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Journal Abstract Search
429 related items for PubMed ID: 20698142
1. Familial hemophagocytic lymphohistiocytosis in a 6-week-old male infant. Jakovljević G, Kardum-Skelin I, Rogosić S, Culić S, Stepan J, Gagro A, Skarić I, Mikecin L, Bonevski A, Barisić I, Nakić M. Coll Antropol; 2010 Jun; 34(2):631-4. PubMed ID: 20698142 [Abstract] [Full Text] [Related]
5. UNC13D is the predominant causative gene with recurrent splicing mutations in Korean patients with familial hemophagocytic lymphohistiocytosis. Yoon HS, Kim HJ, Yoo KH, Sung KW, Koo HH, Kang HJ, Shin HY, Ahn HS, Kim JY, Lim YT, Bae KW, Lee KO, Shin JS, Lee ST, Chung HS, Kim SH, Park CJ, Chi HS, Im HJ, Seo JJ. Haematologica; 2010 Apr; 95(4):622-6. PubMed ID: 20015888 [Abstract] [Full Text] [Related]
13. Unusual functional manifestations of a novel STX11 frameshift mutation in two infants with familial hemophagocytic lymphohistiocytosis type 4 (FHL4). Macartney CA, Weitzman S, Wood SM, Bansal D, Steele M, Meeths M, Abdelhaleem M, Bryceson YT. Pediatr Blood Cancer; 2011 Apr; 56(4):654-7. PubMed ID: 21298754 [Abstract] [Full Text] [Related]
17. Hematopoietic stem cell transplantation for familial hemophagocytic lymphohistiocytosis and Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis in Japan. Ohga S, Kudo K, Ishii E, Honjo S, Morimoto A, Osugi Y, Sawada A, Inoue M, Tabuchi K, Suzuki N, Ishida Y, Imashuku S, Kato S, Hara T. Pediatr Blood Cancer; 2010 Feb; 54(2):299-306. PubMed ID: 19827139 [Abstract] [Full Text] [Related]
18. [The study of gene mutations in unknown refractory viral infection and primary hemophagocytic lymphohistiocytosis]. Tong CR, Liu HX, Xie JJ, Wang F, Cai P, Wang H, Zhu J, Teng W, Zhang X, Yang JF, Zhang YL, Fei XH, Zhao J, Yin YM, Wu T, Wang JB, Sun Y, Liu R, Shi XD, Lu DP. Zhonghua Nei Ke Za Zhi; 2011 Apr; 50(4):280-3. PubMed ID: 21600143 [Abstract] [Full Text] [Related]