Zobrazeno 1 - 10 of 184 pro vyhledávání: '"D. A. Isenberg"'
1
Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypes
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
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0bcd9c6902e2b96ed557a87be46c59d
https://doi.org/10.1038/gene.2015.28
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2
Oral Abstracts 3: Adolescent and Young Adult * O13. Hypermobility is a Risk Factor for Musculoskeletal Pain in Adolescence: Findings From a Prospective Cohort Study
Autor: J. Tobias, K. Deere, S. Palmer, E. Clark, J. Clinch, A. Fikree, R. Aktar, G. Wellstead, C. Knowles, R. Grahame, Q. Aziz, B. Amaral, G. Murphy, Y. Ioannou, D. A. Isenberg, S. L. Tansley, Z. E. Betteridge, H. Gunawardena, G. Shaddick, H. Varsani, L. Wedderburn, N. McHugh, F. De Benedetti, N. Ruperto, G. Espada, V. Gerloni, B. Flato, G. Horneff, B. L. Myones, K. Onel, J. Frane, A. Kenwright, T. H. Lipman, K. N. Bharucha, A. Martini, D. J. Lovell, E. Baildam, H. Brunner, Z. Zuber, C. Keane, O. Harari, R. J. Cuttica, V. Keltsev, R. Xavier, I. C. Penades, I. Nikishina, N. Rubio-Perez, E. Alekseeva, V. Chasnyk, J. Chavez, V. Opoka-Winiarska, P. Quartier, C. A. Silva, E. D. Silverman, A. Spindler, G. J. Hendry, G. F. Watt, M. Brandon, L. Friel, D. Turner, P. K. Lorgelly, J. Gardner-Medwin, R. D. Sturrock, J. Woodburn, J. Firth, R. Waxman, G. Law, H. Siddle, A. E. Nelson, P. Helliwell, S. Otter, V. Butters, L. Loughrey, B. Alcacer-Pitarch, J. Tranter, S. Davies, R. Hryniw, S. Lewis, L. Baker, E. Dures, S. Hewlett, N. Ambler, J. Clarke, R. Gooberman-Hill, R. Jenkins, R. Wilkie, M. Bucknall, K. Jordan, J. McBeth, S. Norton, D. Walsh, P. Kiely, R. Williams, A. Young, J. E. Harkess, K. McAlarey, L. Chesterton, D. A. van der Windt, J. Sim, M. Lewis, C. D. Mallen, E. Mason, E. Hay, L. E. Clarson, S. L. Hider, J. Belcher, C. Heneghan, E. Roddy, J. Gibson, S. Whiteford, E. Williamson, S. Beatty, N. Hamilton-Dyer, E. L. Healey, S. Ryan, G. A. McHugh, C. J. Main, M. Porcheret, B. Nio Ong, A. Pushpa-Rajah, K. S. Dziedzic, C. S. MacRae, A. Shortland, J. Lewis, M. Morrissey, D. Critchley, S. Muller, T. Helliwell, Z. Cole, C. Parsons, S. Crozier, S. Robinson, P. Taylor, H. Inskip, K. Godfrey, E. Dennison, N. C. Harvey, C. Cooper, D. Prieto Alhambra, A. Lalmohamed, B. Abrahamsen, N. Arden, A. de Boer, P. Vestergaard, F. de Vries, A. Kendal, A. Carr, D. Prieto-Alhambra, A. Judge, R. Chapurlat, N. Bellamy, E. Czerwinski, J. Pierre Devogelaer, L. March, K. Pavelka, J.-Y. Reginster, A. Kiran, M. K. Javaid, J. S. Sundy, H. S. Baraf, M. Becker, E. L. Treadwell, R. Yood, F. D. Ottery
Publikováno v: Rheumatology. 52:i33-i43
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5b129125d04a2118279d5833806941d8
https://doi.org/10.1093/rheumatology/ket200
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3
International consensus for a definition of disease flare in lupus
Autor: N, Ruperto, L M, Hanrahan, G S, Alarcón, H M, Belmont, R L, Brey, P, Brunetta, J P, Buyon, M I, Costner, M E, Cronin, M A, Dooley, G, Filocamo, D, Fiorentino, P R, Fortin, A G, Franks, G, Gilkeson, E, Ginzler, C, Gordon, J, Grossman, B, Hahn, D A, Isenberg, K C, Kalunian, M, Petri, L, Sammaritano, J, Sánchez-Guerrero, R D, Sontheimer, V, Strand, M, Urowitz, J M, von Feldt, V P, Werth, J T, Merrill, Asad A, Zoma
Publikováno v: Lupus. 20:453-462
The Lupus Foundation of America (LFA) convened an international working group to obtain a consensus definition of disease flare in lupus. With help from the Paediatric Rheumatology International Trials Organization (PRINTO), two web-based Delphi surv
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99151cc15f8228b0ae7566ef672fc033
https://doi.org/10.1177/0961203310388445
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5
Differences in disease phenotype and severity in SLE across age groups
Autor: N, Ambrose, T A, Morgan, J, Galloway, Y, Ionnoau, M W, Beresford, D A, Isenberg
Publikováno v: Lupus. 25(14)
Significant differences have been reported in disease phenotype and severity of systemic lupus erythematosus (SLE) presenting in different age groups. Most indicate a more severe phenotype in juvenile-onset SLE (JSLE). There have been limited studies
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::31e2baf383d87ad638d77788952f38ca
https://pubmed.ncbi.nlm.nih.gov/27305850
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6
Antiphospholipid syndrome
Autor: J J, Manson, D A, Isenberg
Publikováno v: The International Journal of Biochemistry & Cell Biology. 35:1015-1020
Antiphospholipid syndrome (APS) is defined as the presence of venous or arterial thromboses, and/or recurrent miscarriage, with evidence of antiphospholipid antibodies (aPL). Central to the disease, is the development of the antibodies to phospholipi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8477f72430cb9335a4b4c1ade3fe6e47
https://doi.org/10.1016/s1357-2725(02)00313-8
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7
Antibodies to high-density lipoprotein and ?2-glycoprotein I are inversely correlated with paraoxonase activity in systemic lupus erythematosus and primary antiphospholipid syndrome
Autor: J, Delgado Alves, P R J, Ames, S, Donohue, L, Stanyer, J, Nourooz-Zadeh, C, Ravirajan, D A, Isenberg, J, Noorouz-Zadeh
Publikováno v: Arthritis & Rheumatism. 46:2686-2694
Objective To determine the prevalence of anti–high-density lipoprotein (anti-HDL) antibodies and to establish a possible relationship between anti-HDL, anticardiolipin antibodies (aCL), anti–β2-glycoprotein I (anti-β2GPI), and paraoxonase (PON)
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ec1e33fbb8f24d4f9a72f508c22ce5f
https://doi.org/10.1002/art.10542
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9
Effects of rituximab-based B-cell depletion therapy on skin manifestations of lupus erythematosus--report of 17 cases and review of the literature
Autor: S C, Hofmann, M J, Leandro, S D, Morris, D A, Isenberg
Publikováno v: Lupus
Cutaneous manifestations occur frequently in systemic lupus erythematosus (SLE) and are pathognomonic in subacute-cutaneous lupus erythematosus (SCLE) and chronic cutaneous lupus erythematosus (CCLE). Although B-cell depletion therapy (BCDT) has demo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::2806403d30cd796011df7e9dbd76791c
https://pubmed.ncbi.nlm.nih.gov/23894047
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10
Heart failure in a woman with SLE, anti-phospholipid syndrome and Fabry's disease
Autor: A, Nandagudi, E C, Jury, D, Alonzi, T D, Butters, S, Hughes, D A, Isenberg
Publikováno v: Lupus
We describe a female patient with systemic lupus erythematosus (SLE) also diagnosed with Fabry’s disease and anti-phospholipid antibody syndrome (APS). SLE and Fabry’s disease are both systemic diseases with variable clinical presentations. Recen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::db1be8439730a2a8ef9a4780e182c53a
https://pubmed.ncbi.nlm.nih.gov/23864039
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