BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

289 related articles for article (PubMed ID: 17164654)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 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. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 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. 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]  

  • 12. Hemophagocytic lymphohistiocytosis with isolated central nervous system reactivation and optic nerve involvement.
    Chong KW; Lee JH; Choong CT; Paeds MM; Chan DW; Fortier MV; Chan MY
    J Child Neurol; 2012 Oct; 27(10):1336-9. PubMed ID: 22378674
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Successful treatment with liposteroid followed by reduced intensity stem cell transplantation in an infant with perforin deficiency presenting with hemophagocytic lymphohistiocytosis.
    Kobayashi Y; Salih HM; Kajiume T; Nakamura K; Miyagawa S; Sato T; Nishimura S; Kobayashi M
    J Pediatr Hematol Oncol; 2007 Mar; 29(3):178-82. PubMed ID: 17356398
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 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. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 15.