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Items: 1 to 20 of 97

1.

Quality in molecular biology testing for inherited thrombophilia disorders.

Cooper PC, Goodeve AC, Beauchamp NJ.

Semin Thromb Hemost. 2012 Sep;38(6):600-12. doi: 10.1055/s-0032-1321491. Epub 2012 Aug 20. Review.

PMID:
22907670
2.

Deficiencies of antithrombin, protein C and protein S - practical experience in genetic analysis of a large patient cohort.

Caspers M, Pavlova A, Driesen J, Harbrecht U, Klamroth R, Kadar J, Fischer R, Kemkes-Matthes B, Oldenburg J.

Thromb Haemost. 2012 Aug;108(2):247-57. doi: 10.1160/TH11-12-0875. Epub 2012 May 25.

PMID:
22627591
3.

Development of a simple multiplex polymerase chain reaction for the simultaneous detection of factor V Leiden and prothrombin 20210A mutations.

Dubreuil Lastrucci RM, Dawson DA, Bowden JH, Marion Münster M.

Mol Diagn. 1999 Sep;4(3):247-50.

PMID:
10553025
4.

Prevalence of thrombophilia in women with severe ovarian hyperstimulation syndrome and cost-effectiveness of screening.

Fábregues F, Tàssies D, Reverter JC, Carmona F, Ordinas A, Balasch J.

Fertil Steril. 2004 Apr;81(4):989-95.

PMID:
15066453
5.

External quality assurance of DNA testing for thrombophilia mutations.

Hertzberg M, Neville S, Favaloro E, McDonald D.

Am J Clin Pathol. 2005 Feb;123(2):189-93.

6.
7.

Laboratory diagnosis of hereditary thrombophilia.

Michiels JJ, Hamulyák K.

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

PMID:
9763348
8.

Molecular diagnostic testing for inherited thrombophilia using Invader.

Keller MA.

Methods Mol Med. 2005;114:107-19.

PMID:
16156100
9.

Multilaboratory testing of thrombophilia: current and past practice in Australasia as assessed through the Royal College of Pathologists of Australasia Quality Assurance Program for Hematology.

Favaloro EJ, Bonar R, Sioufi J, Wheeler M, Low J, Aboud M, Duncan E, Smith J, Exner T, Lloyd J, Marsden K; RCPA QAP in Haematology.

Semin Thromb Hemost. 2005 Feb;31(1):49-58.

PMID:
15706475
10.

Role of the geneticist in testing and counseling for inherited thrombophilia.

Reich LM, Bower M, Key NS.

Genet Med. 2003 May-Jun;5(3):133-43. Review.

PMID:
12792420
11.

Genetic testing for thrombophilia mutations.

Hertzberg MS.

Semin Thromb Hemost. 2005 Feb;31(1):33-8. Review.

PMID:
15706473
12.
13.

[Diagnosis of thrombophilia based on coagulation and genetic studies].

Bałszan-Kowalska I.

Ann Acad Med Stetin. 2002;48:179-93. Polish.

PMID:
14601477
15.

Molecular diagnosis of inherited bleeding disorders and thrombophilia.

Lillicrap D.

Semin Hematol. 1999 Oct;36(4):340-51. Review.

PMID:
10530716
16.
17.

[Screening methods in genetic diagnosis of hereditary protein C deficiency].

Dávid M, Losonczy H, Nagy A, Kutscher G, Meyer M.

Orv Hetil. 1999 Jan 17;140(3):125-32. Review. Hungarian.

PMID:
9990817
18.

Screening for thrombophilia in high-risk situations: systematic review and cost-effectiveness analysis. The Thrombosis: Risk and Economic Assessment of Thrombophilia Screening (TREATS) study.

Wu O, Robertson L, Twaddle S, Lowe GD, Clark P, Greaves M, Walker ID, Langhorne P, Brenkel I, Regan L, Greer I.

Health Technol Assess. 2006 Apr;10(11):1-110. Review.

19.

Preconception counseling for women with thrombophilia.

Silver RM, Warren JE.

Clin Obstet Gynecol. 2006 Dec;49(4):906-19. Review.

PMID:
17082685
20.

Contribution of prothrombin 20210A allele and factor V Leiden mutation to thrombosis risk in thrombophilic families with other hemostatic deficiencies.

Tirado I, Mateo J, Soria JM, Oliver A, Borrell M, Coll I, Vallvé C, Souto JC, Martínez-Sánchez E, Fontcuberta J.

Haematologica. 2001 Nov;86(11):1200-8.

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