A series of 10 Polish patients with thromboembolic events and antithrombin deficiency

Author:

Wójcik Magdalena,de la Morena-Barrio María E.,Michalik Justyna,Wypasek Ewa,Kopytek Magdalena,Corral Javier,Undas Anetta

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hematology,General Medicine

Reference35 articles.

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

2. Prevalence of hereditary antithrombin mutations is higher than estimated in patients with thrombotic events;Fischer;Blood Coagul Fibrinolysis,2013

3. Deficiencies of antithrombin, protein C and protein S – practical experience in genetic analysis of a large patient cohort;Caspers;Thromb Haemost,2012

4. Genetic characterization of antithrombin, protein C and protein S deficiencies in Polish patients;Wypasek;Pol Arch Intern Med,2017

5. Homozygous antithrombin deficiency type II (99 Leu to Phe mutation) and childhood thromboembolism;Kuhle;Thromb Haemost,2001

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