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Journal Abstract Search

183 related items for PubMed ID: 11212803

  • 21. 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
    [Abstract] [Full Text] [Related]

  • 22. 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
    [Abstract] [Full Text] [Related]

  • 23. [Two brothers with familial hemophagocytic lymphohistiocytosis, treated by transplantation of stem cells from a single unrelated donor].
    Kraal KC, Bredius RG, Lankester AC, Granzen B, Oudshoorn M, Egeler RM.
    Ned Tijdschr Geneeskd; 2002 Nov 30; 146(48):2309-12. PubMed ID: 12497761
    [Abstract] [Full Text] [Related]

  • 24. Acute inflammatory demyelinating polyradiculoneuropathy associated with perforin-deficient familial haemophagocytic lymphohistiocytosis.
    Del Giudice E, Savoldi G, Notarangelo LD, Di Benedetto L, Manganelli F, Bruzzese E, Romano A, Santoro L.
    Acta Paediatr; 2003 Nov 30; 92(3):398-401. PubMed ID: 12725560
    [Abstract] [Full Text] [Related]

  • 25. Familial hemophagocytic lymphohistiocytosis: too little cell death can seriously damage your health.
    Fadeel B, Orrenius S, Henter JI.
    Leuk Lymphoma; 2001 Jun 30; 42(1-2):13-20. PubMed ID: 11699200
    [Abstract] [Full Text] [Related]

  • 26. Gene abnormalities in patients with hemophagocytic lymphohistiocytosis.
    Grunebaum E, Roifman CM.
    Isr Med Assoc J; 2002 May 30; 4(5):366-9. PubMed ID: 12040827
    [Abstract] [Full Text] [Related]

  • 27. Pathogenesis of haemophagocytic lymphohistiocytosis.
    Aricò M, Danesino C, Pende D, Moretta L.
    Br J Haematol; 2001 Sep 30; 114(4):761-9. PubMed ID: 11564062
    [No Abstract] [Full Text] [Related]

  • 28. [Familial hemophagocytic lymphohistiocytosis].
    Tsunamoto K, Kasubuchi Y, Hibi S, Imashuku S.
    Ryoikibetsu Shokogun Shirizu; 1998 Sep 30; (22 Pt 3):347-51. PubMed ID: 9851158
    [No Abstract] [Full Text] [Related]

  • 29. [Hemophagocytic syndrome: diagnostic problems].
    Czogała M, Czogała W, Balwierz W.
    Przegl Lek; 2006 Sep 30; 63(1):47-52. PubMed ID: 16892901
    [Abstract] [Full Text] [Related]

  • 30. Perforin defects of primary haemophagocytic lymphohistiocytosis in Japan.
    Suga N, Takada H, Nomura A, Ohga S, Ishii E, Ihara K, Ohshima K, Hara T.
    Br J Haematol; 2002 Feb 30; 116(2):346-9. PubMed ID: 11841437
    [Abstract] [Full Text] [Related]

  • 31. Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis.
    Feldmann J, Le Deist F, Ouachée-Chardin M, Certain S, Alexander S, Quartier P, Haddad E, Wulffraat N, Casanova JL, Blanche S, Fischer A, de Saint Basile G.
    Br J Haematol; 2002 Jun 30; 117(4):965-72. PubMed ID: 12060139
    [Abstract] [Full Text] [Related]

  • 32. No mutations of SAP/SH2D1A/DSHP and perforin genes in patients with Epstein-Barr virus-associated hemophagocytic syndrome in Japan.
    Ma X, Okamura A, Yosioka M, Ishiguro N, Kikuta H, Kobayashi K.
    J Med Virol; 2001 Oct 30; 65(2):358-61. PubMed ID: 11536244
    [Abstract] [Full Text] [Related]

  • 33. Severe and progressive encephalitis as a presenting manifestation of a novel missense perforin mutation and impaired cytolytic activity.
    Feldmann J, Ménasché G, Callebaut I, Minard-Colin V, Bader-Meunier B, Le Clainche L, Fischer A, Le Deist F, Tardieu M, de Saint Basile G.
    Blood; 2005 Apr 01; 105(7):2658-63. PubMed ID: 15598808
    [Abstract] [Full Text] [Related]

  • 34. 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 01; 4(2):122-6. PubMed ID: 17652853
    [Abstract] [Full Text] [Related]

  • 35. [Diagnosis and treatment of hemophagocytic syndrome].
    Kawa K, Sakata A, Takeshita Y, Inoue M.
    Rinsho Ketsueki; 2005 Jun 01; 46(6):418-23. PubMed ID: 16447723
    [No Abstract] [Full Text] [Related]

  • 36. Adult onset and atypical presentation of hemophagocytic lymphohistiocytosis in siblings carrying PRF1 mutations.
    Clementi R, Emmi L, Maccario R, Liotta F, Moretta L, Danesino C, Aricó M.
    Blood; 2002 Sep 15; 100(6):2266-7. PubMed ID: 12229880
    [No Abstract] [Full Text] [Related]

  • 37. Genetic subtypes of familial hemophagocytic lymphohistiocytosis: correlations with clinical features and cytotoxic T lymphocyte/natural killer cell functions.
    Ishii E, Ueda I, Shirakawa R, Yamamoto K, Horiuchi H, Ohga S, Furuno K, Morimoto A, Imayoshi M, Ogata Y, Zaitsu M, Sako M, Koike K, Sakata A, Takada H, Hara T, Imashuku S, Sasazuki T, Yasukawa M.
    Blood; 2005 May 01; 105(9):3442-8. PubMed ID: 15632205
    [Abstract] [Full Text] [Related]

  • 38. [Difficulties in the diagnosis of familial hemophagocytic lymphohistiocytosis].
    Astigarraga Aguirre I, Navajas Gutiérrez A, Fernández-Teijeiro Alvarez A, Latorre García J, Aldamiz-Echevarria Azuara L.
    An Esp Pediatr; 2002 Feb 01; 56(2):168-70. PubMed ID: 11827656
    [Abstract] [Full Text] [Related]

  • 39. [Familial hemophagocytic lymphohistiocytosis: diagnosis, treatment and pathophysiological mechanisms].
    Henter JI, Samuelsson A, Ericson K, Nilsson-Ardnor S, Elinder G, Fadeel B.
    Lakartidningen; 2000 Mar 22; 97(12):1405-8. PubMed ID: 10765622
    [Abstract] [Full Text] [Related]

  • 40. 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]

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