Zobrazeno 1 - 10
of 36
pro vyhledávání: '"L M, Pachman"'
Autor:
F W, Miller, W, Chen, T P, O'Hanlon, R G, Cooper, J, Vencovsky, L G, Rider, K, Danko, L R, Wedderburn, I E, Lundberg, L M, Pachman, A M, Reed, S R, Ytterberg, L, Padyukov, A, Selva-O'Callaghan, T R, Radstake, D A, Isenberg, H, Chinoy, W E R, Ollier, P, Scheet, B, Peng, A, Lee, J, Byun, J A, Lamb, P K, Gregersen, C I, Amos, Hemlata, Varsani
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
Publikováno v:
Arthritis care and research : the official journal of the Arthritis Health Professions Association. 13(6)
To perform a cost-identification and cost-effectiveness analysis comparing oral corticosteroids (OCS) with high-dose intermittent intravenous corticosteroid (IVCS) regimens in the treatment of juvenile dermatomyositis (JDM).Children previously diagno
Autor:
L M, Pachman, M R, Liotta-Davis, D K, Hong, T R, Kinsella, E P, Mendez, J M, Kinder, E H, Chen
Publikováno v:
Arthritis and rheumatism. 43(10)
To characterize the association between the TNFalpha-308A allele and 1) duration of active disease, 2) peripheral blood mononuclear cell (PBMC) synthesis of tumor necrosis factor alpha (TNFalpha) in vitro, and 3) pathologic calcifications in patients
Autor:
X, Dong, J, Wang, F N, Kabir, M, Shaw, A M, Reed, L, Stein, L E, Andrade, V F, Trevisani, M L, Miller, T, Fujii, M, Akizuki, L M, Pachman, M, Satoh, W H, Reeves
Publikováno v:
Arthritis and rheumatism. 43(1)
To evaluate the specificity of anti-DEK antibodies for juvenile rheumatoid arthritis (JRA).Anti-DEK autoantibodies were measured by enzyme-linked immunosorbent assay (ELISA) using affinity-purified his6-DEK fusion protein. Sera from 639 subjects (417
Autor:
D J, Lovell, C B, Lindsley, R M, Rennebohm, S H, Ballinger, S L, Bowyer, E H, Giannini, J E, Hicks, J E, Levinson, R, Mier, L M, Pachman, M H, Passo, M D, Perez, A M, Reed, K N, Schikler, M, Smith, L S, Zemel, L G, Rider
Publikováno v:
Arthritis and rheumatism. 42(10)
To develop, validate, and determine the measurement characteristics of a quantitative tool for assessing the severity of muscle involvement in children with idiopathic inflammatory myopathies.The Childhood Myositis Assessment Scale (CMAS) was develop
Publikováno v:
American journal of medical genetics. 80(3)
We describe a 9-year-old girl who initially presented at age 4 with evidence of arthritis in her hands, feet, and large joints. Although she had a partial response to anti-inflammatory medications and had some laboratory results consistent with infla
Autor:
M S, Klein-Gitelman, L M, Pachman
Publikováno v:
The Journal of rheumatology. 25(10)
To determine the frequency and severity of adverse reactions associated with high dose intermittent intravenous corticosteroids (IVCS) in children with rheumatic disease.Prospective documentation of adverse reactions associated with IVCS given to 213
Autor:
L M, Pachman, J R, Hayford, A, Chung, C A, Daugherty, M A, Pallansch, C W, Fink, H L, Gewanter, R, Jerath, B A, Lang, J, Sinacore, I S, Szer, A R, Dyer, M C, Hochberg
Publikováno v:
The Journal of rheumatology. 25(6)
To evaluate demographic and clinical characteristics, duration of time between disease onset (date of first rash and/or weakness), and diagnosis/therapy, as well as socioeconomic status, of children with newly diagnosed juvenile dermatomyositis (JDM)
Publikováno v:
The Journal of rheumatology. 25(5)
We reported an association between juvenile dermatomyositis (JDMS) and the HLA-DQA1*0501 allele. The purpose of this study was to determine whether there is evidence for linkage between JDMS and the DQA1*0501 allele in JDMS families.The study populat
Publikováno v:
Pediatric pathologylaboratory medicine : journal of the Society for Pediatric Pathology, affiliated with the International Paediatric Pathology Association. 18(1)
Children with hyper-immunoglobulin M (hyper-IgM) syndrome are at increased risk for Pneumocystis carinii pneumonia (PCP), an opportunistic infection often found in immunodeficient hosts. PCP can present with increasing hypoxia, fever, cough, and resp