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Items: 1 to 20 of 91

1.

Absence of thrombosis in subjects with heterozygous protein C deficiency.

Miletich J, Sherman L, Broze G Jr.

N Engl J Med. 1987 Oct 15;317(16):991-6.

PMID:
3657866
2.

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 25;59(1):18-22.

PMID:
2966450
3.

Protein C deficiency in a controlled series of unselected outpatients: an infrequent but clear risk factor for venous thrombosis (Leiden Thrombophilia Study)

Koster T, Rosendaal FR, Briët E, van der Meer FJ, Colly LP, Trienekens PH, Poort SR, Reitsma PH, Vandenbroucke JP.

Blood. 1995 May 15;85(10):2756-61.

4.

Clinical relevance of protein C.

Pabinger I.

Blut. 1986 Aug;53(2):63-75. Review.

PMID:
3524711
5.

Congenital protein C deficiency and venous thromboembolism. A study of three Dutch families.

Broekmans AW, Veltkamp JJ, Bertina RM.

N Engl J Med. 1983 Aug 11;309(6):340-4.

PMID:
6688122
7.
8.

Resistance to activated protein C as a basis for venous thrombosis.

Svensson PJ, Dahlbäck B.

N Engl J Med. 1994 Feb 24;330(8):517-22.

11.

Heterozygous protein C deficiency and coumarin necrosis of the skin.

Cucuianu M, Hagău N, Cotul M, Cardan E, Giurgea I.

Rom J Intern Med. 1992 Apr-Jun;30(2):105-11.

PMID:
1496262
12.

Factor V Leiden, protein C, and lipoprotein (a) in catheter-related thrombosis in childhood: a prospective study.

Nowak-Göttl U, Dübbers A, Kececioglu D, Koch HG, Kotthoff S, Runde J, Vielhaber H.

J Pediatr. 1997 Oct;131(4):608-12.

PMID:
9386668
13.

No evidence for an increased risk of venous thrombosis in patients with factor V Leiden by the homozygous 677 C to T mutation in the methylenetetrahydrofolate-reductase gene.

Rintelen C, Mannhalter C, Lechner K, Eichinger S, Kyrle PA, Papagiannopoulos M, Schneider B, Pabinger I.

Blood Coagul Fibrinolysis. 1999 Mar;10(2):101-5.

PMID:
10192659
14.

Increased risk of venous thrombosis in carriers of hereditary protein C deficiency defect.

Allaart CF, Poort SR, Rosendaal FR, Reitsma PH, Bertina RM, Briët E.

Lancet. 1993 Jan 16;341(8838):134-8.

PMID:
8093743
15.

Hereditary thrombophilia among 217 consecutive patients with thromboembolic disease in Jordan.

Awidi AS, Abu-Khalaf M, Herzallah U, Abu-Rajab A, Shannak MM, Abu-Obeid T, al-Taher I, Anshasi B.

Am J Hematol. 1993 Oct;44(2):95-100.

PMID:
8266926
16.

Hereditary protein C deficiency caused by the Ala267Thr mutation in the protein C gene is associated with symptomatic and asymptomatic venous thrombosis.

Tjeldhorn L, Sandset PM, Haugbro K, Skretting G.

Thromb Res. 2010 Mar;125(3):230-4. doi: 10.1016/j.thromres.2009.05.013. Epub 2009 Jun 17.

PMID:
19535131
18.

Different risks of thrombosis in four coagulation defects associated with inherited thrombophilia: a study of 150 families.

Martinelli I, Mannucci PM, De Stefano V, Taioli E, Rossi V, Crosti F, Paciaroni K, Leone G, Faioni EM.

Blood. 1998 Oct 1;92(7):2353-8.

19.

Analysis of 45 episodes of arterial occlusive disease in Japanese patients with congenital protein C deficiency.

Sakata T, Kario K, Katayama Y, Matsuyama T, Kato H, Miyata T.

Thromb Res. 1999 Apr 15;94(2):69-78.

PMID:
10230891
20.

Two novel (R(-11)C; T394D) and two repeat missense mutations in the protein C gene associated with venous thrombosis in six kindreds.

Ireland HA, Boisclair MD, Taylor J, Thompson E, Thein SL, Girolami A, De Caterina M, Scopacasa F, De Stefano V, Leone G, Finazzi G, Cohen H, Lane DA.

Hum Mutat. 1996;7(2):176-9. No abstract available.

PMID:
8829639

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