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Journal Abstract Search

313 related items for PubMed ID: 18024374

  • 1. Characterization of seven novel mutations causing factor XI deficiency.
    Zucker M, Zivelin A, Landau M, Salomon O, Kenet G, Bauduer F, Samama M, Conard J, Denninger MH, Hani AS, Berruyer M, Feinstein D, Seligsohn U.
    Haematologica; 2007 Oct; 92(10):1375-80. PubMed ID: 18024374
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  • 4. Structural analysis of eight novel and 112 previously reported missense mutations in the interactive FXI mutation database reveals new insight on FXI deficiency.
    Saunders RE, Shiltagh N, Gomez K, Mellars G, Cooper C, Perry DJ, Tuddenham EG, Perkins SJ.
    Thromb Haemost; 2009 Aug; 102(2):287-301. PubMed ID: 19652879
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  • 5. Identification of five novel mutations in the factor XI gene (F11) of patients with factor XI deficiency.
    Quélin F, Mathonnet F, Potentini-Esnault C, Trigui N, Peynet J, Bastenaire B, Guillon L, Bigel ML, Sauger A, Mazurier C, de Mazancourt P.
    Blood Coagul Fibrinolysis; 2006 Jan; 17(1):69-73. PubMed ID: 16607084
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  • 7. Severe factor XI deficiency in a Korean woman with a novel missense mutation (Val498Met) and duplication G mutation in exon 13 of the F11 gene.
    Kwon MJ, Kim HJ, Bang SH, Kim SH.
    Blood Coagul Fibrinolysis; 2008 Oct; 19(7):679-83. PubMed ID: 18832909
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  • 8. Factor XI deficiency in Southern Iran: identification of a novel missense mutation.
    Karimi M, Jafari H, Lahsaeizadeh S, Afrasiabi A, Akbari A, Dehbozorgian J, Ardeshiri R, Guella I, Asselta R, Peyvandi F.
    Ann Hematol; 2009 Apr; 88(4):359-63. PubMed ID: 18758779
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  • 9. Three dominant-negative mutations in factor XI-deficient patients.
    Dai L, Rangarajan S, Mitchell M.
    Haemophilia; 2011 Sep; 17(5):e919-22. PubMed ID: 21457405
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  • 10. Molecular genetic analysis of severe coagulation factor XI deficiency in six Italian patients.
    Zadra G, Asselta R, Malcovati M, Santagostino E, Peyvandi F, Mannucci PM, Tenchini ML, Duga S.
    Haematologica; 2004 Nov; 89(11):1332-40. PubMed ID: 15531455
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  • 12. Factor XI deficiency: identification of six novel missense mutations (P23L, P69T, C92G, E243D, W497C and E547K).
    Quélin F, François D, d'Oiron R, Guillet B, de Raucourt E, de Mazancourt P.
    Haematologica; 2005 Aug; 90(8):1149-50. PubMed ID: 16079124
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  • 13. Seven novel point mutations in the F11 gene in Iranian FXI-deficient patients.
    Fard-Esfahani P, Lari GR, Ravanbod S, Mirkhani F, Allahyari M, Rassoulzadegan M, Ala F.
    Haemophilia; 2008 Jan; 14(1):91-5. PubMed ID: 18005151
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  • 15. Factor XI gene mutations in factor XI deficient patients of the Czech Republic.
    Castaman G, Giacomelli SH, Habart D, Asselta R, Duga S, Rodeghiero F.
    Am J Hematol; 2008 Dec; 83(12):916-9. PubMed ID: 18839438
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  • 16. Molecular characterization of FXI deficiency.
    Berber E.
    Clin Appl Thromb Hemost; 2011 Feb; 17(1):27-32. PubMed ID: 20308231
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  • 17. Coagulation factor XI gene analysis in three factor XI deficient Austrian patients.
    Dossenbach-Glaninger A, Hopmeier P.
    Eur J Haematol; 2006 Apr; 76(4):317-21. PubMed ID: 16519703
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  • 18. Genetic analysis in Factor XI deficient patients from central China: identification of one novel and seven recurrent mutations.
    Liu H, Wang HF, Tang L, Yang Y, Wang QY, Zeng W, Wu YY, Cheng ZP, Hu B, Guo T, Hu Y.
    Gene; 2015 Apr 25; 561(1):101-6. PubMed ID: 25681615
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  • 19. Factor XI Deficiency.
    Duga S, Salomon O.
    Semin Thromb Hemost; 2009 Jun 25; 35(4):416-25. PubMed ID: 19598070
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  • 20. Factor XI deficiency database: an interactive web database of mutations, phenotypes, and structural analysis tools.
    Saunders RE, O'Connell NM, Lee CA, Perry DJ, Perkins SJ.
    Hum Mutat; 2005 Sep 25; 26(3):192-8. PubMed ID: 16086308
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