Longitudinal community walking activity in Duchenne muscular dystrophy-Reference-Cited by-同舟云学术

Longitudinal community walking activity in Duchenne muscular dystrophy

Published:2017-07-28 Issue:3 Volume:57 Page:401-406
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Fowler Eileen G.¹,Staudt Loretta A.¹,Heberer Kent R.¹,Sienko Susan E.²,Buckon Cathleen E.²,Bagley Anita M.³,Sussman Michael D.²,McDonald Craig M.³⁴

Affiliation:

1. Department of Orthopaedic Surgery; University of California Los Angeles; 22-70 Rehab Center, 1000 Veteran Avenue, Los Angeles California 90095-1795 USA

2. Shriners Hospitals for Children Portland; Portland Oregon USA

3. Shriners Hospitals for Children Northern California; Sacramento California USA

4. University of California Davis Medical Center; Sacramento California USA

Funder

Shriners Hospitals for Children

Publisher

Wiley

Subject

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

Reference32 articles.

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3. The cooperative international neuromuscular research group Duchenne natural history study: glucocorticoid treatment preserves clinically meaningful functional milestones and reduces rate of disease progression as measured by manual muscle testing and other commonly used clinical trial outcome measures;Henricson;Muscle Nerve,2013

4. Corticosteroid treatment and functional improvement in Duchenne muscular dystrophy: long-term effect;Balaban;Am J Phys Med Rehabil,2005

5. Randomized, double-blind six-month trial of prednisone in Duchenne's muscular dystrophy;Mendell;N Engl J Med,1989

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