Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 8

1.

Recurrent deletion in the human antithrombin III gene.

Grundy CB, Thomas F, Millar DS, Krawczak M, Melissari E, Lindo V, Moffat E, Kakkar VV, Cooper DN.

Blood. 1991 Aug 15;78(4):1027-32.

2.

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
3.

Molecular genetics of inherited antithrombin III deficiencies.

Prochownik EV.

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

PMID:
2572168
4.

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
5.

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

Lane DA, Caso R.

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

PMID:
2688761
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.

SerpinC1/Antithrombin III in kidney-related diseases.

Lu Z, Wang F, Liang M.

Clin Sci (Lond). 2017 May 1;131(9):823-831. doi: 10.1042/CS20160669. Review.

8.

Clinical aspects of antithrombin III deficiency.

Hathaway WE.

Semin Hematol. 1991 Jan;28(1):19-23. Review. No abstract available.

PMID:
2017687

Supplemental Content

Support Center