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Items: 1 to 20 of 136

1.

Clinical and genetic features of protein C deficiency in 23 unrelated Chinese patients.

Ding Q, Shen W, Ye X, Wu Y, Wang X, Wang H.

Blood Cells Mol Dis. 2013 Jan;50(1):53-8. doi: 10.1016/j.bcmd.2012.08.004. Epub 2012 Aug 27.

PMID:
22951146
2.

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.

3.

Molecular basis and thrombotic manifestations of antithrombin deficiency in 15 unrelated Chinese patients.

Ding Q, Wang M, Xu G, Ye X, Xi X, Yu T, Wang X, Wang H.

Thromb Res. 2013 Sep;132(3):367-73. doi: 10.1016/j.thromres.2013.07.013. Epub 2013 Aug 8.

PMID:
23932013
4.
5.

PROC c.574_576del polymorphism: a common genetic risk factor for venous thrombosis in the Chinese population.

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

J Thromb Haemost. 2012 Oct;10(10):2019-26. doi: 10.1111/j.1538-7836.2012.04862.x.

6.
7.

Risk factors of venous thromboembolism in thai patients.

Angchaisuksiri P, Atichartakarn V, Aryurachai K, Archararit N, Rachakom B, Atamasirikul K, Tiraganjana A.

Int J Hematol. 2007 Dec;86(5):397-402. doi: 10.1532/IJH97.A20715.

PMID:
18192106
8.

Prevalence of genetic mutations in protein S, protein C and antithrombin genes in Japanese patients with deep vein thrombosis.

Miyata T, Sato Y, Ishikawa J, Okada H, Takeshita S, Sakata T, Kokame K, Kimura R, Honda S, Kawasaki T, Suehisa E, Tsuji H, Madoiwa S, Sakata Y, Kojima T, Murata M, Ikeda Y.

Thromb Res. 2009 May;124(1):14-8. doi: 10.1016/j.thromres.2008.08.020. Epub 2008 Oct 26.

PMID:
18954896
9.

[A survey of 20 inherited protein C deficiencies in the patients with venous thromboembolism].

Shen W, Gu Y, Zhang L, Zhang JW, Ying CM, Fu QH.

Zhonghua Yi Xue Za Zhi. 2012 Jun 19;92(23):1603-6. Chinese.

PMID:
22944127
10.
11.

Compound heterozygous protein C deficiency in a family with venous thrombosis: Identification and in vitro study of p.Asp297His and p.Val420Leu mutations.

Liu H, Wang HF, Tang L, Yang Y, Wang QY, Zeng W, Wu YY, Cheng ZP, Hu B, Guo T, Hu Y.

Gene. 2015 May 25;563(1):35-40. doi: 10.1016/j.gene.2015.03.002. Epub 2015 Mar 4.

PMID:
25748729
12.

Deficiency of antithrombin and protein C gene in 202 Chinese venous thromboembolism patients.

Gu Y, Shen W, Zhang L, Zhang J, Ying C.

Int J Lab Hematol. 2014 Apr;36(2):151-5. doi: 10.1111/ijlh.12146. Epub 2013 Sep 13.

PMID:
24028705
13.

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 14;118(16):1659-67. doi: 10.1161/CIRCULATIONAHA.108.780759. Epub 2008 Sep 29.

14.

Acroangiodermatitis of Mali in protein C deficiency due to a novel PROC gene mutation.

Wei-Min Tan A, Lee JS, Pramono ZA, Chong WS.

Am J Dermatopathol. 2012 Apr;34(2):e19-21. doi: 10.1097/DAD.0b013e3182169528.

PMID:
22441373
15.

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.

16.

Protein C deficiency.

Goldenberg NA, Manco-Johnson MJ.

Haemophilia. 2008 Nov;14(6):1214-21. doi: 10.1111/j.1365-2516.2008.01838.x.

PMID:
19141162
17.

Familial thrombophilia is an oligogenetic disease: involvement of the prothrombin G20210A, PROC and PROS gene mutations.

Boinot C, Borgel D, Kitzis A, Guicheteau M, Aiach M, Alhenc-Gelas M.

Blood Coagul Fibrinolysis. 2003 Feb;14(2):191-6.

PMID:
12632031
18.
19.

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
20.

Hereditary protein C deficiency in Indian patients with venous thrombosis.

Pai N, Ghosh K, Shetty S.

Ann Hematol. 2012 Sep;91(9):1471-6. doi: 10.1007/s00277-012-1483-5. Epub 2012 May 11.

PMID:
22576310

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