Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Adult-onset Stillʼs disease"'
Autor:
Winston Wing-Shing Fung, Amelia Chien-Wei Chao, Wing-Fai Pang, Raymond Siu-Ming Wong, Kai-Ming Chow, Cheuk-Chun Szeto
Publikováno v:
BMC Nephrology, Vol 25, Iss 1, Pp 1-6 (2024)
Abstract Background Atypical haemolytic uremic syndrome (aHUS) is an uncommon form of thrombotic microangiopathy (TMA). However, it remains difficult to diagnose the disease early, given its non-specific and overlapping presentation to other conditio
Externí odkaz:
https://doaj.org/article/209cee6430e749dc86e0c5e76bdf57d9
Akademický článek
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Autor:
Hana Malcova, Tomas Milota, Zuzana Strizova, Dita Cebecauerova, Ilja Striz, Anna Sediva, Rudolf Horvath
Publikováno v:
Frontiers in Pharmacology, Vol 11 (2021)
Polygenic autoinflammatory diseases (AIDs), such as systemic juvenile idiopathic arthritis (sJIA), adult-onset Still's disease, Kawasaki disease, idiopathic recurrent pericarditis (IRP), Behçet’s Syndrome, Crystal-induced arthropatihes such as gou
Externí odkaz:
https://doaj.org/article/01a244f96caf4555a9d5b87636f26659
Publikováno v:
The Pan African Medical Journal, Vol 34, Iss 17 (2019)
Adult-onset Still's disease (AOSD) has been recognized as a cause of fevers of unknown origin. Malignancies are the most important differential diagnoses of AOSD which has been rarely reported in association with cancer. The present paper undertakes
Externí odkaz:
https://doaj.org/article/80c66a4f7c6c41c58f85feda1de0f2fe
Autor:
Mutlu Hayran, Kenan Aksu, Hakan Emmungil, Emre Bilgin, Cemal Bes, Abdulsamet Erden, Ediz Dalkilic, Servet Akar, Ahmet Omma, Orhan Küçükşahin, Selime Ermurat, Umut Kalyoncu, Nilüfer Alpay Kanıtez, Timuçin Kaşifoğlu, Fatih Yildiz, Muhammet Cinar
Background/Aim: Adult-onset Still’s disease (AOSD) is a multi-systemic, autoinflammatory disorder. Several activity scores have been proposed but none of them have been adopted universally. Our aim was to create a clinician-friendly activity scorin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab3677bd3d91597788f6ea3a413f8f77
https://hdl.handle.net/11454/76625
https://hdl.handle.net/11454/76625
Akademický článek
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Autor:
Anne Pankow, Eugen Feist, Ulrich Baumann, Martin Kirschstein, Gerd-Rüdiger Burmester, Annette Doris Wagner
Publikováno v:
Der Internist
In the last 20 years the clarification of monogenic periodic febrile diseases has led to the independent concept of autoinflammation. In this heterogeneous group polygenic complex diseases are also now included. The spectrum of symptoms is continuous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdb075571333523643f0cf00b683ecd5
http://europepmc.org/articles/PMC8653393
http://europepmc.org/articles/PMC8653393
Akademický článek
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Publikováno v:
The Pan African Medical Journal, Vol 22, Iss 77 (2015)
The adult onset Still's disease is a rare inflammatory pathology of unknown pathogeny. The clinical features are variable. The diagnosis is difficult since exclusion of infectious, systemic and tumoral pathologies should be done. The articular compli
Externí odkaz:
https://doaj.org/article/22a195f8aa3d44279e6e660e078a957d
Autor:
Cláudia Diniz Lopes Marques, Patrícia Souza Nunes, Ângela Luzia Branco Pinto Duarte, Fernando S. Cavalcanti
Publikováno v:
Revista Brasileira de Reumatologia, Vol 45, Iss 5, Pp 331-334 (2005)
A doença de Castleman (DC) é uma doença linfoproliferativa não neoplásica rara, de etiologia desconhecida, que se caracteriza clinicamente por adenomegalias isoladas ou múltiplas, podendo ou não estar associada a sintomas sistêmicos, como feb
Externí odkaz:
https://doaj.org/article/73da66fe78d545a1ad737e7d9fe543d3