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Items: 1 to 20 of 24


Endocardial Endothelial Dysfunction Progressively Disrupts Initially Anti then Pro-Thrombotic Pathways in Heart Failure Mice.

Schoner A, Tyrrell C, Wu M, Gelow JM, Hayes AA, Lindner JR, Thornburg KL, Hasan W.

PLoS One. 2015 Nov 13;10(11):e0142940. doi: 10.1371/journal.pone.0142940. eCollection 2015.


Global assays of hemostasis in the diagnostics of hypercoagulation and evaluation of thrombosis risk.

Lipets EN, Ataullakhanov FI.

Thromb J. 2015 Jan 23;13(1):4. doi: 10.1186/s12959-015-0038-0. eCollection 2015.


Genetic markers associated with plasma protein C level in African Americans: the atherosclerosis risk in communities (ARIC) study.

Munir MS, Weng LC, Tang W, Basu S, Pankow JS, Matijevic N, Cushman M, Boerwinkle E, Folsom AR.

Genet Epidemiol. 2014 Dec;38(8):709-13. doi: 10.1002/gepi.21868. Epub 2014 Nov 5.


Study of associated genetic variants in Indian subjects reveals the basis of ethnicity related differences in susceptibility to venous thromboembolism.

Kumari B, Srivastava S, Chatterjee T, Vardhan R, Tyagi T, Gupta N, Sahu A, Chandra K, Ashraf MZ.

Thrombosis. 2014;2014:182762. doi: 10.1155/2014/182762. Epub 2014 Sep 30.


Testing for thrombophilia: clinical update.

Graham N, Rashiq H, Hunt BJ.

Br J Gen Pract. 2014 Feb;64(619):e120-2. doi: 10.3399/bjgp14X677310. No abstract available.


Omental gangrene and porto-mesenteric thrombosis in a patient of protein C and protein s deficiency.

Patle NM, Tantia O, Das PC, Mukherjee J, Prasad P.

Indian J Surg. 2013 Jun;75(Suppl 1):409-11. doi: 10.1007/s12262-012-0751-x. Epub 2012 Sep 22.


Protein-C deficiency presenting as pulmonary embolism and myocardial infarction in the same patient.

Maqbool S, Rastogi V, Seth A, Singh S, Kumar V, Mustaqueem A.

Thromb J. 2013 Oct 1;11(1):19. doi: 10.1186/1477-9560-11-19.


Distinct frequencies and mutation spectrums of genetic thrombophilia in Korea in comparison with other Asian countries both in patients with thromboembolism and in the general population.

Kim HJ, Seo JY, Lee KO, Bang SH, Lee ST, Ki CS, Kim JW, Jung CW, Kim DK, Kim SH.

Haematologica. 2014 Mar;99(3):561-9. doi: 10.3324/haematol.2013.092023. Epub 2013 Oct 25.


Endothelial cell protein C receptor gene 6936A/G polymorphism is associated with venous thromboembolism.

Yin G, Jin X, Ming H, Zheng X, Zhang D.

Exp Ther Med. 2012 Jun;3(6):989-992. Epub 2012 Mar 12.


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.


Limited ability to activate protein C confers left atrial endocardium a thrombogenic phenotype: a role in cardioembolic stroke?

Cerveró J, Montes R, España F, Esmon CT, Hermida J.

Stroke. 2011 Sep;42(9):2622-4. doi: 10.1161/STROKEAHA.111.614420. Epub 2011 Jun 23.


Normal ranges and genetic variants of antithrombin, protein C and protein S in the general Chinese population. Results of the Chinese Hemostasis Investigation on Natural Anticoagulants Study I Group.

Zhu T, Ding Q, Bai X, Wang X, Kaguelidou F, Alberti C, Wei X, Hua B, Yang R, Wang X, Wang Z, Ruan C, Schlegel N, Zhao Y.

Haematologica. 2011 Jul;96(7):1033-40. doi: 10.3324/haematol.2010.037515. Epub 2011 Apr 12.


Evidence-based approach to thrombophilia testing.

Middeldorp S.

J Thromb Thrombolysis. 2011 Apr;31(3):275-81. doi: 10.1007/s11239-011-0572-y. Review.


Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study.

Tang W, Basu S, Kong X, Pankow JS, Aleksic N, Tan A, Cushman M, Boerwinkle E, Folsom AR.

Blood. 2010 Dec 2;116(23):5032-6. doi: 10.1182/blood-2010-05-283739. Epub 2010 Aug 27.


Case report: perioperative use of protein c concentrate for protein C deficiency in THA.

Thakkar SC, Streiff MB, Bruley DF, Mears SC.

Clin Orthop Relat Res. 2010 Jul;468(7):1986-90. doi: 10.1007/s11999-009-1189-8. Epub 2009 Dec 10.


Low protein C and incidence of ischemic stroke and coronary heart disease: the Atherosclerosis Risk in Communities (ARIC) Study.

Folsom AR, Ohira T, Yamagishi K, Cushman M.

J Thromb Haemost. 2009 Nov;7(11):1774-8. doi: 10.1111/j.1538-7836.2009.03577.x. Epub 2009 Aug 19.


Risk-assessment algorithm and recommendations for venous thromboembolism prophylaxis in medical patients.

Rocha AT, Paiva EF, Lichtenstein A, Milani R Jr, Cavalheiro CF, Maffei FH.

Vasc Health Risk Manag. 2007;3(4):533-53. Review.


Hereditary thrombophilia.

Khan S, Dickerman JD.

Thromb J. 2006 Sep 12;4:15.


Thrombophilia in pregnancy.

Walker ID.

J Clin Pathol. 2000 Aug;53(8):573-80. Review.


Thrombophilia: a genetic predisposition to thrombosis.

Sacher RA.

Trans Am Clin Climatol Assoc. 1999;110:51-60; discussion 60-1. Review. No abstract available.

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