138 related articles for article (PubMed ID: 24915913)
1. [Advances in studies on hemophagocytic lymphohistiocytosis].
Luo Z; Tang Y
Zhonghua Er Ke Za Zhi; 2014 Apr; 52(4):267-70. PubMed ID: 24915913
[No Abstract] [Full Text] [Related]
2. 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]
3. [Etiology analysis of 38 patients with hemophagocytic syndrome].
Wang JS; Wang Z; Wu L; Chen X; Feng CC
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2010 Oct; 18(5):1316-20. PubMed ID: 21129284
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Remission and relapse of hemophagocytic lymphohistiocytosis in a patient harboring a PRF1 homozygous mutation: a case report.
Huang Z; Wang Y; Xie Z; Shen K
J Pediatr Hematol Oncol; 2014 Jan; 36(1):e5-8. PubMed ID: 23073044
[TBL] [Abstract][Full Text] [Related]
6. Perforin gene mutations in adult-onset hemophagocytic lymphohistiocytosis.
Nagafuji K; Nonami A; Kumano T; Kikushige Y; Yoshimoto G; Takenaka K; Shimoda K; Ohga S; Yasukawa M; Horiuchi H; Ishii E; Harada M
Haematologica; 2007 Jul; 92(7):978-81. PubMed ID: 17606450
[TBL] [Abstract][Full Text] [Related]
7. Surprisingly variable "dangers, toils, and snares" faced by humans and mice.
Trapani JA; Voskoboinik I
Blood; 2013 Jan; 121(4):568-70. PubMed ID: 23349371
[No Abstract] [Full Text] [Related]
8. PRF1 gene mutation in a Saudi patient with haemophagocytic lymphohistiocytosis.
Al Balwi MA; Al Harbi T; Al Abdulkareem I; Hajeer AH
Br J Biomed Sci; 2010; 67(2):88-9. PubMed ID: 20669767
[No Abstract] [Full Text] [Related]
9. 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]
10. Defective cytotoxic lymphocyte degranulation in syntaxin-11 deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients.
Bryceson YT; Rudd E; Zheng C; Edner J; Ma D; Wood SM; Bechensteen AG; Boelens JJ; Celkan T; Farah RA; Hultenby K; Winiarski J; Roche PA; Nordenskjöld M; Henter JI; Long EO; Ljunggren HG
Blood; 2007 Sep; 110(6):1906-15. PubMed ID: 17525286
[TBL] [Abstract][Full Text] [Related]
11. Perforin gene analaysis in an Iranian family with familial hemophagocytic lymphohistiocytosis.
Galehdari H; Mohammadi E; Andashti B; Naderi A; Molavi MA
Iran J Immunol; 2007 Jun; 4(2):122-6. PubMed ID: 17652853
[TBL] [Abstract][Full Text] [Related]
12. Unusual clinical presentations of familial hemophagocytic lymphohistiocytosis type-2.
Mhatre S; Madkaikar M; Jijina F; Ghosh K
J Pediatr Hematol Oncol; 2014 Nov; 36(8):e524-7. PubMed ID: 24390453
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. A novel perforin gene mutation in a Japanese family with hemophagocytic lymphohistiocytosis.
Ueda I; Kohdera U; Hibi S; Inaba T; Yamamoto K; Sugimoto T; Morimoto A; Ishii E; Imashuku S
Int J Hematol; 2006 Jan; 83(1):51-4. PubMed ID: 16443553
[TBL] [Abstract][Full Text] [Related]
15. Hemophagocytic lymphohistiocytosis in infants: a single center experience from India.
Ramzan M; Yadav SP; Kharya G; Chinnabhandar V; Enteserian M; Henter JI; Sachdeva A
Pediatr Hematol Oncol; 2014 Apr; 31(3):285-92. PubMed ID: 24383954
[TBL] [Abstract][Full Text] [Related]
16. 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]
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. Familial hemophagocytic lymphohistiocytosis: a model for understanding the human machinery of cellular cytotoxicity.
Sieni E; Cetica V; Mastrodicasa E; Pende D; Moretta L; Griffiths G; Aricò M
Cell Mol Life Sci; 2012 Jan; 69(1):29-40. PubMed ID: 21990010
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Familial haemophagocytic lymphohistiocytosis in patients who are heterozygous for the A91V perforin variation is often associated with other genetic defects.
Zhang K; Johnson JA; Biroschak J; Villanueva J; Lee SM; Bleesing JJ; Risma KA; Wenstrup RJ; Filipovich AH
Int J Immunogenet; 2007 Aug; 34(4):231-3. PubMed ID: 17627755
[No Abstract] [Full Text] [Related]
[Next] [New Search]