Zobrazeno 1 - 10
of 5 435
pro vyhledávání: '"adult still's disease"'
Autor:
Kaneko, Yuko1 (AUTHOR) ykaneko.z6@keio.jp, Kameda, Hideto2 (AUTHOR), Ikeda, Kei3,4 (AUTHOR), Yamashita, Katsuhisa5 (AUTHOR), Ozaki, Ryoto5 (AUTHOR), Tanaka, Yoshiya6 (AUTHOR)
Publikováno v:
International Journal of Rheumatic Diseases. Oct2023, Vol. 26 Issue 10, p1967-1978. 12p.
Autor:
Masias-León, Yuderleys1 yumale97@hotmail.com, García, Diego Fernando2, Ruíz-González, Carlos Eduardo1, Criado-Villamizar, Juan Daniel1, Centeno-Hurtado, Katherine3, Badillo-Abril, Reynaldo4,5
Publikováno v:
Medicina Interna de Mexico. Jan/Feb2023, Vol. 39 Issue 1, p213-218. 6p.
Autor:
Kusaka, Katsuhide1 (AUTHOR), Miyagawa, Ippei1 (AUTHOR), Kosaka, Shunpei1 (AUTHOR), Matsunaga, Satsuki1 (AUTHOR), Nakayamada, Shingo1 (AUTHOR) s-nakaya@med.uoeh-u.ac.jp, Tanaka, Yoshiya1 (AUTHOR)
Publikováno v:
Modern Rheumatology Case Reports. Jan2023, Vol. 7 Issue 1, p182-187. 6p.
Autor:
Anastasia D. Strutynskaya, Maria A. Karnaushkina, Dmitriy Y. Ovsyannikov, Sergey A. Filippov, Igor E. Tyurin
Publikováno v:
Alʹmanah Kliničeskoj Mediciny, Vol 50, Iss 2, Pp 127-132 (2022)
Adult Still's disease is a rare systemic disorder of unknown etiology. Its course is often complicated by interstitial pneumonia and fulminant hepatitis. Published data have indicated some common mechanisms of systemic inflammation in patients with a
Externí odkaz:
https://doaj.org/article/e00c5dc4db584604a103ac00fe11cabf
Akademický článek
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Publikováno v:
Global Rheumatology, Vol 4, Iss 1 (2023)
Introduction: Still's disease is a rare autoinflammatory disorder that affects mostly young adults, with an unknown cause and difficult to diagnose. This study describes four cases of adult-onset Still's disease in Guatemala, providing valuable infor
Externí odkaz:
https://doaj.org/article/894203825a6d4c4ea9ab28d9445ff9cb
Autor:
E. L. Nasonov, E. Feist
Publikováno v:
Научно-практическая ревматология, Vol 59, Iss 6, Pp 645-665 (2021)
Still's disease in children (systemic juvenile idiopathic arthritis - JIA) and adult Still's disease (ASD) are considered as systemic autoinflammatory diseases of unknown etiology, which are based on similar immunopathogenetic mechanisms associated w
Externí odkaz:
https://doaj.org/article/3cc5b08c5b264333b68e9cfebc84bcb4
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Autor:
Leonid I. DVORETSKY, Daria V. NOVIKOVA, Anna V. TORGASHNA, Alla M. KOVRIGINA, Tatiana N. MOISEEVA, Roza M. VAKOLYUK, Maria A. KARNAUSHKINA
Publikováno v:
Archives of the Balkan Medical Union, Vol 56, Iss 3, Pp 363-369 (2021)
Introduction. Adult-onset Still’s disease is a rare systemic autoinflammatory disorder of unknown etiology, characterized by persistent fever, maculopapular skin rash, and arthritis or arthralgia. This triad of symptoms is usually accompanied by ly
Externí odkaz:
https://doaj.org/article/69dd83e603b746c08bad98a204607d75
Publikováno v:
Case Reports in Ophthalmology, Vol 12, Iss 2, Pp 531-537 (2021)
Adult Still’s disease (ASD) is a rare systemic inflammatory disorder in which ocular manifestations have rarely been described. We report a 29-year-old Japanese woman with a rare case of refractory ASD complicated by Purtscher-like retinopathy. She
Externí odkaz:
https://doaj.org/article/050f8ec188d143a1bbad2467b2a67df3