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7021“…Cerebral vasospasm and vasculitis are considered as potential mechanisms of dermoid cyst rupture-related cerebral ischemia. …”
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7022por Grzybowska-Chlebowczyk, Urszula, Horowska-Ziaja, Sabina, Kajor, Maciej, Więcek, Sabina, Chlebowczyk, Wojciech, Woś, Halina“…INTRODUCTION: Eosinophilic colitis, which is a rare form of eosinophilic gastrointestinal diseases, occurs as primary and secondary allergic eosinophilic colitis of the gastrointestinal tract infection, inflammatory bowel disease, celiac disease, and vasculitis. The diagnosis is based on a significant amount of eosinophils in the inflammatory infiltrate of the colon wall. …”
Publicado 2017
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7023por Aykan, Ahmet Çağrı, Hatem, Engin, Kalaycıoğlu, Ezgi, Karabay, Can Yücel, Zehir, Regayip, Gökdeniz, Tayyar, Aykan, Duygun Altıntaş, Çelik, Şükrü“…Patients with previous peripheral revascularizations, acute coronary syndrome, vasculitis, non-atherosclerotic stenosis, and malignancy were excluded. …”
Publicado 2016
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7024por Lauletta, Gianfranco, Russi, Sabino, Pavone, Fabio, Vacca, Angelo, Dammacco, Franco“…BACKGROUND: The efficacy and safety of direct-acting antiviral agents (DAAs) were evaluated in a cohort of prospectively enrolled patients with hepatitis C virus (HCV)-related mixed cryoglobulinaemia (MC), an immune complex-mediated vasculitis of small and medium vessels in which the pathogenetic role of HCV has been clearly established. …”
Publicado 2017
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7025por Dietz, S. M., Kuipers, I. M., Koole, J. C. D., Breur, J. M. P. J., Fejzic, Z., Frerich, S., Dalinghaus, M., Roest, A. A. W., Hutten, B. A., Kuijpers, T. W.“…Kawasaki disease (KD) is a pediatric vasculitis. Its main complication is the development of coronary artery aneurysms (CAA), with giant CAA at the end of the spectrum. …”
Publicado 2017
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7026por Lehur, A. C., Zielinski, M., Pluvy, J., Grégoire, V., Diamantis, S., Bleibtreu, A., Rioux, C., Picard, A., Vallois, D.“…Differential diagnoses such as malignant tumors, cocaine use, granulomatosis, vasculitis and infections are more frequently observed and could delay and/or bias the final diagnosis. …”
Publicado 2017
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7027por Morgan, Matthew David, Szeto, Matthew, Walsh, Michael, Jayne, David, Westman, Kerstin, Rasmussen, Niels, Hiemstra, Thomas F., Flossmann, Oliver, Berden, Annelies, Höglund, Peter, Harper, Lorraine“…BACKGROUND: Relapse of disease is frequent in anti-neutrophil cytoplasm antibody (ANCA)-associated vasculitis (AAV). It is unclear whether persistent ANCA when starting maintenance therapy increases the risk of relapse. …”
Publicado 2017
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7028por Kwon, Young-Chang, Kim, Jae-Jung, Yun, Sin Weon, Yu, Jeong Jin, Yoon, Kyung Lim, Lee, Kyung-Yil, Kil, Hong-Ryang, Kim, Gi Beom, Han, Myung-Ki, Song, Min Seob, Lee, Hyoung Doo, Ha, Kee-Soo, Sohn, Sejung, Ebata, Ryota, Hamada, Hiromichi, Suzuki, Hiroyuki, Ito, Kaoru, Onouchi, Yoshihiro, Hong, Young Mi, Jang, Gi Young, Lee, Jong-Keuk“…Kawasaki disease (KD) is an acute systemic vasculitis that can potentially cause coronary artery aneurysms in some children. …”
Publicado 2017
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7029por Glasner, Corinna, de Goffau, Marcus C., van Timmeren, Mirjan M., Schulze, Mirja L., Jansen, Benita, Tavakol, Mehri, van Wamel, Willem J. B., Stegeman, Coen A., Kallenberg, Cees G. M., Arends, Jan P., Rossen, John W., Heeringa, Peter, van Dijl, Jan Maarten“…The proteinase 3 (PR3)-positive anti-neutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis (AAV) granulomatosis with polyangiitis (GPA) has been associated with chronic nasal S. aureus carriage, which is a risk factor for disease relapse. …”
Publicado 2017
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7030por Sittner, Assa, Bar-David, Elad, Glinert, Itai, Ben-Shmuel, Amir, Weiss, Shay, Schlomovitz, Josef, Kobiler, David, Levy, Haim“…Erythrocytes were present within the meningeal space but no clear vasculitis could be detected. Histology of the brain stem indicates meningitis, edema and hemorrhages that might explain death from suffocation due to direct damage to the respiratory center. …”
Publicado 2017
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7031por Kim, Kyu Yeun, Bae, Yoon-Sun, Ji, Woohyuk, Shin, Dongjik, Kim, Ho-Seong, Kim, Dong Soo“…PURPOSE: Kawasaki disease (KD) is an acute systemic vasculitis. Both the etiology of KD and the erythema of Bacille Calmette-Guérin (BCG) injection sites observed in the disease are poorly understood. …”
Publicado 2018
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7032por Perez, Mariana O., Oliveira, Ricardo M., Levy-Neto, Mauricio, Caparbo, Valeria F., Pereira, Rosa M.R.“…Disease activity was assessed by the Birmingham Vasculitis Activity Score Modified for Wegener’s Granulomatosis (BVAS/WG) and antineutrophil cytoplasmic antibody (ANCA) positivity. …”
Publicado 2017
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7033por Mohr, Emma L., Block, Lindsey N., Newman, Christina M., Stewart, Laurel M., Koenig, Michelle, Semler, Matthew, Breitbach, Meghan E., Teixeira, Leandro B. C., Zeng, Xiankun, Weiler, Andrea M., Barry, Gabrielle L., Thoong, Troy H., Wiepz, Gregory J., Dudley, Dawn M., Simmons, Heather A., Mejia, Andres, Morgan, Terry K., Salamat, M. Shahriar, Kohn, Sarah, Antony, Kathleen M., Aliota, Matthew T., Mohns, Mariel S., Hayes, Jennifer M., Schultz-Darken, Nancy, Schotzko, Michele L., Peterson, Eric, Capuano, Saverio, Osorio, Jorge E., O’Connor, Shelby L., Friedrich, Thomas C., O’Connor, David H., Golos, Thaddeus G.“…Significant pathology at the maternal-fetal interface included acute chorioamnionitis, placental infarcts, and leukocytoclastic vasculitis of the myometrial radial arteries. ZIKV RNA was disseminated throughout fetal tissues and maternal immune system tissues at necropsy, as assessed by quantitative RT-PCR for viral RNA. …”
Publicado 2018
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7034“…Our previous study revealed that the circulating S1P levels and renal expression of S1PRs correlated with disease activity and renal damage in patients with antineutrophil cytoplasmic antibody (ANCA)‐associated vasculitis (AAV). This study investigated the role of S1P and its receptors in myeloperoxidase (MPO)‐ANCA‐positive IgG‐mediated glomerular endothelial cell (GEnC) activation. …”
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7035por Lamprecht, Peter, Kerstein, Anja, Klapa, Sebastian, Schinke, Susanne, Karsten, Christian M., Yu, Xinhua, Ehlers, Marc, Epplen, Jörg T., Holl-Ulrich, Konstanze, Wiech, Thorsten, Kalies, Kathrin, Lange, Tanja, Laudien, Martin, Laskay, Tamas, Gemoll, Timo, Schumacher, Udo, Ullrich, Sebastian, Busch, Hauke, Ibrahim, Saleh, Fischer, Nicole, Hasselbacher, Katrin, Pries, Ralph, Petersen, Frank, Weppner, Gesche, Manz, Rudolf, Humrich, Jens Y., Nieberding, Relana, Riemekasten, Gabriela, Müller, Antje“…Anti-neutrophil cytoplasmic autoantibodies (ANCA) targeting proteinase 3 (PR3) and myeloperoxidase expressed by innate immune cells (neutrophils and monocytes) are salient diagnostic and pathogenic features of small vessel vasculitis, comprising granulomatosis with polyangiitis (GPA), microscopic polyangiitis, and eosinophilic GPA. …”
Publicado 2018
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7036por Rodríguez-Carrio, Javier, Mozo, Lourdes, López, Patricia, Nikiphorou, Elena, Suárez, Ana“…METHODS: Serum IgG anti-HDL antibodies, PON1 activity, and total antioxidant capacity (TAC) were quantified in 381 patients with different immune-driven diseases [18 mixed connective tissue disease (MCTD), 35 primary Sjögren syndrome (pSS), 38 systemic sclerosis (SSc), 33 ANCA-associated vasculitis (AAV), 60 diabetes mellitus 1, 29 autoimmune B12 deficiency/pernicious anemia, 29 primary biliary cirrhosis, 46 IBD/Crohn, 54 IBD/UC, and 39 celiac disease (CD)] and 138 healthy controls. …”
Publicado 2018
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7037“…A leptospirosis and a vasculitis screen were both negative. Symptoms had slowly improved but he was left with a left arm motor weakness, and the team was left puzzled as to what could have caused his signs and symptoms. …”
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7038por Pacholczak, Renata, Bazan-Socha, Stanisława, Iwaniec, Teresa, Zaręba, Lech, Kielczewski, Stan, Walocha, Jerzy A., Musiał, Jacek, Dropiński, Jerzy“…BACKGROUND: Granulomatosis with polyangiitis (GPA) is a rare granulomatous vasculitis affecting small- and medium-sized blood vessels. …”
Publicado 2018
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7039por Iwasaki, Kazuma, Morimoto, Mitsuaki, Ota, Gaku, Koinuma, Koji, Horie, Hisanaga, Sata, Naohiro, Nakaya, Takeo“…Histopathology evaluation revealed marked inflammatory cell infiltration in the intestinal tract wall and recanalization of the vessels, suggesting a circulatory disorder caused by vasculitis and antiphospholipid syndrome. Postoperatively, the clinical course was good. …”
Publicado 2018
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7040“…In addition, subgroup analysis based on disease type has indicated that the serum/plasma HMGB1 levels in patients with small vessel vasculitis, systemic lupus erythematosus, rheumatoid arthritis, ankylosing spondylitis and sjogren syndrome were significantly higher, compared to healthy controls. …”
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