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Items: 1 to 20 of 214

1.

An unknown genetic defect increases venous thrombosis risk, through interaction with protein C deficiency.

Hasstedt SJ, Bovill EG, Callas PW, Long GL.

Am J Hum Genet. 1998 Aug;63(2):569-76.

2.

Clarification of the risk for venous thrombosis associated with hereditary protein S deficiency by investigation of a large kindred with a characterized gene defect.

Simmonds RE, Ireland H, Lane DA, Zöller B, García de Frutos P, Dahlbäck B.

Ann Intern Med. 1998 Jan 1;128(1):8-14.

PMID:
9424998
3.
4.

Genetic background analysis of protein C deficiency demonstrates a recurrent mutation associated with venous thrombosis in Chinese population.

Tang L, Guo T, Yang R, Mei H, Wang H, Lu X, Yu J, Wang Q, Hu Y.

PLoS One. 2012;7(4):e35773. doi: 10.1371/journal.pone.0035773. Epub 2012 Apr 24.

5.

Increased lipoprotein(a) is an important risk factor for venous thromboembolism in childhood.

Nowak-Göttl U, Junker R, Hartmeier M, Koch HG, Münchow N, Assmann G, von Eckardstein A.

Circulation. 1999 Aug 17;100(7):743-8.

6.

[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 Jan-Feb;127(1-2):21-7. Serbian.

PMID:
10377836
7.

Genetic risk factors of venous thrombosis.

Franco RF, Reitsma PH.

Hum Genet. 2001 Oct;109(4):369-84. Review.

PMID:
11702218
8.

Genome scan of venous thrombosis in a pedigree with protein C deficiency.

Hasstedt SJ, Scott BT, Callas PW, Vossen CY, Rosendaal FR, Long GL, Bovill EG.

J Thromb Haemost. 2004 Jun;2(6):868-73.

9.

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.

PMID:
19132194
10.

Sudden infant death syndrome, childhood thrombosis, and presence of genetic risk factors for thrombosis.

Larsen TB, Nørgaard-Pedersen B, Lundemose JB, Rüdiger N, Gaustadnes M, Brandslund I.

Thromb Res. 2000 May 15;98(4):233-9.

PMID:
10822069
11.

Silent cerebral infarcts in basal ganglia are advanced in congenital protein C-deficient heterozygotes with hypertension.

Kario K, Sakata T, Higashikawa M, Katayama Y, Hoshide S, Shimada K, Miyata T.

Am J Hypertens. 2001 Aug;14(8 Pt 1):818-22.

PMID:
11497200
12.

Studies on congenital protein C deficiency in Japanese: prevalence, genetic analysis, and relevance to the onset of arterial occlusive diseases.

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

Semin Thromb Hemost. 2000;26(1):11-6.

PMID:
10805275
13.

[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
14.

Protein C/S ratio, an accurate and simple tool to identify carriers of a protein C gene mutation.

Libourel EJ, Meinardi JR, de Kam PJ, Veenstra R, van der Schaaf W, Ruiters MH, van der Meer J.

Br J Haematol. 2002 Aug;118(2):615-8.

PMID:
12139756
15.

Hereditary basis of protein C deficiency (PCD) in thrombosis patients: first report from India.

Pai N, Shetty S, Idicula-Thomas S, Kulkarni B, Ghosh K.

Thromb Haemost. 2009 Apr;101(4):785-7. No abstract available.

PMID:
19350130
16.

Prevalence of protein C deficiency in the healthy population.

Tait RC, Walker ID, Reitsma PH, Islam SI, McCall F, Poort SR, Conkie JA, Bertina RM.

Thromb Haemost. 1995 Jan;73(1):87-93.

PMID:
7740502
17.

Severe perinatal thrombosis in double and triple heterozygous offspring of a family segregating two independent protein S mutations and a protein C mutation.

Formstone CJ, Hallam PJ, Tuddenham EG, Voke J, Layton M, Nicolaides K, Hann IM, Cooper DN.

Blood. 1996 May 1;87(9):3731-7.

18.

Chronic venous abnormalities in symptomatic and asymptomatic protein C deficiency.

Emmerich J, Vossen CY, Callas PW, Demers C, Naud S, Long GL, Couture P, Rosendaal FR, Bovill EG.

J Thromb Haemost. 2005 Jul;3(7):1428-31.

19.

Factor V Leiden, prothrombin G20210A, and protein C mutation frequency in Turkish venous thrombosis patients.

Altinisik J, Ates O, Ulutin T, Cengiz M, Buyru N.

Clin Appl Thromb Hemost. 2008 Oct;14(4):415-20. Epub 2007 Dec 26.

PMID:
18160601
20.

[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. Review. Spanish.

PMID:
1596402

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