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6161por Arooj, Mahwish, Malik, Arif, Basit, Abdul, Husain Qazi, Mahmood, Asif, Muhammad, Sarwar Jamal, Mohammad, Mostafa Mahmoud, Maged, Choudhry, Hani, Natesan Pushparaj, Peter, Rasool, Mahmood“…Interferon (IFN) therapy can cause vasculitis, glomerulonephritis, cryoglobulinemia and certain other autoimmune diseases such as sialoadentitis, lichen planus and thyroiditis. …”
Publicado 2016
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6162“…OBJECTIVES: Henoch-Schonlein Purpura (HSP) is the most widespread systemic vasculitis during childhood. Gastrointestinal tract retention and gastrointestinal bleeding are among its major complications. …”
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6163por Ueno, Kentaro, Ninomiya, Yumiko, Hazeki, Daisuke, Masuda, Kiminori, Nomura, Yuichi, Kawano, Yoshifumi“…We sought to clarify the poorly understood pathogenic role of endothelial cell survival and death in KD vasculitis. Human umbilical vein endothelial cells (HUVECs) stimulated with sera from KD patients, compared with sera from patients with bacterial infections, exhibited significant increases in cytotoxicity, high mobility group box protein 1 (HMGB-1), and caspase-3/7 and a decrease in phosphorylated Akt/Akt (pAkt/Akt) ratios. …”
Publicado 2017
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6164por Kimura, Yayoi, Yanagimachi, Masakatsu, Ino, Yoko, Aketagawa, Mao, Matsuo, Michie, Okayama, Akiko, Shimizu, Hiroyuki, Oba, Kunihiro, Morioka, Ichiro, Imagawa, Tomoyuki, Kaneko, Tetsuji, Yokota, Shumpei, Hirano, Hisashi, Mori, Masaaki“…Kawasaki disease (KD) is a systemic vasculitis and childhood febrile disease that can lead to cardiovascular complications. …”
Publicado 2017
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6165“…PURPOSE: Kawasaki disease (KD) is an immune-related multisystemic vasculitis that occurs in children, especially ensuing from a coronary artery abnormality. …”
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6166por Wolfe, Bryce, Wiepz, Gregory J., Schotzko, Michele, Bondarenko, Gennadiy I., Durning, Maureen, Simmons, Heather A., Mejia, Andres, Faith, Nancy G., Sampene, Emmanuel, Suresh, Marulasiddappa, Kathariou, Sophia, Czuprynski, Charles J., Golos, Thaddeus G.“…Histopathology indicated vasculitis, fibrinoid necrosis, and thrombosis of the decidual spiral arteries, acute chorioamnionitis and villitis in the placenta, and hematogenous infection of the fetus. …”
Publicado 2017
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6167por Sirikudta, Wararat, Tuchinda, Papapit, Chularojanamontri, Leena, Kulthanan, Kanokvalai, Pinkaew, Samruay“…The most common diagnosis was CNTD (79%) followed by vasculitis (10.1%). Lupus erythematosus was the most common diagnosis among CNTD (78%). …”
Publicado 2017
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6168Association of FCGR2A/FCGR3A variant rs2099684 with Takayasu arteritis in the Han Chinese populationpor Chen, Si, Wen, Xiaoting, Li, Jing, Li, Yuan, Li, Liubing, Tian, Xinping, Yuan, Hui, Zhang, Fengchun, Li, Yongzhe“…Takayasu arteritis (TA) is a chronic large-vessel vasculitis of unclear pathogenesis. A recent genome-wide association study (GWAS) has revealed that the FCGR2A/FCGR3A, EEFSEC, RPS9/LILRB3, RIPPLY2 and MLX genes confer susceptibility to TA. …”
Publicado 2016
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6169por Panda, Rachita, Krieger, Thorsten, Hopf, Luke, Renné, Thomas, Haag, Friedrich, Röber, Nadja, Conrad, Karsten, Csernok, Elena, Fuchs, Tobias A.“…Using NETs as a substrate for IIF, we characterized ANCAs in sera of patients with ANCA-associated vasculitis (AAV). Furthermore, we inhibited serine proteases by diisopropylfluorophosphate to prevent chromatin unfolding and the release of NETs and thus generated neutrophils with MPO-positive nuclei and PR3-positive cytoplasm, which resembled the appearance of ethanol-fixed neutrophils. …”
Publicado 2017
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6170“…BACKGROUND: Kawasaki disease (KD) is a febrile childhood vasculitis of unknown etiology. The diagnosis is highly concerning as over a quarter of children who fail to receive timely treatment with intravenous immunoglobulin (IVIG) will develop coronary aneurysms. …”
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6171por Takeuchi, Yoichi, Saito, Ayako, Ojima, Yoshie, Kagaya, Saeko, Fukami, Hirotaka, Sato, Hiroyuki, Matsuda, Ken, Nagasawa, Tasuku“…BACKGROUND: Antineutrophil cytoplasmic antibody-associated vasculitis is triggered by environmental factors, including silica dust exposure. …”
Publicado 2017
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6172por Nagashima, Takamitsu, Ishihara, Mami, Shibuya, Etsuko, Nakamura, Satoshi, Mizuki, Nobuhisa“…Case 3: The patient developed bilateral panuveitis, retinal vasculitis, and macular edema, which were initially suspected to be sarcoidosis. …”
Publicado 2016
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6173por Ferraz de Campos, Fernando Peixoto, Felipe-Silva, Aloísio, Lopes, Ana Claudia Frota Machado de Melo, Passadore, Lilian Ferri, Guida, Stella Maria, Balabakis, Angélica Jean, Martines, João Augusto dos Santos“…The autopsy findings confirmed a hemorrhagic necrotizing pneumonia with bacteria-invading vasculitis and thrombosis. A culture of the metalworking fluid of the factory was also positive for P. aeruginosa. …”
Publicado 2014
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6174por Sadeghi, Alireza, Davatchi, Fereydoun, Shahram, Farhad, Karimimoghadam, Arezoo, Alikhani, Majid, Pezeshgi, Aiyoub, Mazloomzadeh, Saeideh, Sadeghi-Abdollahi, Bahar, Asadi-Khiavi, Masoud“…Introduction: Behcet’s disease (BD) is a chronic systemic autoinflammatory vasculitis which is handled by the variety of proteins like cytokines. …”
Publicado 2017
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6175por Ohmiya, Naoki, Horiguchi, Noriyuki, Tahara, Tomomitsu, Nagasaka, Mitsuo, Nakagawa, Yoshihito, Shibata, Tomoyuki, Tsukamoto, Tetsuya, Kuroda, Makoto“…Hereditary hemorrhagic telangiectasia and angiodysplasia contained anastomosis of capillary vessels of different calibers. In IgA vasculitis, segmental capillary strictures were observed. …”
Publicado 2017
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6176“…BACKGROUND AND OBJECTIVES: Behçet's disease (BD) is a systemic vasculitis that is characterized by genital, oral, or skin lesions, uveitis, and vascular complications. …”
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6177por GHATEE, Mohammad Amin, KANANNEJAD, Zahra, SHARIFI, Iraj, ASKARI, Asma, BAMOROVAT, Mehdi“…METHODS: Ninety-two urine samples from autoimmune patients including systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), scleroderma, autoimmune vasculitis, vitiligo, pemphigus and Wagner cases and 20 urine samples from healthy individuals were collected from Kerman Province in Southeastern Iran in 2010–2011. …”
Publicado 2017
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6178por Chandra, Sadanandavalli Retnaswami, Viswanathan, Lakshminarayanapuram Gopal, Pai, Anupama Ramakanth, Wahatule, Rahul, Alladi, Suvarna“…PATIENTS AND METHODS: All patients underwent all mandatory tests for dementia including brain imaging. Complete vasculitis workup, autoimmune encephalitis profile including Voltage Gated Potassium Channel, N-methyl-D-aspartic acid receptor, glutamic acid-decarboxylase, thyroid-peroxidase antibody, cerebrospinal fluid, and other special tests such as duodenal biopsy and paraneoplastic workup were done based on clinical indications. …”
Publicado 2017
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6179por Sugimoto, Koichi, Nakazato, Kazuhiko, Sato, Akihiko, Suzuki, Satoshi, Yoshihisa, Akiomi, Machida, Takeshi, Saitoh, Shu-ichi, Sekine, Hideharu, Takeishi, Yasuchika“…MRL/lpr mice, which have hypergammaglobulinemia, produce various autoimmune antibodies, and develop vasculitis and nephritis spontaneously. However, little is known about pulmonary circulation in these mice. …”
Publicado 2017
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6180por Esposito, Daniela, Trimpou, Penelope, Giugliano, Dario, Dehlin, Mats, Ragnarsson, Oskar“…PURPOSE: Granulomatosis with polyangiitis (GPA) is a multisystem disease, characterized by necrotizing small-vessel vasculitis, which mainly affects the respiratory tract and the kidneys. …”
Publicado 2017
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