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Results: 1 to 20 of 32

Related Articles by Review for PubMed (Select 6895379)

1.

Deficiency of protein C in congenital thrombotic disease.

Griffin JH, Evatt B, Zimmerman TS, Kleiss AJ, Wideman C.

J Clin Invest. 1981 Nov;68(5):1370-3.

2.

Recurrent venous thrombosis and hypercoagulable states.

Bolan CD, Alving BM.

Am Fam Physician. 1991 Nov;44(5):1741-51. Review.

PMID:
1835274
3.

[The genetics of thrombosis].

Girolami A, Simioni P, Zanardi S, Coser E, Signora S.

Haematologica. 1991 Jun;76 Suppl 3:249-60. Review. Italian. No abstract available.

PMID:
1836447
4.

Familial venous thromboembolism and inherited abnormalities of the blood clotting system.

Gallus AS.

Aust N Z J Med. 1984 Dec;14(6):807-10. Review. No abstract available.

PMID:
6398051
5.

Antithrombin III, protein C, and protein S. Naturally occurring anticoagulant proteins.

High KA.

Arch Pathol Lab Med. 1988 Jan;112(1):28-36. Review.

PMID:
2962557
6.

The molecular genetics of familial venous thrombosis.

Cooper DN.

Blood Rev. 1991 Mar;5(1):55-70. Review.

PMID:
1674436
7.

Familial venous thrombosis.

Winter JH, Douglas AS.

Postgrad Med J. 1983 Nov;59(697):677-89. Review. No abstract available.

8.

Hereditary disorders predisposing to thrombosis.

Comp PC.

Prog Hemost Thromb. 1986;8:71-102. Review. No abstract available.

PMID:
3031738
9.

[Significance of hereditary thrombophilia for risk of thrombosis with oral contraceptives].

Bauersachs R, Lindhoff-Last E, Ehrly AM, Kuhl H.

Zentralbl Gynakol. 1996;118(5):262-70. Review. German.

PMID:
8701622
10.

Clinical studies of protein C.

Griffin JH.

Semin Thromb Hemost. 1984 Apr;10(2):162-6. Review.

PMID:
6377499
11.

Activated protein C resistance--a major risk factor for thrombosis.

Rosén SB, Sturk A.

Eur J Clin Chem Clin Biochem. 1997 Jul;35(7):501-16. Review.

PMID:
9263726
12.

Congenital thrombotic disorders.

Rodgers GM, Shuman MA.

Am J Hematol. 1986 Apr;21(4):419-30. Review.

PMID:
2937290
13.

[Role of the hemostasis laboratory in the etiologic approach to deep vein thrombosis].

De Maistre E, Briquel ME, Andre E, Regnault V, Whal D, Perret C, Laprevote MC, Lecompte T.

J Mal Vasc. 1996;21(1):1-6. Review. French.

PMID:
8656085
14.

Familial thrombophilia: a complex genetic disorder.

Koeleman BP, Reitsma PH, Bertina RM.

Semin Hematol. 1997 Jul;34(3):256-64. Review.

PMID:
9241710
15.

Inherited resistance to activated protein C caused by presence of the FV:Q506 allele as a basis of venous thrombosis.

Dahlbäck B, Zöller B, Hillarp A.

Haemostasis. 1996 Oct;26 Suppl 4:301-14. Review.

PMID:
8979136
16.
17.

[Protein C: a priority factor to be determined in recurrent venous thrombosis].

Muñiz-Díaz E, Fontcuberta J, Sala N, Félez J.

Med Clin (Barc). 1984 Nov 10;83(15):640-3. Review. Spanish. No abstract available.

PMID:
6441089
18.

[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 9;146(41):2121-5. Review. Hungarian.

PMID:
16304806
19.
20.

Incidence of thromboembolism in association with congenital disorders in coagulation and fibrinolysis.

Conard J, Horellou MH, Samama M.

Acta Chir Scand Suppl. 1988;543:15-25. Review. No abstract available.

PMID:
2973199
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