An inflammatory, familial, inclusion body myositis with autoimmune features and a phenotype identical to sporadic inclusion body myositis. Studies in three families

Brain

Volumn 120, Issue 4, 1997, Pages 653-661

  Sivakumar, Kumaraswamy ^a   Semino Mora, Christina ^a   Dalakas, Marinos C ^a  

^a NATIONAL INSTITUTES OF HEALTH   (United States)

Author keywords

Autoimmune disease; HLA antigens; Inclusion body myositis; Inherited susceptibility; Myositis

Indexed keywords

AMYLOID; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 1;

ADULT; AGED; ALLELE; ARTICLE; AUTOIMMUNITY; CLINICAL ARTICLE; CONGENITAL DISORDER; DIAGNOSIS; ETIOLOGY; EXTENSOR MUSCLE; FAMILIAL DISEASE; FAMILY STUDY; FEMALE; FINGER; FLEXOR MUSCLE; FOOT; FOREARM; GENETIC SUSCEPTIBILITY; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOCYTOCHEMISTRY; INCLUSION BODY MYOSITIS; MALE; MUSCLE BIOPSY; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPE; PRIORITY JOURNAL; QUADRICEPS FEMORIS MUSCLE; SIBLING; T LYMPHOCYTE SUBPOPULATION; TRICEPS BRACHII MUSCLE;

EID: 0031002684     PISSN: 00068950     EISSN: None     Source Type: Journal    
DOI: 10.1093/brain/120.4.653     Document Type: Article

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