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Journal Abstract Search

319 related items for PubMed ID: 17849042

  • 1. Molecular basis of protein S deficiency.
    García de Frutos P, Fuentes-Prior P, Hurtado B, Sala N.
    Thromb Haemost; 2007 Sep; 98(3):543-56. PubMed ID: 17849042
    [Abstract] [Full Text] [Related]

  • 2. Protein S gene analysis reveals the presence of a cosegregating mutation in most pedigrees with type I but not type III PS deficiency.
    Espinosa-Parrilla Y, Morell M, Souto JC, Tirado I, Fontcuberta J, Estivill X, Sala N.
    Hum Mutat; 1999 Sep; 14(1):30-9. PubMed ID: 10447256
    [Abstract] [Full Text] [Related]

  • 3. One novel and one recurrent mutation in the PROS1 gene cause type I protein S deficiency in patients with pulmonary embolism associated with deep vein thrombosis.
    Mizukami K, Nakabayashi T, Naitoh S, Takeda M, Tarumi T, Mizoguchi I, Ieko M, Koike T.
    Am J Hematol; 2006 Oct; 81(10):787-97. PubMed ID: 16868938
    [Abstract] [Full Text] [Related]

  • 4. Identification of a novel PROS1 c.1113T-->GG frameshift mutation in a family with mixed type I/type III protein S deficiency.
    ten Kate MK, Mulder R, Platteel M, Brouwer JL, van der Steege G, van der Meer J.
    Haematologica; 2006 Aug; 91(8):1151-2. PubMed ID: 16885060
    [Abstract] [Full Text] [Related]

  • 5. Optimization of a simple and rapid single-strand conformation analysis for detection of mutations in the PROS1 gene: identification of seven novel mutations and three novel, apparently neutral, variants.
    Espinosa-Parrilla Y, Morell M, Borrell M, Souto JC, Fontcuberta J, Estivill X, Sala N.
    Hum Mutat; 2000 Aug; 15(5):463-73. PubMed ID: 10790208
    [Abstract] [Full Text] [Related]

  • 6. Characterization and structural impact of five novel PROS1 mutations in eleven protein S-deficient families.
    Andersen BD, Bisgaard ML, Lind B, Philips M, Villoutreix B, Thorsen S.
    Thromb Haemost; 2001 Dec; 86(6):1392-9. PubMed ID: 11776305
    [Abstract] [Full Text] [Related]

  • 7. [Hereditary protein S deficiency and familial thrombosis. A review with description of a Danish family with protein S deficiency].
    Ingerslev J, Ingerslev J, Thelle T.
    Ugeskr Laeger; 1993 May 31; 155(22):1703-7. PubMed ID: 8317013
    [Abstract] [Full Text] [Related]

  • 8. [Protein S deficiency, acute phase reaction and thrombosis].
    Odegaard OR, Try K, Ly B, Gundersen T, Linnebo S.
    Tidsskr Nor Laegeforen; 1993 Nov 20; 113(28):3460-3. PubMed ID: 7505957
    [Abstract] [Full Text] [Related]

  • 9. Low cut-off values increase diagnostic performance of protein S assays.
    Mulder R, Ten Kate MK, Kluin-Nelemans HC, Mulder AB.
    Thromb Haemost; 2010 Sep 20; 104(3):618-25. PubMed ID: 20539904
    [Abstract] [Full Text] [Related]

  • 10. Three-dimensional model of the SHBG-like region of anticoagulant protein S: new structure-function insights.
    Villoutreix BO, Dahlbäck B, Borgel D, Gandrille S, Muller YA.
    Proteins; 2001 May 01; 43(2):203-16. PubMed ID: 11276089
    [Abstract] [Full Text] [Related]

  • 11. Protein C and protein S assessment in hospital laboratories: which strategy and what role for DNA sequencing?
    Labrouche S, Reboul MP, Guérin V, Vergnes C, Freyburger G.
    Blood Coagul Fibrinolysis; 2003 Sep 01; 14(6):531-8. PubMed ID: 12960605
    [Abstract] [Full Text] [Related]

  • 12. Homozygosity for the protein S Heerlen allele is associated with type I PS deficiency in a thrombophilic pedigree with multiple risk factors.
    Espinosa-Parrilla Y, Navarro G, Morell M, Abella E, Estivill X, Sala N.
    Thromb Haemost; 2000 Jan 01; 83(1):102-6. PubMed ID: 10669162
    [Abstract] [Full Text] [Related]

  • 13. Functional characterization of twelve natural PROS1 mutations associated with anticoagulant protein S deficiency.
    Hurtado B, Muñoz X, Mulero MC, Navarro G, Domènech P, García de Frutos P, Pérez-Riba M, Sala N.
    Haematologica; 2008 Apr 01; 93(4):574-80. PubMed ID: 18322254
    [Abstract] [Full Text] [Related]

  • 14. Protein C and protein S deficiency - practical diagnostic issues.
    Wypasek E, Undas A.
    Adv Clin Exp Med; 2013 Apr 01; 22(4):459-67. PubMed ID: 23986205
    [Abstract] [Full Text] [Related]

  • 15. Difference in absolute risk of venous and arterial thrombosis between familial protein S deficiency type I and type III. Results from a family cohort study to assess the clinical impact of a laboratory test-based classification.
    Brouwer JL, Veeger NJ, van der Schaaf W, Kluin-Nelemans HC, van der Meer J.
    Br J Haematol; 2005 Mar 01; 128(5):703-10. PubMed ID: 15725093
    [Abstract] [Full Text] [Related]

  • 16. Coagulation factor V and thrombophilia: background and mechanisms.
    Segers K, Dahlbäck B, Nicolaes GA.
    Thromb Haemost; 2007 Sep 01; 98(3):530-42. PubMed ID: 17849041
    [Abstract] [Full Text] [Related]

  • 17. Thrombophilia: a genetic predisposition to thrombosis.
    Sacher RA.
    Trans Am Clin Climatol Assoc; 1999 Sep 01; 110():51-60; discussion 60-1. PubMed ID: 10344006
    [No Abstract] [Full Text] [Related]

  • 18. Hereditary protein S deficiency leads to ischemic stroke.
    Wang ZH, Zhao ZJ, Xu K, Sun GB, Song L, Yin HX, Chen XQ.
    Mol Med Rep; 2015 Sep 01; 12(3):3279-3284. PubMed ID: 25997409
    [Abstract] [Full Text] [Related]

  • 19. Confirmation of inherited protein S deficiency by PROS1 mutational screening: Identification of three novel PROS1 mutations and haplotype analysis of p.Q279X recurrence.
    Hurtado B, Abasolo N, Domènech-Santasusana P, Fuentes-Prior P, García de Frutos P, Sala N.
    Thromb Haemost; 2008 Oct 01; 100(4):721-4. PubMed ID: 18841302
    [No Abstract] [Full Text] [Related]

  • 20. Protein S deficiency.
    D'Angelo A, Viganò D'Angelo S.
    Haematologica; 2008 Apr 01; 93(4):498-501. PubMed ID: 18379009
    [No Abstract] [Full Text] [Related]

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