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Journal Abstract Search

137 related items for PubMed ID: 16358309

  • 1. 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; 49(6):856-8. PubMed ID: 16358309
    [Abstract] [Full Text] [Related]

  • 2. 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; 83(1):51-4. PubMed ID: 16443553
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  • 4. 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
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  • 5. Subtypes of familial hemophagocytic lymphohistiocytosis in Japan based on genetic and functional analyses of cytotoxic T lymphocytes.
    Nagai K, Yamamoto K, Fujiwara H, An J, Ochi T, Suemori K, Yasumi T, Tauchi H, Koh K, Sato M, Morimoto A, Heike T, Ishii E, Yasukawa M.
    PLoS One; 2010 Nov 30; 5(11):e14173. PubMed ID: 21152410
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  • 7. Hematopoietic stem cell transplantation for familial hemophagocytic lymphohistiocytosis and Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis in Japan.
    Ohga S, Kudo K, Ishii E, Honjo S, Morimoto A, Osugi Y, Sawada A, Inoue M, Tabuchi K, Suzuki N, Ishida Y, Imashuku S, Kato S, Hara T.
    Pediatr Blood Cancer; 2010 Feb 30; 54(2):299-306. PubMed ID: 19827139
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  • 9. [Familial haemophagocytic lymphohistiocytosis caused by perforin deficit can be successfully treated by haematopoietic stem cell transplantation--the first diagnosed case in the Czech Republic].
    Spísek R, Mejstríková E, Formánková R, Zizková H, Vávra V, Hrusák O, Sedivá A, Sedlácek P, Starý J.
    Cas Lek Cesk; 2006 Feb 30; 145(1):50-4. PubMed ID: 16468242
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  • 11. Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A.
    Zur Stadt U, Beutel K, Kolberg S, Schneppenheim R, Kabisch H, Janka G, Hennies HC.
    Hum Mutat; 2006 Jan 30; 27(1):62-8. PubMed ID: 16278825
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  • 12. 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 30; 4(2):122-6. PubMed ID: 17652853
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  • 13. Perforin gene mutations in adult-onset hemophagocytic lymphohistiocytosis.
    Nagafuji K, Nonami A, Kumano T, Kikushige Y, Yoshimoto G, Takenaka K, Shimoda K, Ohga S, Yasukawa M, Horiuchi H, Ishii E, Harada M.
    Haematologica; 2007 Jul 30; 92(7):978-81. PubMed ID: 17606450
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  • 14. 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 30; 28(12):831-3. PubMed ID: 17164654
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  • 15. Familial hemophagocytic lymphohistiocytosis in a girl with a novel homozygous mutation of STX11: A case report.
    Guo X, Jiang M, Tang X, Li Q.
    Medicine (Baltimore); 2019 Nov 30; 98(48):e18107. PubMed ID: 31770233
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  • 16. Allogeneic hematopoietic stem cell transplant for familial hemophagocytic lymphohistiocytosis: a case report and literature review.
    Bingjie L, Linlin Z, Futian M, Fan X, Huan D, Wu X, Zhou L, Fuxu W, Xuejun Z, Ying W.
    Front Immunol; 2024 Nov 30; 15():1391074. PubMed ID: 38887297
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  • 17. Remission and relapse of hemophagocytic lymphohistiocytosis in a patient harboring a PRF1 homozygous mutation: a case report.
    Huang Z, Wang Y, Xie Z, Shen K.
    J Pediatr Hematol Oncol; 2014 Jan 30; 36(1):e5-8. PubMed ID: 23073044
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  • 18. Review of hemophagocytic lymphohistiocytosis (HLH) in children with focus on Japanese experiences.
    Ishii E, Ohga S, Imashuku S, Kimura N, Ueda I, Morimoto A, Yamamoto K, Yasukawa M.
    Crit Rev Oncol Hematol; 2005 Mar 30; 53(3):209-23. PubMed ID: 15718147
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  • 19. Fatal sibling cases of familial hemophagocytic lymphohistiocytosis (FHL) with MUNC13-4 mutations: case reports.
    Nakao T, Shimizu T, Fukushima T, Saito M, Okamoto M, Sugiura M, Yamamoto K, Ueda I, Imashuku S, Kobayashi C, Koike K, Tsuchida M, Sumazaki R, Matsui A.
    Pediatr Hematol Oncol; 2008 Mar 30; 25(3):171-80. PubMed ID: 18432499
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  • 20. 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 30; 22(7):863-8. PubMed ID: 17715280
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