd.iisc.ernet.in/abstracts/4470/G27158-Abs.pdf.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Madan, Aditi. “Developmental and Functional Roles of Troponin-T Isoforms, and Exploring Genome-Wide Alterations in Drosophila Indirect Flight Muscle Mutants.” 2015. Web. 23 Apr 2019.

Vancouver:

Madan A. Developmental and Functional Roles of Troponin-T Isoforms, and Exploring Genome-Wide Alterations in Drosophila Indirect Flight Muscle Mutants. [Internet] [Thesis]. Indian Institute of Science; 2015. [cited 2019 Apr 23]. Available from: http://etd.iisc.ernet.in/2005/3601 ; http://etd.iisc.ernet.in/abstracts/4470/G27158-Abs.pdf.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Madan A. Developmental and Functional Roles of Troponin-T Isoforms, and Exploring Genome-Wide Alterations in Drosophila Indirect Flight Muscle Mutants. [Thesis]. Indian Institute of Science; 2015. Available from: http://etd.iisc.ernet.in/2005/3601 ; http://etd.iisc.ernet.in/abstracts/4470/G27158-Abs.pdf

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

29. Marilita Falangola Accioly. Efeito de exercÃcio fÃsico e estatinas no perfil lipÃdico e na funÃÃo muscular em ratos dislipidÃmicos.

Degree: 2007, Faculdade de Medicina de São José do Rio Preto

 Statins are used to treat dislipidemias with great tolerance, however, several side effects can occur, specially myopathies. The regular practice of physical exercise (PE) produce… (more)

Subjects/Keywords: EDUCACAO FISICA; Estatinas; ExercÃcio FÃsico; Miopatia; Perfil LipÃdico; Educação Física e Treinamento; Doença Musculares; statins; physical exercise; myopathies; lipidic profile; Educaci?n y Entrenamiento F?sico; Physical Education and Training; Enfermedades Musculares; Muscular Diseases

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APA (6th Edition):

Accioly, M. F. (2007). Efeito de exercÃcio fÃsico e estatinas no perfil lipÃdico e na funÃÃo muscular em ratos dislipidÃmicos. (Thesis). Faculdade de Medicina de São José do Rio Preto. Retrieved from http://bdtd.famerp.br//tde_busca/arquivo.php?codArquivo=206

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Accioly, Marilita Falangola. “Efeito de exercÃcio fÃsico e estatinas no perfil lipÃdico e na funÃÃo muscular em ratos dislipidÃmicos.” 2007. Thesis, Faculdade de Medicina de São José do Rio Preto. Accessed April 23, 2019. http://bdtd.famerp.br//tde_busca/arquivo.php?codArquivo=206.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Accioly, Marilita Falangola. “Efeito de exercÃcio fÃsico e estatinas no perfil lipÃdico e na funÃÃo muscular em ratos dislipidÃmicos.” 2007. Web. 23 Apr 2019.

Vancouver:

Accioly MF. Efeito de exercÃcio fÃsico e estatinas no perfil lipÃdico e na funÃÃo muscular em ratos dislipidÃmicos. [Internet] [Thesis]. Faculdade de Medicina de São José do Rio Preto; 2007. [cited 2019 Apr 23]. Available from: http://bdtd.famerp.br//tde_busca/arquivo.php?codArquivo=206.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Accioly MF. Efeito de exercÃcio fÃsico e estatinas no perfil lipÃdico e na funÃÃo muscular em ratos dislipidÃmicos. [Thesis]. Faculdade de Medicina de São José do Rio Preto; 2007. Available from: http://bdtd.famerp.br//tde_busca/arquivo.php?codArquivo=206

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

30. Abath Neto, Osório Lopes. Estudo clínico, histológico e molecular da miopatia centronuclear.

Degree: PhD, Neurologia, 2014, University of São Paulo

 Introdução: A miopatia centronuclear é uma doença muscular congênita com apresentação clínica heterogênea, caracterizada histologicamente pela proeminência de fibras musculares com núcleos centralizados. Três formas… (more)

Subjects/Keywords: Biópsia; Biopsy; Canal de liberação de cálcio do receptor de rianodina; Dinamina II; Dynamin II; Exoma; Exome; Highthroughput nucleotide sequencing; Hipotonia muscular; Miopatia centronuclear; Muscle hypotonia; Myopathies structural congenital; Ryanodine receptor calcium release channel; Sequenciamento de nucleotídeos em larga escala

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Abath Neto, O. L. (2014). Estudo clínico, histológico e molecular da miopatia centronuclear. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5138/tde-13012015-113703/ ;

Chicago Manual of Style (16th Edition):

Abath Neto, Osório Lopes. “Estudo clínico, histológico e molecular da miopatia centronuclear.” 2014. Doctoral Dissertation, University of São Paulo. Accessed April 23, 2019. http://www.teses.usp.br/teses/disponiveis/5/5138/tde-13012015-113703/ ;.

MLA Handbook (7th Edition):

Abath Neto, Osório Lopes. “Estudo clínico, histológico e molecular da miopatia centronuclear.” 2014. Web. 23 Apr 2019.

Vancouver:

Abath Neto OL. Estudo clínico, histológico e molecular da miopatia centronuclear. [Internet] [Doctoral dissertation]. University of São Paulo; 2014. [cited 2019 Apr 23]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5138/tde-13012015-113703/ ;.

Council of Science Editors:

Abath Neto OL. Estudo clínico, histológico e molecular da miopatia centronuclear. [Doctoral Dissertation]. University of São Paulo; 2014. Available from: http://www.teses.usp.br/teses/disponiveis/5/5138/tde-13012015-113703/ ;

[1] [2]

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