BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

147 related articles for article (PubMed ID: 659588)

  • 21. Familial dysfunction of protein S.
    Mannucci PM; Valsecchi C; Krachmalnicoff A; Faioni EM; Tripodi A
    Thromb Haemost; 1989 Sep; 62(2):763-6. PubMed ID: 2530648
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A family with an abnormal protein C and a thrombotic tendency.
    Girolami A; Simioni P; Lazzaro AR; Girolami B; Prandoni P
    Haematologia (Budap); 1993; 25(1):25-33. PubMed ID: 8339996
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [A heterozygous point mutation G13328A in antithrombin gene causes thrombosis].
    Zhou RF; Shi GC; Fu QH; Wang WB; Xie S; Dai J; Ding QL; Hu YQ; Wang XF; Deng WW; Wang HL
    Zhonghua Xue Ye Xue Za Zhi; 2005 Nov; 26(11):661-4. PubMed ID: 16620552
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Abnormal plasminogen: a genetically determined cause of hypercoagulability.
    Towne JB; Bandyk DF; Hussey CV; Tollack VT
    J Vasc Surg; 1984 Nov; 1(6):896-902. PubMed ID: 6208389
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Is plasminogen deficiency a thrombotic risk factor? A study on 23 thrombophilic patients and their family members.
    Demarmels Biasiutti F; Sulzer I; Stucki B; Wuillemin WA; Furlan M; Lämmle B
    Thromb Haemost; 1998 Jul; 80(1):167-70. PubMed ID: 9684804
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Homozygous (or double heterozygous) antithrombin III defect: AT-III, Budapest 4].
    Csurgay E; Petö I; Samu A; Sas G
    Orv Hetil; 1991 May; 132(18):967-70. PubMed ID: 2027669
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Purification and characterization of hereditary abnormal antithrombin III with impaired thrombin binding.
    Jørgensen M; Petersen LC; Thorsen S
    J Lab Clin Med; 1984 Aug; 104(2):245-56. PubMed ID: 6747440
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Dysfunctional activated protein C (PC Cádiz) in a patient with thrombotic disease.
    Sala N; Borrell M; Bauer KA; Viganò-D'Angelo S; Fontcuberta J; Félez J; Rutllant ML
    Thromb Haemost; 1987 Apr; 57(2):183-6. PubMed ID: 3037717
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Fibrinogen Nijmegen: congenital dysfibrinogenemia associated with impaired t-PA mediated plasminogen activation and decreased binding of t-PA.
    Engesser L; Koopman J; de Munk G; Haverkate F; Nováková I; Verheijen JH; Briët E; Brommer EJ
    Thromb Haemost; 1988 Aug; 60(1):113-20. PubMed ID: 3142089
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mild haemostatic problems associated with congenital heterozygous alpha 2-antiplasmin deficiency.
    Leebeek FW; Stibbe J; Knot EA; Kluft C; Gomes MJ; Beudeker M
    Thromb Haemost; 1988 Feb; 59(1):96-100. PubMed ID: 3363537
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Release of tissue plasminogen activator and its fast-acting inhibitor in defective fibrinolysis.
    Pizzo SV; Fuchs HE; Doman KA; Petruska DB; Berger H
    Arch Intern Med; 1986 Jan; 146(1):188-91. PubMed ID: 2935105
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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; 79(4):802-7. PubMed ID: 9569196
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Type I congenital plasminogen deficiency is not a risk factor for thrombosis.
    Shigekiyo T; Uno Y; Tomonari A; Satoh K; Hondo H; Ueda S; Saito S
    Thromb Haemost; 1992 Feb; 67(2):189-92. PubMed ID: 1621238
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [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; 146(41):2121-5. PubMed ID: 16304806
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Factor VII Mie: homozygous asymptomatic type I deficiency caused by an amino acid substitution of His (CAC) for Arg(247) (CGC) in the catalytic domain.
    Ohiwa M; Hayashi T; Wada H; Minamikawa K; Shirakawa S; Suzuki K
    Thromb Haemost; 1994 Jun; 71(6):773-7. PubMed ID: 7974346
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [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; 155(22):1703-7. PubMed ID: 8317013
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Antithrombin III Padua: a "new" congenital antithrombin III abnormality with normal or near normal activity, normal antigen, abnormal migration and no thrombotic disease.
    Girolami A; Pengo V; Cappellato G; Vianello C; Procidano M; Cartei C
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1983; 110(1):98-111. PubMed ID: 6192061
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Absence of inhibition by lipoprotein (a) inhibition of tPA induced thrombolysis in a patient's plasma milieu.
    Lu H; Bruckert J; Soria J; Li H; de Gennes JL; Legrand A; Peynet J; Soria C
    Blood Coagul Fibrinolysis; 1990 Oct; 1(4-5):513-6. PubMed ID: 1966796
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Acute sensorineural hearing loss and vertigo in a young adult with congenital plasminogen disorder.
    Ishida T; Kitamura K; Tanaka H; Ichimura K; Mimuro J; Madoiwa S; Sakata Y
    Auris Nasus Larynx; 2006 Jun; 33(2):187-90. PubMed ID: 16500059
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.