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Journal Abstract Search

145 related items for PubMed ID: 21418834

  • 1. [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; 50(2):132-5. PubMed ID: 21418834
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  • 2. 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; 4(2):122-6. PubMed ID: 17652853
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  • 3. 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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  • 4. [The study of gene mutations in unknown refractory viral infection and primary hemophagocytic lymphohistiocytosis].
    Tong CR, Liu HX, Xie JJ, Wang F, Cai P, Wang H, Zhu J, Teng W, Zhang X, Yang JF, Zhang YL, Fei XH, Zhao J, Yin YM, Wu T, Wang JB, Sun Y, Liu R, Shi XD, Lu DP.
    Zhonghua Nei Ke Za Zhi; 2011 Apr; 50(4):280-3. PubMed ID: 21600143
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  • 10. [Analysis of clinical phenotype and genetic mutations of a pedigree of familial hemophagocytic lymphohistiocytosis].
    Sun S, Guo X, Zhu Y, Yang X, Li Q, Gao J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):570-3. PubMed ID: 25297583
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  • 11. Mutations in the perforin gene in children with hemophagocytic lymphohistiocytosis.
    Lu G, Xie ZD, Shen KL, Ye LJ, Wu RH, Liu CY, Jin YK, Yang S.
    Chin Med J (Engl); 2009 Dec 05; 122(23):2851-5. PubMed ID: 20092789
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  • 12. 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 05; 27(1):62-8. PubMed ID: 16278825
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  • 13. 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 05; 53(3):209-23. PubMed ID: 15718147
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  • 15. Successful treatment with liposteroid followed by reduced intensity stem cell transplantation in an infant with perforin deficiency presenting with hemophagocytic lymphohistiocytosis.
    Kobayashi Y, Salih HM, Kajiume T, Nakamura K, Miyagawa S, Sato T, Nishimura S, Kobayashi M.
    J Pediatr Hematol Oncol; 2007 Mar 05; 29(3):178-82. PubMed ID: 17356398
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  • 16. 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 05; 22(7):863-8. PubMed ID: 17715280
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  • 17. [Expression of porforin and granzyme B in familial hemophagocytic lymphohistiocytosis].
    Zhou XH, Luo JM, Bin Q, Huang XH.
    Zhonghua Xue Ye Xue Za Zhi; 2016 Mar 05; 37(3):227-32. PubMed ID: 27033761
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  • 18. 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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  • 19. Late-onset cases of familial hemophagocytic lymphohistiocytosis with missense perforin gene mutations.
    Ueda I, Kurokawa Y, Koike K, Ito S, Sakata A, Matsumora T, Fukushima T, Morimoto A, Ishii E, Imashuku S.
    Am J Hematol; 2007 Jun 30; 82(6):427-32. PubMed ID: 17266056
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  • 20. Unusual clinical presentations of familial hemophagocytic lymphohistiocytosis type-2.
    Mhatre S, Madkaikar M, Jijina F, Ghosh K.
    J Pediatr Hematol Oncol; 2014 Nov 30; 36(8):e524-7. PubMed ID: 24390453
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