How I treat patients with hereditary antithrombin deficiency-Reference-Cited by-同舟云学术

How I treat patients with hereditary antithrombin deficiency

Published:2019-12-26 Issue:26 Volume:134 Page:2346-2353
ISSN:0006-4971
Container-title:Blood
language:en
Short-container-title:

Author:

Pabinger Ingrid¹,Thaler Johannes¹^ORCID

Affiliation:

1. Clinical Division of Hematology and Hemostaseology, Department of Medicine I, Medical University of Vienna, Vienna, Austria

Abstract

This issue’s How I Treat article offers valuable insights to clinicians caring for patients with congenital antithrombin deficiency and is likely to be especially helpful for clinicians who only see a few cases in their career.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

http://ashpublications.org/blood/article-pdf/134/26/2346/1549626/bloodbld2019002927c.pdf

Reference81 articles.

1. Antithrombin deficiency and its laboratory diagnosis;Muszbek;Clin Chem Lab Med,2010

2. Investigation and management of heritable thrombophilia;Haemostasis and Thrombosis Task Force, British Committee for Standards in Haematology;Br J Haematol,2001

3. Inherited antithrombin deficiency: a review;Patnaik;Haemophilia,2008

4. Antithrombin: in control of coagulation;Quinsey;Int J Biochem Cell Biol,2004

5. Serpins in thrombosis, hemostasis and fibrinolysis;Rau;J Thromb Haemost,2007

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3. Familial onset of venous thromboembolism due to inherited antithrombin deficiency with a novel gene variant (p.Arg14Gly);Journal of Cardiology Cases;2024-07

4. Long-range and real-time PCR identification of a large SERPINC1 deletion in a patient with antithrombin deficiency;International Journal of Hematology;2024-05-27

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