429 related articles for article (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
[TBL] [Abstract][Full Text] [Related]
2. Characterization of PRF1, STX11 and UNC13D genotype-phenotype correlations in familial hemophagocytic lymphohistiocytosis.
Horne A; Ramme KG; Rudd E; Zheng C; Wali Y; al-Lamki Z; Gürgey A; Yalman N; Nordenskjöld M; Henter JI
Br J Haematol; 2008 Oct; 143(1):75-83. PubMed ID: 18710388
[TBL] [Abstract][Full Text] [Related]
3. Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosis.
Rudd E; Bryceson YT; Zheng C; Edner J; Wood SM; Ramme K; Gavhed S; Gürgey A; Hellebostad M; Bechensteen AG; Ljunggren HG; Fadeel B; Nordenskjöld M; Henter JI
J Med Genet; 2008 Mar; 45(3):134-41. PubMed ID: 17993578
[TBL] [Abstract][Full Text] [Related]
4. [Familial haemophagocytic lymphohistiocytosis caused by perforin deficit can be successfully treated by haematopoietic stem cell transplantation--the first diagnosed case in the Czech Republic].
Spísek R; Mejstríková E; Formánková R; Zizková H; Vávra V; Hrusák O; Sedivá A; Sedlácek P; Starý J
Cas Lek Cesk; 2006; 145(1):50-4. PubMed ID: 16468242
[TBL] [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
[TBL] [Abstract][Full Text] [Related]
6. Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A.
Zur Stadt U; Beutel K; Kolberg S; Schneppenheim R; Kabisch H; Janka G; Hennies HC
Hum Mutat; 2006 Jan; 27(1):62-8. PubMed ID: 16278825
[TBL] [Abstract][Full Text] [Related]
7. A neurologic presentation of familial hemophagocytic lymphohistiocytosis which mimicked septic emboli to the brain.
Turtzo LC; Lin DD; Hartung H; Barker PB; Arceci R; Yohay K
J Child Neurol; 2007 Jul; 22(7):863-8. PubMed ID: 17715280
[TBL] [Abstract][Full Text] [Related]
8. Prolonged course of familial hemophagocytic lymphohistiocytosis.
Steinberg O; Yacobovich J; Dgany O; Kodman Y; Livni G; Rachmel A; Stein J; Yaniv I; Tamary H
J Pediatr Hematol Oncol; 2006 Dec; 28(12):831-3. PubMed ID: 17164654
[TBL] [Abstract][Full Text] [Related]
9. Angeborene hämophagozytische Lymphohistiozytose (HLH).
Pachlopnik Schmid J; de Saint Basile G
Klin Padiatr; 2010 Nov; 222(6):345-50. PubMed ID: 20458667
[TBL] [Abstract][Full Text] [Related]
10. Mutations of the hemophagocytic lymphohistiocytosis-associated gene UNC13D in a patient with systemic juvenile idiopathic arthritis.
Hazen MM; Woodward AL; Hofmann I; Degar BA; Grom A; Filipovich AH; Binstadt BA
Arthritis Rheum; 2008 Feb; 58(2):567-70. PubMed ID: 18240215
[TBL] [Abstract][Full Text] [Related]
11. Familial Hemophagocytic Lymphohistiocytosis secondary to UNC13D mutation: a report of two cases.
Sadeghi P; Esslami GG; Rokni-Zadeh H; Changi-Ashtiani M; Mohsenipour R
BMC Pediatr; 2022 Nov; 22(1):667. PubMed ID: 36401200
[TBL] [Abstract][Full Text] [Related]
12. Screening the PRF1, UNC13D, STX11, SH2D1A, XIAP, and ITK gene mutations in Chinese children with Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis.
Zhizhuo H; Junmei X; Yuelin S; Qiang Q; Chunyan L; Zhengde X; Kunling S
Pediatr Blood Cancer; 2012 Mar; 58(3):410-4. PubMed ID: 21674762
[TBL] [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
[TBL] [Abstract][Full Text] [Related]
14. Hematopoietic stem cell transplantation for hemophagocytic lymphohistiocytosis: a retrospective analysis of data from the Italian Association of Pediatric Hematology Oncology (AIEOP).
Cesaro S; Locatelli F; Lanino E; Porta F; Di Maio L; Messina C; Prete A; Ripaldi M; Maximova N; Giorgiani G; Rondelli R; Aricò M; Fagioli F
Haematologica; 2008 Nov; 93(11):1694-701. PubMed ID: 18768529
[TBL] [Abstract][Full Text] [Related]
15. Fatal sibling cases of familial hemophagocytic lymphohistiocytosis (FHL) with MUNC13-4 mutations: case reports.
Nakao T; Shimizu T; Fukushima T; Saito M; Okamoto M; Sugiura M; Yamamoto K; Ueda I; Imashuku S; Kobayashi C; Koike K; Tsuchida M; Sumazaki R; Matsui A
Pediatr Hematol Oncol; 2008; 25(3):171-80. PubMed ID: 18432499
[TBL] [Abstract][Full Text] [Related]
16. 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
[TBL] [Abstract][Full Text] [Related]
17. [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
[TBL] [Abstract][Full Text] [Related]
18. Fatal Epstein-Barr virus infection in a case of familial hemophagocytic lymphohistiocytosis with syntaxin-11 mutation.
Albayrak M; Kaya Z; Yilmaz-Keskin E; Stadt UZ; Koçak U; Gürsel T
Turk J Pediatr; 2009; 51(4):371-4. PubMed ID: 19950846
[TBL] [Abstract][Full Text] [Related]
19. Review of hemophagocytic lymphohistiocytosis (HLH) in children with focus on Japanese experiences.
Ishii E; Ohga S; Imashuku S; Kimura N; Ueda I; Morimoto A; Yamamoto K; Yasukawa M
Crit Rev Oncol Hematol; 2005 Mar; 53(3):209-23. PubMed ID: 15718147
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
