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Items: 17

1.

3' end processing of the prothrombin mRNA in thrombophilia.

Danckwardt S, Hartmann K, Gehring NH, Hentze MW, Kulozik AE.

Acta Haematol. 2006;115(3-4):192-7. Review.

PMID:
16549895
2.

Review article: inherited thrombophilia in inflammatory bowel disease.

Papa A, Danese S, Grillo A, Gasbarrini G, Gasbarrini A.

Am J Gastroenterol. 2003 Jun;98(6):1247-51. Review.

PMID:
12818264
3.

Human gene mutations affecting RNA processing and translation.

Cooper DN.

Ann Med. 1993 Feb;25(1):11-7. Review.

PMID:
8435181
4.

[Genomic diagnosis of thrombophilia in women: clinical relevance].

Luxembourg B, Lindhoff-Last E.

Hamostaseologie. 2007 Feb;27(1):22-31. Review. German.

PMID:
17279273
5.

The molecular mechanisms of inherited thrombophilia.

März W, Nauck M, Wieland H.

Z Kardiol. 2000 Jul;89(7):575-86. Review.

PMID:
10957782
6.

Clinical and laboratory management of the prothrombin G20210A mutation.

McGlennen RC, Key NS.

Arch Pathol Lab Med. 2002 Nov;126(11):1319-25. Review.

PMID:
12421139
7.

Risk of recurrent venous thromboembolism in patients with common thrombophilia: a systematic review.

Ho WK, Hankey GJ, Quinlan DJ, Eikelboom JW.

Arch Intern Med. 2006 Apr 10;166(7):729-36. Review.

PMID:
16606808
8.

Review and management of patients with the prothrombin G20210A polymorphism.

Nguyen A.

Clin Appl Thromb Hemost. 2000 Apr;6(2):94-9. Review.

PMID:
10775030
9.

A patient homozygous for mutation 20210A in the prothrombin gene with venous thrombosis and transient ischemic attacks of thrombotic origin.

González Ordóñez AJ, Medina Rodriguez JM, Fernández Alvarez CR, Macias Robles MD, Coto García E.

Haematologica. 1998 Nov;83(11):1050-1. Review.

10.

DNA technology for the detection of common genetic variants that predispose to thrombophilia.

Pecheniuk NM, Walsh TP, Marsh NA.

Blood Coagul Fibrinolysis. 2000 Dec;11(8):683-700. Review.

PMID:
11132646
11.

Role of hemostatic gene polymorphisms in venous and arterial thrombotic disease.

Lane DA, Grant PJ.

Blood. 2000 Mar 1;95(5):1517-32. Review. No abstract available.

12.

Inherited thrombophilias in pregnant patients: detection and treatment paradigm.

Lockwood CJ.

Obstet Gynecol. 2002 Feb;99(2):333-41. Review.

PMID:
11814516
13.

Venous thromboembolism: implications for gene-based diagnosis and technology development.

Hooper WC, De Staercke C.

Expert Rev Mol Diagn. 2002 Nov;2(6):576-86. Review.

PMID:
12465454
15.

The role of inherited thrombophilia in venous thromboembolism associated with pregnancy.

McColl MD, Walker ID, Greer IA.

Br J Obstet Gynaecol. 1999 Aug;106(8):756-66. Review.

PMID:
10453824
16.

Thrombophilia: a genetic predisposition to thrombosis.

Sacher RA.

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

17.

Understanding the contribution of synonymous mutations to human disease.

Sauna ZE, Kimchi-Sarfaty C.

Nat Rev Genet. 2011 Aug 31;12(10):683-91. doi: 10.1038/nrg3051. Review.

PMID:
21878961

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