Motor Function Measure: Validation of a Short Form for Young Children With Neuromuscular Diseases-Reference-Cited by-同舟云学术

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Motor Function Measure: Validation of a Short Form for Young Children With Neuromuscular Diseases

Published:2013-11 Issue:11 Volume:94 Page:2218-2226
ISSN:0003-9993
Container-title:Archives of Physical Medicine and Rehabilitation
language:en
Short-container-title:Archives of Physical Medicine and Rehabilitation

Author:

de Lattre Capucine,Payan Christine,Vuillerot Carole,Rippert Pascal,de Castro Denis,Bérard Carole,Poirot Isabelle

Publisher

Elsevier BV

Subject

Rehabilitation,Physical Therapy, Sports Therapy and Rehabilitation

Reference27 articles.

1. Reliability of 4 outcome measures in pediatric spinal muscular atrophy;Iannaccone;Arch Neurol,2003

2. Current methodological issues in the study of children with inherited neuromuscular disorders;Mercuri;Dev Med Child Neurol,2008

3. Quantitation of muscle function in children: a prospective study in Duchenne muscular dystrophy;Scott;Muscle Nerve,1982

4. Prospective study of spinal muscular atrophy before age 6 years. DCN/SMA Group;Iannaccone;Pediatr Neurol,1993

5. Clinical trial in Duchenne dystrophy. I. The design of the protocol;Brooke;Muscle Nerve,1981

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1. Relationship Between Hand Strength and Function in Duchenne Muscular Dystrophy and Spinal Muscular Atrophy: Implications for Clinical Trials;Journal of Neuromuscular Diseases;2024-07-02

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3. Association between protein intake and muscle wasting in critically ill children: A prospective cohort study;Journal of Parenteral and Enteral Nutrition;2024-03-30

4. Correlations between clinical motor scores and CMAP in patients with type 2 spinal muscular amyotrophy treated with nusinersen;Archives de Pédiatrie;2024-01

5. Nusinersen demonstrates effectiveness in treating spinal muscular atrophy: findings from a three-year nationwide study in Korea;Frontiers in Neurology;2023-12-20

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