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Links from PubMed

Items: 8

1.

Evidence linking familial thrombosis with a defective antithrombin III gene in two British kindreds.

Sacks SH, Old JM, Reeders ST, Weatherall DJ, Douglas AS, Winter JH, Rizza CR.

J Med Genet. 1988 Jan;25(1):20-4.

2.

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
3.

Molecular genetics of inherited antithrombin III deficiencies.

Prochownik EV.

Am J Med. 1989 Sep 11;87(3B):15S-18S. Review.

PMID:
2572168
4.

Familial thrombophilia: a complex genetic disorder.

Koeleman BP, Reitsma PH, Bertina RM.

Semin Hematol. 1997 Jul;34(3):256-64. Review.

PMID:
9241710
5.

[The diagnosis of congenital antithrombin III deficiency and abnormality].

Takahashi K, Yamagishi R, Sakuragawa N.

Rinsho Byori. 1987 May;35(5):505-10. Review. Japanese. No abstract available.

PMID:
3302410
6.

Molecular genetics of antithrombin deficiency.

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

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

PMID:
8813337
7.

Antithrombin and its inherited deficiency states.

van Boven HH, Lane DA.

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

PMID:
9241705
8.

Progressing ischemic stroke in a homozygote with variant antithrombin III.

Ueyama H, Hashimoto Y, Uchino M, Sasaki Y, Uyama E, Okajima K, Araki S.

Stroke. 1989 Jun;20(6):815-8. Review.

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