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Journal Abstract Search

217 related items for PubMed ID: 17356398

  • 21. Prolonged course of familial hemophagocytic lymphohistiocytosis.
    Steinberg O, Yacobovich J, Dgany O, Kodman Y, Livni G, Rachmel A, Stein J, Yaniv I, Tamary H.
    J Pediatr Hematol Oncol; 2006 Dec; 28(12):831-3. PubMed ID: 17164654
    [Abstract] [Full Text] [Related]

  • 22. Infective, neoplastic, and homeostatic sequelae of the loss of perforin function in humans.
    Trapani JA, Voskoboinik I.
    Adv Exp Med Biol; 2007 Dec; 601():235-42. PubMed ID: 17713010
    [Abstract] [Full Text] [Related]

  • 23. Defective cytotoxic lymphocyte degranulation in syntaxin-11 deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients.
    Bryceson YT, Rudd E, Zheng C, Edner J, Ma D, Wood SM, Bechensteen AG, Boelens JJ, Celkan T, Farah RA, Hultenby K, Winiarski J, Roche PA, Nordenskjöld M, Henter JI, Long EO, Ljunggren HG.
    Blood; 2007 Sep 15; 110(6):1906-15. PubMed ID: 17525286
    [Abstract] [Full Text] [Related]

  • 24. Unusual clinical presentations of familial hemophagocytic lymphohistiocytosis type-2.
    Mhatre S, Madkaikar M, Jijina F, Ghosh K.
    J Pediatr Hematol Oncol; 2014 Nov 15; 36(8):e524-7. PubMed ID: 24390453
    [Abstract] [Full Text] [Related]

  • 25. Immunotherapy of familial hemophagocytic lymphohistiocytosis with antithymocyte globulins: a single-center retrospective report of 38 patients.
    Mahlaoui N, Ouachée-Chardin M, de Saint Basile G, Neven B, Picard C, Blanche S, Fischer A.
    Pediatrics; 2007 Sep 15; 120(3):e622-8. PubMed ID: 17698967
    [Abstract] [Full Text] [Related]

  • 26. 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 15; 82(12):1099-102. PubMed ID: 17674359
    [Abstract] [Full Text] [Related]

  • 27. [An analysis of etiological and genetic factors of a patient with familial hemophagocytic lymphohistiocytosis].
    Liu HX, Tong CR, Wang H, Zhu J, Wang F, Cai P, Teng W, Yang JF, Zhang YL, Lu DP.
    Zhonghua Nei Ke Za Zhi; 2011 Feb 15; 50(2):132-5. PubMed ID: 21418834
    [Abstract] [Full Text] [Related]

  • 28. Novel mutation of the perforin gene and maternal uniparental disomy 10 in a patient with familial hemophagocytic lymphohistiocytosis.
    Al-Jasmi F, Abdelhaleem M, Stockley T, Lee KS, Clarke JT.
    J Pediatr Hematol Oncol; 2008 Aug 15; 30(8):621-4. PubMed ID: 18799942
    [Abstract] [Full Text] [Related]

  • 29. Perforin and lymphohistiocytic proliferative disorders.
    Katano H, Cohen JI.
    Br J Haematol; 2005 Mar 15; 128(6):739-50. PubMed ID: 15755277
    [Abstract] [Full Text] [Related]

  • 30. Perforin deficiency and susceptibility to cancer.
    Brennan AJ, Chia J, Trapani JA, Voskoboinik I.
    Cell Death Differ; 2010 Apr 15; 17(4):607-15. PubMed ID: 20075937
    [Abstract] [Full Text] [Related]

  • 31. [Flow cytometry in the diagnosis of hemophagocytic lymphohistiocytosis in a case with fatal outcome].
    Pállinger E, Erdélyi D, Kovács G, Kriván G, Korponay Z, Fekete G, Szabó A, Falus A, Dérfalvi B.
    Orv Hetil; 2014 Mar 09; 155(10):389-95. PubMed ID: 24583560
    [Abstract] [Full Text] [Related]

  • 32. Central nervous system involvement in a case of familial hemophagocytic lymphohistiocytosis with perforin mutation.
    Akbayram S, Akgun C, Dogan M, Caksen H, Okur H, Oner AF.
    Genet Couns; 2011 Mar 09; 22(3):281-5. PubMed ID: 22029169
    [Abstract] [Full Text] [Related]

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  • 34. Neonatal primary hemophagocytic lymphohistiocytosis in Turkish children.
    Gurgey A, Unal S, Okur H, Orhan D, Yurdakok M.
    J Pediatr Hematol Oncol; 2008 Dec 09; 30(12):871-6. PubMed ID: 19131769
    [Abstract] [Full Text] [Related]

  • 35. Pathology of the liver in familial hemophagocytic lymphohistiocytosis.
    Chen JH, Fleming MD, Pinkus GS, Pinkus JL, Nichols KE, Mo JQ, Perez-Atayde AR.
    Am J Surg Pathol; 2010 Jun 09; 34(6):852-67. PubMed ID: 20442642
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  • 37. The clinical spectrum and treatment options of macrophage activation syndrome in the pediatric age.
    Stabile A, Bertoni B, Ansuini V, La Torraca I, Sallì A, Rigante D.
    Eur Rev Med Pharmacol Sci; 2006 Jun 09; 10(2):53-9. PubMed ID: 16705949
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  • 39. Gene-expression signatures differ between different clinical forms of familial hemophagocytic lymphohistiocytosis.
    Sumegi J, Nestheide SV, Barnes MG, Villanueva J, Zhang K, Grom AA, Filipovich AH.
    Blood; 2013 Feb 14; 121(7):e14-24. PubMed ID: 23264592
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