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You searched for subject:(Muscular Diseases). Showing records 1 – 30 of 62 total matches.

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1. Zukosky, Kristen. Molecular basis of congenital disorders of muscle: from genetic diagnosis to cellular modeling of actinopathies and alpha- dystroglycanopathies.

Degree: PhD, Neuroscience, 2015, Brown University

 The aim of this thesis research is to identify and model neuromuscular diseases. I focused on two particular congenital neuromuscular diseases. Among the many genes… (more)

Subjects/Keywords: congenital muscular diseases

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

APA (6th Edition):

Zukosky, K. (2015). Molecular basis of congenital disorders of muscle: from genetic diagnosis to cellular modeling of actinopathies and alpha- dystroglycanopathies. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:419380/

Chicago Manual of Style (16th Edition):

Zukosky, Kristen. “Molecular basis of congenital disorders of muscle: from genetic diagnosis to cellular modeling of actinopathies and alpha- dystroglycanopathies.” 2015. Doctoral Dissertation, Brown University. Accessed April 19, 2019. https://repository.library.brown.edu/studio/item/bdr:419380/.

MLA Handbook (7th Edition):

Zukosky, Kristen. “Molecular basis of congenital disorders of muscle: from genetic diagnosis to cellular modeling of actinopathies and alpha- dystroglycanopathies.” 2015. Web. 19 Apr 2019.

Vancouver:

Zukosky K. Molecular basis of congenital disorders of muscle: from genetic diagnosis to cellular modeling of actinopathies and alpha- dystroglycanopathies. [Internet] [Doctoral dissertation]. Brown University; 2015. [cited 2019 Apr 19]. Available from: https://repository.library.brown.edu/studio/item/bdr:419380/.

Council of Science Editors:

Zukosky K. Molecular basis of congenital disorders of muscle: from genetic diagnosis to cellular modeling of actinopathies and alpha- dystroglycanopathies. [Doctoral Dissertation]. Brown University; 2015. Available from: https://repository.library.brown.edu/studio/item/bdr:419380/

2. Escorcio, Renata. Elaboração e análise de confiabilidade de escala de avaliação funcional  da manobra de Gowers e da passagem de bipedestação para sedestação no solo para portadores de distrofia muscular de Duchenne (DMD).

Degree: Mestrado, Movimento, Postura e Ação Humana, 2009, University of São Paulo

Objetivo: Construir Escala de Avaliação Funcional do Sentar e Levantar do Solo para Portadores de DMD (EAF-2) e testar sua confiabilidade intra e interexaminadores. Método:… (more)

Subjects/Keywords: Avaliação; Distrofia muscular de Duchenne; Doenças musculares; Evaluation; Exame físico; Muscular diseases; Muscular dystrophy Duchenne; Physical examination

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APA (6th Edition):

Escorcio, R. (2009). Elaboração e análise de confiabilidade de escala de avaliação funcional  da manobra de Gowers e da passagem de bipedestação para sedestação no solo para portadores de distrofia muscular de Duchenne (DMD). (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5163/tde-09122009-162729/ ;

Chicago Manual of Style (16th Edition):

Escorcio, Renata. “Elaboração e análise de confiabilidade de escala de avaliação funcional  da manobra de Gowers e da passagem de bipedestação para sedestação no solo para portadores de distrofia muscular de Duchenne (DMD).” 2009. Masters Thesis, University of São Paulo. Accessed April 19, 2019. http://www.teses.usp.br/teses/disponiveis/5/5163/tde-09122009-162729/ ;.

MLA Handbook (7th Edition):

Escorcio, Renata. “Elaboração e análise de confiabilidade de escala de avaliação funcional  da manobra de Gowers e da passagem de bipedestação para sedestação no solo para portadores de distrofia muscular de Duchenne (DMD).” 2009. Web. 19 Apr 2019.

Vancouver:

Escorcio R. Elaboração e análise de confiabilidade de escala de avaliação funcional  da manobra de Gowers e da passagem de bipedestação para sedestação no solo para portadores de distrofia muscular de Duchenne (DMD). [Internet] [Masters thesis]. University of São Paulo; 2009. [cited 2019 Apr 19]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5163/tde-09122009-162729/ ;.

Council of Science Editors:

Escorcio R. Elaboração e análise de confiabilidade de escala de avaliação funcional  da manobra de Gowers e da passagem de bipedestação para sedestação no solo para portadores de distrofia muscular de Duchenne (DMD). [Masters Thesis]. University of São Paulo; 2009. Available from: http://www.teses.usp.br/teses/disponiveis/5/5163/tde-09122009-162729/ ;


University of Florida

3. Millette, Alexandre R. Impact of Physical Activity on Muscles of People with Collagen-VI Myopathies.

Degree: 2013, University of Florida

 Collagen-6 myopathy (COL6) is a congenital neuromuscular disorder with major complications including joint contractures, muscle weakness, and limited mobility. This study assessed the relationship between… (more)

Subjects/Keywords: Collagens; Exercise; Legs; Magnetic resonance imaging; Medical conditions; Muscles; Muscular diseases; Muscular dystrophies; Skeletal muscle; Torque; Exercise; Muscles; Neuromuscular diseases

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APA (6th Edition):

Millette, A. R. (2013). Impact of Physical Activity on Muscles of People with Collagen-VI Myopathies. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00060993

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):

Millette, Alexandre R. “Impact of Physical Activity on Muscles of People with Collagen-VI Myopathies.” 2013. Thesis, University of Florida. Accessed April 19, 2019. http://ufdc.ufl.edu/AA00060993.

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

MLA Handbook (7th Edition):

Millette, Alexandre R. “Impact of Physical Activity on Muscles of People with Collagen-VI Myopathies.” 2013. Web. 19 Apr 2019.

Vancouver:

Millette AR. Impact of Physical Activity on Muscles of People with Collagen-VI Myopathies. [Internet] [Thesis]. University of Florida; 2013. [cited 2019 Apr 19]. Available from: http://ufdc.ufl.edu/AA00060993.

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

Council of Science Editors:

Millette AR. Impact of Physical Activity on Muscles of People with Collagen-VI Myopathies. [Thesis]. University of Florida; 2013. Available from: http://ufdc.ufl.edu/AA00060993

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


University of Florida

4. Pecoraro, Karen. Quality of Life in Families with Duchenne Muscular Dystrophy.

Degree: 2010, University of Florida

 As the most common, fatal form of muscular dystrophy, Duchenne muscular dystrophy (DMD) has a significant lack of current research related to quality of life… (more)

Subjects/Keywords: Age groups; Child psychology; Children; Diseases; Duchenne muscular dystrophy; Electronics; Muscular dystrophies; Parents; Pediatrics; Quality of life; Duchenne muscular dystrophy; Duchenne muscular dystrophy – Patients; Quality of life

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APA (6th Edition):

Pecoraro, K. (2010). Quality of Life in Families with Duchenne Muscular Dystrophy. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00059976

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):

Pecoraro, Karen. “Quality of Life in Families with Duchenne Muscular Dystrophy.” 2010. Thesis, University of Florida. Accessed April 19, 2019. http://ufdc.ufl.edu/AA00059976.

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

MLA Handbook (7th Edition):

Pecoraro, Karen. “Quality of Life in Families with Duchenne Muscular Dystrophy.” 2010. Web. 19 Apr 2019.

Vancouver:

Pecoraro K. Quality of Life in Families with Duchenne Muscular Dystrophy. [Internet] [Thesis]. University of Florida; 2010. [cited 2019 Apr 19]. Available from: http://ufdc.ufl.edu/AA00059976.

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

Council of Science Editors:

Pecoraro K. Quality of Life in Families with Duchenne Muscular Dystrophy. [Thesis]. University of Florida; 2010. Available from: http://ufdc.ufl.edu/AA00059976

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


Universidade do Rio Grande do Sul

5. Pinto, João Paulo Nascimento e Silva. Associação entre doença periodontal e dano muscular induzido pelo exercício : resultados preliminares de um estudo longitudinal.

Degree: 2017, Universidade do Rio Grande do Sul

O dano muscular induzido pelo exercício (DMIE) e os diferentes elementos envolvidos em seu processo têm sido amplamente estudados. A doença periodontal (DP), por sua… (more)

Subjects/Keywords: Periodontal diseases; Doenças periodontais; Dano muscular; Muscle damage; Muscle strenght

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APA (6th Edition):

Pinto, J. P. N. e. S. (2017). Associação entre doença periodontal e dano muscular induzido pelo exercício : resultados preliminares de um estudo longitudinal. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/151433

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):

Pinto, João Paulo Nascimento e Silva. “Associação entre doença periodontal e dano muscular induzido pelo exercício : resultados preliminares de um estudo longitudinal.” 2017. Thesis, Universidade do Rio Grande do Sul. Accessed April 19, 2019. http://hdl.handle.net/10183/151433.

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

MLA Handbook (7th Edition):

Pinto, João Paulo Nascimento e Silva. “Associação entre doença periodontal e dano muscular induzido pelo exercício : resultados preliminares de um estudo longitudinal.” 2017. Web. 19 Apr 2019.

Vancouver:

Pinto JPNeS. Associação entre doença periodontal e dano muscular induzido pelo exercício : resultados preliminares de um estudo longitudinal. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2017. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/10183/151433.

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

Council of Science Editors:

Pinto JPNeS. Associação entre doença periodontal e dano muscular induzido pelo exercício : resultados preliminares de um estudo longitudinal. [Thesis]. Universidade do Rio Grande do Sul; 2017. Available from: http://hdl.handle.net/10183/151433

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

6. Fridman, Leticia. Histopathological Characterization of the Dystrophic Phenotype and Development of Therapeutic Candidates for a Gene Therapy Pre-Clinical Study in Dysferlin Deficient Mice.

Degree: Translational Science, Neurology, 2016, U of Massachusetts : Med

  Dysferlin deficient muscular dystrophy is a devastating disease that leads to loss of mobility and quality of life in patients. Dysferlin is a 230… (more)

Subjects/Keywords: dysferlin; muscular dystrophy; membrane resealing; Cell Biology; Nervous System Diseases; Neurology

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APA (6th Edition):

Fridman, L. (2016). Histopathological Characterization of the Dystrophic Phenotype and Development of Therapeutic Candidates for a Gene Therapy Pre-Clinical Study in Dysferlin Deficient Mice. (Masters Thesis). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/881

Chicago Manual of Style (16th Edition):

Fridman, Leticia. “Histopathological Characterization of the Dystrophic Phenotype and Development of Therapeutic Candidates for a Gene Therapy Pre-Clinical Study in Dysferlin Deficient Mice.” 2016. Masters Thesis, U of Massachusetts : Med. Accessed April 19, 2019. http://escholarship.umassmed.edu/gsbs_diss/881.

MLA Handbook (7th Edition):

Fridman, Leticia. “Histopathological Characterization of the Dystrophic Phenotype and Development of Therapeutic Candidates for a Gene Therapy Pre-Clinical Study in Dysferlin Deficient Mice.” 2016. Web. 19 Apr 2019.

Vancouver:

Fridman L. Histopathological Characterization of the Dystrophic Phenotype and Development of Therapeutic Candidates for a Gene Therapy Pre-Clinical Study in Dysferlin Deficient Mice. [Internet] [Masters thesis]. U of Massachusetts : Med; 2016. [cited 2019 Apr 19]. Available from: http://escholarship.umassmed.edu/gsbs_diss/881.

Council of Science Editors:

Fridman L. Histopathological Characterization of the Dystrophic Phenotype and Development of Therapeutic Candidates for a Gene Therapy Pre-Clinical Study in Dysferlin Deficient Mice. [Masters Thesis]. U of Massachusetts : Med; 2016. Available from: http://escholarship.umassmed.edu/gsbs_diss/881


UCLA

7. Kwok, Yuk Wah. Isolation of Primary Myoblasts and Characterization of the Endoplasmic Reticulum Stress Response in Wild-type and mdx Mice.

Degree: Physiological Science, 2014, UCLA

 Duchenne Muscular Dystrophy (DMD) is a devastating muscle disease caused by a recessive X- linked mutation in the dystrophin gene. This mutation leads to a… (more)

Subjects/Keywords: Biology; Biochemistry; Animal diseases; Duchenne muscular dystrophy; mdx; Unfolded protein response

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APA (6th Edition):

Kwok, Y. W. (2014). Isolation of Primary Myoblasts and Characterization of the Endoplasmic Reticulum Stress Response in Wild-type and mdx Mice. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/4g3968vq

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):

Kwok, Yuk Wah. “Isolation of Primary Myoblasts and Characterization of the Endoplasmic Reticulum Stress Response in Wild-type and mdx Mice.” 2014. Thesis, UCLA. Accessed April 19, 2019. http://www.escholarship.org/uc/item/4g3968vq.

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

MLA Handbook (7th Edition):

Kwok, Yuk Wah. “Isolation of Primary Myoblasts and Characterization of the Endoplasmic Reticulum Stress Response in Wild-type and mdx Mice.” 2014. Web. 19 Apr 2019.

Vancouver:

Kwok YW. Isolation of Primary Myoblasts and Characterization of the Endoplasmic Reticulum Stress Response in Wild-type and mdx Mice. [Internet] [Thesis]. UCLA; 2014. [cited 2019 Apr 19]. Available from: http://www.escholarship.org/uc/item/4g3968vq.

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

Council of Science Editors:

Kwok YW. Isolation of Primary Myoblasts and Characterization of the Endoplasmic Reticulum Stress Response in Wild-type and mdx Mice. [Thesis]. UCLA; 2014. Available from: http://www.escholarship.org/uc/item/4g3968vq

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

8. El-Aloul, Basmah. Fatigue in Children and Adolescents with Duchenne Muscular Dystrophy.

Degree: 2017, University of Western Ontario

 Fatigue was recently reported to be the largest predictor of poor health-related quality of life (HRQOL) in children and adolescents with Duchenne muscular dystrophy (DMD).… (more)

Subjects/Keywords: Duchenne muscular dystrophy; children; adolescents; fatigue; Musculoskeletal Diseases

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APA (6th Edition):

El-Aloul, B. (2017). Fatigue in Children and Adolescents with Duchenne Muscular Dystrophy. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/4626

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):

El-Aloul, Basmah. “Fatigue in Children and Adolescents with Duchenne Muscular Dystrophy.” 2017. Thesis, University of Western Ontario. Accessed April 19, 2019. https://ir.lib.uwo.ca/etd/4626.

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

MLA Handbook (7th Edition):

El-Aloul, Basmah. “Fatigue in Children and Adolescents with Duchenne Muscular Dystrophy.” 2017. Web. 19 Apr 2019.

Vancouver:

El-Aloul B. Fatigue in Children and Adolescents with Duchenne Muscular Dystrophy. [Internet] [Thesis]. University of Western Ontario; 2017. [cited 2019 Apr 19]. Available from: https://ir.lib.uwo.ca/etd/4626.

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

Council of Science Editors:

El-Aloul B. Fatigue in Children and Adolescents with Duchenne Muscular Dystrophy. [Thesis]. University of Western Ontario; 2017. Available from: https://ir.lib.uwo.ca/etd/4626

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


University of Edinburgh

9. Le, Thanh Phu. Nuclear envelope transmembrane proteins as mediators of tissue-specific diseases.

Degree: PhD, 2017, University of Edinburgh

 Many tissue-restricted diseases are linked to mutations in lamins and nuclear envelope transmembrane proteins (NETs). How these mutations in ubiquitously expressed proteins cause such defined… (more)

Subjects/Keywords: NE proteins; NE-linked diseases; muscular dystrophy; lamins; NETs distribution

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APA (6th Edition):

Le, T. P. (2017). Nuclear envelope transmembrane proteins as mediators of tissue-specific diseases. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/28905

Chicago Manual of Style (16th Edition):

Le, Thanh Phu. “Nuclear envelope transmembrane proteins as mediators of tissue-specific diseases.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed April 19, 2019. http://hdl.handle.net/1842/28905.

MLA Handbook (7th Edition):

Le, Thanh Phu. “Nuclear envelope transmembrane proteins as mediators of tissue-specific diseases.” 2017. Web. 19 Apr 2019.

Vancouver:

Le TP. Nuclear envelope transmembrane proteins as mediators of tissue-specific diseases. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/1842/28905.

Council of Science Editors:

Le TP. Nuclear envelope transmembrane proteins as mediators of tissue-specific diseases. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/28905


University of British Columbia

10. Cooper, Ann. Histological and ultrastructural study of mice with hereditary muscular dystrophy .

Degree: 1962, University of British Columbia

 The history of human muscular dystrophy with reference to clinical, histological and biochemical studies is reviewed. The value of the recent discovery of an experimental… (more)

Subjects/Keywords: Laboratory animals  – Diseases; Muscular dystrophy

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APA (6th Edition):

Cooper, A. (1962). Histological and ultrastructural study of mice with hereditary muscular dystrophy . (Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/39292

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):

Cooper, Ann. “Histological and ultrastructural study of mice with hereditary muscular dystrophy .” 1962. Thesis, University of British Columbia. Accessed April 19, 2019. http://hdl.handle.net/2429/39292.

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

MLA Handbook (7th Edition):

Cooper, Ann. “Histological and ultrastructural study of mice with hereditary muscular dystrophy .” 1962. Web. 19 Apr 2019.

Vancouver:

Cooper A. Histological and ultrastructural study of mice with hereditary muscular dystrophy . [Internet] [Thesis]. University of British Columbia; 1962. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/2429/39292.

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

Council of Science Editors:

Cooper A. Histological and ultrastructural study of mice with hereditary muscular dystrophy . [Thesis]. University of British Columbia; 1962. Available from: http://hdl.handle.net/2429/39292

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


East Carolina University

11. Whitworth, Hoke B. Paired Effects of Dietary Leucine Supplementation and Overload on Protein Translational Signaling and Hypertrophy in Aged Rat Skeletal Muscle.

Degree: 2012, East Carolina University

 Sarcopenia is an age-associated disorder that causes loss of skeletal muscle mass particularly in type II (fast-twitch) muscle fibers. This loss in muscle mass can… (more)

Subjects/Keywords: Muscles – Diseases – Age factors; Muscular atrophy; Leucine; Dietary supplements

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APA (6th Edition):

Whitworth, H. B. (2012). Paired Effects of Dietary Leucine Supplementation and Overload on Protein Translational Signaling and Hypertrophy in Aged Rat Skeletal Muscle. (Masters Thesis). East Carolina University. Retrieved from http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=14401

Chicago Manual of Style (16th Edition):

Whitworth, Hoke B. “Paired Effects of Dietary Leucine Supplementation and Overload on Protein Translational Signaling and Hypertrophy in Aged Rat Skeletal Muscle.” 2012. Masters Thesis, East Carolina University. Accessed April 19, 2019. http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=14401.

MLA Handbook (7th Edition):

Whitworth, Hoke B. “Paired Effects of Dietary Leucine Supplementation and Overload on Protein Translational Signaling and Hypertrophy in Aged Rat Skeletal Muscle.” 2012. Web. 19 Apr 2019.

Vancouver:

Whitworth HB. Paired Effects of Dietary Leucine Supplementation and Overload on Protein Translational Signaling and Hypertrophy in Aged Rat Skeletal Muscle. [Internet] [Masters thesis]. East Carolina University; 2012. [cited 2019 Apr 19]. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=14401.

Council of Science Editors:

Whitworth HB. Paired Effects of Dietary Leucine Supplementation and Overload on Protein Translational Signaling and Hypertrophy in Aged Rat Skeletal Muscle. [Masters Thesis]. East Carolina University; 2012. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=14401


Columbia University

12. Lee, Justin. Characterization of motor pool selectivity of neuromuscular degeneration and identification of molecular correlates of disease resistance in Type I spinal muscular atrophy.

Degree: 2015, Columbia University

 Selective neuronal loss in response to loss or dysfunction of a ubiquitously expressed protein is a hallmark of neurodegenerative disease. Proximal spinal muscular atrophy (SMA)… (more)

Subjects/Keywords: Spinal muscular atrophy; Nervous system – Degeneration; Neuromuscular diseases; Neurosciences; Pathology; Biology

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APA (6th Edition):

Lee, J. (2015). Characterization of motor pool selectivity of neuromuscular degeneration and identification of molecular correlates of disease resistance in Type I spinal muscular atrophy. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8513XBQ

Chicago Manual of Style (16th Edition):

Lee, Justin. “Characterization of motor pool selectivity of neuromuscular degeneration and identification of molecular correlates of disease resistance in Type I spinal muscular atrophy.” 2015. Doctoral Dissertation, Columbia University. Accessed April 19, 2019. https://doi.org/10.7916/D8513XBQ.

MLA Handbook (7th Edition):

Lee, Justin. “Characterization of motor pool selectivity of neuromuscular degeneration and identification of molecular correlates of disease resistance in Type I spinal muscular atrophy.” 2015. Web. 19 Apr 2019.

Vancouver:

Lee J. Characterization of motor pool selectivity of neuromuscular degeneration and identification of molecular correlates of disease resistance in Type I spinal muscular atrophy. [Internet] [Doctoral dissertation]. Columbia University; 2015. [cited 2019 Apr 19]. Available from: https://doi.org/10.7916/D8513XBQ.

Council of Science Editors:

Lee J. Characterization of motor pool selectivity of neuromuscular degeneration and identification of molecular correlates of disease resistance in Type I spinal muscular atrophy. [Doctoral Dissertation]. Columbia University; 2015. Available from: https://doi.org/10.7916/D8513XBQ

13. Alves, Marcelo Mendes. Ventilação não-invasiva com pressão positiva (BIPAP) em cães da raça Golden  Retriever afetados pela distrofia muscular.

Degree: Mestrado, Anatomia dos Animais Domésticos e Silvestres, 2008, University of São Paulo

A Distrofia Muscular dos cães Golden Retriever (GRMD) é uma miopatia degenerativa causada pela ausência da proteína distrofina na superfície da membrana da célula muscular.… (more)

Subjects/Keywords: Bipap; Bipap; Cão Golden Retriever; Distrofia muscular; Doenças neuromusculares; Golden retriever dog; Insuficiência respiratória; Muscular dystrophy; Neuromuscular diseases; Respiratory failure

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APA (6th Edition):

Alves, M. M. (2008). Ventilação não-invasiva com pressão positiva (BIPAP) em cães da raça Golden  Retriever afetados pela distrofia muscular. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/10/10132/tde-14072011-164329/ ;

Chicago Manual of Style (16th Edition):

Alves, Marcelo Mendes. “Ventilação não-invasiva com pressão positiva (BIPAP) em cães da raça Golden  Retriever afetados pela distrofia muscular.” 2008. Masters Thesis, University of São Paulo. Accessed April 19, 2019. http://www.teses.usp.br/teses/disponiveis/10/10132/tde-14072011-164329/ ;.

MLA Handbook (7th Edition):

Alves, Marcelo Mendes. “Ventilação não-invasiva com pressão positiva (BIPAP) em cães da raça Golden  Retriever afetados pela distrofia muscular.” 2008. Web. 19 Apr 2019.

Vancouver:

Alves MM. Ventilação não-invasiva com pressão positiva (BIPAP) em cães da raça Golden  Retriever afetados pela distrofia muscular. [Internet] [Masters thesis]. University of São Paulo; 2008. [cited 2019 Apr 19]. Available from: http://www.teses.usp.br/teses/disponiveis/10/10132/tde-14072011-164329/ ;.

Council of Science Editors:

Alves MM. Ventilação não-invasiva com pressão positiva (BIPAP) em cães da raça Golden  Retriever afetados pela distrofia muscular. [Masters Thesis]. University of São Paulo; 2008. Available from: http://www.teses.usp.br/teses/disponiveis/10/10132/tde-14072011-164329/ ;


University of Florida

14. Min, Kisuk. Doxorubicin-Induced Cardiac and Skeletal Myopathy the Role of Mitochondrial Reactive Oxygen Species Emission and Calpain Activation.

Degree: PhD, Health and Human Performance - Applied Physiology and Kinesiology, 2012, University of Florida

 Doxorubicin (DOX) is an antitumor agent used to treat a variety of cancers. Although DOX is a highly effective anti-tumor treatment, DOX has been shown… (more)

Subjects/Keywords: Apoptosis; Diaphragm; Mitochondria; Muscles; Muscular atrophy; Muscular diseases; Myocardium; Reactive oxygen species; Skeletal muscle; Ubiquitins; calpain  – doxorubicin  – mitochondria  – ros

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

APA (6th Edition):

Min, K. (2012). Doxorubicin-Induced Cardiac and Skeletal Myopathy the Role of Mitochondrial Reactive Oxygen Species Emission and Calpain Activation. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0044927

Chicago Manual of Style (16th Edition):

Min, Kisuk. “Doxorubicin-Induced Cardiac and Skeletal Myopathy the Role of Mitochondrial Reactive Oxygen Species Emission and Calpain Activation.” 2012. Doctoral Dissertation, University of Florida. Accessed April 19, 2019. http://ufdc.ufl.edu/UFE0044927.

MLA Handbook (7th Edition):

Min, Kisuk. “Doxorubicin-Induced Cardiac and Skeletal Myopathy the Role of Mitochondrial Reactive Oxygen Species Emission and Calpain Activation.” 2012. Web. 19 Apr 2019.

Vancouver:

Min K. Doxorubicin-Induced Cardiac and Skeletal Myopathy the Role of Mitochondrial Reactive Oxygen Species Emission and Calpain Activation. [Internet] [Doctoral dissertation]. University of Florida; 2012. [cited 2019 Apr 19]. Available from: http://ufdc.ufl.edu/UFE0044927.

Council of Science Editors:

Min K. Doxorubicin-Induced Cardiac and Skeletal Myopathy the Role of Mitochondrial Reactive Oxygen Species Emission and Calpain Activation. [Doctoral Dissertation]. University of Florida; 2012. Available from: http://ufdc.ufl.edu/UFE0044927


University of Florida

15. Stewart, Oliver. MRI Assessment of Heterogeneity of Muscles across Three Models of Muscular Dystrophy.

Degree: 2015, University of Florida

 Introduction: Duchenne muscular dystrophy (DMD) is a progressive neuromuscular disease caused by lack of dystrophin, and several models have been utilized to test interventions in… (more)

Subjects/Keywords: Animal models; Canines; Disease models; Diseases; Duchenne muscular dystrophy; Gene therapy; Legs; Magnetic resonance imaging; Muscles; Muscular dystrophies

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

APA (6th Edition):

Stewart, O. (2015). MRI Assessment of Heterogeneity of Muscles across Three Models of Muscular Dystrophy. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00037463

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):

Stewart, Oliver. “MRI Assessment of Heterogeneity of Muscles across Three Models of Muscular Dystrophy.” 2015. Thesis, University of Florida. Accessed April 19, 2019. http://ufdc.ufl.edu/AA00037463.

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

MLA Handbook (7th Edition):

Stewart, Oliver. “MRI Assessment of Heterogeneity of Muscles across Three Models of Muscular Dystrophy.” 2015. Web. 19 Apr 2019.

Vancouver:

Stewart O. MRI Assessment of Heterogeneity of Muscles across Three Models of Muscular Dystrophy. [Internet] [Thesis]. University of Florida; 2015. [cited 2019 Apr 19]. Available from: http://ufdc.ufl.edu/AA00037463.

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

Council of Science Editors:

Stewart O. MRI Assessment of Heterogeneity of Muscles across Three Models of Muscular Dystrophy. [Thesis]. University of Florida; 2015. Available from: http://ufdc.ufl.edu/AA00037463

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


University of Florida

16. Crawford, Rachel. Non-invasive Analysis of Muscle Quality in Patients with Duchenne Muscular Dystrophy.

Degree: 2011, University of Florida

 Duchenne Muscular Dystrophy (DMD) is a fatal disease that results in progressive muscle degeneration, which is primarily due to a loss of contractile tissue and… (more)

Subjects/Keywords: Disease progression; Diseases; Duchenne muscular dystrophy; Exercise; Fats; Legs; Lipids; Muscles; Skeletal muscle; Torque; Boys; Duchenne muscular dystrophy; Leg – Muscles

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

APA (6th Edition):

Crawford, R. (2011). Non-invasive Analysis of Muscle Quality in Patients with Duchenne Muscular Dystrophy. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00057488

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):

Crawford, Rachel. “Non-invasive Analysis of Muscle Quality in Patients with Duchenne Muscular Dystrophy.” 2011. Thesis, University of Florida. Accessed April 19, 2019. http://ufdc.ufl.edu/AA00057488.

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

MLA Handbook (7th Edition):

Crawford, Rachel. “Non-invasive Analysis of Muscle Quality in Patients with Duchenne Muscular Dystrophy.” 2011. Web. 19 Apr 2019.

Vancouver:

Crawford R. Non-invasive Analysis of Muscle Quality in Patients with Duchenne Muscular Dystrophy. [Internet] [Thesis]. University of Florida; 2011. [cited 2019 Apr 19]. Available from: http://ufdc.ufl.edu/AA00057488.

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

Council of Science Editors:

Crawford R. Non-invasive Analysis of Muscle Quality in Patients with Duchenne Muscular Dystrophy. [Thesis]. University of Florida; 2011. Available from: http://ufdc.ufl.edu/AA00057488

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


University of Western Australia

17. Fragall, Clayton Travis. Peripheral tolerance, regulatory T cells and myoblast transfer therapy.

Degree: PhD, 2009, University of Western Australia

[Truncated abstract] Of the 700 neuromuscular diseases currently described in man Duchenne Muscular Dystrophy (DMD) is both the most common and most severe of those… (more)

Subjects/Keywords: Duchenne muscular dystrophy; Muscular dystrophy; Myoblast transfer therapy; Neuromuscular diseases; T cells; Duchenne muscular dystrophy; Regulatory T cells; Myoblast transfer therapy; Immune response

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

APA (6th Edition):

Fragall, C. T. (2009). Peripheral tolerance, regulatory T cells and myoblast transfer therapy. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=13206&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Fragall, Clayton Travis. “Peripheral tolerance, regulatory T cells and myoblast transfer therapy.” 2009. Doctoral Dissertation, University of Western Australia. Accessed April 19, 2019. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=13206&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Fragall, Clayton Travis. “Peripheral tolerance, regulatory T cells and myoblast transfer therapy.” 2009. Web. 19 Apr 2019.

Vancouver:

Fragall CT. Peripheral tolerance, regulatory T cells and myoblast transfer therapy. [Internet] [Doctoral dissertation]. University of Western Australia; 2009. [cited 2019 Apr 19]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=13206&local_base=GEN01-INS01.

Council of Science Editors:

Fragall CT. Peripheral tolerance, regulatory T cells and myoblast transfer therapy. [Doctoral Dissertation]. University of Western Australia; 2009. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=13206&local_base=GEN01-INS01


University of Florida

18. Iglesias, Kelsey. Parent’s Experience with Healthcare Providers within their Child’s Diagnosis of Duchenne Muscular Dystrophy.

Degree: 2013, University of Florida

 Duchenne Muscular Dystrophy (DMD) is a severe, progressive muscle disease in male children that results in abnormal muscle function affecting early mobility and overall development.… (more)

Subjects/Keywords: Child psychology; Diseases; Duchenne muscular dystrophy; Health care industry; Muscular dystrophies; Neurology; Parents; Quality of life; Sons; Symptomatology; Diagnosis; Duchenne muscular dystrophy; Medical care; Parents

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

APA (6th Edition):

Iglesias, K. (2013). Parent’s Experience with Healthcare Providers within their Child’s Diagnosis of Duchenne Muscular Dystrophy. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00060243

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):

Iglesias, Kelsey. “Parent’s Experience with Healthcare Providers within their Child’s Diagnosis of Duchenne Muscular Dystrophy.” 2013. Thesis, University of Florida. Accessed April 19, 2019. http://ufdc.ufl.edu/AA00060243.

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

MLA Handbook (7th Edition):

Iglesias, Kelsey. “Parent’s Experience with Healthcare Providers within their Child’s Diagnosis of Duchenne Muscular Dystrophy.” 2013. Web. 19 Apr 2019.

Vancouver:

Iglesias K. Parent’s Experience with Healthcare Providers within their Child’s Diagnosis of Duchenne Muscular Dystrophy. [Internet] [Thesis]. University of Florida; 2013. [cited 2019 Apr 19]. Available from: http://ufdc.ufl.edu/AA00060243.

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

Council of Science Editors:

Iglesias K. Parent’s Experience with Healthcare Providers within their Child’s Diagnosis of Duchenne Muscular Dystrophy. [Thesis]. University of Florida; 2013. Available from: http://ufdc.ufl.edu/AA00060243

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

19. Gomes-Santos, Igor Lucas. Angiotensina II e treinamento físico na insuficiência cardíaca: implicações para a miopatia esquelética.

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

 INTRODUÇÃO: Capítulo 1. A Insuficiência Cardíaca (IC) é acompanhada de uma hiperativação simpática e do sistema renina-angiotensina (SRA). As ações deletérias do SRA são atribuídas… (more)

Subjects/Keywords: Angiotensin II; Angiotensina II; Atrofia muscular/patologia; Atrofia muscular/reabilitação; Doenças musculares; Exercício/fisiologia; Exercise therapy; Exercise/physiology; Heart failure; Insuficiência cardíaca; Muscular atrophy/pathology; Muscular atrophy/rehabilitation; Muscular diseases; Ratos Wistar; Rats Wistar; Renin-angiotensin system; Sistema renina-angiotensina; Terapia por exercício; Ubiquitin/genetics; Ubiquitina/genética

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

APA (6th Edition):

Gomes-Santos, I. L. (2014). Angiotensina II e treinamento físico na insuficiência cardíaca: implicações para a miopatia esquelética. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5131/tde-04042014-162601/ ;

Chicago Manual of Style (16th Edition):

Gomes-Santos, Igor Lucas. “Angiotensina II e treinamento físico na insuficiência cardíaca: implicações para a miopatia esquelética.” 2014. Doctoral Dissertation, University of São Paulo. Accessed April 19, 2019. http://www.teses.usp.br/teses/disponiveis/5/5131/tde-04042014-162601/ ;.

MLA Handbook (7th Edition):

Gomes-Santos, Igor Lucas. “Angiotensina II e treinamento físico na insuficiência cardíaca: implicações para a miopatia esquelética.” 2014. Web. 19 Apr 2019.

Vancouver:

Gomes-Santos IL. Angiotensina II e treinamento físico na insuficiência cardíaca: implicações para a miopatia esquelética. [Internet] [Doctoral dissertation]. University of São Paulo; 2014. [cited 2019 Apr 19]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5131/tde-04042014-162601/ ;.

Council of Science Editors:

Gomes-Santos IL. Angiotensina II e treinamento físico na insuficiência cardíaca: implicações para a miopatia esquelética. [Doctoral Dissertation]. University of São Paulo; 2014. Available from: http://www.teses.usp.br/teses/disponiveis/5/5131/tde-04042014-162601/ ;


University of Florida

20. Mangieri, Gianna Marie. Use of MRI to characterize the DBA/2J-mdx mouse model of Duchenne muscular dystrophy.

Degree: 2017, University of Florida

 Duchenne muscular dystrophy (DMD) is a debilitating disease caused by a mutation of the gene encoding dystrophin protein. This study evaluated a mouse model, DBA/2Jmdx,… (more)

Subjects/Keywords: Diseases; Duchenne muscular dystrophy; Magnetic resonance imaging; Metabolites; Muscles; Myocardium; Phenotypes; Phosphorus; T tests; Treadmills

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

APA (6th Edition):

Mangieri, G. M. (2017). Use of MRI to characterize the DBA/2J-mdx mouse model of Duchenne muscular dystrophy. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00057956

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):

Mangieri, Gianna Marie. “Use of MRI to characterize the DBA/2J-mdx mouse model of Duchenne muscular dystrophy.” 2017. Thesis, University of Florida. Accessed April 19, 2019. http://ufdc.ufl.edu/AA00057956.

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

MLA Handbook (7th Edition):

Mangieri, Gianna Marie. “Use of MRI to characterize the DBA/2J-mdx mouse model of Duchenne muscular dystrophy.” 2017. Web. 19 Apr 2019.

Vancouver:

Mangieri GM. Use of MRI to characterize the DBA/2J-mdx mouse model of Duchenne muscular dystrophy. [Internet] [Thesis]. University of Florida; 2017. [cited 2019 Apr 19]. Available from: http://ufdc.ufl.edu/AA00057956.

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

Council of Science Editors:

Mangieri GM. Use of MRI to characterize the DBA/2J-mdx mouse model of Duchenne muscular dystrophy. [Thesis]. University of Florida; 2017. Available from: http://ufdc.ufl.edu/AA00057956

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


Michigan State University

21. Husic, Harold David. Circulatory clearance of muscle enzymes in normal and dystrophic chickens.

Degree: PhD, Department of Biochemistry, 1982, Michigan State University

Subjects/Keywords: Chickens – Diseases – Diagnosis; Poultry – Diseases – Diagnosis; Muscular dystrophy; Muscles

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

APA (6th Edition):

Husic, H. D. (1982). Circulatory clearance of muscle enzymes in normal and dystrophic chickens. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:18334

Chicago Manual of Style (16th Edition):

Husic, Harold David. “Circulatory clearance of muscle enzymes in normal and dystrophic chickens.” 1982. Doctoral Dissertation, Michigan State University. Accessed April 19, 2019. http://etd.lib.msu.edu/islandora/object/etd:18334.

MLA Handbook (7th Edition):

Husic, Harold David. “Circulatory clearance of muscle enzymes in normal and dystrophic chickens.” 1982. Web. 19 Apr 2019.

Vancouver:

Husic HD. Circulatory clearance of muscle enzymes in normal and dystrophic chickens. [Internet] [Doctoral dissertation]. Michigan State University; 1982. [cited 2019 Apr 19]. Available from: http://etd.lib.msu.edu/islandora/object/etd:18334.

Council of Science Editors:

Husic HD. Circulatory clearance of muscle enzymes in normal and dystrophic chickens. [Doctoral Dissertation]. Michigan State University; 1982. Available from: http://etd.lib.msu.edu/islandora/object/etd:18334


University of Florida

22. Rundall, Amber. Effective Health Measures for Boys.

Degree: 2012, University of Florida

 Duchenne Muscular Dystrophy (DMD) is a progressive muscle disease in males. Clinical studies in DMD have focused exclusively on clinically based physiological and functional measures.… (more)

Subjects/Keywords: Disabilities; Diseases; Duchenne muscular dystrophy; Exercise; Health care outcome assessment; Health status; Longitudinal studies; Motor ability; Self reports; Statistical significance; Boys; Duchenne muscular dystrophy; Motor ability; Participation

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

APA (6th Edition):

Rundall, A. (2012). Effective Health Measures for Boys. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00060168

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):

Rundall, Amber. “Effective Health Measures for Boys.” 2012. Thesis, University of Florida. Accessed April 19, 2019. http://ufdc.ufl.edu/AA00060168.

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

MLA Handbook (7th Edition):

Rundall, Amber. “Effective Health Measures for Boys.” 2012. Web. 19 Apr 2019.

Vancouver:

Rundall A. Effective Health Measures for Boys. [Internet] [Thesis]. University of Florida; 2012. [cited 2019 Apr 19]. Available from: http://ufdc.ufl.edu/AA00060168.

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

Council of Science Editors:

Rundall A. Effective Health Measures for Boys. [Thesis]. University of Florida; 2012. Available from: http://ufdc.ufl.edu/AA00060168

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

23. Chakouch, Mashhour. Viscoelastic properties of in vivo thigh muscle and in vivo phantom using magnetic resonance elastography (MRE) : Propriétés viscoélastiques des muscles in vivo de la cuisse et d'un fantôme in vitro avec la technique d'élastographie par résonance magnétique (ERM).

Degree: Docteur es, Biomechanics and Bioengineering, 2015, Compiègne

 Résumé de l'étude in vitro. L'objectif de cette étude in vitro était de créer un fantôme avec la même architecture musculaire (fibre, aponévrose ...) et… (more)

Subjects/Keywords: Fantôme; Élastographie par résonance magnétique; ERM; Modèles rhéologiques; Longueur d'onde; Myopathie de Duchenne; Phantom; Muscular Diseases; Noninvasive diagnosis; Elasticity; Viscoelasticity; Rheology; Muscular dystrophy

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

APA (6th Edition):

Chakouch, M. (2015). Viscoelastic properties of in vivo thigh muscle and in vivo phantom using magnetic resonance elastography (MRE) : Propriétés viscoélastiques des muscles in vivo de la cuisse et d'un fantôme in vitro avec la technique d'élastographie par résonance magnétique (ERM). (Doctoral Dissertation). Compiègne. Retrieved from http://www.theses.fr/2015COMP2236

Chicago Manual of Style (16th Edition):

Chakouch, Mashhour. “Viscoelastic properties of in vivo thigh muscle and in vivo phantom using magnetic resonance elastography (MRE) : Propriétés viscoélastiques des muscles in vivo de la cuisse et d'un fantôme in vitro avec la technique d'élastographie par résonance magnétique (ERM).” 2015. Doctoral Dissertation, Compiègne. Accessed April 19, 2019. http://www.theses.fr/2015COMP2236.

MLA Handbook (7th Edition):

Chakouch, Mashhour. “Viscoelastic properties of in vivo thigh muscle and in vivo phantom using magnetic resonance elastography (MRE) : Propriétés viscoélastiques des muscles in vivo de la cuisse et d'un fantôme in vitro avec la technique d'élastographie par résonance magnétique (ERM).” 2015. Web. 19 Apr 2019.

Vancouver:

Chakouch M. Viscoelastic properties of in vivo thigh muscle and in vivo phantom using magnetic resonance elastography (MRE) : Propriétés viscoélastiques des muscles in vivo de la cuisse et d'un fantôme in vitro avec la technique d'élastographie par résonance magnétique (ERM). [Internet] [Doctoral dissertation]. Compiègne; 2015. [cited 2019 Apr 19]. Available from: http://www.theses.fr/2015COMP2236.

Council of Science Editors:

Chakouch M. Viscoelastic properties of in vivo thigh muscle and in vivo phantom using magnetic resonance elastography (MRE) : Propriétés viscoélastiques des muscles in vivo de la cuisse et d'un fantôme in vitro avec la technique d'élastographie par résonance magnétique (ERM). [Doctoral Dissertation]. Compiègne; 2015. Available from: http://www.theses.fr/2015COMP2236


University of Florida

24. Zink, Kasie. Participation and Quality of Life of Boys with Duchenne Muscular Dystrophy.

Degree: 2010, University of Florida

 Background: Duchenne Muscular Dystrophy (DMD) is a progressive disease affecting males that rapidly deteriorates muscles and limits their ability to participate in many activities, possibly… (more)

Subjects/Keywords: Child psychology; Children; Correlations; Disabilities; Diseases; Duchenne muscular dystrophy; Exercise; Pediatrics; Quality of life; Self reports; Duchenne muscular dystrophy; Participation; Quality of life

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

APA (6th Edition):

Zink, K. (2010). Participation and Quality of Life of Boys with Duchenne Muscular Dystrophy. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00060025

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):

Zink, Kasie. “Participation and Quality of Life of Boys with Duchenne Muscular Dystrophy.” 2010. Thesis, University of Florida. Accessed April 19, 2019. http://ufdc.ufl.edu/AA00060025.

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

MLA Handbook (7th Edition):

Zink, Kasie. “Participation and Quality of Life of Boys with Duchenne Muscular Dystrophy.” 2010. Web. 19 Apr 2019.

Vancouver:

Zink K. Participation and Quality of Life of Boys with Duchenne Muscular Dystrophy. [Internet] [Thesis]. University of Florida; 2010. [cited 2019 Apr 19]. Available from: http://ufdc.ufl.edu/AA00060025.

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

Council of Science Editors:

Zink K. Participation and Quality of Life of Boys with Duchenne Muscular Dystrophy. [Thesis]. University of Florida; 2010. Available from: http://ufdc.ufl.edu/AA00060025

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


University of Florida

25. Hugi, Sheila. Relationships Between Contractile Tissue, Physical Activity, and Functional Ability in Ambulatory Boys with Duchenne Muscular Dystrophy.

Degree: 2013, University of Florida

 Duchenne Muscular Dystrophy (DMD) is a genetic muscle wasting disease, primarily affecting males and is usually diagnosed around five years of age. Researchers have used… (more)

Subjects/Keywords: Control groups; Diseases; Duchenne muscular dystrophy; Exercise; Metabolic equivalent; Muscle contraction; Muscle tissues; Muscles; Quadriceps muscle; Trucks; Duchenne muscular dystrophy; Exercise; Motor abilty; Muscles

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

APA (6th Edition):

Hugi, S. (2013). Relationships Between Contractile Tissue, Physical Activity, and Functional Ability in Ambulatory Boys with Duchenne Muscular Dystrophy. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00061065

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):

Hugi, Sheila. “Relationships Between Contractile Tissue, Physical Activity, and Functional Ability in Ambulatory Boys with Duchenne Muscular Dystrophy.” 2013. Thesis, University of Florida. Accessed April 19, 2019. http://ufdc.ufl.edu/AA00061065.

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

MLA Handbook (7th Edition):

Hugi, Sheila. “Relationships Between Contractile Tissue, Physical Activity, and Functional Ability in Ambulatory Boys with Duchenne Muscular Dystrophy.” 2013. Web. 19 Apr 2019.

Vancouver:

Hugi S. Relationships Between Contractile Tissue, Physical Activity, and Functional Ability in Ambulatory Boys with Duchenne Muscular Dystrophy. [Internet] [Thesis]. University of Florida; 2013. [cited 2019 Apr 19]. Available from: http://ufdc.ufl.edu/AA00061065.

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

Council of Science Editors:

Hugi S. Relationships Between Contractile Tissue, Physical Activity, and Functional Ability in Ambulatory Boys with Duchenne Muscular Dystrophy. [Thesis]. University of Florida; 2013. Available from: http://ufdc.ufl.edu/AA00061065

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


University of Southern California

26. Gustavo, Gutierrez. Rare diseases.

Degree: MA, Journalism (Broadcast Journalism), 2012, University of Southern California

 Rare diseases or also commonly known as orphan diseases are devastating for the person dealing with them, but also for the entire family. They are… (more)

Subjects/Keywords: spinal muscular atrophy; cystic fibrosis; type II; diseases; rare; U.S. Congress; funding; Madison'; s Foundation; Children'; s Hospital; Spinal Muscular Atrophy research.

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

APA (6th Edition):

Gustavo, G. (2012). Rare diseases. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/37380/rec/5399

Chicago Manual of Style (16th Edition):

Gustavo, Gutierrez. “Rare diseases.” 2012. Masters Thesis, University of Southern California. Accessed April 19, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/37380/rec/5399.

MLA Handbook (7th Edition):

Gustavo, Gutierrez. “Rare diseases.” 2012. Web. 19 Apr 2019.

Vancouver:

Gustavo G. Rare diseases. [Internet] [Masters thesis]. University of Southern California; 2012. [cited 2019 Apr 19]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/37380/rec/5399.

Council of Science Editors:

Gustavo G. Rare diseases. [Masters Thesis]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/37380/rec/5399


University of Oxford

27. Benson, Matthew Arnold. Cloning and characterisation of myospryn, a novel dysbindin-binding protein in muscle.

Degree: 2005, University of Oxford

Subjects/Keywords: 616.748; Protein binding : Muscle : Diseases : Duchenne muscular dystrophy : Myocardium

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

APA (6th Edition):

Benson, M. A. (2005). Cloning and characterisation of myospryn, a novel dysbindin-binding protein in muscle. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:efb3191c-504e-4e74-86c3-b3b789d8bb15 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.419265

Chicago Manual of Style (16th Edition):

Benson, Matthew Arnold. “Cloning and characterisation of myospryn, a novel dysbindin-binding protein in muscle.” 2005. Doctoral Dissertation, University of Oxford. Accessed April 19, 2019. http://ora.ox.ac.uk/objects/uuid:efb3191c-504e-4e74-86c3-b3b789d8bb15 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.419265.

MLA Handbook (7th Edition):

Benson, Matthew Arnold. “Cloning and characterisation of myospryn, a novel dysbindin-binding protein in muscle.” 2005. Web. 19 Apr 2019.

Vancouver:

Benson MA. Cloning and characterisation of myospryn, a novel dysbindin-binding protein in muscle. [Internet] [Doctoral dissertation]. University of Oxford; 2005. [cited 2019 Apr 19]. Available from: http://ora.ox.ac.uk/objects/uuid:efb3191c-504e-4e74-86c3-b3b789d8bb15 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.419265.

Council of Science Editors:

Benson MA. Cloning and characterisation of myospryn, a novel dysbindin-binding protein in muscle. [Doctoral Dissertation]. University of Oxford; 2005. Available from: http://ora.ox.ac.uk/objects/uuid:efb3191c-504e-4e74-86c3-b3b789d8bb15 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.419265


Technical University of Lisbon

28. Rodrigues, Rita Vaz. Otimização da caracterização de fibras musculares estriadas em cão (Canis familiaris) por histoquímica e imunohistoquímica com potencial aplicação ao diagnóstico.

Degree: 2016, Technical University of Lisbon

Dissertação de Mestrado Integrado em Medicina Veterinária

As técnicas histoquímicas permitem melhorar o conhecimento sobre o tecido muscular e suas alterações patológicas e, juntamente com… (more)

Subjects/Keywords: cão; músculo estriado; fibras musculares; histoquímica; imunohistoquímica; doenças musculares; dog; striated muscle; muscle fibers; histochemistry; immunohistochemistry; muscular diseases

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

APA (6th Edition):

Rodrigues, R. V. (2016). Otimização da caracterização de fibras musculares estriadas em cão (Canis familiaris) por histoquímica e imunohistoquímica com potencial aplicação ao diagnóstico. (Thesis). Technical University of Lisbon. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:www.repository.utl.pt:10400.5/11840

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):

Rodrigues, Rita Vaz. “Otimização da caracterização de fibras musculares estriadas em cão (Canis familiaris) por histoquímica e imunohistoquímica com potencial aplicação ao diagnóstico.” 2016. Thesis, Technical University of Lisbon. Accessed April 19, 2019. http://www.rcaap.pt/detail.jsp?id=oai:www.repository.utl.pt:10400.5/11840.

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

MLA Handbook (7th Edition):

Rodrigues, Rita Vaz. “Otimização da caracterização de fibras musculares estriadas em cão (Canis familiaris) por histoquímica e imunohistoquímica com potencial aplicação ao diagnóstico.” 2016. Web. 19 Apr 2019.

Vancouver:

Rodrigues RV. Otimização da caracterização de fibras musculares estriadas em cão (Canis familiaris) por histoquímica e imunohistoquímica com potencial aplicação ao diagnóstico. [Internet] [Thesis]. Technical University of Lisbon; 2016. [cited 2019 Apr 19]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:www.repository.utl.pt:10400.5/11840.

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

Council of Science Editors:

Rodrigues RV. Otimização da caracterização de fibras musculares estriadas em cão (Canis familiaris) por histoquímica e imunohistoquímica com potencial aplicação ao diagnóstico. [Thesis]. Technical University of Lisbon; 2016. Available from: http://www.rcaap.pt/detail.jsp?id=oai:www.repository.utl.pt:10400.5/11840

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


University of Florida

29. Arpan, Ishu. Non-Invasive Monitoring of Muscle Response to Disease Progression and Therapeutic Interventions in Duchenne Muscular Dystrophy Using MRI and MRS.

Degree: PhD, Rehabilitation Science, 2014, University of Florida

 Duchenne muscular dystrophy DMD is an inherited neuromuscular disorder characterized by progressive muscle degeneration and weakness. Boys with DMD experience gradual disability; with loss of… (more)

Subjects/Keywords: Corticosteroids; Disease progression; Diseases; Duchenne muscular dystrophy; Fats; Legs; Magnetic resonance imaging; Muscles; Pixels; Skeletal muscle; biomarker  – dmd  – mri  – mrs

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

APA (6th Edition):

Arpan, I. (2014). Non-Invasive Monitoring of Muscle Response to Disease Progression and Therapeutic Interventions in Duchenne Muscular Dystrophy Using MRI and MRS. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0046559

Chicago Manual of Style (16th Edition):

Arpan, Ishu. “Non-Invasive Monitoring of Muscle Response to Disease Progression and Therapeutic Interventions in Duchenne Muscular Dystrophy Using MRI and MRS.” 2014. Doctoral Dissertation, University of Florida. Accessed April 19, 2019. http://ufdc.ufl.edu/UFE0046559.

MLA Handbook (7th Edition):

Arpan, Ishu. “Non-Invasive Monitoring of Muscle Response to Disease Progression and Therapeutic Interventions in Duchenne Muscular Dystrophy Using MRI and MRS.” 2014. Web. 19 Apr 2019.

Vancouver:

Arpan I. Non-Invasive Monitoring of Muscle Response to Disease Progression and Therapeutic Interventions in Duchenne Muscular Dystrophy Using MRI and MRS. [Internet] [Doctoral dissertation]. University of Florida; 2014. [cited 2019 Apr 19]. Available from: http://ufdc.ufl.edu/UFE0046559.

Council of Science Editors:

Arpan I. Non-Invasive Monitoring of Muscle Response to Disease Progression and Therapeutic Interventions in Duchenne Muscular Dystrophy Using MRI and MRS. [Doctoral Dissertation]. University of Florida; 2014. Available from: http://ufdc.ufl.edu/UFE0046559


Kansas State University

30. Mueller, Robert Edward. Brown Swiss weaver syndrome : studies of muscle pathology.

Degree: 1980, Kansas State University

Subjects/Keywords: Muscles – Hypertrophy; Cattle – Diseases; Muscular atrophy; Lameness in cattle

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

APA (6th Edition):

Mueller, R. E. (1980). Brown Swiss weaver syndrome : studies of muscle pathology. (Thesis). Kansas State University. Retrieved from http://hdl.handle.net/2097/11842

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):

Mueller, Robert Edward. “Brown Swiss weaver syndrome : studies of muscle pathology.” 1980. Thesis, Kansas State University. Accessed April 19, 2019. http://hdl.handle.net/2097/11842.

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

MLA Handbook (7th Edition):

Mueller, Robert Edward. “Brown Swiss weaver syndrome : studies of muscle pathology.” 1980. Web. 19 Apr 2019.

Vancouver:

Mueller RE. Brown Swiss weaver syndrome : studies of muscle pathology. [Internet] [Thesis]. Kansas State University; 1980. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/2097/11842.

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

Council of Science Editors:

Mueller RE. Brown Swiss weaver syndrome : studies of muscle pathology. [Thesis]. Kansas State University; 1980. Available from: http://hdl.handle.net/2097/11842

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

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