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Cited by 431

The DOI matches its Crossref record; 77 of the 77 references it cites were found in a registry or an index.

Rhabdomyolysis: A review

Warren, Jason D., Blumbergs, Peter C., Thompson, Philip D.·2002·Muscle & Nerve

Abstract

Rhabdomyolysis, a syndrome of skeletal muscle breakdown with leakage of muscle contents, is frequently accompanied by myoglobinuria, and if sufficiently severe, acute renal failure with potentially life‐threatening metabolic derangements may ensue. A diverse spectrum of inherited and acquired disorders affecting muscle membranes, membrane ion channels, and muscle energy supply causes rhabdomyolysis. Common final pathophysiological mechanisms among these causes of rhabdomyolysis include an uncontrolled rise in free intracellular calcium and activation of calcium‐dependent proteases, which lead to destruction of myofibrils and lysosomal digestion of muscle fiber contents. Recent advances in molecular genetics and muscle enzyme histochemistry may enable a specific metabolic diagnosis in many patients with idiopathic recurrent rhabdomyolysis. © 2002 Wiley Periodicals, Inc. Muscle Nerve 25: 000–000, 2002

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Metadata

Authors
Warren, J. D., Blumbergs, P. C., & Thompson, P. D.
Venue
Muscle & Nerve
Publisher
Wiley
Published
2002-02-19
Volume
25
Issue
3
Pages
332-347
ISSN
  • 0148-639X (ISSN-L)
  • 1097-4598
OpenAlex
W2069462877
Cited by
431
References
77
FWCI
13.91
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Rhabdomyolysis: A review. https://app.cochat.ai/papers/10.1002/mus.10053
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Warren, J. D., Blumbergs, P. C., & Thompson, P. D. (2002). Rhabdomyolysis: A review. Muscle & Nerve. https://doi.org/10.1002/mus.10053

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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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