BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

279 related articles for article (PubMed ID: 19141160)

  • 1. Combined FV and FVIII deficiency.
    Spreafico M; Peyvandi F
    Haemophilia; 2008 Nov; 14(6):1201-8. PubMed ID: 19141160
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Combined Factor V and Factor VIII Deficiency.
    Spreafico M; Peyvandi F
    Semin Thromb Hemost; 2009 Jun; 35(4):390-9. PubMed ID: 19598067
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in India.
    Jayandharan G; Spreafico M; Viswabandya A; Chandy M; Srivastava A; Peyvandi F
    Haemophilia; 2007 Jul; 13(4):413-9. PubMed ID: 17610559
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Combined deficiency of coagulation factors V and VIII: an update.
    Zheng C; Zhang B
    Semin Thromb Hemost; 2013 Sep; 39(6):613-20. PubMed ID: 23852824
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Recent developments in the understanding of the combined deficiency of FV and FVIII.
    Zhang B
    Br J Haematol; 2009 Apr; 145(1):15-23. PubMed ID: 19183188
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genotype-phenotype correlation in combined deficiency of factor V and factor VIII.
    Zhang B; Spreafico M; Zheng C; Yang A; Platzer P; Callaghan MU; Avci Z; Ozbek N; Mahlangu J; Haw T; Kaufman RJ; Marchant K; Tuddenham EG; Seligsohn U; Peyvandi F; Ginsburg D
    Blood; 2008 Jun; 111(12):5592-600. PubMed ID: 18391077
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel missense mutation causing abnormal LMAN1 in a Japanese patient with combined deficiency of factor V and factor VIII.
    Yamada T; Fujimori Y; Suzuki A; Miyawaki Y; Takagi A; Murate T; Sano M; Matsushita T; Saito H; Kojima T
    Am J Hematol; 2009 Nov; 84(11):738-42. PubMed ID: 19787799
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations in the MCFD2 gene and a novel mutation in the LMAN1 gene in Indian families with combined deficiency of factor V and VIII.
    Mohanty D; Ghosh K; Shetty S; Spreafico M; Garagiola I; Peyvandi F
    Am J Hematol; 2005 Aug; 79(4):262-6. PubMed ID: 16044454
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular analysis in two Tunisian families with combined factor V and factor VIII deficiency.
    Abdallah HE; Gouider E; Amor MB; Jlizi A; Meddeb B; Elgaaied A
    Haemophilia; 2010 Sep; 16(5):801-4. PubMed ID: 20491958
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Low factor V level ameliorates bleeding diathesis in patients with combined deficiency of factor V and factor VIII.
    Shao Y; Wu W; Xu G; Wang X; Ding Q
    Blood; 2019 Nov; 134(20):1745-1754. PubMed ID: 31558466
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Combined deficiency of factor V and factor VIII is due to mutations in either LMAN1 or MCFD2.
    Zhang B; McGee B; Yamaoka JS; Guglielmone H; Downes KA; Minoldo S; Jarchum G; Peyvandi F; de Bosch NB; Ruiz-Saez A; Chatelain B; Olpinski M; Bockenstedt P; Sperl W; Kaufman RJ; Nichols WC; Tuddenham EG; Ginsburg D
    Blood; 2006 Mar; 107(5):1903-7. PubMed ID: 16304051
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genotype and phenotype report on patients with combined deficiency of factor V and factor VIII in Iran.
    Karimi M; Cairo A; Safarpour MM; Haghpanah S; Ekramzadeh M; Afrasiabi A; Shahriari M; Menegatti M
    Blood Coagul Fibrinolysis; 2014 Jun; 25(4):360-3. PubMed ID: 24389588
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Desmopressin acetate as a haemostatic elevator in individuals with combined deficiency of factors V and VIII: a clinical trial.
    Mansouritorghabeh H; Shirdel A
    J Thromb Haemost; 2016 Feb; 14(2):336-9. PubMed ID: 26599105
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Combined deficiency of factors V and VIII caused by a novel compound heterozygous mutation of gene Lman1].
    Ge J; Xue F; Gu DS; DU WT; Zhao HF; Sui T; Li HY; Ma L; Zhang L; Yang RC
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2010 Feb; 18(1):185-90. PubMed ID: 20137144
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Two new mutations at ERGIC-53 gene in a Turkish family.
    Torun D; Yilmaz E; Atay A; Kürekçi E; Akar N
    Clin Appl Thromb Hemost; 2011 Jun; 17(3):248-50. PubMed ID: 20460353
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of newly detected mutations in the MCFD2 gene giving rise to combined deficiency of coagulation factors V and VIII.
    Elmahmoudi H; Wigren E; Laatiri A; Jlizi A; Elgaaied A; Gouider E; Lindqvist Y
    Haemophilia; 2011 Sep; 17(5):e923-7. PubMed ID: 21492322
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Structural basis for the cooperative interplay between the two causative gene products of combined factor V and factor VIII deficiency.
    Nishio M; Kamiya Y; Mizushima T; Wakatsuki S; Sasakawa H; Yamamoto K; Uchiyama S; Noda M; McKay AR; Fukui K; Hauri HP; Kato K
    Proc Natl Acad Sci U S A; 2010 Mar; 107(9):4034-9. PubMed ID: 20142513
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mice deficient in LMAN1 exhibit FV and FVIII deficiencies and liver accumulation of α1-antitrypsin.
    Zhang B; Zheng C; Zhu M; Tao J; Vasievich MP; Baines A; Kim J; Schekman R; Kaufman RJ; Ginsburg D
    Blood; 2011 Sep; 118(12):3384-91. PubMed ID: 21795745
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial multiple coagulation factor deficiencies: new biologic insight from rare genetic bleeding disorders.
    Zhang B; Ginsburg D
    J Thromb Haemost; 2004 Sep; 2(9):1564-72. PubMed ID: 15333032
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Altered phenotype in LMAN1-deficient mice with low levels of residual LMAN1 expression.
    Everett LA; Khoriaty RN; Zhang B; Ginsburg D
    Blood Adv; 2020 Nov; 4(22):5635-5643. PubMed ID: 33196840
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.