109 related articles for article (PubMed ID: 21157897)
1. A665G mutation in PRF1 in a Turkish infant with familial hemophagocytic lymphohistiocytosis.
Aslan D
Pediatr Blood Cancer; 2011 Feb; 56(2):319-20. PubMed ID: 21157897
[No Abstract] [Full Text] [Related]
2. 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]
3. 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]
4. Mutations in the perforin gene in children with hemophagocytic lymphohistiocytosis.
Lu G; Xie ZD; Shen KL; Ye LJ; Wu RH; Liu CY; Jin YK; Yang S
Chin Med J (Engl); 2009 Dec; 122(23):2851-5. PubMed ID: 20092789
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. Adult onset of primary hemophagocytic syndrome in subjects carrying PRF1 mutations.
Wang Y; Wang Z; Chen H; Wang X
Ann Hematol; 2012 Sep; 91(9):1489-90. PubMed ID: 22249210
[No Abstract] [Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. 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]
13. Fatal hemophagocytic lymphohistiocytosis in X-linked chronic granulomatous disease associated with a perforin gene variant.
van Montfrans JM; Rudd E; van de Corput L; Henter JI; Nikkels P; Wulffraat N; Boelens JJ
Pediatr Blood Cancer; 2009 Apr; 52(4):527-9. PubMed ID: 19058215
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Functional impact of A91V mutation of the PRF1 perforin gene.
Martínez-Pomar N; Lanio N; Romo N; Lopez-Botet M; Matamoros N
Hum Immunol; 2013 Jan; 74(1):14-7. PubMed ID: 23073290
[TBL] [Abstract][Full Text] [Related]
16. Association of nonimmune hydrops fetalis with familial hemophagocytic lymphohistiocytosis in identical twin neonates with perforin His222Arg (c665A>G) mutation.
Balta G; Topcuoglu S; Gursoy T; Gurgey A; Ovali F
J Pediatr Hematol Oncol; 2013 Nov; 35(8):e332-4. PubMed ID: 23073042
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Hemophagocytic lymphohistiocytosis associated with parechovirus 3 infection.
Aviner S; Sofer D; Shulman LM; Bibi H; Weitzman S
J Pediatr Hematol Oncol; 2014 May; 36(4):e251-3. PubMed ID: 24072243
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]
