247 related articles for article (PubMed ID: 19595804)
1. 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]
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. 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]
4. Fulminant neonatal liver failure in siblings: probable congenital hemophagocytic lymphohistiocytosis.
Stapp J; Wilkerson S; Stewart D; Coventry S; Mo JQ; Bove KE
Pediatr Dev Pathol; 2006; 9(3):239-44. PubMed ID: 16944969
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. 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]
9. Transaldolase deficiency: a new cause of hydrops fetalis and neonatal multi-organ disease.
Valayannopoulos V; Verhoeven NM; Mention K; Salomons GS; Sommelet D; Gonzales M; Touati G; de Lonlay P; Jakobs C; Saudubray JM
J Pediatr; 2006 Nov; 149(5):713-7. PubMed ID: 17095351
[TBL] [Abstract][Full Text] [Related]
10. Familial hemophagocytic lymphohistiocytosis in a pediatric patient diagnosed by brain magnetic resonance imaging.
van Egmond ME; Vermeulen RJ; Peeters-Scholte CM; Augoustides-Savvopoulou P; Abbink F; Boelens JJ; van der Knaap MS
Neuropediatrics; 2011 Oct; 42(5):191-3. PubMed ID: 21959744
[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. A teenage boy with late onset hemophagocytic lymphohistiocytosis with predominant neurologic disease and perforin deficiency.
Beaty AD; Weller C; Levy B; Vogler C; Ferguson WS; Bicknese A; Knutsen AP
Pediatr Blood Cancer; 2008 May; 50(5):1070-2. PubMed ID: 18074390
[TBL] [Abstract][Full Text] [Related]
13. A91V perforin variation in healthy subjects and FHLH patients.
Busiello R; Fimiani G; Miano MG; Aricò M; Santoro A; Ursini MV; Pignata C
Int J Immunogenet; 2006 Apr; 33(2):123-5. PubMed ID: 16611257
[TBL] [Abstract][Full Text] [Related]
14. Hemophagocytic lymphohistiocytosis after lung transplant: report of 2 cases and a literature review.
Diaz-Guzman E; Dong B; Hobbs SB; Kesler MV; Hayes D
Exp Clin Transplant; 2011 Jun; 9(3):217-22. PubMed ID: 21649574
[TBL] [Abstract][Full Text] [Related]
15. Prolonged neurologic course of familial hemophagocytic lymphohistiocytosis.
Puliyel MM; Rose W; Kumar S; Moses PD; Gibikote S
Pediatr Neurol; 2009 Sep; 41(3):207-10. PubMed ID: 19664539
[TBL] [Abstract][Full Text] [Related]
16. An unusual cause of multiple organ dysfunction syndrome in the pediatric intensive care unit: hemophagocytic lymphohistiocytosis.
Karapinar B; Yilmaz D; Balkan C; Akin M; Ay Y; Kvakli K
Pediatr Crit Care Med; 2009 May; 10(3):285-90. PubMed ID: 19433941
[TBL] [Abstract][Full Text] [Related]
17. Atypical familial hemophagocytic lymphohistiocytosis responding to non-cytotoxic therapy.
Vlacha V; Feketea G
Pediatr Blood Cancer; 2007 Jan; 48(1):118. PubMed ID: 16724310
[No Abstract] [Full Text] [Related]
18. Pathology of the liver in familial hemophagocytic lymphohistiocytosis.
Chen JH; Fleming MD; Pinkus GS; Pinkus JL; Nichols KE; Mo JQ; Perez-Atayde AR
Am J Surg Pathol; 2010 Jun; 34(6):852-67. PubMed ID: 20442642
[TBL] [Abstract][Full Text] [Related]
19. Novel mutation of the perforin gene and maternal uniparental disomy 10 in a patient with familial hemophagocytic lymphohistiocytosis.
Al-Jasmi F; Abdelhaleem M; Stockley T; Lee KS; Clarke JT
J Pediatr Hematol Oncol; 2008 Aug; 30(8):621-4. PubMed ID: 18799942
[TBL] [Abstract][Full Text] [Related]
20. Diffuse multifocal chorangiomatosis of the placenta with multiple intestinal stenosis of the fetus: combination of rare causes for nonimmune hydrops fetalis.
Chopra A; Iyer VK; Thapar R; Singh N
Indian J Pathol Microbiol; 2006 Oct; 49(4):600-2. PubMed ID: 17183871
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]