Strength training in patients with myotonic dystrophy and hereditary motor and sensory neuropathy: A randomized clinical trial-Reference-Cited by-同舟云学术

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Strength training in patients with myotonic dystrophy and hereditary motor and sensory neuropathy: A randomized clinical trial

Published:1995-07 Issue:7 Volume:76 Page:612-620
ISSN:0003-9993
Container-title:Archives of Physical Medicine and Rehabilitation
language:en
Short-container-title:Archives of Physical Medicine and Rehabilitation

Author:

Lindeman Eline,Leffers Pieter,Spaans Frank,Drukker Jan,Reulen Jos,Kerckhoffs Maria,Köke Albere

Publisher

Elsevier BV

Subject

Rehabilitation,Physical Therapy, Sports Therapy and Rehabilitation

Reference59 articles.

1. Physical models of rehabilitation in neuromuscular disease;Vignos;Muscle Nerve,1983

2. Exercise in neuromuscular disease: Statement of the problem;Vignos,1984

3. Management of musculoskeletal complications in neuromuscular diseases: weakness and the role of exercise;Fowler;Physic Med Rehabil: STARs,1988

4. The effect of exercise in muscular dystrophy;Vignos;JAMA,1966

5. Effect on maximal strength of submaximal exercises in Duchenne muscular dystrophy;deLateur;Am J Phys Med,1979

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1. Changes in Physiopathological Markers in Myotonic Dystrophy Type 1 Skeletal Muscle: A 3-Year Follow-up Study;Journal of Neuromuscular Diseases;2024-09-03

2. Physiotherapeutic Interventions for Patients With Rare Genetic Muscle-Wasting Disorders: A Systematic Review and Meta-Analysis;Cureus;2024-08-07

3. Decreased and Improved Movement Abilities in a Case of Myotonic Dystrophy Type 1: Examining Longitudinal Characteristics Based on Repeated Evaluations;Cureus;2024-05-21

4. Telecoaching: a potential new training model for Charcot-Marie-Tooth patients: a systematic review;Frontiers in Neurology;2024-05-09

5. Myotone Dystrophien, nichtdystrophe Myotonien und periodische Paralysen;DGNeurologie;2024-04-18

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