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6541por Carlton-Conway, Daniel, Ahluwalia, Raju, Henry, Lucy, Michie, Colin, Wood, Louise, Tulloh, Robert“…BACKGROUND: Kawasaki disease is a systemic vasculitis and may affect cerebral function acutely. …”
Publicado 2005
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6542por Flendrie, Marcel, Vissers, Wynand HPM, Creemers, Marjonne CW, de Jong, Elke MGJ, van de Kerkhof, Peter CM, van Riel, Piet LCM“…Other events with a possible relation to TNF-α-blocking therapy included vasculitis, psoriasis, drug-induced systemic lupus erythematosus, dermatomyositis, and a lymphomatoid-papulosis-like eruption. …”
Publicado 2005
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6543por Turesson, Carl, Schaid, Daniel J, Weyand, Cornelia M, Jacobsson, Lennart TH, Goronzy, Jörg J, Petersson, Ingemar F, Sturfelt, Gunnar, Nyhäll-Wåhlin, Britt-Marie, Truedsson, Lennart, Dechant, Sonja A, Matteson, Eric L“…The presence of two HLA-DRB1*04 alleles encoding the shared epitope (SE) was associated with ExRA (overall odds ratio 1.79, 95% confidence interval 1.04–3.08) and with rheumatoid vasculitis (odds ratio 2.44, 95% confidence interval 1.22–4.89). …”
Publicado 2005
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6544Heterogeneity of CD4 and CD8(+) memory T cells in localized and generalized Wegener's granulomatosispor Lamprecht, Peter, Erdmann, Anika, Mueller, Antje, Csernok, Elena, Reinhold-Keller, Eva, Holl-Ulrich, Konstanze, Feller, Alfred C, Bruehl, Hilke, Gross, Wolfgang L“…CCR5 and CCR3 expression on CD4(+) and CD8(+) memory T cells indicates a potential to respond to chemotactic gradients and might be important in T cell migration contributing to granuloma formation and vasculitis in WG.…”
Publicado 2003
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6545por Alexopoulos, Efstathios, Gionanlis, Lazaros, Papayianni, Ekaterini, Kokolina, Elizabeth, Leontsini, Maria, Memmos, Dimitrios“…CONCLUSION: Patients with ANCA-associated renal vasculitis seem to respond better to the treatment. …”
Publicado 2006
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6546por Hegewisch-Becker, S., Fliegner, M., Tsuruo, T., Zander, A., Zeller, W., Hossfeld, D. K.“…Bone marrow aspirates were obtained as part of a routine diagnostic programme in bone marrow donors or in patients presenting with a variety of diagnoses such as unexplained gammopathy, fever, anaemia, other changes in peripheral blood smear, rheumatoid arthritis, vasculitis, or urticaria pigmentosa. Morphologically the bone marrow was normal in 23 patients, a megaloblastic erythropoiesis was seen in two patients and unspecific changes were seen in 28 patients. …”
Publicado 1993
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6547por Zimmer, Jacques, Bausinger, Huguette, Andrès, Emmanuel, Donato, Lionel, Hanau, Daniel, Hentges, François, Moretta, Alessandro, de la Salle, Henri“…We further investigated TAP-deficient NK cells in these patients and compared them to NK cells from two other TAP-deficient patients with no clinical symptoms and to individuals with chronic inflammatory diseases other than TAP deficiency (chronic lung diseases or vasculitis). Peripheral blood mononuclear cells isolated from venous blood were stained with fluorochrome-conjugated antibodies and the phenotype of NK cells was analyzed by flow cytometry. …”
Publicado 2007
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6548“…In very rare cases, necrotizing panniculitis and secondary vasculitis may occur. AATD is caused by mutations in the SERPINA1 gene encoding AAT, and is inherited as an autosomal recessive trait. …”
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6549por Willcocks, Lisa C., Lyons, Paul A., Clatworthy, Menna R., Robinson, James I., Yang, Wanling, Newland, Stephen A., Plagnol, Vincent, McGovern, Naomi N., Condliffe, Alison M., Chilvers, Edwin R., Adu, Dwomoa, Jolly, Elaine C., Watts, Richard, Lau, Yu Lung, Morgan, Ann W., Nash, Gerard, Smith, Kenneth G.C.“…In contrast, antineutrophil cytoplasmic antibody–associated systemic vasculitis (AASV), a disease not associated with immune complex deposition, is associated with high FCGR3B CN. …”
Publicado 2008
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6550por Quartuccio, Luca, Fabris, Martina, Moretti, Massimo, Barone, Francesca, Bombardieri, Michele, Rupolo, Maurizio, Lombardi, Sandra, Pitzalis, Costantino, Beltrami, Carlo Alberto, Curcio, Francesco, De Vita, Salvatore“…PATIENT AND METHODS: We describe the treatments employed, with particular regards to rituximab therapy, and the histopathologic and biologic studies, in particular BAFF levels in serum and in pathologic tissues before and after B-cell depletion therapy, and the characterization of the cultured epithelial cells obtained by the parotid gland MALT-lymphoma, in a case of a 51-year old woman with primary SS and mixed cryoglobulinaemia type II with features of systemic vasculitis, who developed a bilateral parotid MALT-type lymphoma. …”
Publicado 2008
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6551“…Specifically, AML was associated with rheumatoid arthritis (OR 1.28), systemic lupus erythematosus (OR 1.92), polymyalgia rheumatica (OR 1.73), autoimmune haemolytic anaemia (OR 3.74), systemic vasculitis (OR 6.23), ulcerative colitis (OR 1.72) and pernicious anaemia (OR 1.57). …”
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6552por Vasil, Michael L., Stonehouse, Martin J., Vasil, Adriana I., Wadsworth, Sandra J., Goldfine, Howard, Bolcome, Robert E., Chan, Joanne“…Taken together, these observations are pertinent to the distinctive vasculitis and poor wound healing associated with P. aeruginosa sepsis and suggest that the potent antiangiogenic properties of PlcHR are worthy of further investigation for the treatment of diseases where angiogenesis contributes pathological conditions (e.g., vascularization of tumors, diabetic retinopathy).…”
Publicado 2009
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6553por Hersh, Aimee O, Pang, Shirley, Curran, Megan L, Milojevic, Diana S, von Scheven, Emily“…Subject diagnoses included systemic lupus erythematosus (52%), mixed connective tissue disease (16%), juvenile idiopathic arthritis (16%), antiphospholipid antibody syndrome (13%) and vasculitis (3%). Nearly 30% of subjects were hospitalized for disease treatment or management of flares in the year prior to transfer, and 58% had active disease at the time of transfer. …”
Publicado 2009
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6554por Meier-Trummer, Claudia S., Rehrauer, Hubert, Franchini, Marco, Patrignani, Andrea, Wagner, Ulrich, Ackermann, Mathias“…BACKGROUND: Malignant catarrhal fever (MCF) is a lethal disease of cattle, characterized by vasculitis, necrosis, and accumulation of activated, dysregulated cytotoxic lymphocytes in various tissues. …”
Publicado 2009
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6555por Bossart, Katharine N., Zhu, Zhongyu, Middleton, Deborah, Klippel, Jessica, Crameri, Gary, Bingham, John, McEachern, Jennifer A., Green, Diane, Hancock, Timothy J., Chan, Yee-Peng, Hickey, Andrew C., Dimitrov, Dimiter S., Wang, Lin-Fa, Broder, Christopher C.“…The underlying pathology seen in the ferret closely resembles that seen in Nipah virus infected humans, characterized as a widespread multisystemic vasculitis, with virus replicating in highly vascular tissues including lung, spleen and brain, with recoverable virus from a variety of tissues. …”
Publicado 2009
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6556por Motulsky, Elie, Koch, Philippe, Janssens, Sarah, Liénart, Maité, Vanbellinghen, Anne-Marie, Bolaky, Nargis, Chan, Chi-Chao, Caspers, Laure, Martin-Martinez, Maria-Dolores, Xu, Heping, Delporte, Christine, Willermain, François“…Retinal endothelial cells never expressed AQP1. In vasculitis and intraretinal inflammatory infiltrates, decreased AQP1 expression was observed due to the loss of photoreceptors and the characteristic radial labeling of AQP4 was lost. …”
Publicado 2010
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6557“…BACKGROUND: Scrub typhus is a mite-borne bacterial infection of humans caused by Orientia tsutsugamushi that causes a generalized vasculitis that may involve the tissues of any organ system. …”
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6558por Cheriyath, Pramil, Gorrepati, Venkata Subhash, Peters, Ian, Nookala, Vinod, Murphy, Megan E, Srouji, Nadine, Fischman, Daniel“…This finding supports the hypothesis that the antioxidant nature of TBili, demonstrating a protective effect with regard to the risk of stroke, atherosclerosis, and vasculitis in prior research, also extends to DM risk. …”
Publicado 2010
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6559“…BACKGROUND AND OBJECTIVES: Kawasaki disease (KD) is a multi-systemic vasculitis with coronary artery involvement. Serum interleukin (IL)-6 levels during acute phase showed a significant correlation with the duration of fever in patients with KD who were not treated with intravenous immunoglobulin (IVIG), suggesting that the regulation of IL-6 expression in KD patients may differ from that in normal children. …”
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6560Publicado 2011“…DESIGN, SETTING AND PATIENTS: A case–control analysis was performed as part of surveillance of children hospitalised through the emergency departments of eight paediatric hospitals/wards for ILI, neurological disorders, non-infectious muco-cutaneous diseases and vasculitis, thrombocytopaenia and gastroduodenal lesions. …”
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