Women with homozygous AT deficiency type II heparin-binding site (HBS) are at high risk of pregnancy loss and pregnancy complications-Reference-Cited by-同舟云学术

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Women with homozygous AT deficiency type II heparin-binding site (HBS) are at high risk of pregnancy loss and pregnancy complications

Published:2017-03-30 Issue:6 Volume:96 Page:1023-1031
ISSN:0939-5555
Container-title:Annals of Hematology
language:en
Short-container-title:Ann Hematol

Author:

Kraft Julia,Sunder-Plassmann Raute,Mannhalter Christine,Quehenberger Peter,Tews Gernot,Langer Martin,Pabinger Ingrid

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00277-017-2965-2.pdf

Reference21 articles.

1. Lockwood CJ (2002) Inherited thrombophilias in pregnant patients: detection and treatment paradigm. Obstet Gynecol 99(2):333–341

2. Patnaik MM, Moll S (2008) Inherited antithrombin deficiency: a review. Haemophilia: the official journal of the World Federation of Hemophilia 14(6):1229–1239. doi: 10.1111/j.1365-2516.2008.01830.x

3. Kuhle S, Lane DA, Jochmanns K, Male C, Quehenberger P, Lechner K, Pabinger I (2001) Homozygous antithrombin deficiency type II (99 Leu to Phe mutation) and childhood thromboembolism. Thromb Haemost 86(4):1007–1011

4. Tait RC, Walker ID, Perry DJ, Islam SI, Daly ME, McCall F, Conkie JA, Carrell RW (1994) Prevalence of antithrombin deficiency in the healthy population. Br J Haematol 87(1):106–112

5. Middeldorp S (2007) Thrombophilia and pregnancy complications: cause or association? Journal of thrombosis and haemostasis: JTH 5:276–282

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3. Thrombin Generation Decrease After LMWH Administration in an Antithrombin-Deficient Pregnant Woman With a Homozygous HBS II Mutation;Clinical and Applied Thrombosis/Hemostasis;2023-01

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5. Antithrombin Deficiency: Frequency in Patients with Thrombosis and Thrombophilic Families;Acta Medica (Hradec Kralove, Czech Republic);2023

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