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Cited by 451

The DOI matches its Crossref record; 15 of the 15 references it cites were found in a registry or an index.

A clinical review

Siegel, Irwin M.·1978·Muscle & Nerve

Abstract

The optimal management of muscular dystrophy is multidisciplinary and aggressive in nature. Serial assessment aids in determining the functional stage of the disease and in indicating specific therapies. Physical therapy can augment strength through exercise and relieve contracture through passive stretching. Occupational therapy is employed to help the patient manage his activities of daily living within the restrictions imposed on him by his disease. Progressive disability can be delayed through a variety of physiatric and orthopedic techniques, including surgical release of lower‐extremity contracture, repair of foot and ankle deformity, and correction of scoliosis. Appropriate orthoses are available, as are a variety of special devices to facilitate ongoing care for postambulatory patients. Physicians treating the muscular dystrophies should be aware of the complications of these diseases, particularly cardiomyopathy, pulmonary failure, and psychological and social problems.

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Metadata

Authors
Siegel, I. M.
Venue
Muscle & Nerve
Publisher
Wiley
Published
1978-11
Volume
1
Issue
6
Pages
453-460
ISSN
  • 0148-639X (ISSN-L)
  • 1097-4598
OpenAlex
W2063816661
Cited by
451
References
15
FWCI
2.15
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: A clinical review. https://app.cochat.ai/papers/10.1002/mus.880010603
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Siegel, I. M. (1978). A clinical review. Muscle & Nerve. https://doi.org/10.1002/mus.880010603

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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