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313 related items for PubMed ID: 12935978

  • 1. Complexity of the genetic contribution to factor VII deficiency in two Spanish families: clinical and biological implications.
    Sabater-Lleal M, Martínez-Marchán E, Martínez-Sánchez E, Coll M, Vallvé C, Mateo J, Souto JC, Fontcuberta J, Soria JM.
    Haematologica; 2003 Aug; 88(8):906-13. PubMed ID: 12935978
    [Abstract] [Full Text] [Related]

  • 2. Twenty two novel mutations of the factor VII gene in factor VII deficiency.
    Wulff K, Herrmann FH.
    Hum Mutat; 2000 Aug; 15(6):489-96. PubMed ID: 10862079
    [Abstract] [Full Text] [Related]

  • 3. The paradoxical association between inherited factor VII deficiency and venous thrombosis.
    Marty S, Barro C, Chatelain B, Fimbel B, Tribout B, Reynaud J, Schved JF, Giansily-Blaizot M.
    Haemophilia; 2008 May; 14(3):564-70. PubMed ID: 18282149
    [Abstract] [Full Text] [Related]

  • 4. Characterisation of a large complex intragenic re-arrangement in the FVII gene (F7) avoiding misdiagnosis in inherited factor VII deficiency.
    Giansily-Blaizot M, Thorel D, Khau Van Kien P, Behar C, Romey MC, Mugneret F, Schved JF, Claustres M.
    Br J Haematol; 2007 Aug; 138(3):359-65. PubMed ID: 17614823
    [Abstract] [Full Text] [Related]

  • 5. Prevalence of factor VII deficiency and molecular characterization of the F7 gene in Brazilian patients.
    Rodrigues DN, Siqueira LH, Galizoni AM, Arruda VR, Annichino-Bizzacchi JM.
    Blood Coagul Fibrinolysis; 2003 Apr; 14(3):289-92. PubMed ID: 12695753
    [Abstract] [Full Text] [Related]

  • 6. Genetic architecture of the F7 gene in a Spanish population: implication for mapping complex diseases and for functional assays.
    Sabater-Lleal M, Almasy L, Martínez-Marchán E, Martínez-Sánchez E, Souto R, Blangero J, Souto J, Fontcuberta J, Soria JM.
    Clin Genet; 2006 May; 69(5):420-8. PubMed ID: 16650081
    [Abstract] [Full Text] [Related]

  • 7. [Studies on inherited coagulation factor VII deficiency and tissue factor abnormality in a pedigree].
    Ding QL, Wang XF, Xu GQ, Huang XP, Hu YQ, Wu WM, Fu QH, Wang HL, Wang ZY.
    Zhonghua Xue Ye Xue Za Zhi; 2006 Mar; 27(3):150-3. PubMed ID: 16792912
    [Abstract] [Full Text] [Related]

  • 8. A two adenine insertion polymorphism in the 3' untranslated region of factor VII gene is associated with peripheral arterial disease but not with venous thrombosis. Results of case-control studies.
    Serve E, Reny JL, Akhavan S, Emmerich J, Fischer AM, Tapon-Bretaudière J.
    Thromb Haemost; 2007 Oct; 98(4):733-7. PubMed ID: 17938795
    [Abstract] [Full Text] [Related]

  • 9. Inherited factor VII deficiency: identification of two novel mutations (A191V and T239P) in the catalytic domain.
    Borensztajn K, Chafa O, Le Bonniec B, Wajcman H, Reghis A, Fischer AM, Tapon-Bretaudière J.
    Thromb Res; 2005 Oct; 116(2):115-20. PubMed ID: 15907525
    [Abstract] [Full Text] [Related]

  • 10. [Novel double heterozygous mutations on Met306Val and Thr181Asn related to a hereditary coagulation factor VII deficiency].
    Tu CQ, Deng CY, Wu JZ, Pan CY, Xie CY.
    Zhonghua Yi Xue Za Zhi; 2006 Jan 10; 86(2):124-7. PubMed ID: 16620721
    [Abstract] [Full Text] [Related]

  • 11. Prevalence in a Tunisian Arabic population of factor VII DNA variants and relation to factor VII plasma levels.
    Nour M, Slama FB, Monastiri K, Hammami M, Helal AN.
    Clin Chim Acta; 2004 Nov 10; 349(1-2):199-202. PubMed ID: 15469874
    [Abstract] [Full Text] [Related]

  • 12. Characterization of mild coagulation factor VII deficiency: activity and clearance of the Arg315Trp and Arg315Lys variants in the Cys310-Cys329 loop (c170s).
    Furlan Freguia C, Toso R, Pollak ES, Arruda VR, Pinotti M, Bernardi F.
    Haematologica; 2004 Dec 10; 89(12):1504-9. PubMed ID: 15590402
    [Abstract] [Full Text] [Related]

  • 13. [Two novel mutations in one pedigree with hereditary Factor VII deficiency].
    Xing ZF, Wang XF, Dai J, Lu YL, Xu GQ, Xi XD, Wang HL.
    Zhonghua Xue Ye Xue Za Zhi; 2011 Mar 10; 32(3):158-62. PubMed ID: 21535952
    [Abstract] [Full Text] [Related]

  • 14. Factor VII gene polymorphisms contribute about one third of the factor VII level variation in plasma.
    Bernardi F, Marchetti G, Pinotti M, Arcieri P, Baroncini C, Papacchini M, Zepponi E, Ursicino N, Chiarotti F, Mariani G.
    Arterioscler Thromb Vasc Biol; 1996 Jan 10; 16(1):72-6. PubMed ID: 8548429
    [Abstract] [Full Text] [Related]

  • 15. F7 gene variants modulate protein levels in a large cohort of patients with factor VII deficiency. Results from a genotype-phenotype study.
    Quintavalle G, Riccardi F, Rivolta GF, Martorana D, Di Perna C, Percesepe A, Tagliaferri A, Ad-Hoc Study Group.
    Thromb Haemost; 2017 Aug 01; 117(8):1455-1464. PubMed ID: 28447100
    [Abstract] [Full Text] [Related]

  • 16. Molecular characterization of a factor VII deficient patient supports the importance of the second epidermal growth factor-like domain.
    D'Andrea G, Bossone A, Lupone MR, Peyvandi F, Maisto G, Perricone F, Grandone E, Margaglione M.
    Haematologica; 2004 Aug 01; 89(8):979-84. PubMed ID: 15339682
    [Abstract] [Full Text] [Related]

  • 17. [Analysis of an inherited FVII deficiency pedigree caused by homozygosity of Thr359Met].
    Chu HY, Wang HL, Ding QL, Wang XF, Qu B, Wu F, Kang WY, Duan BH, Yin J, Fu QH, Wu WM, Wang ZY.
    Zhonghua Xue Ye Xue Za Zhi; 2003 Mar 01; 24(3):134-7. PubMed ID: 12697124
    [Abstract] [Full Text] [Related]

  • 18. Analysis of the genotypes and phenotypes of 37 unrelated patients with inherited factor VII deficiency.
    Giansily-Blaizot M, Aguilar-Martinez P, Biron-Andreani C, Jeanjean P, Igual H, Schved JF, Study Group of Factor Seven Deficiency.
    Eur J Hum Genet; 2001 Feb 01; 9(2):105-12. PubMed ID: 11313743
    [Abstract] [Full Text] [Related]

  • 19. Molecular characterisation and three-dimensional structural analysis of mutations in 21 unrelated families with inherited factor VII deficiency.
    Peyvandi F, Jenkins PV, Mannucci PM, Billio A, Zeinali S, Perkins SJ, Perry DJ.
    Thromb Haemost; 2000 Aug 01; 84(2):250-7. PubMed ID: 10959697
    [Abstract] [Full Text] [Related]

  • 20. [Genetic analysis of hereditary factor VII deficiency from a Chinese pedigree].
    Wu Y, Yang W, Fang G.
    Zhonghua Yi Xue Za Zhi; 2000 Dec 01; 80(12):904-6. PubMed ID: 11236630
    [Abstract] [Full Text] [Related]

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