Format
Items per page
Sort by

Send to:

Choose Destination

Results: 11

Related Articles by Review for PubMed (Select 2983542)

1.

Hereditary thrombosis in a Utah kindred is caused by a dysfunctional antithrombin III gene.

Bock SC, Harris JF, Schwartz CE, Ward JH, Hershgold EJ, Skolnick MH.

Am J Hum Genet. 1985 Jan;37(1):32-41.

2.

Molecular genetics of inherited antithrombin III deficiencies.

Prochownik EV.

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

PMID:
2572168
3.

Clinical experience with antithrombin III concentrate in treatment of congenital and acquired deficiency of antithrombin. The Antithrombin III Study Group.

Schwartz RS, Bauer KA, Rosenberg RD, Kavanaugh EJ, Davies DC, Bogdanoff DA.

Am J Med. 1989 Sep 11;87(3B):53S-60S. Review.

PMID:
2679072
4.

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
5.

Thrombosis in antithrombin-III-deficient persons. Report of a large kindred and literature review.

Demers C, Ginsberg JS, Hirsh J, Henderson P, Blajchman MA.

Ann Intern Med. 1992 May 1;116(9):754-61. Review.

PMID:
1489375
6.

[Congenital antithrombin III deficiency associated with pulmonary thromboembolism].

Katayama T, Akiba Y, Nishigaki Y, Morimoto H, Yamaguchi S, Fujiuchi S, Yamazaki Y, Nakano H, Ohsaki Y, Kikuchi K.

Nihon Kyobu Shikkan Gakkai Zasshi. 1997 Jul;35(7):790-5. Review. Japanese.

PMID:
9341285
7.

[Antithrombin III. Physiologic, physiopathologic and laboratory aspects].

de Sousa JC, Ferreira R, CarriƧo F, Nunes V, Geraldes MJ, Parreira F, Ribeiro C.

Rev Port Cardiol. 1991 Sep;10(9):693-9. Review. Portuguese.

PMID:
1747261
8.

Congenital antithrombin III deficiency. Incidence and clinical features.

Hirsh J, Piovella F, Pini M.

Am J Med. 1989 Sep 11;87(3B):34S-38S. Review.

PMID:
2679068
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.
11.

Prenatal diagnosis of hemoglobinopathies by DNA analysis.

Boehm C, Kazazian HH Jr.

Crit Rev Oncol Hematol. 1985;4(2):155-67. Review.

PMID:
2998637
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk