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Items: 11

1.

Antithrombin Morioka (Cys 95-Arg): a novel missense mutation causing type I antithrombin deficiency.

Ozawa T, Takikawa Y, Niiya K, Fujiwara T, Suzuki K, Sato S, Sakuragawa N.

Thromb Haemost. 1997 Feb;77(2):403. No abstract available.

PMID:
9157604
2.

Homozygous antithrombin deficiency: report of two new cases (99 Leu to Phe) associated with arterial and venous thrombosis.

Chowdhury V, Lane DA, Mille B, Auberger K, Gandenberger-Bachem S, Pabinger I, Olds RJ, Thein SL.

Thromb Haemost. 1994 Aug;72(2):198-202. Review.

PMID:
7831651
3.

Homozygous antithrombin deficiency type II (99 Leu to Phe mutation) and childhood thromboembolism.

Kuhle S, Lane DA, Jochmanns K, Male C, Quehenberger P, Lechner K, Pabinger I.

Thromb Haemost. 2001 Oct;86(4):1007-11. Review.

PMID:
11686316
4.

The molecular genetics of antithrombin deficiency.

Olds RJ, Lane DA, Thein SL.

Br J Haematol. 1994 Jun;87(2):221-6. Review. No abstract available.

PMID:
7947262
5.

Antithrombin: molecular basis of deficiency.

Bayston TA, Lane DA.

Thromb Haemost. 1997 Jul;78(1):339-43. Review.

PMID:
9198176
6.

Antithrombin and its inherited deficiency states.

van Boven HH, Lane DA.

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

PMID:
9241705
7.

Antithrombin and heparin.

Carrell R, Skinner R, Warden M, Whisstock J.

Mol Med Today. 1995 Aug;1(5):226-31. Review.

PMID:
17607884
8.

Antithrombin: the principal inhibitor of thrombin.

Olds RJ, Lane DA, Mille B, Chowdhury V, Thein SL.

Semin Thromb Hemost. 1994;20(4):353-72. Review. No abstract available.

PMID:
7899868
9.

[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
10.

Annotation. The unhinged antithrombins.

Carrell RW, Perry DJ.

Br J Haematol. 1996 May;93(2):253-7. Review. No abstract available.

PMID:
8639413
11.

[Congenital antithrombin III deficiency].

Ohke M.

Ryoikibetsu Shokogun Shirizu. 1996;(15):460-3. Review. Japanese. No abstract available.

PMID:
9048069

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