Twenty-year follow-up of newborn screening for patients with muscular dystrophy-Reference-Cited by-同舟云学术

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Twenty-year follow-up of newborn screening for patients with muscular dystrophy

Published:2015-09-10 Issue:4 Volume:53 Page:570-578
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Chung Jeffrey¹,Smith Andrea L.¹,Hughes Sarah C.¹,Niizawa Gabriela¹,Abdel-Hamid Hoda Z.²,Naylor Edwin W.³,Hughes Timothy⁴,Clemens Paula R.¹⁵

Affiliation:

1. Department of Neurology; University of Pittsburgh, S520 Biomedical Science Tower; 200 Lothrop Street Pittsburgh Pennsylvania 15213 USA

2. Department of Pediatrics; University of Pittsburgh; Pittsburgh Pennsylvania USA

3. Department of Pediatrics, Medical University of South Carolina; Charleston South Carolina USA

4. Department of Internal Medicine, School of Medicine; Wake Forest University; Winston-Salem North Carolina USA

5. Neurology Service, Department of Veterans Affairs Medical Center; Pittsburgh Pennsylvania USA

Funder

BioChem Genetics, LLC

U.S. Department of Health and Human Services to the University of Utah

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Reference26 articles.

1. A systematic review and meta-analysis on the epidemiology of Duchenne and Becker muscular dystrophy;Mah;Neuromuscul Disord,2014

2. Function and genetics of dystrophin and dystrophin-related proteins in muscle;Blake;Physiol Rev,2002

3. Delayed diagnosis in Duchenne muscular dystrophy: data from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet);Ciafaloni;J Pediatr,2009

4. Failure of early diagnosis in symptomatic Duchenne muscular dystrophy;Bushby;Lancet,1999

5. Dystrophin and mutations: one gene, several proteins, multiple phenotypes;Muntoni;Lancet Neurol,2003

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