Congenital myopathy with central cores and fingerprint bodies in association with malignant hyperthermia susceptibility

Neuromuscular Disorders

Volumn 11, Issue 6-7, 2001, Pages 538-541

  Stojkovic, T ^a   Maurage, C A ^a   Moerman, A ^a   Hurtevent, J F ^a   Krivosic Horber, R ^a   Pellissier, J F ^b   Vermersch, P ^a  

^a LILLE UNIVERSITY HOSPITAL   (France)

^b TIMONE HOSPITAL   (France)

Author keywords

Central cores; Congenital myopathy; Fingerprint bodies; Malignant hyperthermia

Indexed keywords

CAFFEINE; HALOTHANE; RYANODINE RECEPTOR;

ARTICLE; CASE REPORT; CELL INCLUSION; DISEASE PREDISPOSITION; HISTOLOGY; HUMAN; MALE; MALIGNANT HYPERTHERMIA; MUSCLE BIOPSY; MUSCLE CELL; MUSCLE CONTRACTURE; MUSCLE POTENTIAL; MUSCLE WEAKNESS; MYOPATHY; NERVE CONDUCTION; PHENOTYPE; PRIORITY JOURNAL;

ADULT; ANESTHETICS, INHALATION; BIOPSY; CAFFEINE; CENTRAL NERVOUS SYSTEM STIMULANTS; HALOTHANE; HUMANS; INCLUSION BODIES; MALE; MALIGNANT HYPERTHERMIA; MICROSCOPY, ELECTRON; MUSCLE CONTRACTION; MUSCLE FIBERS; MYOPATHY, CENTRAL CORE; NUCLEAR FAMILY;

EID: 0034893873     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-8966(01)00196-1     Document Type: Article

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6. Ryanodine receptor mutations in malignant hyperthermia and central core disease
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15. In vitro contracture tests in patients with various neuromuscular diseases