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Items: 10

2.

Antithrombin: structure, genomic organization, function and inherited deficiency.

Lane DA, Caso R.

Baillieres Clin Haematol. 1989 Oct;2(4):961-98. Review.

PMID:
2688761
3.

Antithrombin and its inherited deficiencies.

Perry DJ.

Blood Rev. 1994 Mar;8(1):37-55. Review.

PMID:
8205009
4.

The molecular pathology of inherited human antithrombin III deficiency.

Manson HE, Austin RC, Fernandez-Rachubinski F, Rachubinski RA, Blajchman MA.

Transfus Med Rev. 1989 Oct;3(4):264-81. Review. No abstract available. Erratum in: Transfus Med Rev. 1990 Jan;4(1):83-4.

PMID:
2520560
5.

Antithrombin III Kumamoto: identification of a point mutation and genotype analysis of the family.

Ueyama H, Murakami T, Nishiguchi S, Maeda S, Hashimoto Y, Okajima K, Shimada K, Araki S.

Thromb Haemost. 1990 Apr 12;63(2):231-4. Review.

PMID:
2194315
6.

Antithrombin and its deficiency states.

Lane DA, Olds RR, Thein SL.

Blood Coagul Fibrinolysis. 1992 Jun;3(3):315-41. Review.

PMID:
1643210
7.

An overview of the mechanism of action of antithrombin and its inherited deficiency states.

Blajchman MA.

Blood Coagul Fibrinolysis. 1994 Jan;5 Suppl 1:S5-11; discussion S59-64. Review.

PMID:
8186357
8.

Molecular genetics of antithrombin deficiency.

Lane DA, Kunz G, Olds RJ, Thein SL.

Blood Rev. 1996 Jun;10(2):59-74. Review.

PMID:
8813337
9.

Molecular genetics of human antithrombin deficiency.

Perry DJ, Carrell RW.

Hum Mutat. 1996;7(1):7-22. Review.

PMID:
8664906
10.

A review of mutations causing deficiencies of antithrombin, protein C and protein S.

Aiach M, Gandrille S, Emmerich J.

Thromb Haemost. 1995 Jul;74(1):81-9. Review.

PMID:
8578531

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