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Articles (8)

Journals (0)

1-8 of 8 results for sarcoglycanopathy

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Select article: Sarcoglycanopathies: From clinical diagnosis to new promising therapies

Open access

Review article

First published 2025-7

Sarcoglycanopathies: From clinical diagnosis to new promising therapies

Holly Borland, Jordi Diaz-Manera

Journal of Neuromuscular Diseases

Select article: γ-Sarcoglycanopathy in Two Palestinian-American Siblings

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Other

First published 2001-02

γ-Sarcoglycanopathy in Two Palestinian-American Siblings

Sergio R. Russo Buzzini, Carol Macmillan

Clinical Pediatrics

Select article: Skin Biopsy

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Research article

First published 2014-8

Skin Biopsy

Biswaroop Chakrabarty, M.C. Sharma, Sheffali Gulati [...]

Journal of Child Neurology

Select article: A Pediatric Neurologist's Clinical Experiences in Saudi Arabia

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Other

First published 2005-03

A Pediatric Neurologist's Clinical Experiences in Saudi Arabia

Enrique Chaves-Carballo

Journal of Child Neurology

Select article: Pharmacokinetic and Pharmacodynamic Evaluation of Bidridistrogene Xeboparvovec in an Aged Murine Model of Limb-Girdle Muscular Dystrophy Type 2E/R4

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Research article

First published 2026-2

Pharmacokinetic and Pharmacodynamic Evaluation of Bidridistrogene Xeboparvovec in an Aged Murine Model of Limb-Girdle Muscular Dystrophy Type 2E/R4

Stephen Baine, Jared Cui, Young-Eun Seo [...]

Human Gene Therapy

Select article: Delivery of α - and β -Sarcoglycan by Recombinant Adeno-Associated Virus: Efficient Rescue of Muscle,but Differential Toxicity

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Research article

First published 2002-09

Delivery of α - and β -Sarcoglycan by Recombinant Adeno-Associated Virus: Efficient Rescue of Muscle,but Differential Toxicity

D. Dressman, K. Araishi, M. Imamura [...]

Human Gene Therapy

Select article: Carrier Frequency of the c.525delT Mutation in the SGCG Gene and Estimated Prevalence of Limb Girdle Muscular Dystrophy Type 2C Among the Moroccan Population

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Research article

First published 2014-04

Carrier Frequency of the c.525delT Mutation in the SGCG Gene and Estimated Prevalence of Limb Girdle Muscular Dystrophy Type 2C Among the Moroccan Population

Fatiha El Kerch, Ilham Ratbi, Aziza Sbiti [...]

Genetic Testing and Molecular Biomarkers

Select article: Elucidation of the Genetic Cause in Dutch Limb Girdle Muscular Dystrophy Families: A 27-Year’s Journey

Open access

Research article

First published 2021-03-02

Elucidation of the Genetic Cause in Dutch Limb Girdle Muscular Dystrophy Families: A 27-Year’s Journey

L. ten Dam, M. de Visser, Ieke B. Ginjaar [...]

Journal of Neuromuscular Diseases

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