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Items: 1 to 20 of 103

1.

Laboratory tests for antithrombin deficiency.

Khor B, Van Cott EM.

Am J Hematol. 2010 Dec;85(12):947-50. doi: 10.1002/ajh.21893. Review.

2.

Laboratory tests for protein C deficiency.

Khor B, Van Cott EM.

Am J Hematol. 2010 Jun;85(6):440-2. doi: 10.1002/ajh.21679. Review.

3.

Early graft thrombosis due to antithrombin III deficiency following CABG.

Kovacevic P, Velicki L, Komazec N, Vujin B, Ivanovic V, Golubovic M.

Herz. 2011 Mar;36(2):144-6. doi: 10.1007/s00059-011-3430-y. Epub 2011 Feb 18.

PMID:
21327876
4.

Inherited antithrombin deficiency: a review.

Patnaik MM, Moll S.

Haemophilia. 2008 Nov;14(6):1229-39. doi: 10.1111/j.1365-2516.2008.01830.x. Review.

PMID:
19141163
5.

Antithrombin.

Hepner M, Karlaftis V.

Methods Mol Biol. 2013;992:355-64. doi: 10.1007/978-1-62703-339-8_28.

PMID:
23546728
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.

Laboratory diagnosis of hereditary thrombophilia.

Michiels JJ, Hamulyák K.

Semin Thromb Hemost. 1998;24(4):309-20. Review.

PMID:
9763348
8.

Role of antithrombin concentrate in treatment of hereditary antithrombin deficiency. An update.

Rodgers GM.

Thromb Haemost. 2009 May;101(5):806-12. Review.

PMID:
19404531
9.

The prevalence of hereditary antithrombin-III deficiency in patients with a history of venous thromboembolism.

Vikydal R, Korninger C, Kyrle PA, Niessner H, Pabinger I, Thaler E, Lechner K.

Thromb Haemost. 1985 Dec 17;54(4):744-5.

PMID:
4089808
10.

[A novel mutation in antithrombin gene results in hereditary antithrombin deficiency].

Zhang FH, Ding QL, Wu JS, Zhou RF, Wang XF, Xu XC.

Zhonghua Xue Ye Xue Za Zhi. 2006 Sep;27(9):598-601. Chinese.

PMID:
17278425
11.
12.

The hypercoagulable states.

Schafer AI.

Ann Intern Med. 1985 Jun;102(6):814-28. Review.

PMID:
3158262
13.
14.

[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
15.

Detection of large deletion mutations in the SERPINC1 gene causing hereditary antithrombin deficiency by multiplex ligation-dependent probe amplification (MLPA).

Lee ST, Kim HJ, Kim DK, Schuit RJ, Kim SH.

J Thromb Haemost. 2008 Apr;6(4):701-3. doi: 10.1111/j.1538-7836.2008.02905.x. Epub 2008 Jan 15. No abstract available.

17.

Hereditary antithrombin III deficiency and pregnancy: report of two cases and review of the literature.

Nelson DM, Stempel LE, Brandt JT.

Obstet Gynecol. 1985 Jun;65(6):848-53.

PMID:
4039808
18.

Genetic analysis should be included in clinical practice when screening for antithrombin deficiency.

Zeng W, Tang L, Jian XR, Li YQ, Guo T, Wang QY, Liu H, Wu YY, Cheng ZP, Hu B, Lu X, Yu JM, Deng J, Wang HF, Sun CY, Yang Y, Hu Y.

Thromb Haemost. 2015 Feb;113(2):262-71. doi: 10.1160/TH14-05-0446. Epub 2014 Oct 9.

PMID:
25298121
19.

Assessment of interference by heparin cofactor II in the DuPont aca antithrombin-III assay.

Hortin GL, Tollefsen DM, Santoro SA.

Am J Clin Pathol. 1988 Apr;89(4):515-7.

20.

Pathophysiology of antithrombin III deficiency.

Green RA.

Vet Clin North Am Small Anim Pract. 1988 Jan;18(1):95-104. Review.

PMID:
3282388
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