These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

183 related items for PubMed ID: 11212803

  • 61. Functional significance of the perforin/granzyme cell death pathway.
    Trapani JA, Smyth MJ.
    Nat Rev Immunol; 2002 Oct; 2(10):735-47. PubMed ID: 12360212
    [Abstract] [Full Text] [Related]

  • 62.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 63.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 64. A91V is a polymorphism in the perforin gene not causative of an FHLH phenotype.
    Zur Stadt U, Beutel K, Weber B, Kabisch H, Schneppenheim R, Janka G.
    Blood; 2004 Sep 15; 104(6):1909; author reply 1910. PubMed ID: 15342365
    [No Abstract] [Full Text] [Related]

  • 65. Effect of chemotherapy and stem cell transplantation on T lymphocyte clones in familial haemophagocytic lymphohistiocytosis.
    Kimura N, Ishii E, Sako M, Yoshida T, Nagano M, Takada H, Imashuku S, Tamura K.
    Br J Haematol; 2001 Jun 15; 113(3):822-31. PubMed ID: 11380476
    [Abstract] [Full Text] [Related]

  • 66. Characterisation of diverse PRF1 mutations leading to decreased natural killer cell activity in North American families with haemophagocytic lymphohistiocytosis.
    Molleran Lee S, Villanueva J, Sumegi J, Zhang K, Kogawa K, Davis J, Filipovich AH.
    J Med Genet; 2004 Feb 15; 41(2):137-44. PubMed ID: 14757862
    [No Abstract] [Full Text] [Related]

  • 67. Primary hemophagocytic syndromes point to a direct link between lymphocyte cytotoxicity and homeostasis.
    Ménasché G, Feldmann J, Fischer A, de Saint Basile G.
    Immunol Rev; 2005 Feb 15; 203():165-79. PubMed ID: 15661029
    [Abstract] [Full Text] [Related]

  • 68. Perforin-mediated target-cell death and immune homeostasis.
    Voskoboinik I, Smyth MJ, Trapani JA.
    Nat Rev Immunol; 2006 Dec 15; 6(12):940-52. PubMed ID: 17124515
    [Abstract] [Full Text] [Related]

  • 69. Natural killer cell dysfunction in patients with systemic-onset juvenile rheumatoid arthritis and macrophage activation syndrome.
    Grom AA, Villanueva J, Lee S, Goldmuntz EA, Passo MH, Filipovich A.
    J Pediatr; 2003 Mar 15; 142(3):292-6. PubMed ID: 12640378
    [Abstract] [Full Text] [Related]

  • 70. Hemophagocytic lymphohistiocytosis: when the immune system runs amok.
    Janka G.
    Klin Padiatr; 2009 Sep 15; 221(5):278-85. PubMed ID: 19707989
    [Abstract] [Full Text] [Related]

  • 71. Mutations of perforin and Munc13-4 do not mark HLH by NK defects.
    Schneider EM.
    Pediatr Blood Cancer; 2006 Apr 15; 46(4):409-11. PubMed ID: 16365870
    [No Abstract] [Full Text] [Related]

  • 72. Familial hemophagocytic lymphohistiocytosis macrophages showing immunohistochemical properties of activated macrophages and T-accessory cells.
    Hansmann ML, Rontogianni D, Janka-Schaub GE, Wacker HH, Hinkeldey K, Radzun HJ.
    Pediatr Hematol Oncol; 1989 Apr 15; 6(3):237-46. PubMed ID: 2642082
    [No Abstract] [Full Text] [Related]

  • 73. Six novel mutations in the PRF1 gene in children with haemophagocytic lymphohistiocytosis.
    Clementi R, zur Stadt U, Savoldi G, Varoitto S, Conter V, De Fusco C, Notarangelo LD, Schneider M, Klersy C, Janka G, Danesino C, Aricò M.
    J Med Genet; 2001 Sep 15; 38(9):643-6. PubMed ID: 11565555
    [No Abstract] [Full Text] [Related]

  • 74. Sensorineural hearing loss in a case of familial hemophagocytic lymphohistiocytosis.
    Imashuku S, Kohdera U, Teramura T, Ueda I, Morimoto A, Naya M, Kuroda H.
    Pediatr Blood Cancer; 2007 Nov 15; 49(6):856-8. PubMed ID: 16358309
    [Abstract] [Full Text] [Related]

  • 75. A91V perforin variation in healthy subjects and FHLH patients.
    Busiello R, Fimiani G, Miano MG, Aricò M, Santoro A, Ursini MV, Pignata C.
    Int J Immunogenet; 2006 Apr 15; 33(2):123-5. PubMed ID: 16611257
    [Abstract] [Full Text] [Related]

  • 76. High frequency of QPY allele and linkage disequilibrium of granzyme-B in Epstein-Barr-virus-associated hemophagocytic lymphohistiocytosis.
    Zaitsu M, Yamamoto K, Ishii E, Teramura T, Nakadate N, Sako M, Sakata N, Wakiguchi H, Hirose M, Imayoshi M, Ogata Y, Imashuku S, Hamasaki Y, Yasukawa M.
    Tissue Antigens; 2004 Nov 15; 64(5):611-5. PubMed ID: 15496206
    [Abstract] [Full Text] [Related]

  • 77. Clinical and epidemiologic studies of familial hemophagocytic lymphohistiocytosis in Japan. Japan LCH Study Group.
    Ishii E, Ohga S, Tanimura M, Imashuku S, Sako M, Mizutani S, Miyazaki S.
    Med Pediatr Oncol; 1998 May 15; 30(5):276-83. PubMed ID: 9544223
    [Abstract] [Full Text] [Related]

  • 78.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 79.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 80. Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 28-2004. Newborn twins with thrombocytopenia, coagulation defects, and hepatosplenomegaly.
    Lipton JM, Westra S, Haverty CE, Roberts D, Harris NL.
    N Engl J Med; 2004 Sep 09; 351(11):1120-30. PubMed ID: 15356310
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 10.