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Journal Abstract Search

252 related items for PubMed ID: 15609274

  • 1. An inframe perforin gene deletion in familial hemophagocytic lymphohistiocytosis is associated with perforin expression.
    Muralitharan S, Al Lamki Z, Dennison D, Christie BS, Wali YA, Zachariah M, Romana M, Bayoumi R, Krishnamoorthy R.
    Am J Hematol; 2005 Jan; 78(1):59-63. PubMed ID: 15609274
    [Abstract] [Full Text] [Related]

  • 2. Biology and treatment of familial hemophagocytic lymphohistiocytosis: importance of perforin in lymphocyte-mediated cytotoxicity and triggering of apoptosis.
    Henter JI.
    Med Pediatr Oncol; 2002 May; 38(5):305-9. PubMed ID: 11979453
    [Abstract] [Full Text] [Related]

  • 3. Sequence analysis of the granulysin and granzyme B genes in familial hemophagocytic lymphohistiocytosis.
    Ericson KG, Fadeel B, Andersson M, Gudmundsson GH, Gürgey A, Yalman N, Janka G, Nordenskjöld M, Henter JI.
    Hum Genet; 2003 Jan; 112(1):98-9. PubMed ID: 12483306
    [Abstract] [Full Text] [Related]

  • 4. The functional basis for hemophagocytic lymphohistiocytosis in a patient with co-inherited missense mutations in the perforin (PFN1) gene.
    Voskoboinik I, Thia MC, De Bono A, Browne K, Cretney E, Jackson JT, Darcy PK, Jane SM, Smyth MJ, Trapani JA.
    J Exp Med; 2004 Sep 20; 200(6):811-6. PubMed ID: 15365097
    [Abstract] [Full Text] [Related]

  • 5. 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 20; 22(7):863-8. PubMed ID: 17715280
    [Abstract] [Full Text] [Related]

  • 6. 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 20; 46(4):482-8. PubMed ID: 16365863
    [Abstract] [Full Text] [Related]

  • 7. Novel spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis in ethnic Omani patients.
    Muralitharan S, Wali YA, Dennison D, Lamki ZA, Zachariah M, Nagwa el B, Pathare A, Krishnamoorthy R.
    Am J Hematol; 2007 Dec 20; 82(12):1099-102. PubMed ID: 17674359
    [Abstract] [Full Text] [Related]

  • 8. 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 20; 91(9):1257-60. PubMed ID: 16956828
    [Abstract] [Full Text] [Related]

  • 9. 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 20; 4(2):122-6. PubMed ID: 17652853
    [Abstract] [Full Text] [Related]

  • 10. [Familial hemophagocytic lymphohistiocytosis(FHL)].
    Kawa K.
    Ryoikibetsu Shokogun Shirizu; 2000 Jun 20; (32):553-6. PubMed ID: 11212803
    [No Abstract] [Full Text] [Related]

  • 11. 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; 20(8):603-9. PubMed ID: 14578030
    [Abstract] [Full Text] [Related]

  • 12. Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis.
    Göransdotter Ericson K, Fadeel B, Nilsson-Ardnor S, Söderhäll C, Samuelsson A, Janka G, Schneider M, Gürgey A, Yalman N, Révész T, Egeler R, Jahnukainen K, Storm-Mathiesen I, Haraldsson A, Poole J, de Saint Basile G, Nordenskjöld M, Henter J.
    Am J Hum Genet; 2001 Mar 20; 68(3):590-7. PubMed ID: 11179007
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  • 14. Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11.
    zur Stadt U, Schmidt S, Kasper B, Beutel K, Diler AS, Henter JI, Kabisch H, Schneppenheim R, Nürnberg P, Janka G, Hennies HC.
    Hum Mol Genet; 2005 Mar 15; 14(6):827-34. PubMed ID: 15703195
    [Abstract] [Full Text] [Related]

  • 15. Review of hemophagocytic lymphohistiocytosis (HLH) in children with focus on Japanese experiences.
    Ishii E, Ohga S, Imashuku S, Kimura N, Ueda I, Morimoto A, Yamamoto K, Yasukawa M.
    Crit Rev Oncol Hematol; 2005 Mar 15; 53(3):209-23. PubMed ID: 15718147
    [Abstract] [Full Text] [Related]

  • 16. [Familial haemophagocytic lymphohistiocytosis caused by perforin deficit can be successfully treated by haematopoietic stem cell transplantation--the first diagnosed case in the Czech Republic].
    Spísek R, Mejstríková E, Formánková R, Zizková H, Vávra V, Hrusák O, Sedivá A, Sedlácek P, Starý J.
    Cas Lek Cesk; 2006 Mar 15; 145(1):50-4. PubMed ID: 16468242
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  • 18. Perforin and lymphohistiocytic proliferative disorders.
    Katano H, Cohen JI.
    Br J Haematol; 2005 Mar 15; 128(6):739-50. PubMed ID: 15755277
    [Abstract] [Full Text] [Related]

  • 19. Perforin expression can define CD8 positive lymphocyte subsets in pigs allowing phenotypic and functional analysis of natural killer, cytotoxic T, natural killer T and MHC un-restricted cytotoxic T-cells.
    Denyer MS, Wileman TE, Stirling CM, Zuber B, Takamatsu HH.
    Vet Immunol Immunopathol; 2006 Apr 15; 110(3-4):279-92. PubMed ID: 16325923
    [Abstract] [Full Text] [Related]

  • 20. Perforin expression in cytotoxic lymphocytes from patients with hemophagocytic lymphohistiocytosis and their family members.
    Kogawa K, Lee SM, Villanueva J, Marmer D, Sumegi J, Filipovich AH.
    Blood; 2002 Jan 01; 99(1):61-6. PubMed ID: 11756153
    [Abstract] [Full Text] [Related]

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