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Links from PubMed

Items: 11

1.

Antithrombin III deficiency in an Australian family.

Pitney WR, Manoharan A, Dean S.

Br J Haematol. 1980 Sep;46(1):147-9. No abstract available.

PMID:
7426446
2.

[Genetic analysis of congenital antithrombin deficiencies].

Masuda H, Tsuji H, Nakahara Y, Nishimura H, Kasahara T, Sugano T, Nakagawa M.

Rinsho Byori. 1997 Feb;Suppl 104:187-94. Review. Japanese. No abstract available.

PMID:
9128381
3.

Inherited antithrombin III deficiency in the neonate.

Seguin J, Weatherstone K, Nankervis C.

Arch Pediatr Adolesc Med. 1994 Apr;148(4):389-93. Review.

PMID:
8148939
4.

[Type I antithrombin deficiency as a cause of arterial and venous thrombosis in a family with severe thrombophilia].

Tóth O, Dávid M, Habon T, Nagy A, Keszthelyi Z, Kovács N, Losonczy H.

Orv Hetil. 2005 Oct 9;146(41):2121-5. Review. Hungarian.

PMID:
16304806
5.

Plasma antithrombin III deficiency in ischaemic stroke in the young.

Nagaraja D, Christopher R, Tripathi M.

Neurol India. 1999 Jun;47(2):155-6. Review.

6.

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
7.

[Inherited thrombophilia].

Lopaciuk S.

Acta Haematol Pol. 1994;25(2 Suppl 2):41-54. Review. Polish.

PMID:
7998473
8.

[Mesenteric venous infarction and antithrombin III deficiency: description of 2 cases and literature review].

Lurquin P, Mendes da Costa P.

Rev Med Brux. 1993 Sep;14(7):203-6. Review. French.

PMID:
8235184
9.

Familial thrombophilia: a complex genetic disorder.

Koeleman BP, Reitsma PH, Bertina RM.

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

PMID:
9241710
10.

Inherited thrombophilia: Part 1.

Lane DA, Mannucci PM, Bauer KA, Bertina RM, Bochkov NP, Boulyjenkov V, Chandy M, Dahlbäck B, Ginter EK, Miletich JP, Rosendaal FR, Seligsohn U.

Thromb Haemost. 1996 Nov;76(5):651-62. Review. No abstract available.

PMID:
8950768
11.

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