HuGE Literature Finder
Rare Disease
Records 1-12
Hypoalbuminemia on admission in COVID-19 infection: An early predictor of mortality and adverse events. A retrospective observational study.
Medicina clinica 2021 2 . Viana-Llamas María C, Arroyo-Espliguero Ramón, Silva-Obregón J Alberto, Uribe-Heredia Giovanna, Núñez-Gil Iván, García-Magallón Belén, Torán-Martínez Claudio G, Castillo-Sandoval Alicia, Díaz-Caraballo Eva, Rodríguez-Guinea Itsaso, Domínguez-López Jes |
Serum amyloid A1 (SAA1) gene polymorphisms in Japanese patients with adult-onset Still's disease.
Medicine 2018 Dec 97 (49): e13394. Yashiro Makiko, Furukawa Hiroshi, Asano Tomoyuki, Sato Shuzo, Kobayashi Hiroko, Watanabe Hiroshi, Suzuki Eiji, Nakamura Tadashi, Koga Tomohiro, Shimizu Toshimasa, Umeda Masataka, Nonaka Fumiaki, Ueki Yukitaka, Eguchi Katsumi, Kawakami Atsushi, Migita Kiyos |
Association of IRF5 polymorphisms with susceptibility to hemophagocytic lymphohistiocytosis in children.
Journal of clinical immunology 2011 Dec 31 (6): 946-51. Yanagimachi Masakatsu, Goto Hiroaki, Miyamae Takako, Kadota Keisuke, Imagawa Tomoyuki, Mori Masaaki, Sato Hidenori, Yanagisawa Ryu, Kaneko Tetsuji, Morita Satoshi, Ishii Eiichi, Yokota Shump |
Association of IRF5 polymorphisms with susceptibility to macrophage activation syndrome in patients with juvenile idiopathic arthritis.
The Journal of rheumatology 2011 Apr 38 (4): 769-74. Yanagimachi Masakatsu, Naruto Takuya, Miyamae Takako, Hara Takuma, Kikuchi Masako, Hara Ryoki, Imagawa Tomoyuki, Mori Masaaki, Sato Hidenori, Goto Hiroaki, Yokota Shump |
Mutations in the perforin gene can be linked to macrophage activation syndrome in patients with systemic onset juvenile idiopathic arthritis.
Rheumatology (Oxford, England) 2010 Mar 49 (3): 441-9. Vastert Sebastiaan J, van Wijk Richard, D'Urbano Leila E, de Vooght Karen M K, de Jager Wilco, Ravelli Angelo, Magni-Manzoni Silvia, Insalaco Antonella, Cortis Elisabetta, van Solinge Wouter W, Prakken Berent J, Wulffraat Nico M, de Benedetti Fabrizio, Kuis Wiet |
Macrophage activation syndrome in patients with systemic juvenile idiopathic arthritis is associated with MUNC13-4 polymorphisms.
Arthritis and rheumatism 2008 Sep 58 (9): 2892-6. Zhang Kejian, Biroschak Jennifer, Glass David N, Thompson Susan D, Finkel Terri, Passo Murray H, Binstadt Bryce A, Filipovich Alexandra, Grom Alexei |
- Page last reviewed:Oct 1, 2020
- Page last updated:Mar 05, 2021
- Content source: