A series of 10 Polish patients with thromboembolic events and antithrombin deficiency-Reference-Cited by-同舟云学术

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

Published:2019-07 Issue:5 Volume:30 Page:193-198
ISSN:0957-5235
Container-title:Blood Coagulation & Fibrinolysis
language:en
Short-container-title:

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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1. Identification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiency;Thrombosis Journal;2023-01-09

2. Analysis of phenotype and gene mutation in three pedigrees with inherited antithrombin deficiency;Journal of Clinical Laboratory Analysis;2022-10-21

3. Generation of a human iPSC line ZZUNEUi014-A from a patient with antithrombin deficiency caused by mutation in SERPINC1 gene;Stem Cell Research;2022-03

4. Type II antithrombin deficiency caused by a novel missense mutation (p.Leu417Gln) in a Chinese family;Blood Coagulation & Fibrinolysis;2021-01

5. Investigation of genetic factors leading to cardiovascular diseases in persons with risk of sudden cardiac death;Genes & Cells;2020-06-15

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