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Journal Abstract Search

183 related items for PubMed ID: 11212803

  • 41. [Familial lymphohistiocytosis. Evolution of management apropos of 3 cases].
    Mikhael R, Gerbaka B, Melki I, Akatcherian C, Naman R.
    J Med Liban; 2000; 48(2):100-3. PubMed ID: 11028159
    [Abstract] [Full Text] [Related]

  • 42. Perforin deficiency: fighting unarmed?
    Arnaout RA.
    Immunol Today; 2000 Nov; 21(11):592; author reply 593-4. PubMed ID: 11221684
    [No Abstract] [Full Text] [Related]

  • 43. 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; 82(12):1099-102. PubMed ID: 17674359
    [Abstract] [Full Text] [Related]

  • 44. Familial haemophagocytic lymphohistiocytosis in patients who are heterozygous for the A91V perforin variation is often associated with other genetic defects.
    Zhang K, Johnson JA, Biroschak J, Villanueva J, Lee SM, Bleesing JJ, Risma KA, Wenstrup RJ, Filipovich AH.
    Int J Immunogenet; 2007 Aug; 34(4):231-3. PubMed ID: 17627755
    [No Abstract] [Full Text] [Related]

  • 45. Apoptosis induced by the lymphocyte effector molecule perforin.
    Bolitho P, Voskoboinik I, Trapani JA, Smyth MJ.
    Curr Opin Immunol; 2007 Jun; 19(3):339-47. PubMed ID: 17442557
    [Abstract] [Full Text] [Related]

  • 46. Unusual immunophenotype of CD8+ T cells in familial hemophagocytic lymphohistiocytosis.
    Karandikar NJ, Kroft SH, Yegappan S, Rogers BB, Aquino VM, Lee KM, Kumar V, Guenaga FJ, Jaffe ES, Douek DC, McKenna RW.
    Blood; 2004 Oct 01; 104(7):2007-9. PubMed ID: 15205266
    [Abstract] [Full Text] [Related]

  • 47. Near fatal cerebellar swelling in familial hemophagocytic lymphohistiocytosis.
    Astigarraga I, Prats JM, Navajas A, Fernández-Teijeiro A, Urberuaga A.
    Pediatr Neurol; 2004 May 01; 30(5):361-4. PubMed ID: 15165642
    [Abstract] [Full Text] [Related]

  • 48. [Familial hemophagocytic lymphohistiocytosis: report of two new cases].
    Perez-Caballero Macarrón C, Couselo Sánchez JM, Maldonado Regalado MS, Muñoz Villa A.
    An Esp Pediatr; 1998 Jul 01; 49(1):71-4. PubMed ID: 9718772
    [No Abstract] [Full Text] [Related]

  • 49. Development of hemophagocytic lymphohistiocytosis in triplets infected with HHV-8.
    Grossman WJ, Radhi M, Schauer D, Gerday E, Grose C, Goldman FD.
    Blood; 2005 Aug 15; 106(4):1203-6. PubMed ID: 15840696
    [Abstract] [Full Text] [Related]

  • 50. On the pathogenesis of perforin defects and related immunodeficiencies.
    Moretta L, Moretta A, Hengartner H, Zinkernagel RM.
    Immunol Today; 2000 Nov 15; 21(11):593-4. PubMed ID: 11221685
    [No Abstract] [Full Text] [Related]

  • 51. Hemophagocytic lymphohistiocytosis: diagnosis, pathophysiology, treatment, and future perspectives.
    Verbsky JW, Grossman WJ.
    Ann Med; 2006 Nov 15; 38(1):20-31. PubMed ID: 16448985
    [Abstract] [Full Text] [Related]

  • 52. 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]

  • 53. Identification of novel MUNC13-4 mutations in familial haemophagocytic lymphohistiocytosis and functional analysis of MUNC13-4-deficient cytotoxic T lymphocytes.
    Yamamoto K, Ishii E, Sako M, Ohga S, Furuno K, Suzuki N, Ueda I, Imayoshi M, Yamamoto S, Morimoto A, Takada H, Hara T, Imashuku S, Sasazuki T, Yasukawa M.
    J Med Genet; 2004 Oct 01; 41(10):763-7. PubMed ID: 15466010
    [Abstract] [Full Text] [Related]

  • 54. [Diagnosis and pathogenesis of primary (familial) hemophagocytic lymphohistiocytosis].
    Ishii E, Kimura N.
    Rinsho Ketsueki; 1999 Feb 01; 40(2):83-7. PubMed ID: 10199197
    [No Abstract] [Full Text] [Related]

  • 55. A functional analysis of the putative polymorphisms A91V and N252S and 22 missense perforin mutations associated with familial hemophagocytic lymphohistiocytosis.
    Voskoboinik I, Thia MC, Trapani JA.
    Blood; 2005 Jun 15; 105(12):4700-6. PubMed ID: 15755897
    [Abstract] [Full Text] [Related]

  • 56. Familial hemophagocytic lymphohistiocytosis in two brothers.
    Gan GG, Eow GI, Teh A, Ng SC, Sangkar JV.
    Med J Malaysia; 2004 Mar 15; 59(1):100-2. PubMed ID: 15535343
    [Abstract] [Full Text] [Related]

  • 57. A novel perforin gene mutation in a Japanese family with hemophagocytic lymphohistiocytosis.
    Ueda I, Kohdera U, Hibi S, Inaba T, Yamamoto K, Sugimoto T, Morimoto A, Ishii E, Imashuku S.
    Int J Hematol; 2006 Jan 15; 83(1):51-4. PubMed ID: 16443553
    [Abstract] [Full Text] [Related]

  • 58.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 59. [Familial lymphohistiocytosis--a second Tunisian case].
    Trabelsi M, Bennaceur B, Damergi R, Gorji Y, Ben Jilani S.
    Tunis Med; 1990 Dec 15; 68(12):751-5. PubMed ID: 2089757
    [No Abstract] [Full Text] [Related]

  • 60. Novel perforin mutation in a patient with hemophagocytic lymphohistiocytosis and CD45 abnormal splicing.
    McCormick J, Flower DR, Strobel S, Wallace DL, Beverley PC, Tchilian EZ.
    Am J Med Genet A; 2003 Mar 15; 117A(3):255-60. PubMed ID: 12599189
    [Abstract] [Full Text] [Related]

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