These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

231 related articles for article (PubMed ID: 23682803)

  • 1. Use of global assays to understand clinical phenotype in congenital factor VII deficiency.
    Greene LA; Goldenberg NA; Simpson ML; Villalobos-Menuey E; Bombardier C; Acharya SS; Santiago-Borrero PJ; Cambara A; DiMichele DM
    Haemophilia; 2013 Sep; 19(5):765-72. PubMed ID: 23682803
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Use of thromboelastography and thrombin generation assay to predict clinical phenotype in patients with severe FVII deficiency.
    Tran HT; Tjønnfjord GE; Holme PA
    Haemophilia; 2014 Jan; 20(1):141-6. PubMed ID: 23992369
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Analysis of biological phenotypes from 42 patients with inherited factor VII deficiency: can biological tests predict the bleeding risk?
    Giansily-Blaizot M; Verdier R; Biron-Adréani C; Schved JF; Bertrand MA; Borg JY; Le Cam-Duchez V; Briquel ME; Chambost H; Pouymayou K; Dutrillaux F; Favier R; Martin-Toutain I; Verdy E; Gay V; Goudemand J; Navarro R; Durin A; d'Oiron R; Lambert T; Pernod G; Barrot C; Peynet J; Bastenaire B; Sie P; Stieltjes N; Torchet MF; de Moerloose P;
    Haematologica; 2004 Jun; 89(6):704-9. PubMed ID: 15194538
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pharmacodynamics of recombinant activated factor VII and plasma-derived factor VII in a cohort of severe FVII deficient patients.
    van Geffen M; Mathijssen NC; Holme PA; Laros-van Gorkom BA; van Kraaij MG; Masereeuw R; Peyvandi F; van Heerde WL
    Thromb Res; 2013 Jul; 132(1):116-22. PubMed ID: 23731565
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Bleeding manifestations in heterozygotes with congenital FVII deficiency: a comparison with unaffected family members during a long observation period.
    Girolami A; Cosi E; Ferrari S; Girolami B; Lombardi AM
    Hematology; 2017 Jul; 22(6):375-379. PubMed ID: 28176610
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Evaluation of Bleeding Phenotype of Inherited Factor VII Deficiency in Children With a Bleeding Assessment Tool and Global Assays.
    Toret E; Ay Y; Karapinar TH; Oymak Y; Kavakli K; Vergin RC
    J Pediatr Hematol Oncol; 2020 Aug; 42(6):e527-e530. PubMed ID: 31343480
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Challenges in the laboratory analyses of bleeding disorders.
    Chitlur M
    Thromb Res; 2012 Jul; 130(1):1-6. PubMed ID: 22483776
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Bleeding symptoms at disease presentation and prediction of ensuing bleeding in inherited FVII deficiency.
    Di Minno MN; Dolce A; Mariani G;
    Thromb Haemost; 2013 Jun; 109(6):1051-9. PubMed ID: 23571462
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene.
    Herrmann FH; Wulff K; Auerswald G; Schulman S; Astermark J; Batorova A; Kreuz W; Pollmann H; Ruiz-Saez A; De Bosch N; Salazar-Sanchez L;
    Haemophilia; 2009 Jan; 15(1):267-80. PubMed ID: 18976247
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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;
    Thromb Haemost; 2017 Aug; 117(8):1455-1464. PubMed ID: 28447100
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular analysis in a patient with severe factor VII deficiency and an inhibitor: report of a novel mutation (S103G).
    Pruthi RK; Rodriguez V; Allen C; Slaby JA; Schmidt KA; Plumhoff EA
    Eur J Haematol; 2007 Oct; 79(4):354-9. PubMed ID: 17692102
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Potential predictors of bleeding risk in inherited factorVII deficiency. Clinical, biological and molecular criteria.
    Giansily-Blaizot M; Schved JF
    Thromb Haemost; 2005 Nov; 94(5):901-6. PubMed ID: 16363229
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genotypic heterogeneity may explain phenotypic variations in inherited factor VII deficiency.
    Giansily-Blaizot M; Aguilar-Martinez P; Schved JF
    Haematologica; 2002 Mar; 87(3):328-9. PubMed ID: 11869950
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Replacement therapy for bleeding episodes in factor VII deficiency. A prospective evaluation.
    Mariani G; Napolitano M; Dolce A; Pérez Garrido R; Batorova A; Karimi M; Platokouki H; Auerswald G; Bertrand AM; Di Minno G; Schved JF; Bjerre J; Ingerslev J; Sørensen B; Ruiz-Saez A; ;
    Thromb Haemost; 2013 Feb; 109(2):238-47. PubMed ID: 23238632
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A comparison between recombinant activated factor VII (Aryoseven) and Novoseven in patients with congenital factor VII deficiency.
    Faranoush M; Abolghasemi H; Toogeh G; Karimi M; Eshghi P; Managhchi M; Hoorfar H; Dehdezi BK; Mehrvar A; Khoeiny B; Kamyar K; Heshmat R; Baghaeipour MR; Mirbehbahani NB; Fayazfar R; Ahmadinejad M; Naderi M
    Clin Appl Thromb Hemost; 2015 Nov; 21(8):724-8. PubMed ID: 24651301
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 116(2):115-20. PubMed ID: 15907525
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Primary prophylaxis for children with severe congenital factor VII deficiency - Clinical and laboratory assessment.
    Kuperman AA; Barg AA; Fruchtman Y; Shaoul E; Rosenberg N; Kenet G; Livnat T
    Blood Cells Mol Dis; 2017 Sep; 67():86-90. PubMed ID: 28038846
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Heterozygous congenital Factor VII deficiency with the 9729del4 mutation, associated with severe spontaneous intracranial bleeding in an adolescent male.
    Cramer TJ; Anderson K; Navaz K; Brown JM; Mosnier LO; von Drygalski A
    Blood Cells Mol Dis; 2016 Mar; 57():8-12. PubMed ID: 26852649
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pregnancy in women with congenital factor VII deficiency.
    Kulkarni AA; Lee CA; Kadir RA
    Haemophilia; 2006 Jul; 12(4):413-6. PubMed ID: 16834743
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Significant decrease in factor VII activity by tissue thromboplastin derived from rabbit brain in a patient with congenital factor VII deficiency (FVII Padua)].
    Sekiya A; Morishita E; Maruyama K; Asakura H; Nakao S; Ohtake S
    Rinsho Ketsueki; 2012 Mar; 53(3):357-60. PubMed ID: 22499055
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.