188 related articles for article (PubMed ID: 23073042)
1. 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]
2. Hemophagocytic lymphohistiocytosis with Munc13-4 mutation: a cause of recurrent fatal hydrops fetalis.
Bechara E; Dijoud F; de Saint Basile G; Bertrand Y; Pondarré C
Pediatrics; 2011 Jul; 128(1):e251-4. PubMed ID: 21646258
[TBL] [Abstract][Full Text] [Related]
3. Hydrops fetalis and early neonatal multiple organ failure in familial hemophagocytic lymphohistiocytosis.
Vermeulen MJ; de Haas V; Mulder MF; Flohil C; Fetter WP; van de Kamp JM
Eur J Med Genet; 2009; 52(6):417-20. PubMed ID: 19595804
[TBL] [Abstract][Full Text] [Related]
4. Hemophagocytic lymphohistiocytosis presenting with nonimmune hydrops fetalis.
Malloy CA; Polinski C; Alkan S; Manera R; Challapalli M
J Perinatol; 2004 Jul; 24(7):458-60. PubMed ID: 15224121
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Familial hemophagocytic lymphohistiocytosis in an adult patient homozygous for A91V in the perforin gene, with tuberculosis infection.
Mancebo E; Allende LM; Guzmán M; Paz-Artal E; Gil J; Urrea-Moreno R; Fernández-Cruz E; Gayà A; Calvo J; Arbós A; Durán MA; Canet R; Balanzat J; Udina MA; Vercher FJ
Haematologica; 2006 Sep; 91(9):1257-60. PubMed ID: 16956828
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. 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]
12. Nonimmune hydrops fetalis in two cases of consanguineous parents and associated with hereditary spherocytosis and hemophagocytic hystiocytosis.
Yetgin S; Aytac S; Gurakan F; Yurdakok M
J Perinatol; 2007 Apr; 27(4):252-4. PubMed ID: 17377610
[TBL] [Abstract][Full Text] [Related]
13. Correlation between phenotypic heterogeneity and gene mutational characteristics in familial hemophagocytic lymphohistiocytosis (FHL).
Ueda I; Ishii E; Morimoto A; Ohga S; Sako M; Imashuku S
Pediatr Blood Cancer; 2006 Apr; 46(4):482-8. PubMed ID: 16365863
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. Clinical and genetic studies of familial hemophagocytic lymphohistiocytosis in Oman: need for early treatment.
Al-Lamki Z; Wali YA; Pathare A; Ericson KG; Henter JI
Pediatr Hematol Oncol; 2003 Dec; 20(8):603-9. PubMed ID: 14578030
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Central nervous system involvement in a case of familial hemophagocytic lymphohistiocytosis with perforin mutation.
Akbayram S; Akgun C; Dogan M; Caksen H; Okur H; Oner AF
Genet Couns; 2011; 22(3):281-5. PubMed ID: 22029169
[TBL] [Abstract][Full Text] [Related]
20. Late-onset cases of familial hemophagocytic lymphohistiocytosis with missense perforin gene mutations.
Ueda I; Kurokawa Y; Koike K; Ito S; Sakata A; Matsumora T; Fukushima T; Morimoto A; Ishii E; Imashuku S
Am J Hematol; 2007 Jun; 82(6):427-32. PubMed ID: 17266056
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
