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Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypes

Publikováno v: Genes & Immunity. 16:470-480

Autoimmune muscle diseases (myositis) comprise a group of complex phenotypes influenced by genetic and environmental factors. To identify genetic risk factors in patients of European ancestry, we conducted a genome-wide association study (GWAS) of th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0bcd9c6902e2b96ed557a87be46c59d
https://doi.org/10.1038/gene.2015.28

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Validation of the Childhood Health Assessment Questionnaire in the juvenile idiopathic myopathies. Juvenile Dermatomyositis Disease Activity Collaborative Study Group

Autor: A M, Huber, J E, Hicks, P A, Lachenbruch, M D, Perez, L S, Zemel, R M, Rennebohm, C A, Wallace, C B, Lindsley, M H, Passo, S H, Ballinger, S L, Bowyer, A M, Reed, P H, White, I M, Katona, F W, Miller, L G, Rider, B M, Feldman

Publikováno v: The Journal of rheumatology. 28(5)

To examine the validity of the Childhood Health Assessment Questionnaire (CHAQ) in patients with juvenile idiopathic inflammatory myopathy (IIM).One hundred fifteen patients were enrolled in a multicenter collaborative study, during which subjects we

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::eb3ce02d7eb3f65a424f26789841958a
https://pubmed.ncbi.nlm.nih.gov/11361197

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Magnetic resonance imaging detection of occult skin and subcutaneous abnormalities in juvenile dermatomyositis. Implications for diagnosis and therapy

Autor: A B, Kimball, R M, Summers, M, Turner, E M, Dugan, J, Hicks, F W, Miller, L G, Rider

Publikováno v: Arthritis and rheumatism. 43(8)

To assess the utility of magnetic resonance imaging (MRI) of skin, subcutaneous tissue, and fascia in evaluating disease activity in juvenile dermatomyositis (DM).Short tau inversion recovery (STIR) MRI of the proximal thighs and buttocks, cutaneous

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::50e69e73671f9326c5e015c0a6baf8ac
https://pubmed.ncbi.nlm.nih.gov/10943878

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Genetic risk and protective factors for idiopathic inflammatory myopathy in Koreans and American whites: a tale of two loci

Autor: L G, Rider, E, Shamim, S, Okada, J P, Pandey, I N, Targoff, T P, O'Hanlon, H A, Kim, Y S, Lim, H, Han, Y W, Song, F W, Miller

Publikováno v: Arthritis and rheumatism. 42(6)

To better understand genetic contributions to autoimmunity, immunogenetic markers were studied in two racially discrete and geographically isolated populations of patients with idiopathic inflammatory myopathy (IIM).Clinical characteristics, as well

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c28f6e77d2f8b692c4142f569d288787
https://pubmed.ncbi.nlm.nih.gov/10366124

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Clinical, serologic, and immunogenetic features of familial idiopathic inflammatory myopathy

Autor: L G, Rider, R C, Gurley, J P, Pandey, I, Garcia de la Torre, A E, Kalovidouris, T P, O'Hanlon, L A, Love, R C, Hennekam, L L, Baumbach, H E, Neville, C A, Garcia, J, Klingman, M, Gibbs, M H, Weisman, I N, Targoff, F W, Miller

Publikováno v: Arthritis and rheumatism. 41(4)

To describe the clinical, serologic, and immunogenetic features of familial idiopathic inflammatory myopathy (IIM) and to compare these with the features of sporadic IIM.Clinical signs and symptoms, autoantibodies, HLA-DRB1 and DQA1 alleles, and GM/K

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e2ca359b4f03825de614f83bceccbb3d
https://pubmed.ncbi.nlm.nih.gov/9550481

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Development of validated disease activity and damage indices for the juvenile idiopathic inflammatory myopathies: I. Physician, parent, and patient global assessments. Juvenile Dermatomyositis Disease Activity Collaborative Study Group

Autor: L G, Rider, B M, Feldman, M D, Perez, R M, Rennebohm, C B, Lindsley, L S, Zemel, C A, Wallace, S H, Ballinger, S L, Bowyer, A M, Reed, M H, Passo, I M, Katona, F W, Miller, P A, Lachenbruch

Publikováno v: Arthritis and rheumatism. 40(11)

To determine the reliability, content validity, and responsiveness of physician global assessments of disease activity and damage in the juvenile idiopathic inflammatory myopathies (IIM), and to investigate concordance among physician, parent, and pa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::517a010e92df20762bae21983503e8f5
https://pubmed.ncbi.nlm.nih.gov/9365086

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NIH conference. Myositis: immunologic contributions to understanding cause, pathogenesis, and therapy

Autor: P H, Plotz, L G, Rider, I N, Targoff, N, Raben, T P, O'Hanlon, F W, Miller

Publikováno v: Annals of internal medicine. 122(9)

The myositis syndromes, the most common forms of which are polymyositis and dermatomyositis, are defined by idiopathic chronic inflammation in skeletal muscle. Although initially described more than a century ago, these diseases are so rare and heter

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9c52c37de51fc860c0c5cf1171078549
https://pubmed.ncbi.nlm.nih.gov/7702234

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Diacylglycerol accumulation and superoxide anion production in stimulated human neutrophils

Autor: L G, Rider, J E, Niedel

Publikováno v: The Journal of biological chemistry. 262(12)

Exogenous diacylglycerols stimulate neutrophil superoxide anion production, suggesting that endogenous diacylglycerols may function as second messengers for this biological response. We have measured the diacylglycerol mass in human neutrophils stimu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f12510b75262f94dfc92f4b5ef459cb9
https://pubmed.ncbi.nlm.nih.gov/3032939

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