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 *

90 related articles for article (PubMed ID: 2109456)

  • 21. [Hereditary protein C deficiency and portal vein thrombosis].
    dos Santos JN; Mello e Silva A; Alexandrino P; Saldanha T; Carreira MO; Ferreira E; de Pádua F
    Acta Med Port; 1990; 3(1):27-30. PubMed ID: 2333774
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Hereditary homozygous heparin cofactor II deficiency and the risk of developing venous thrombosis.
    Villa P; Aznar J; Vaya A; España F; Ferrando F; Mira Y; Estellés A
    Thromb Haemost; 1999 Sep; 82(3):1011-4. PubMed ID: 10494755
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Constitutional protein C deficiency in 57 patients from 22 non-related families].
    Horellou MH; Conard J; Van Dreden P; Samama M
    Ann Med Interne (Paris); 1986; 137(6):465-70. PubMed ID: 3813281
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Homozygous antithrombin deficiency: report of two new cases (99 Leu to Phe) associated with arterial and venous thrombosis.
    Chowdhury V; Lane DA; Mille B; Auberger K; Gandenberger-Bachem S; Pabinger I; Olds RJ; Thein SL
    Thromb Haemost; 1994 Aug; 72(2):198-202. PubMed ID: 7831651
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [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]  

  • 26. The significance of F139V mutation on thrombotic events in compound heterozygous and homozygous protein C deficiency.
    Yang LH; Zheng FX; Chen Y; Jin YH; Zhang Z; Xie HX; Yang XL; Wang MS; Chen BC
    Blood Coagul Fibrinolysis; 2014 Dec; 25(8):824-30. PubMed ID: 24911457
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [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]  

  • 28. Familial thrombotic risk based on the genetic background of Protein C Deficiency in a Portuguese Study.
    Fidalgo T; Martinho P; Salvado R; Manco L; Oliveira AC; Pinto CS; Gonçalves E; Marques D; Sevivas T; Martins N; Ribeiro ML
    Eur J Haematol; 2015 Oct; 95(4):294-307. PubMed ID: 25533856
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Hereditary protein S deficiency in a large New Jersey kindred.
    Wilkerson DK; Burrell L; Cisar LA; Graham AM; Kim H
    J Vasc Surg; 1993 Dec; 18(6):932-7; discussion 937-8. PubMed ID: 8264049
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Thrombovascular disease and familial plasminogen deficiency: a report of three kindreds.
    Dolan G; Greaves M; Cooper P; Preston FE
    Br J Haematol; 1988 Dec; 70(4):417-21. PubMed ID: 3219292
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genetic screening of candidate genes for a prothrombotic interaction with type I protein C deficiency in a large kindred.
    Scott BT; Bovill EG; Callas PW; Hasstedt SJ; Leppert MF; Valliere JE; Varvil TS; Long GL
    Thromb Haemost; 2001 Jan; 85(1):82-7. PubMed ID: 11204593
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The G20210A prothrombin polymorphism is not associated with increased thromboembolic risk in a large protein C deficient kindred.
    Bovill EG; Hasstedt SJ; Callas PW; Valliere JE; Scott BT; Bauer KA; Long GL
    Thromb Haemost; 2000 Mar; 83(3):366-70. PubMed ID: 10744139
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Activation-resistant homozygous protein C R229W mutation causing familial perinatal intracranial hemorrhage and delayed onset of thrombosis.
    Alsultan A; Gale AJ; Kurban K; Khalifah M; Albadr FB; Griffin JH
    Thromb Res; 2016 Jul; 143():17-21. PubMed ID: 27172833
    [TBL] [Abstract][Full Text] [Related]  

  • 34. SELDI-TOF plasma profiles distinguish individuals in a protein C-deficient family with thrombotic episodes occurring before age 40.
    Svensson AM; Whiteley GR; Callas PW; Bovill EG
    Thromb Haemost; 2006 Dec; 96(6):725-30. PubMed ID: 17139365
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Childhood thrombosis.
    Nuss R; Hays T; Manco-Johnson M
    Pediatrics; 1995 Aug; 96(2 Pt 1):291-4. PubMed ID: 7630687
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Different impact of two mutations of a novel compound heterozygous protein C deficiency with late onset thrombosis.
    Yang LH; Wang MS; Zheng FX; Li J; Chen Y; Jin YH; Xie HX; Yang XL; Chen BC
    Genet Mol Res; 2014 Apr; 13(2):2969-77. PubMed ID: 24782131
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Protein C and protein S deficiencies.
    Aiach M; Borgel D; Gaussem P; Emmerich J; Alhenc-Gelas M; Gandrille S
    Semin Hematol; 1997 Jul; 34(3):205-16. PubMed ID: 9241706
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [The clinical characteristics, complications and therapeutic problems of protein C deficiency].
    Barkagan ZS; Belykh SI; Karpenko AA
    Ter Arkh; 1993; 65(7):58-62. PubMed ID: 8211782
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Homozygous type I protein C deficiency in two unrelated families exhibiting thrombophilia related to Ala136-->Pro or Arg286-->His mutations.
    Long GL; Tomczak JA; Rainville IR; Dreyfus M; Schramm W; Schwarz HP
    Thromb Haemost; 1994 Oct; 72(4):526-33. PubMed ID: 7878626
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Thrombophilia caused by a type II protein-C defect].
    Vogel G; Machulik M; Lauten G
    Z Gesamte Inn Med; 1987 Oct; 42(19):550-1. PubMed ID: 3424887
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.