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Results: 1 to 20 of 105

Similar articles for PubMed (Select 7423286)

1.

A South African family with antithrombin III deficiency.

Beukes CA, Heyns AD.

S Afr Med J. 1980 Sep 27;58(13):528-30.

PMID:
7423286
2.

[Molecular mechanisms of antithrombin gene mutations in 3 pedigrees with hereditary antithrombin deficiency].

Sun L, Yu ZQ, Wang CR.

Zhonghua Xue Ye Xue Za Zhi. 2013 Mar;34(3):253-5. doi: 10.3760/cma.j.issn.0253-2727.2013.03.016. Chinese. No abstract available.

3.

Antithrombin.

Hepner M, Karlaftis V.

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

PMID:
23546728
4.

[Acquired antithrombin III deficiency in cardiac surgery: an update].

Muedra V.

Rev Esp Anestesiol Reanim. 2012 Aug-Sep;59(7):347-9. doi: 10.1016/j.redar.2012.05.026. Epub 2012 Jun 29. Spanish. No abstract available.

PMID:
22749326
5.

Regulatory regions of SERPINC1 gene: identification of the first mutation associated with antithrombin deficiency.

de la Morena-Barrio ME, Antón AI, Martínez-Martínez I, Padilla J, Miñano A, Navarro-Fernández J, Águila S, López MF, Fontcuberta J, Vicente V, Corral J.

Thromb Haemost. 2012 Mar;107(3):430-7. doi: 10.1160/TH11-10-0701. Epub 2012 Jan 11.

PMID:
22234719
6.

Arterial and venous thrombosis and prothrombotic fibrin clot phenotype in a Polish family with type 1 antithrombin deficiency (antithrombin Krakow).

Celinska-Lowenhoff M, Iwaniec T, Alhenc-Gelas M, Musial J, Undas A.

Thromb Haemost. 2011 Aug;106(2):379-81. doi: 10.1160/TH11-02-0066. Epub 2011 Jun 9. No abstract available.

PMID:
21655678
7.

A heparin binding site Arg79Cys missense mutation in the SERPINC1 gene in a Korean patient with hereditary antithrombin deficiency.

Yoo JH, Maeng HY, Kim HJ, Lee KA, Choi JR, Song J.

Ann Clin Lab Sci. 2011 Fall;41(1):89-92.

PMID:
21325262
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.

[Antithrombin deficiency due to heterozygous antithrombin gene mutation and a pedigree study].

Ye X, Feng Y, Jin PP, Zhou XH, Ding QL, Wang XF.

Zhonghua Xue Ye Xue Za Zhi. 2007 Sep;28(9):587-9. Chinese.

PMID:
18246812
10.

Report of a novel kindred with antithrombin heparin-binding site variant (47 Arg to His): demand for an automated progressive antithrombin assay to detect molecular variants with low thrombotic risk.

Rossi E, Chiusolo P, Za T, Marietti S, Ciminello A, Leone G, De Stefano V.

Thromb Haemost. 2007 Sep;98(3):695-7. No abstract available. Erratum in: Thromb Haemost. 2007 Oct;98(4):915.

PMID:
17849067
11.

[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
12.
13.

[Role of newly developed technology in blood coagulation disorders].

Matsuo T.

Rinsho Byori. 2002 May;50(5):506-12. Japanese.

PMID:
12078050
14.

Discrepancy between antithrombin activity methods revealed in Antithrombin Stockholm: do factor Xa-based methods overestimate antithrombin activity in some patients?

Ungerstedt JS, Schulman S, Egberg N, Antovic J, Blombäck N.

Blood. 2002 Mar 15;99(6):2271-2. No abstract available.

15.

[Combined hemostatic defects in family members of symptomatic carriers of Leiden mutations of factor V].

Lewandowski K, Rozek M, Turowiecka Z, Markiewicz WT, Zawilska K.

Pol Arch Med Wewn. 1998 Mar;99(3):211-7. Polish.

PMID:
9760807
16.

Uses of antithrombin III concentrate in congenital and acquired deficiency states.

Bucur SZ, Levy JH, Despotis GJ, Spiess BD, Hillyer CD.

Transfusion. 1998 May;38(5):481-98. Review. No abstract available.

PMID:
9633563
17.

[Genetic diagnosis of hereditary coagulation disorders].

Ozawa T.

Rinsho Byori. 1998 Jan;46(1):43-8. Review. Japanese.

PMID:
9492537
18.

Index of suspicion. Case 3. Antithrombin III deficiency.

Nussbaum D 2nd.

Pediatr Rev. 1997 Aug;18(8):283, 285-6. No abstract available.

PMID:
9255997
19.

Antithrombin and its inherited deficiency states.

van Boven HH, Lane DA.

Semin Hematol. 1997 Jul;34(3):188-204. Review.

PMID:
9241705
20.

[Epidemiology of hereditary thrombophilia].

Rozendal FR.

Vestn Ross Akad Med Nauk. 1997;(1):5-9. Review. Russian. No abstract available.

PMID:
9064024
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