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A. Shahein

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ZINCARE

R. Roda

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Muscular Dystrophy Association

C. 'Chris' Weihl

Non-Dystrophin Muscular Dystrophies: Gene Variants & Clinical Featur…

ZINCARE

D. Leung

Enhancing Glycosylation With Ribitol for Treating LGMD2I: A Metaboli…

Muscular Dystrophy Association

Q. Lu

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The France Foundation

P. B. Kang

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The France Foundation

C. D. Zingariello

Upcoming Therapies for LGMD

The France Foundation

J. Brandsema, A. Veerapandiyan

Pathogenesis and Therapeutics of Calpainopathy (LGMDR1/2A)

Muscular Dystrophy Association

M. Spencer

Case Discussion: DMD

The France Foundation

C. Proud, A. Veerapandiyan, C. Mcdonald

DMD Management in the Era of Gene Therapy

The France Foundation

A. Veerapandiyan, C. Zaidman

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Impact of Combination Therapies and Exercise Programs for Neuromuscu…

The France Foundation

A. Veerapandiyan, J. Brandsema, L. Servais

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The France Foundation

H. Abdel-Hamid, A. Veerapandiyan

Emerging Therapies for Neuromuscular Diseases in 2021: ALS, Dystroph…

Houston Methodist

E. Greene

Approach to a Child with Delayed Walking

UCSF School of Medicine

Y. Mitsuya

The Technology Will See You Now: Digital Endpoints and AI Applicatio…

Henry J. Kaminski

Cell-Based Therapies for Neuromuscular Diseases

Houston Methodist

B. Liao

Principles of AAV Gene Therapy for Inherited Neurological Disorders:…

American Neurological Association

S. G. Kaler, B. Traynor

Newborn Screening for Duchenne Muscular Dystrophy

United Scientific Group

R. Rodney Howell