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Journal Abstract Search

250 related items for PubMed ID: 8317013

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  • 2. [Hereditary deficiency of antithrombin III, protein C, protein S and factor XII in 121 patients with venous or arterial thrombosis].
    Miljić P, Rolović Z, Elezović I, Antunović P, Stanojević M, Colović M.
    Srp Arh Celok Lek; 1999; 127(1-2):21-7. PubMed ID: 10377836
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  • 8. High incidence of thrombophilia detected in Chinese patients with venous thrombosis.
    Liu HW, Kwong YL, Bourke C, Lam CK, Lie AK, Wei D, Chan LC.
    Thromb Haemost; 1994 Apr; 71(4):416-9. PubMed ID: 8052955
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  • 9. Protein C system defects in Indian children with thrombosis.
    Gupta PK, Ahmed RP, Bhattacharyya M, Kannan M, Biswas A, Kalra V, Saxena R.
    Ann Hematol; 2005 Feb; 84(2):85-8. PubMed ID: 15449030
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  • 10. Familial thrombophilia: a complex genetic disorder.
    Koeleman BP, Reitsma PH, Bertina RM.
    Semin Hematol; 1997 Jul; 34(3):256-64. PubMed ID: 9241710
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  • 11. [Molecular biological analysis of hereditary thrombophilia--genetic characterization of protein S deficiency].
    Yamazaki T.
    Rinsho Ketsueki; 1995 Apr; 36(4):299-302. PubMed ID: 7783333
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  • 13. [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
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  • 16. A common 4G allele in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene as a risk factor for pulmonary embolism and arterial thrombosis in hereditary protein S deficiency.
    Zöller B, García de Frutos P, Dahlbäck B.
    Thromb Haemost; 1998 Apr 20; 79(4):802-7. PubMed ID: 9569196
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  • 17. [Significance of hereditary thrombophilia for risk of thrombosis with oral contraceptives].
    Bauersachs R, Lindhoff-Last E, Ehrly AM, Kuhl H.
    Zentralbl Gynakol; 1996 Apr 20; 118(5):262-70. PubMed ID: 8701622
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  • 18. 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 20; 83(1):102-6. PubMed ID: 10669162
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  • 19. 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 Jan 20; 14(1):30-9. PubMed ID: 10447256
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  • 20. [Type I antithrombin deficiency as a cause of arterial and venous thrombosis in a family with severe thrombophilia].
    Tóth O, Dávid M, Habon T, Nagy A, Keszthelyi Z, Kovács N, Losonczy H.
    Orv Hetil; 2005 Oct 09; 146(41):2121-5. PubMed ID: 16304806
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