Myalgia as the revealing symptom of multicore disease and fibre type disproportion myopathy

Journal of Neurology, Neurosurgery and Psychiatry

Volumn 74, Issue 9, 2003, Pages 1317-1319

  Sobreira, C ^a,b   Marques Jr , W ^a   Barreira, A A ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

^b HC sala 536   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

OXIDOREDUCTASE;

ADOLESCENT; ADULT; ARTICLE; CASE REPORT; CLINICAL FEATURE; CONGENITAL FIBER TYPE DISPROPORTION MYOPATHY; DISEASE EXACERBATION; ENZYME ACTIVITY; EXERCISE; FEMALE; GENETIC COUNSELING; HISTOCHEMISTRY; HISTOPATHOLOGY; HUMAN; HUMAN CELL; HUMAN TISSUE; MALE; MULTIMINICORE DISEASE; MUSCLE BIOPSY; MUSCLE CELL; MUSCLE WEAKNESS; MYALGIA; MYOPATHY; PHYSICAL EXAMINATION; PRIORITY JOURNAL; PROGNOSIS; SKELETAL MUSCLE; SYMPTOM;

ADOLESCENT; ADULT; BIOPSY; FEMALE; HUMANS; MALE; MIDDLE AGED; MUSCLE FIBERS; MUSCLE WEAKNESS; MUSCLE, SKELETAL; MYOPATHY, CENTRAL CORE; PAIN; PHENOTYPE; PROGNOSIS;

EID: 0141740663     PISSN: 00223050     EISSN: None     Source Type: Journal    
DOI: 10.1136/jnnp.74.9.1317     Document Type: Article

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