The association of sporadic inclusion body myositis and Sjögren's syndrome in carriers of HLA-DR3 and the 8.1 MHC ancestral haplotype

Clinical Neurology and Neurosurgery

Volumn 113, Issue 7, 2011, Pages 559-563

  Rojana Udomsart, A ^a,b   Needham, M ^c   Luo, Y B ^a   Fabian, V ^d   Walters, S ^a   Zilko, P J ^a   Mastaglia, F L ^a  

^a UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^b Yala Hospital   (Thailand)

^c ROYAL NORTH SHORE HOSPITAL   (Australia)

^d ROYAL PERTH HOSPITAL   (Australia)

Author keywords

0301,8.1 MHC ancestral haplotype; HLA DR3; HLA DRB1; Sj gren's syndrome; Sporadic inclusion body myositis

Indexed keywords

AZATHIOPRINE; CYCLOPHOSPHAMIDE; CYCLOSPORIN; HLA DR ANTIGEN; HLA DR3 ANTIGEN; HYDROXYCHLOROQUINE; IMMUNOGLOBULIN; METHOTREXATE; PREDNISOLONE;

ARTICLE; DISEASE ASSOCIATION; GENETIC PREDISPOSITION; GENOTYPE; HAPLOTYPE; HUMAN; IMMUNOTHERAPY; INCLUSION BODY MYOSITIS; MAJOR HISTOCOMPATIBILITY COMPLEX; MUSCLE BIOPSY; MUSCLE WEAKNESS; ONSET AGE; SJOEGREN SYNDROME; SPORADIC INCLUSION BODY MYOSITIS; TREATMENT OUTCOME;

AGE OF ONSET; CREATINE KINASE; FEMALE; GENES, MHC CLASS I; GENOTYPE; HAPLOTYPES; HETEROZYGOTE; HLA ANTIGENS; HLA-DR3 ANTIGEN; HUMANS; MIDDLE AGED; MUSCLE STRENGTH; MUSCLE, SKELETAL; MUSCULAR DISEASES; MYOSITIS, INCLUSION BODY; NECROSIS; SJOGREN'S SYNDROME;

EID: 79960540929     PISSN: 03038467     EISSN: 18726968     Source Type: Journal    
DOI: 10.1016/j.clineuro.2011.03.016     Document Type: Article

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