Familial inclusion body myositis with histologically confirmed sensorimotor axonal neuropathy [4]

Journal of Neurology

Volumn 247, Issue 11, 2000, Pages 882-884

  Hengstmann, G J D ^a   Van Engelen, B G M ^a   Ter Laak, H J ^a   Gabreels Festen A A W M ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOANTIBODY; CD4 ANTIGEN; CD8 ANTIGEN; CORTICOSTEROID; CREATINE KINASE; CREATININE; ELECTROLYTE; GLUCOSE; HEMOGLOBIN; UREA;

ACHILLES REFLEX; AGED; AUTOIMMUNE DISEASE; CASE REPORT; CONTROLLED STUDY; DISEASE COURSE; DYSPHAGIA; ELECTROMYOGRAPHY; FAMILIAL DISEASE; FEMALE; HUMAN; HUMAN TISSUE; IMMUNOELECTROPHORESIS; IMMUNOSUPPRESSIVE TREATMENT; INCLUSION BODY MYOSITIS; LETTER; MOTOR UNIT POTENTIAL; MUSCLE ATROPHY; MUSCLE BIOPSY; MUSCLE WEAKNESS; MYOPATHY; NERVE BIOPSY; NERVE CONDUCTION; NEUROPHYSIOLOGY; PERIPHERAL NEUROPATHY; PRIORITY JOURNAL; SENSORIMOTOR NEUROPATHY; SURAL NERVE; TECHNIQUE; THROMBOCYTE COUNT;

AGED; AXONS; CHARCOT-MARIE-TOOTH DISEASE; FEMALE; HUMANS; MYOSITIS, INCLUSION BODY;

EID: 0033666099     PISSN: 03405354     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004150070079     Document Type: Letter

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