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You searched for subject:(Rett Syndrome). Showing records 1 – 30 of 84 total matches.

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University of Illinois – Urbana-Champaign

1. Long, Steven W. A brain-derived MeCP2 complex supports a role for MeCP2 in RNA processing.

Degree: PhD, 4094, 2010, University of Illinois – Urbana-Champaign

 Methyl CpG binding protein 2 (MeCP2) was originally characterized as a transcriptional repressor that preferentially bound methylated DNA, however, recent data indicates MeCP2 is a… (more)

Subjects/Keywords: MeCP2; Prpf3; Sdccag1; Rett Syndrome

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APA (6th Edition):

Long, S. W. (2010). A brain-derived MeCP2 complex supports a role for MeCP2 in RNA processing. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/16960

Chicago Manual of Style (16th Edition):

Long, Steven W. “A brain-derived MeCP2 complex supports a role for MeCP2 in RNA processing.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 24, 2019. http://hdl.handle.net/2142/16960.

MLA Handbook (7th Edition):

Long, Steven W. “A brain-derived MeCP2 complex supports a role for MeCP2 in RNA processing.” 2010. Web. 24 Aug 2019.

Vancouver:

Long SW. A brain-derived MeCP2 complex supports a role for MeCP2 in RNA processing. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/2142/16960.

Council of Science Editors:

Long SW. A brain-derived MeCP2 complex supports a role for MeCP2 in RNA processing. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/16960


University of Edinburgh

2. Kerr, Alison. Critical account of clinical and physiological studies in Rett syndrome.

Degree: Thesis (M.D.), 2006, University of Edinburgh

Rett syndrome is the manifestation of an X linked, mainly female, genetic, neurodevelopmental disorder that usually produces profound intellectual and physical disabilities including abnormal muscle… (more)

Subjects/Keywords: 618.92; Rett syndrome

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APA (6th Edition):

Kerr, A. (2006). Critical account of clinical and physiological studies in Rett syndrome. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/8756

Chicago Manual of Style (16th Edition):

Kerr, Alison. “Critical account of clinical and physiological studies in Rett syndrome.” 2006. Doctoral Dissertation, University of Edinburgh. Accessed August 24, 2019. http://hdl.handle.net/1842/8756.

MLA Handbook (7th Edition):

Kerr, Alison. “Critical account of clinical and physiological studies in Rett syndrome.” 2006. Web. 24 Aug 2019.

Vancouver:

Kerr A. Critical account of clinical and physiological studies in Rett syndrome. [Internet] [Doctoral dissertation]. University of Edinburgh; 2006. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1842/8756.

Council of Science Editors:

Kerr A. Critical account of clinical and physiological studies in Rett syndrome. [Doctoral Dissertation]. University of Edinburgh; 2006. Available from: http://hdl.handle.net/1842/8756


University of Minnesota

3. Dimian, Adele. Using functional analysis to test whether idiosyncratic and challenging behavior in Rett syndrome is sensitive to social reinforcement contingencies.

Degree: MA, Educational psychology, 2012, University of Minnesota

University of Minnesota M.A. thesis. July 2012. Major: Educational psychology. Advisors: Frank J. Symons, LeAnne Johnson. 1 computer file (PDF); v, 31 pages, appendix p.… (more)

Subjects/Keywords: Rett syndrome; Functional analysis; Idiosyncratic behavior

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APA (6th Edition):

Dimian, A. (2012). Using functional analysis to test whether idiosyncratic and challenging behavior in Rett syndrome is sensitive to social reinforcement contingencies. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/140343

Chicago Manual of Style (16th Edition):

Dimian, Adele. “Using functional analysis to test whether idiosyncratic and challenging behavior in Rett syndrome is sensitive to social reinforcement contingencies.” 2012. Masters Thesis, University of Minnesota. Accessed August 24, 2019. http://purl.umn.edu/140343.

MLA Handbook (7th Edition):

Dimian, Adele. “Using functional analysis to test whether idiosyncratic and challenging behavior in Rett syndrome is sensitive to social reinforcement contingencies.” 2012. Web. 24 Aug 2019.

Vancouver:

Dimian A. Using functional analysis to test whether idiosyncratic and challenging behavior in Rett syndrome is sensitive to social reinforcement contingencies. [Internet] [Masters thesis]. University of Minnesota; 2012. [cited 2019 Aug 24]. Available from: http://purl.umn.edu/140343.

Council of Science Editors:

Dimian A. Using functional analysis to test whether idiosyncratic and challenging behavior in Rett syndrome is sensitive to social reinforcement contingencies. [Masters Thesis]. University of Minnesota; 2012. Available from: http://purl.umn.edu/140343


Univerzitet u Beogradu

4. Sarajlija, Adrijan, 1976-. Epidemiološko-klinička studija Retovog sindroma u populaciji Srbije.

Degree: Medicinski fakultet, 2015, Univerzitet u Beogradu

Epidemiologija - Epidemiology

Retov sindrom (RTT) je teţak neurorazvojni poremećaj koji se uglavnom susreće kod osoba ţenskog pola. U različitim delovima sveta RTT ima prevalenciju… (more)

Subjects/Keywords: Rett syndrome; incidence; genotype-phenotype correlation

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APA (6th Edition):

Sarajlija, Adrijan, 1. (2015). Epidemiološko-klinička studija Retovog sindroma u populaciji Srbije. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:9655/bdef:Content/get

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):

Sarajlija, Adrijan, 1976-. “Epidemiološko-klinička studija Retovog sindroma u populaciji Srbije.” 2015. Thesis, Univerzitet u Beogradu. Accessed August 24, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:9655/bdef:Content/get.

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

MLA Handbook (7th Edition):

Sarajlija, Adrijan, 1976-. “Epidemiološko-klinička studija Retovog sindroma u populaciji Srbije.” 2015. Web. 24 Aug 2019.

Vancouver:

Sarajlija, Adrijan 1. Epidemiološko-klinička studija Retovog sindroma u populaciji Srbije. [Internet] [Thesis]. Univerzitet u Beogradu; 2015. [cited 2019 Aug 24]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:9655/bdef:Content/get.

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

Council of Science Editors:

Sarajlija, Adrijan 1. Epidemiološko-klinička studija Retovog sindroma u populaciji Srbije. [Thesis]. Univerzitet u Beogradu; 2015. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:9655/bdef:Content/get

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

5. Brown, Kyla Joy. Molecular basis of R133C Rett syndrome.

Degree: PhD, 2016, University of Edinburgh

Rett syndrome is a debilitating autistic spectrum disorder affecting one in ten thousand girls. Patients develop normally for up to eighteen months before a period… (more)

Subjects/Keywords: 616.85; R133C; Rett syndrome; autistic spectrum

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APA (6th Edition):

Brown, K. J. (2016). Molecular basis of R133C Rett syndrome. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/20412

Chicago Manual of Style (16th Edition):

Brown, Kyla Joy. “Molecular basis of R133C Rett syndrome.” 2016. Doctoral Dissertation, University of Edinburgh. Accessed August 24, 2019. http://hdl.handle.net/1842/20412.

MLA Handbook (7th Edition):

Brown, Kyla Joy. “Molecular basis of R133C Rett syndrome.” 2016. Web. 24 Aug 2019.

Vancouver:

Brown KJ. Molecular basis of R133C Rett syndrome. [Internet] [Doctoral dissertation]. University of Edinburgh; 2016. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1842/20412.

Council of Science Editors:

Brown KJ. Molecular basis of R133C Rett syndrome. [Doctoral Dissertation]. University of Edinburgh; 2016. Available from: http://hdl.handle.net/1842/20412


University of Victoria

6. Bell, Nancy Marie. A Child's "Terminal Illness": An Analysis of Text Mediated Knowing.

Degree: Faculty of Human and Social Development, 2014, University of Victoria

 Several years ago a ten year child with a disability died from "severe malnutrition" according to a Coroners Service inquest jury. The inquest evidence shows… (more)

Subjects/Keywords: children; malnutrition; institutional ethnography; Rett syndrome

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APA (6th Edition):

Bell, N. M. (2014). A Child's "Terminal Illness": An Analysis of Text Mediated Knowing. (Masters Thesis). University of Victoria. Retrieved from http://hdl.handle.net/1828/5561

Chicago Manual of Style (16th Edition):

Bell, Nancy Marie. “A Child's "Terminal Illness": An Analysis of Text Mediated Knowing.” 2014. Masters Thesis, University of Victoria. Accessed August 24, 2019. http://hdl.handle.net/1828/5561.

MLA Handbook (7th Edition):

Bell, Nancy Marie. “A Child's "Terminal Illness": An Analysis of Text Mediated Knowing.” 2014. Web. 24 Aug 2019.

Vancouver:

Bell NM. A Child's "Terminal Illness": An Analysis of Text Mediated Knowing. [Internet] [Masters thesis]. University of Victoria; 2014. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1828/5561.

Council of Science Editors:

Bell NM. A Child's "Terminal Illness": An Analysis of Text Mediated Knowing. [Masters Thesis]. University of Victoria; 2014. Available from: http://hdl.handle.net/1828/5561


University of Minnesota

7. Dimian, Adele. Using functional analysis to test whether idiosyncratic and challenging behavior in Rett syndrome is sensitive to social reinforcement contingencies.

Degree: MA, Educational psychology, 2012, University of Minnesota

Rett syndrome (RS) is a severe neurodevelopmental disability that results in cognitive impairment, loss of functional and communication skills, and an emergence of idiosyncratic behaviors.… (more)

Subjects/Keywords: Rett syndrome; Functional analysis; Idiosyncratic behavior

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APA (6th Edition):

Dimian, A. (2012). Using functional analysis to test whether idiosyncratic and challenging behavior in Rett syndrome is sensitive to social reinforcement contingencies. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/140343

Chicago Manual of Style (16th Edition):

Dimian, Adele. “Using functional analysis to test whether idiosyncratic and challenging behavior in Rett syndrome is sensitive to social reinforcement contingencies.” 2012. Masters Thesis, University of Minnesota. Accessed August 24, 2019. http://purl.umn.edu/140343.

MLA Handbook (7th Edition):

Dimian, Adele. “Using functional analysis to test whether idiosyncratic and challenging behavior in Rett syndrome is sensitive to social reinforcement contingencies.” 2012. Web. 24 Aug 2019.

Vancouver:

Dimian A. Using functional analysis to test whether idiosyncratic and challenging behavior in Rett syndrome is sensitive to social reinforcement contingencies. [Internet] [Masters thesis]. University of Minnesota; 2012. [cited 2019 Aug 24]. Available from: http://purl.umn.edu/140343.

Council of Science Editors:

Dimian A. Using functional analysis to test whether idiosyncratic and challenging behavior in Rett syndrome is sensitive to social reinforcement contingencies. [Masters Thesis]. University of Minnesota; 2012. Available from: http://purl.umn.edu/140343


University of Minnesota

8. Byiers, Breanne J. L. Functional communication training in Rett syndrome.

Degree: PhD, 2013, University of Minnesota

Rett syndrome (RTT) is associated with a range of serious neurodevelopmental consequences including severe impairments in communication. Currently, no evidence-based communication interventions exist for the… (more)

Subjects/Keywords: Functional analysis; Functional communication training; Rett syndrome

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APA (6th Edition):

Byiers, B. J. L. (2013). Functional communication training in Rett syndrome. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/155597

Chicago Manual of Style (16th Edition):

Byiers, Breanne J L. “Functional communication training in Rett syndrome.” 2013. Doctoral Dissertation, University of Minnesota. Accessed August 24, 2019. http://purl.umn.edu/155597.

MLA Handbook (7th Edition):

Byiers, Breanne J L. “Functional communication training in Rett syndrome.” 2013. Web. 24 Aug 2019.

Vancouver:

Byiers BJL. Functional communication training in Rett syndrome. [Internet] [Doctoral dissertation]. University of Minnesota; 2013. [cited 2019 Aug 24]. Available from: http://purl.umn.edu/155597.

Council of Science Editors:

Byiers BJL. Functional communication training in Rett syndrome. [Doctoral Dissertation]. University of Minnesota; 2013. Available from: http://purl.umn.edu/155597


University of Toronto

9. D'Cruz, Jennifer. Alterations of Cortical and Hippocampal Network Activity in MeCP2-Deficient Mice.

Degree: 2010, University of Toronto

Intractable epilepsy remains one of the top issues affecting the quality of living in Rett children. While several MeCP2-deficient mouse models of Rett Syndrome have… (more)

Subjects/Keywords: Rett Syndrome EEG mice MeCP2; 0564

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APA (6th Edition):

D'Cruz, J. (2010). Alterations of Cortical and Hippocampal Network Activity in MeCP2-Deficient Mice. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/24557

Chicago Manual of Style (16th Edition):

D'Cruz, Jennifer. “Alterations of Cortical and Hippocampal Network Activity in MeCP2-Deficient Mice.” 2010. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/24557.

MLA Handbook (7th Edition):

D'Cruz, Jennifer. “Alterations of Cortical and Hippocampal Network Activity in MeCP2-Deficient Mice.” 2010. Web. 24 Aug 2019.

Vancouver:

D'Cruz J. Alterations of Cortical and Hippocampal Network Activity in MeCP2-Deficient Mice. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/24557.

Council of Science Editors:

D'Cruz J. Alterations of Cortical and Hippocampal Network Activity in MeCP2-Deficient Mice. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/24557


Arizona State University

10. Williams, Alison Ann. Drosophila as a Translational Model For MECP2 Gain-of-Function in Neurons.

Degree: Neuroscience, 2015, Arizona State University

 Methyl-CpG binding protein 2 (MECP2) is a widely abundant, multifunctional regulator of gene expression with highest levels of expression in mature neurons. In humans, both… (more)

Subjects/Keywords: Neurosciences; apoptosis; dendrite; Drosophila; MECP2; Rett syndrome

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APA (6th Edition):

Williams, A. A. (2015). Drosophila as a Translational Model For MECP2 Gain-of-Function in Neurons. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/35984

Chicago Manual of Style (16th Edition):

Williams, Alison Ann. “Drosophila as a Translational Model For MECP2 Gain-of-Function in Neurons.” 2015. Doctoral Dissertation, Arizona State University. Accessed August 24, 2019. http://repository.asu.edu/items/35984.

MLA Handbook (7th Edition):

Williams, Alison Ann. “Drosophila as a Translational Model For MECP2 Gain-of-Function in Neurons.” 2015. Web. 24 Aug 2019.

Vancouver:

Williams AA. Drosophila as a Translational Model For MECP2 Gain-of-Function in Neurons. [Internet] [Doctoral dissertation]. Arizona State University; 2015. [cited 2019 Aug 24]. Available from: http://repository.asu.edu/items/35984.

Council of Science Editors:

Williams AA. Drosophila as a Translational Model For MECP2 Gain-of-Function in Neurons. [Doctoral Dissertation]. Arizona State University; 2015. Available from: http://repository.asu.edu/items/35984


University of Edinburgh

11. Kruusvee, Valdeko. The structural basis of MeCP2 interaction with NCoR/SMRT co-repressor complex.

Degree: PhD, 2017, University of Edinburgh

Rett syndrome (RTT) is an X-linked neurological disorder primarily caused by mutations in the MECP2 gene. The majority of RTT mutations disrupt the interaction of… (more)

Subjects/Keywords: Rett syndrome; x-ray; structural biology

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APA (6th Edition):

Kruusvee, V. (2017). The structural basis of MeCP2 interaction with NCoR/SMRT co-repressor complex. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/25703

Chicago Manual of Style (16th Edition):

Kruusvee, Valdeko. “The structural basis of MeCP2 interaction with NCoR/SMRT co-repressor complex.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed August 24, 2019. http://hdl.handle.net/1842/25703.

MLA Handbook (7th Edition):

Kruusvee, Valdeko. “The structural basis of MeCP2 interaction with NCoR/SMRT co-repressor complex.” 2017. Web. 24 Aug 2019.

Vancouver:

Kruusvee V. The structural basis of MeCP2 interaction with NCoR/SMRT co-repressor complex. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1842/25703.

Council of Science Editors:

Kruusvee V. The structural basis of MeCP2 interaction with NCoR/SMRT co-repressor complex. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/25703


Universitat de Barcelona

12. Petazzi, Paolo. Methyl-CpG binding protein 2 deregulation: from Rett syndrome to MeCP2 duplication disorder.

Degree: 2015, Universitat de Barcelona

 Introducción: El síndrome de Rett (RTT, OMIM#312750) fue por primera vez descrito en 1966 por el pediatra austriaco Andreas Rett. El síndrome de Rett causa… (more)

Subjects/Keywords: Síndrome de Rett; Síndrome de Rett; Rett syndrome; Neurobiologia; Neurobiología; Neurobiology; Ciències de la Salut; 616.8

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APA (6th Edition):

Petazzi, P. (2015). Methyl-CpG binding protein 2 deregulation: from Rett syndrome to MeCP2 duplication disorder. (Thesis). Universitat de Barcelona. Retrieved from http://hdl.handle.net/10803/396242

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):

Petazzi, Paolo. “Methyl-CpG binding protein 2 deregulation: from Rett syndrome to MeCP2 duplication disorder.” 2015. Thesis, Universitat de Barcelona. Accessed August 24, 2019. http://hdl.handle.net/10803/396242.

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

MLA Handbook (7th Edition):

Petazzi, Paolo. “Methyl-CpG binding protein 2 deregulation: from Rett syndrome to MeCP2 duplication disorder.” 2015. Web. 24 Aug 2019.

Vancouver:

Petazzi P. Methyl-CpG binding protein 2 deregulation: from Rett syndrome to MeCP2 duplication disorder. [Internet] [Thesis]. Universitat de Barcelona; 2015. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/10803/396242.

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

Council of Science Editors:

Petazzi P. Methyl-CpG binding protein 2 deregulation: from Rett syndrome to MeCP2 duplication disorder. [Thesis]. Universitat de Barcelona; 2015. Available from: http://hdl.handle.net/10803/396242

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


Universidade Presbiteriana Mackenzie

13. Renata de Lima Velloso. Reconhecimento dos conceitos de forma, cor, tamanho e posição em 10 crianças com Síndrome de Rett.

Degree: 2008, Universidade Presbiteriana Mackenzie

Crianças com Síndrome de Rett (SR) apresentam regressão progressiva do desenvolvimento psicomotor e das habilidades de linguagem verbal e perda das habilidades manuais voluntárias, o… (more)

Subjects/Keywords: cognição; visual tracking; cognition; rastreamento visual; Rett syndrome; PSICOLOGIA; síndrome de Rett

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APA (6th Edition):

Velloso, R. d. L. (2008). Reconhecimento dos conceitos de forma, cor, tamanho e posição em 10 crianças com Síndrome de Rett. (Thesis). Universidade Presbiteriana Mackenzie. Retrieved from http://tede.mackenzie.com.br//tde_busca/arquivo.php?codArquivo=725

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):

Velloso, Renata de Lima. “Reconhecimento dos conceitos de forma, cor, tamanho e posição em 10 crianças com Síndrome de Rett.” 2008. Thesis, Universidade Presbiteriana Mackenzie. Accessed August 24, 2019. http://tede.mackenzie.com.br//tde_busca/arquivo.php?codArquivo=725.

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

MLA Handbook (7th Edition):

Velloso, Renata de Lima. “Reconhecimento dos conceitos de forma, cor, tamanho e posição em 10 crianças com Síndrome de Rett.” 2008. Web. 24 Aug 2019.

Vancouver:

Velloso RdL. Reconhecimento dos conceitos de forma, cor, tamanho e posição em 10 crianças com Síndrome de Rett. [Internet] [Thesis]. Universidade Presbiteriana Mackenzie; 2008. [cited 2019 Aug 24]. Available from: http://tede.mackenzie.com.br//tde_busca/arquivo.php?codArquivo=725.

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

Council of Science Editors:

Velloso RdL. Reconhecimento dos conceitos de forma, cor, tamanho e posição em 10 crianças com Síndrome de Rett. [Thesis]. Universidade Presbiteriana Mackenzie; 2008. Available from: http://tede.mackenzie.com.br//tde_busca/arquivo.php?codArquivo=725

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


Universidade Presbiteriana Mackenzie

14. Cristiane Amorosino. Estudo do olhar com intenção comunicativa e vocabulário receptivo de meninas com síndrome de Rett através do instrumento Eyegaze.

Degree: 2006, Universidade Presbiteriana Mackenzie

A Síndrome de Rett (SR) foi descrita pela primeira vez por Andreas Rett (1966). Caracteriza-se por uma desordem neurobiológica que afeta preferentemente o sexo feminino.… (more)

Subjects/Keywords: Síndrome de Rett; vocabulário receptivo; comunicação; Eyegaze; Rett Syndrome; receptive vocabulary; communication; Eyegaze; CLINICA MEDICA

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APA (6th Edition):

Amorosino, C. (2006). Estudo do olhar com intenção comunicativa e vocabulário receptivo de meninas com síndrome de Rett através do instrumento Eyegaze. (Thesis). Universidade Presbiteriana Mackenzie. Retrieved from http://tede.mackenzie.com.br//tde_busca/arquivo.php?codArquivo=8

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):

Amorosino, Cristiane. “Estudo do olhar com intenção comunicativa e vocabulário receptivo de meninas com síndrome de Rett através do instrumento Eyegaze.” 2006. Thesis, Universidade Presbiteriana Mackenzie. Accessed August 24, 2019. http://tede.mackenzie.com.br//tde_busca/arquivo.php?codArquivo=8.

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

MLA Handbook (7th Edition):

Amorosino, Cristiane. “Estudo do olhar com intenção comunicativa e vocabulário receptivo de meninas com síndrome de Rett através do instrumento Eyegaze.” 2006. Web. 24 Aug 2019.

Vancouver:

Amorosino C. Estudo do olhar com intenção comunicativa e vocabulário receptivo de meninas com síndrome de Rett através do instrumento Eyegaze. [Internet] [Thesis]. Universidade Presbiteriana Mackenzie; 2006. [cited 2019 Aug 24]. Available from: http://tede.mackenzie.com.br//tde_busca/arquivo.php?codArquivo=8.

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

Council of Science Editors:

Amorosino C. Estudo do olhar com intenção comunicativa e vocabulário receptivo de meninas com síndrome de Rett através do instrumento Eyegaze. [Thesis]. Universidade Presbiteriana Mackenzie; 2006. Available from: http://tede.mackenzie.com.br//tde_busca/arquivo.php?codArquivo=8

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


University of Vienna

15. Schönegger, Anna Katharina. Development of an ECLIA based assay for MeCP2 protein.

Degree: 2017, University of Vienna

Hintergrund: Das Rett Syndrom ist eine schwere, neurologische Entwicklungsstörung, die bei Mädchen mit einer Prävalenz von 1:10.000 auftritt. Als Ursache für diese Erkrankung wurde eine… (more)

Subjects/Keywords: 30.99 Naturwissenschaften allgemein: Sonstiges; Rett Syndrom / MeCP2 / ECLIA; Rett syndrome / MeCP2 / ECLIA

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APA (6th Edition):

Schönegger, A. K. (2017). Development of an ECLIA based assay for MeCP2 protein. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/47114/

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):

Schönegger, Anna Katharina. “Development of an ECLIA based assay for MeCP2 protein.” 2017. Thesis, University of Vienna. Accessed August 24, 2019. http://othes.univie.ac.at/47114/.

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

MLA Handbook (7th Edition):

Schönegger, Anna Katharina. “Development of an ECLIA based assay for MeCP2 protein.” 2017. Web. 24 Aug 2019.

Vancouver:

Schönegger AK. Development of an ECLIA based assay for MeCP2 protein. [Internet] [Thesis]. University of Vienna; 2017. [cited 2019 Aug 24]. Available from: http://othes.univie.ac.at/47114/.

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

Council of Science Editors:

Schönegger AK. Development of an ECLIA based assay for MeCP2 protein. [Thesis]. University of Vienna; 2017. Available from: http://othes.univie.ac.at/47114/

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


University of Edinburgh

16. Ekiert, Robert. Analysis of partner proteins of MeCP2 and their relevance to Rett syndrome.

Degree: PhD, 2012, University of Edinburgh

 Methyl-CpG binding protein 2 (MeCP2) was discovered as a protein binding to methylated DNA more than 20 years ago. It is very abundant in the… (more)

Subjects/Keywords: 572.8; MeCP2; Methyl-CpG binding protein 2; Rett syndrome; epigenetics

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APA (6th Edition):

Ekiert, R. (2012). Analysis of partner proteins of MeCP2 and their relevance to Rett syndrome. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/9901

Chicago Manual of Style (16th Edition):

Ekiert, Robert. “Analysis of partner proteins of MeCP2 and their relevance to Rett syndrome.” 2012. Doctoral Dissertation, University of Edinburgh. Accessed August 24, 2019. http://hdl.handle.net/1842/9901.

MLA Handbook (7th Edition):

Ekiert, Robert. “Analysis of partner proteins of MeCP2 and their relevance to Rett syndrome.” 2012. Web. 24 Aug 2019.

Vancouver:

Ekiert R. Analysis of partner proteins of MeCP2 and their relevance to Rett syndrome. [Internet] [Doctoral dissertation]. University of Edinburgh; 2012. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1842/9901.

Council of Science Editors:

Ekiert R. Analysis of partner proteins of MeCP2 and their relevance to Rett syndrome. [Doctoral Dissertation]. University of Edinburgh; 2012. Available from: http://hdl.handle.net/1842/9901


UCLA

17. Ohashi, Minori. Modeling Rett Syndrome with Human Induced Pluripotent Stem Cells.

Degree: Molecular Biology, 2017, UCLA

Rett syndrome is a neurodevelopmental disorder that predominately affects females and is one of the most common causes of intellectual disability in females. The syndrome(more)

Subjects/Keywords: Molecular biology; Neurosciences; disease modeling; iPSC; Rett syndrome; telomere

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APA (6th Edition):

Ohashi, M. (2017). Modeling Rett Syndrome with Human Induced Pluripotent Stem Cells. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/6658h6r9

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):

Ohashi, Minori. “Modeling Rett Syndrome with Human Induced Pluripotent Stem Cells.” 2017. Thesis, UCLA. Accessed August 24, 2019. http://www.escholarship.org/uc/item/6658h6r9.

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

MLA Handbook (7th Edition):

Ohashi, Minori. “Modeling Rett Syndrome with Human Induced Pluripotent Stem Cells.” 2017. Web. 24 Aug 2019.

Vancouver:

Ohashi M. Modeling Rett Syndrome with Human Induced Pluripotent Stem Cells. [Internet] [Thesis]. UCLA; 2017. [cited 2019 Aug 24]. Available from: http://www.escholarship.org/uc/item/6658h6r9.

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

Council of Science Editors:

Ohashi M. Modeling Rett Syndrome with Human Induced Pluripotent Stem Cells. [Thesis]. UCLA; 2017. Available from: http://www.escholarship.org/uc/item/6658h6r9

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

18. SHOVLIN, STEPHEN. The molecular determinant of IGF-1(Mecasermin)action in Rett Syndrome Patients.

Degree: School of Medicine. Discipline of Psychiatry, 2018, Trinity College Dublin

 Abstract This is a preliminary investigation of effects of insulin-like growth factor-1 (IGF-1) treatment on differential gene expression (DGE) of whole blood samples from Rett(more)

Subjects/Keywords: Rett syndrome; IGF-1; Mecasermin; Differential Gene Expression

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APA (6th Edition):

SHOVLIN, S. (2018). The molecular determinant of IGF-1(Mecasermin)action in Rett Syndrome Patients. (Thesis). Trinity College Dublin. Retrieved from http://hdl.handle.net/2262/85441

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):

SHOVLIN, STEPHEN. “The molecular determinant of IGF-1(Mecasermin)action in Rett Syndrome Patients.” 2018. Thesis, Trinity College Dublin. Accessed August 24, 2019. http://hdl.handle.net/2262/85441.

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

MLA Handbook (7th Edition):

SHOVLIN, STEPHEN. “The molecular determinant of IGF-1(Mecasermin)action in Rett Syndrome Patients.” 2018. Web. 24 Aug 2019.

Vancouver:

SHOVLIN S. The molecular determinant of IGF-1(Mecasermin)action in Rett Syndrome Patients. [Internet] [Thesis]. Trinity College Dublin; 2018. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/2262/85441.

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

Council of Science Editors:

SHOVLIN S. The molecular determinant of IGF-1(Mecasermin)action in Rett Syndrome Patients. [Thesis]. Trinity College Dublin; 2018. Available from: http://hdl.handle.net/2262/85441

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


Montana Tech

19. Henighan, Carol. Speech-language abilities in Rett syndrome.

Degree: MCSD, 1987, Montana Tech

Subjects/Keywords: Rett syndrome.; Language acquisition.

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

APA (6th Edition):

Henighan, C. (1987). Speech-language abilities in Rett syndrome. (Thesis). Montana Tech. Retrieved from https://scholarworks.umt.edu/etd/8882

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):

Henighan, Carol. “Speech-language abilities in Rett syndrome.” 1987. Thesis, Montana Tech. Accessed August 24, 2019. https://scholarworks.umt.edu/etd/8882.

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

MLA Handbook (7th Edition):

Henighan, Carol. “Speech-language abilities in Rett syndrome.” 1987. Web. 24 Aug 2019.

Vancouver:

Henighan C. Speech-language abilities in Rett syndrome. [Internet] [Thesis]. Montana Tech; 1987. [cited 2019 Aug 24]. Available from: https://scholarworks.umt.edu/etd/8882.

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

Council of Science Editors:

Henighan C. Speech-language abilities in Rett syndrome. [Thesis]. Montana Tech; 1987. Available from: https://scholarworks.umt.edu/etd/8882

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


Clemson University

20. Wells, Jared J. A Sensor Based Approach to Analyzing Motion in Medical Applications: AV Fistula Cannulation and Rett Syndrome.

Degree: MS, Bioengineering, 2018, Clemson University

 Sensor based motion analysis is employed to assess frequency, severity and duration of Rett syndrome hand stereotypies as well as soft tissue palpation of an… (more)

Subjects/Keywords: Cannulation; Hand Stereotypies; Leap Motion Controller; Palpation; Rett Syndrome; Sensors

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APA (6th Edition):

Wells, J. J. (2018). A Sensor Based Approach to Analyzing Motion in Medical Applications: AV Fistula Cannulation and Rett Syndrome. (Masters Thesis). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_theses/2890

Chicago Manual of Style (16th Edition):

Wells, Jared J. “A Sensor Based Approach to Analyzing Motion in Medical Applications: AV Fistula Cannulation and Rett Syndrome.” 2018. Masters Thesis, Clemson University. Accessed August 24, 2019. https://tigerprints.clemson.edu/all_theses/2890.

MLA Handbook (7th Edition):

Wells, Jared J. “A Sensor Based Approach to Analyzing Motion in Medical Applications: AV Fistula Cannulation and Rett Syndrome.” 2018. Web. 24 Aug 2019.

Vancouver:

Wells JJ. A Sensor Based Approach to Analyzing Motion in Medical Applications: AV Fistula Cannulation and Rett Syndrome. [Internet] [Masters thesis]. Clemson University; 2018. [cited 2019 Aug 24]. Available from: https://tigerprints.clemson.edu/all_theses/2890.

Council of Science Editors:

Wells JJ. A Sensor Based Approach to Analyzing Motion in Medical Applications: AV Fistula Cannulation and Rett Syndrome. [Masters Thesis]. Clemson University; 2018. Available from: https://tigerprints.clemson.edu/all_theses/2890


Brandeis University

21. Delaney, Christine. The Impact of Genetic Testing for Rett Syndrome: An Assessment of Parents' Experiences.

Degree: 2011, Brandeis University

Rett syndrome (RTT) is an X-linked disorder diagnosed either clinically or with genetic testing. Approximately 60% of girls with RTT have had genetic testing, most… (more)

Subjects/Keywords: genetic diagnosis; clinical diagnosis; genetic testing; parents; Rett syndrome

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APA (6th Edition):

Delaney, C. (2011). The Impact of Genetic Testing for Rett Syndrome: An Assessment of Parents' Experiences. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/24398

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):

Delaney, Christine. “The Impact of Genetic Testing for Rett Syndrome: An Assessment of Parents' Experiences.” 2011. Thesis, Brandeis University. Accessed August 24, 2019. http://hdl.handle.net/10192/24398.

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

MLA Handbook (7th Edition):

Delaney, Christine. “The Impact of Genetic Testing for Rett Syndrome: An Assessment of Parents' Experiences.” 2011. Web. 24 Aug 2019.

Vancouver:

Delaney C. The Impact of Genetic Testing for Rett Syndrome: An Assessment of Parents' Experiences. [Internet] [Thesis]. Brandeis University; 2011. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/10192/24398.

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

Council of Science Editors:

Delaney C. The Impact of Genetic Testing for Rett Syndrome: An Assessment of Parents' Experiences. [Thesis]. Brandeis University; 2011. Available from: http://hdl.handle.net/10192/24398

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


University of Toronto

22. Lai, Wesley. MECP2e1 Mutation Reduces the Dendritic Complexity of Rett Syndrome Patient iPS Cell-derived Neurons.

Degree: 2014, University of Toronto

The gene MECP2 that is commonly mutated in Rett Syndrome (RTT) can be alternatively spliced in neurons into MeCP2e1 and MECP2e2 isoforms. Fibroblasts from a… (more)

Subjects/Keywords: dendrite complexity; induced pluripotent stem cells; MECP2e1; Ngn2; Rett Syndrome; 0369

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APA (6th Edition):

Lai, W. (2014). MECP2e1 Mutation Reduces the Dendritic Complexity of Rett Syndrome Patient iPS Cell-derived Neurons. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/67925

Chicago Manual of Style (16th Edition):

Lai, Wesley. “MECP2e1 Mutation Reduces the Dendritic Complexity of Rett Syndrome Patient iPS Cell-derived Neurons.” 2014. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/67925.

MLA Handbook (7th Edition):

Lai, Wesley. “MECP2e1 Mutation Reduces the Dendritic Complexity of Rett Syndrome Patient iPS Cell-derived Neurons.” 2014. Web. 24 Aug 2019.

Vancouver:

Lai W. MECP2e1 Mutation Reduces the Dendritic Complexity of Rett Syndrome Patient iPS Cell-derived Neurons. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/67925.

Council of Science Editors:

Lai W. MECP2e1 Mutation Reduces the Dendritic Complexity of Rett Syndrome Patient iPS Cell-derived Neurons. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/67925


University of Toronto

23. Lang, Min. Ubiquitous Reactivation and Targeted Preservation of MeCP2 Expression in a Mouse Model of Rett Syndrome.

Degree: 2012, University of Toronto

Rett syndrome is a neurodevelopmental disorder that is predominately caused by mutations of the MECP2 gene. As neuronal apoptosis is not observed in RTT patients… (more)

Subjects/Keywords: Rett syndrome; MeCP2; behaviour; electroencephalography; catecholamine; thermoregulation; daily rhythmic activity; 0719

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APA (6th Edition):

Lang, M. (2012). Ubiquitous Reactivation and Targeted Preservation of MeCP2 Expression in a Mouse Model of Rett Syndrome. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33301

Chicago Manual of Style (16th Edition):

Lang, Min. “Ubiquitous Reactivation and Targeted Preservation of MeCP2 Expression in a Mouse Model of Rett Syndrome.” 2012. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/33301.

MLA Handbook (7th Edition):

Lang, Min. “Ubiquitous Reactivation and Targeted Preservation of MeCP2 Expression in a Mouse Model of Rett Syndrome.” 2012. Web. 24 Aug 2019.

Vancouver:

Lang M. Ubiquitous Reactivation and Targeted Preservation of MeCP2 Expression in a Mouse Model of Rett Syndrome. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/33301.

Council of Science Editors:

Lang M. Ubiquitous Reactivation and Targeted Preservation of MeCP2 Expression in a Mouse Model of Rett Syndrome. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33301


University of Manitoba

24. Batuwita Liyanage, Vichithra Rasangi. Intrinsic and extrinsic regulation of MeCP2 in brain cell types and their implications in MeCP2-related neurodevelopmental disorders.

Degree: Biochemistry and Medical Genetics, 2013, University of Manitoba

 MeCP2 is a key epigenetic regulator in the brain, which regulates gene expression. There are two Mecp2/MeCP2 isoforms - MeCP2E1 and MeCP2E2 - with both… (more)

Subjects/Keywords: MeCP2; DNA methylation; Epigenetics; FASD; Rett syndrome; Autism; MeCP2 isoforms; Alcohol

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APA (6th Edition):

Batuwita Liyanage, V. R. (2013). Intrinsic and extrinsic regulation of MeCP2 in brain cell types and their implications in MeCP2-related neurodevelopmental disorders. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/32732

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):

Batuwita Liyanage, Vichithra Rasangi. “Intrinsic and extrinsic regulation of MeCP2 in brain cell types and their implications in MeCP2-related neurodevelopmental disorders.” 2013. Thesis, University of Manitoba. Accessed August 24, 2019. http://hdl.handle.net/1993/32732.

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

MLA Handbook (7th Edition):

Batuwita Liyanage, Vichithra Rasangi. “Intrinsic and extrinsic regulation of MeCP2 in brain cell types and their implications in MeCP2-related neurodevelopmental disorders.” 2013. Web. 24 Aug 2019.

Vancouver:

Batuwita Liyanage VR. Intrinsic and extrinsic regulation of MeCP2 in brain cell types and their implications in MeCP2-related neurodevelopmental disorders. [Internet] [Thesis]. University of Manitoba; 2013. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1993/32732.

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

Council of Science Editors:

Batuwita Liyanage VR. Intrinsic and extrinsic regulation of MeCP2 in brain cell types and their implications in MeCP2-related neurodevelopmental disorders. [Thesis]. University of Manitoba; 2013. Available from: http://hdl.handle.net/1993/32732

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


University of Manitoba

25. Pejhan, Shervin. Investigating the MeCP2 (E1/E2) regulatory network in the human control and Rett syndrome brain.

Degree: Biochemistry and Medical Genetics, 2018, University of Manitoba

Rett Syndrome (RTT) is a neurodevelopmental disorder characterized by neurological regression and autism spectrum features, usually in females with mutation in MECP2. Animal and cell… (more)

Subjects/Keywords: MECP2 mutations; Rett syndrome; MeCP2 isoforms; BDNF; miR132; Epigenetics

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APA (6th Edition):

Pejhan, S. (2018). Investigating the MeCP2 (E1/E2) regulatory network in the human control and Rett syndrome brain. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/33663

Chicago Manual of Style (16th Edition):

Pejhan, Shervin. “Investigating the MeCP2 (E1/E2) regulatory network in the human control and Rett syndrome brain.” 2018. Masters Thesis, University of Manitoba. Accessed August 24, 2019. http://hdl.handle.net/1993/33663.

MLA Handbook (7th Edition):

Pejhan, Shervin. “Investigating the MeCP2 (E1/E2) regulatory network in the human control and Rett syndrome brain.” 2018. Web. 24 Aug 2019.

Vancouver:

Pejhan S. Investigating the MeCP2 (E1/E2) regulatory network in the human control and Rett syndrome brain. [Internet] [Masters thesis]. University of Manitoba; 2018. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1993/33663.

Council of Science Editors:

Pejhan S. Investigating the MeCP2 (E1/E2) regulatory network in the human control and Rett syndrome brain. [Masters Thesis]. University of Manitoba; 2018. Available from: http://hdl.handle.net/1993/33663


University of Toronto

26. Popescu, Andreea. Pharmacological Rescue of Nonsense Mutations in Rett Syndrome.

Degree: 2009, University of Toronto

Rett syndrome is a neurological condition that affects primarily girls. Approximately 40% of Rett syndrome cases arise from nonsense mutations. Several studies have shown that… (more)

Subjects/Keywords: Rett syndrome; aminoglycosides; MeCP2; 0719

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APA (6th Edition):

Popescu, A. (2009). Pharmacological Rescue of Nonsense Mutations in Rett Syndrome. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/18985

Chicago Manual of Style (16th Edition):

Popescu, Andreea. “Pharmacological Rescue of Nonsense Mutations in Rett Syndrome.” 2009. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/18985.

MLA Handbook (7th Edition):

Popescu, Andreea. “Pharmacological Rescue of Nonsense Mutations in Rett Syndrome.” 2009. Web. 24 Aug 2019.

Vancouver:

Popescu A. Pharmacological Rescue of Nonsense Mutations in Rett Syndrome. [Internet] [Masters thesis]. University of Toronto; 2009. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/18985.

Council of Science Editors:

Popescu A. Pharmacological Rescue of Nonsense Mutations in Rett Syndrome. [Masters Thesis]. University of Toronto; 2009. Available from: http://hdl.handle.net/1807/18985


Michigan State University

27. Houtaling, Carolyn M. Music and Rett syndrome : a survey from the parental perspective.

Degree: M.M. in Music Therapy, School of Music, 2003, Michigan State University

Subjects/Keywords: Rett syndrome; Music therapy

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APA (6th Edition):

Houtaling, C. M. (2003). Music and Rett syndrome : a survey from the parental perspective. (Masters Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:31990

Chicago Manual of Style (16th Edition):

Houtaling, Carolyn M. “Music and Rett syndrome : a survey from the parental perspective.” 2003. Masters Thesis, Michigan State University. Accessed August 24, 2019. http://etd.lib.msu.edu/islandora/object/etd:31990.

MLA Handbook (7th Edition):

Houtaling, Carolyn M. “Music and Rett syndrome : a survey from the parental perspective.” 2003. Web. 24 Aug 2019.

Vancouver:

Houtaling CM. Music and Rett syndrome : a survey from the parental perspective. [Internet] [Masters thesis]. Michigan State University; 2003. [cited 2019 Aug 24]. Available from: http://etd.lib.msu.edu/islandora/object/etd:31990.

Council of Science Editors:

Houtaling CM. Music and Rett syndrome : a survey from the parental perspective. [Masters Thesis]. Michigan State University; 2003. Available from: http://etd.lib.msu.edu/islandora/object/etd:31990


Georgia State University

28. Arrowood, Colin. GABAergic Inhibition of Brainstem Neurons Involved in Breathing Regulation is Disrupted in Rett Syndrome.

Degree: MS, Biology, 2019, Georgia State University

  GABA is the prominent inhibitory neurotransmitter in the brain and defects in the GABA system are attributable to several genetic diseases including Rett Syndrome(more)

Subjects/Keywords: Locus coeruleus; Optogenetics; Rett Syndrome; MEA; Microelectrode Array; Transgenic; In-vitro

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APA (6th Edition):

Arrowood, C. (2019). GABAergic Inhibition of Brainstem Neurons Involved in Breathing Regulation is Disrupted in Rett Syndrome. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/biology_theses/95

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):

Arrowood, Colin. “GABAergic Inhibition of Brainstem Neurons Involved in Breathing Regulation is Disrupted in Rett Syndrome.” 2019. Thesis, Georgia State University. Accessed August 24, 2019. https://scholarworks.gsu.edu/biology_theses/95.

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

MLA Handbook (7th Edition):

Arrowood, Colin. “GABAergic Inhibition of Brainstem Neurons Involved in Breathing Regulation is Disrupted in Rett Syndrome.” 2019. Web. 24 Aug 2019.

Vancouver:

Arrowood C. GABAergic Inhibition of Brainstem Neurons Involved in Breathing Regulation is Disrupted in Rett Syndrome. [Internet] [Thesis]. Georgia State University; 2019. [cited 2019 Aug 24]. Available from: https://scholarworks.gsu.edu/biology_theses/95.

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

Council of Science Editors:

Arrowood C. GABAergic Inhibition of Brainstem Neurons Involved in Breathing Regulation is Disrupted in Rett Syndrome. [Thesis]. Georgia State University; 2019. Available from: https://scholarworks.gsu.edu/biology_theses/95

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


University of Manchester

29. Handley, Louise. Movement disorders and catatonia-like presentations in rare genetic syndromes.

Degree: 2016, University of Manchester

 The prevalence of Autism Spectrum Disorder (ASD) and its defining features has been increasingly investigated in genetic syndromes associated with intellectual disability, with syndrome specific… (more)

Subjects/Keywords: genetic syndromes; intellectual disabilities; movement; catatonia; cornelia de lange syndrome; fragile x syndrome; angelman syndrome; rett syndrome

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APA (6th Edition):

Handley, L. (2016). Movement disorders and catatonia-like presentations in rare genetic syndromes. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:305214

Chicago Manual of Style (16th Edition):

Handley, Louise. “Movement disorders and catatonia-like presentations in rare genetic syndromes.” 2016. Doctoral Dissertation, University of Manchester. Accessed August 24, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:305214.

MLA Handbook (7th Edition):

Handley, Louise. “Movement disorders and catatonia-like presentations in rare genetic syndromes.” 2016. Web. 24 Aug 2019.

Vancouver:

Handley L. Movement disorders and catatonia-like presentations in rare genetic syndromes. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Aug 24]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:305214.

Council of Science Editors:

Handley L. Movement disorders and catatonia-like presentations in rare genetic syndromes. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:305214


University of Manchester

30. Handley, Louise. Movement disorders and catatonia-like presentations in rare genetic syndromes.

Degree: Thesis (D.Clin.Psy.), 2016, University of Manchester

 The prevalence of Autism Spectrum Disorder (ASD) and its defining features has been increasingly investigated in genetic syndromes associated with intellectual disability, with syndrome specific… (more)

Subjects/Keywords: rett syndrome; angelman syndrome; fragile x syndrome; cornelia de lange syndrome; intellectual disabilities; movement; genetic syndromes; catatonia

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APA (6th Edition):

Handley, L. (2016). Movement disorders and catatonia-like presentations in rare genetic syndromes. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/movement-disorders-and-catatonialike-presentations-in-rare-genetic-syndromes(581c9b5a-0681-4a14-8b49-35fecded2f55).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764403

Chicago Manual of Style (16th Edition):

Handley, Louise. “Movement disorders and catatonia-like presentations in rare genetic syndromes.” 2016. Doctoral Dissertation, University of Manchester. Accessed August 24, 2019. https://www.research.manchester.ac.uk/portal/en/theses/movement-disorders-and-catatonialike-presentations-in-rare-genetic-syndromes(581c9b5a-0681-4a14-8b49-35fecded2f55).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764403.

MLA Handbook (7th Edition):

Handley, Louise. “Movement disorders and catatonia-like presentations in rare genetic syndromes.” 2016. Web. 24 Aug 2019.

Vancouver:

Handley L. Movement disorders and catatonia-like presentations in rare genetic syndromes. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Aug 24]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/movement-disorders-and-catatonialike-presentations-in-rare-genetic-syndromes(581c9b5a-0681-4a14-8b49-35fecded2f55).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764403.

Council of Science Editors:

Handley L. Movement disorders and catatonia-like presentations in rare genetic syndromes. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/movement-disorders-and-catatonialike-presentations-in-rare-genetic-syndromes(581c9b5a-0681-4a14-8b49-35fecded2f55).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764403

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