92 related articles for article (PubMed ID: 1448781)
1. Hereditary protein C-deficiency: laboratory values in transmitters and guidelines for the diagnostic procedure. Report on a study of the SSC Subcommittee on Protein C and Protein S. Protein C Transmitter Study Group.
Pabinger I; Allaart CF; Hermans J; Briët E; Bertina RM
Thromb Haemost; 1992 Oct; 68(4):470-4. PubMed ID: 1448781
[TBL] [Abstract][Full Text] [Related]
2. Diagnosis of protein C deficiency in patients on oral anticoagulant treatment: comparison of three different functional protein C assays.
Pabinger I; Kyrle PA; Speiser W; Stoffels U; Jung M; Lechner K
Thromb Haemost; 1990 Jun; 63(3):407-12. PubMed ID: 2402742
[TBL] [Abstract][Full Text] [Related]
3. The frequency of type I heterozygous protein S and protein C deficiency in 141 unrelated young patients with venous thrombosis.
Gladson CL; Scharrer I; Hach V; Beck KH; Griffin JH
Thromb Haemost; 1988 Feb; 59(1):18-22. PubMed ID: 2966450
[TBL] [Abstract][Full Text] [Related]
4. Thrombotic risk of women with hereditary antithrombin III-, protein C- and protein S-deficiency taking oral contraceptive medication. The GTH Study Group on Natural Inhibitors.
Pabinger I; Schneider B
Thromb Haemost; 1994 May; 71(5):548-52. PubMed ID: 8091378
[TBL] [Abstract][Full Text] [Related]
5. Treatment of hereditary protein C deficiency with stanozolol.
Broekmans AW; Conard J; van Weyenberg RG; Horellou MH; Kluft C; Bertina RM
Thromb Haemost; 1987 Feb; 57(1):20-4. PubMed ID: 3590078
[TBL] [Abstract][Full Text] [Related]
6. Prevalence of factor V Leiden mutation and other hereditary thrombophilic factors in Egyptian children with portal vein thrombosis: results of a single-center case-control study.
El-Karaksy H; El-Koofy N; El-Hawary M; Mostafa A; Aziz M; El-Shabrawi M; Mohsen NA; Kotb M; El-Raziky M; El-Sonoon MA; A-Kader H
Ann Hematol; 2004 Nov; 83(11):712-5. PubMed ID: 15309526
[TBL] [Abstract][Full Text] [Related]
7. [Cerebral venous thrombosis and hereditary protein C deficiency].
Massons J; Arboix A; Oliveres M; Besses C; Muñoz C; Titus F
Neurologia; 1992 Jan; 7(1):34-8. PubMed ID: 1596402
[TBL] [Abstract][Full Text] [Related]
8. Protein C and S deficiency, thrombophilia, and hypofibrinolysis: pathophysiologic causes of Legg-Perthes disease.
Glueck CJ; Glueck HI; Greenfield D; Freiberg R; Kahn A; Hamer T; Stroop D; Tracy T
Pediatr Res; 1994 Apr; 35(4 Pt 1):383-8. PubMed ID: 8047373
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. Hereditary deficiency of protein C or protein S confers increased risk of arterial thromboembolic events at a young age: results from a large family cohort study.
Mahmoodi BK; Brouwer JL; Veeger NJ; van der Meer J
Circulation; 2008 Oct; 118(16):1659-67. PubMed ID: 18824642
[TBL] [Abstract][Full Text] [Related]
11. Hereditary protein S deficiency in young adults with arterial occlusive disease.
Allaart CF; Aronson DC; Ruys T; Rosendaal FR; van Bockel JH; Bertina RM; Briët E
Thromb Haemost; 1990 Oct; 64(2):206-10. PubMed ID: 2148653
[TBL] [Abstract][Full Text] [Related]
12. The use of a functional and immunologic assay for plasma protein C in the study of the heterogeneity of congenital protein C deficiency.
Bertina RM; Broekmans AW; Krommenhoek-van Es C; van Wijngaarden A
Thromb Haemost; 1984 Feb; 51(1):1-5. PubMed ID: 6547008
[TBL] [Abstract][Full Text] [Related]
13. 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; 14(6):531-8. PubMed ID: 12960605
[TBL] [Abstract][Full Text] [Related]
14. A compound heterozygous protein C deficiency with a single nucleotide G deletion encoding Gly-381 and an amino acid substitution of Lys for Gla-26.
Ido M; Ohiwa M; Hayashi T; Nishioka J; Hatada T; Watanabe Y; Wada H; Shirakawa S; Suzuki K
Thromb Haemost; 1993 Oct; 70(4):636-41. PubMed ID: 8115990
[TBL] [Abstract][Full Text] [Related]
15. High long-term absolute risk of recurrent venous thromboembolism in patients with hereditary deficiencies of protein S, protein C or antithrombin.
Brouwer JL; Lijfering WM; Ten Kate MK; Kluin-Nelemans HC; Veeger NJ; van der Meer J
Thromb Haemost; 2009 Jan; 101(1):93-9. PubMed ID: 19132194
[TBL] [Abstract][Full Text] [Related]
16. Laboratory testing for von Willebrand's disease: an assessment of current diagnostic practice and efficacy by means of a multi-laboratory survey. RCPA Quality Assurance Program (QAP) in Haematology Haemostasis Scientific Advisory Panel.
Favaloro EJ; Smith J; Petinos P; Hertzberg M; Koutts J
Thromb Haemost; 1999 Oct; 82(4):1276-82. PubMed ID: 10544913
[TBL] [Abstract][Full Text] [Related]
17. Clinical application of a functional assay for protein C.
Triplett DA; Sandquist DS; Musgrave KA
Hematol Pathol; 1987; 1(4):239-47. PubMed ID: 3143709
[TBL] [Abstract][Full Text] [Related]
18. Antithrombin III, protein C, and protein S. Naturally occurring anticoagulant proteins.
High KA
Arch Pathol Lab Med; 1988 Jan; 112(1):28-36. PubMed ID: 2962557
[TBL] [Abstract][Full Text] [Related]
19. Beta 2-glycoprotein I deficiency and the risk of thrombosis.
Bancsi LF; van der Linden IK; Bertina RM
Thromb Haemost; 1992 Jun; 67(6):649-53. PubMed ID: 1509404
[TBL] [Abstract][Full Text] [Related]
20. Evaluation of a new venom-based clotting assay of protein C.
Cooper PC; Cooper SM; Goodfellow KJ; Hickey KP; Kitchen S; Makris M
Int J Lab Hematol; 2008 Oct; 30(5):437-43. PubMed ID: 19046320
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
