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Journal Abstract Search

183 related items for PubMed ID: 11212803

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

  • 2. 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; 53(3):209-23. PubMed ID: 15718147
    [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. 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]

  • 5. 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]

  • 6. Perforin deficiency and familial hemophagocytic lymphohistiocytosis.
    Zipursky A.
    Pediatr Res; 2001 Jan; 49(1):3. PubMed ID: 11134481
    [No Abstract] [Full Text] [Related]

  • 7. Perforin and lymphohistiocytic proliferative disorders.
    Katano H, Cohen JI.
    Br J Haematol; 2005 Mar; 128(6):739-50. PubMed ID: 15755277
    [Abstract] [Full Text] [Related]

  • 8. 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; 68(3):590-7. PubMed ID: 11179007
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Pathogenesis of hemophagocytic syndrome (HPS).
    Larroche C, Mouthon L.
    Autoimmun Rev; 2004 Feb 20; 3(2):69-75. PubMed ID: 15003190
    [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. [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 Dec 20; 145(1):50-4. PubMed ID: 16468242
    [Abstract] [Full Text] [Related]

  • 13. 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 20; 29(3):178-82. PubMed ID: 17356398
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. Perforin gene defects in familial hemophagocytic lymphohistiocytosis.
    Stepp SE, Dufourcq-Lagelouse R, Le Deist F, Bhawan S, Certain S, Mathew PA, Henter JI, Bennett M, Fischer A, de Saint Basile G, Kumar V.
    Science; 1999 Dec 03; 286(5446):1957-9. PubMed ID: 10583959
    [Abstract] [Full Text] [Related]

  • 16. Prenatal diagnosis of perforin gene mutations in familial hemophagocytic lymphohistiocytosis (FHLH).
    zur Stadt U, Pruggmayer M, Jung H, Henter JI, Schneider M, Kabisch H, Janka G.
    Prenat Diagn; 2002 Jan 03; 22(1):80-1. PubMed ID: 11810660
    [No Abstract] [Full Text] [Related]

  • 17. [Treatment of familial hemophagocytic lymphohistiocytosis].
    Sako M.
    Rinsho Ketsueki; 1999 Feb 03; 40(2):88-91. PubMed ID: 10199198
    [No Abstract] [Full Text] [Related]

  • 18. [Virus-associated hemophagocytic syndrome(VAHS)].
    Kawa K.
    Ryoikibetsu Shokogun Shirizu; 2000 Feb 03; (32):561-3. PubMed ID: 11212806
    [No Abstract] [Full Text] [Related]

  • 19. Primary hemophagocytic lymphohistiocytosis in Turkish children.
    Gürgey A, Göğüş S, Ozyürek E, Aslan D, Gümrük F, Cetin M, Yüce A, Ceyhan M, Seçmeer G, Yetgin S, Hiçsönmez G.
    Pediatr Hematol Oncol; 2003 Feb 03; 20(5):367-71. PubMed ID: 12775534
    [Abstract] [Full Text] [Related]

  • 20. [Pathophysiology of and therapy for hemophagocytic syndrome].
    Kawa K.
    Nihon Naika Gakkai Zasshi; 2004 Aug 10; 93(8):1666-72. PubMed ID: 15384700
    [No Abstract] [Full Text] [Related]

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