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Journal Abstract Search

106 related items for PubMed ID: 15356310

  • 1. 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]

  • 2. Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 37-1994. A newborn boy with petechiae, hepatosplenomegaly, leukocytosis, and thrombocytopenia.
    N Engl J Med; 1994 Oct 13; 331(15):1005-12. PubMed ID: 7521936
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. 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 13; 20(8):603-9. PubMed ID: 14578030
    [Abstract] [Full Text] [Related]

  • 5. 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 13; 38(5):305-9. PubMed ID: 11979453
    [Abstract] [Full Text] [Related]

  • 6. 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 13; 41(2):137-44. PubMed ID: 14757862
    [No Abstract] [Full Text] [Related]

  • 7. [Familial hemophagocytic lymphohistiocytosis. Differential diagnosis with secondary hemophagocytic syndromes].
    Boissy C, Velin P, Michiels JF, Diebold J, Hofman P.
    Arch Anat Cytol Pathol; 1997 Feb 13; 45(4):208-13. PubMed ID: 9406478
    [Abstract] [Full Text] [Related]

  • 8. Perforin and lymphohistiocytic proliferative disorders.
    Katano H, Cohen JI.
    Br J Haematol; 2005 Mar 13; 128(6):739-50. PubMed ID: 15755277
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 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 Sep 15; 20(5):367-71. PubMed ID: 12775534
    [Abstract] [Full Text] [Related]

  • 11. Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 40-1993. A 61-year-old woman with jaundice, anemia, thrombocytopenia, and leukocytosis.
    N Engl J Med; 1993 Oct 07; 329(15):1108-15. PubMed ID: 8257528
    [No Abstract] [Full Text] [Related]

  • 12. Identical twin brothers concordant for Langerhans' cell histiocytosis and discordant for Epstein-Barr virus-associated haemophagocytic syndrome.
    Chen CJ, Ho TY, Lu JJ, Sheu LF, Lee SY, Tien CH, Cheng SN.
    Eur J Pediatr; 2004 Sep 07; 163(9):536-9. PubMed ID: 15243808
    [Abstract] [Full Text] [Related]

  • 13. 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 07; 22(1):80-1. PubMed ID: 11810660
    [No Abstract] [Full Text] [Related]

  • 14. [Familial hemophagocytic lymphohistiocytosis(FHL)].
    Kawa K.
    Ryoikibetsu Shokogun Shirizu; 2000 Jan 07; (32):553-6. PubMed ID: 11212803
    [No Abstract] [Full Text] [Related]

  • 15. Haemophagocytic lymphohistiocytosis: proposal of a diagnostic algorithm based on perforin expression.
    Aricò M, Allen M, Brusa S, Clementi R, Pende D, Maccario R, Moretta L, Danesino C.
    Br J Haematol; 2002 Oct 07; 119(1):180-8. PubMed ID: 12358924
    [Abstract] [Full Text] [Related]

  • 16. Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 4-1979.
    N Engl J Med; 1979 Jan 25; 300(4):184-90. PubMed ID: 759844
    [No Abstract] [Full Text] [Related]

  • 17. Case records of the Massachusetts General Hospital. Case 21-2005. A four-week-old male infant with jaundice and thrombocytopenia.
    Andrews NC, Anupindi S, Badizadegan K.
    N Engl J Med; 2005 Jul 14; 353(2):189-98. PubMed ID: 16014889
    [No Abstract] [Full Text] [Related]

  • 18. [Diagnostic image (137) An infant with fever and pancytopenia. Hemophagocytic lymphohistiocytosis].
    Verhallen-Dantuma JT, Buysse CM.
    Ned Tijdschr Geneeskd; 2003 May 03; 147(18):861. PubMed ID: 12756877
    [Abstract] [Full Text] [Related]

  • 19. Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 20-2003. A nine-year-old girl with hepatosplenomegaly and pain in the thigh.
    Larsen EC, Connolly SA, Rosenberg AE.
    N Engl J Med; 2003 Jun 26; 348(26):2669-77. PubMed ID: 12826642
    [No Abstract] [Full Text] [Related]

  • 20. Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 27-2001. A 50-year-old man with marked splenomegaly and anemia.
    N Engl J Med; 2001 Aug 30; 345(9):682-7. PubMed ID: 11547723
    [No Abstract] [Full Text] [Related]

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