Zsolt Oláh

Founder effect is responsible for the p.Leu131Phe heparin‐binding‐site antithrombin mutation common in Hungary: phenotype analysis in a large cohort

Réka Gindele, Zsolt Oláh, Péter Ilonczai et al. · Journal of Thrombosis and Haemostasis · 2016 · 60 citations · Full text

Medicine, Genetics, Molecular Genetics +12

The Superiority of Anti-FXa Assay Over Anti-FIIa Assay in Detecting Heparin-Binding Site Antithrombin Deficiency

Bettina Kovács, Zsuzsanna Bereczky, Zsolt Oláh et al. · American Journal of Clinical Pathology · 2013 · 32 citations · Full text

Medicine, Genetics, Hematology +17

Stem Cell Therapy: A Promising and Prospective Approach in the Treatment of Patients With Severe Buerger’s Disease

Z Boda, Miklós Udvardy, Katalin Rázsó et al. · Clinical and Applied Thrombosis/Hemostasis · 2008 · 26 citations · Full text

Medicine, Orthopaedic Surgery, Surgery +13

Clinical and laboratory characteristics of antithrombin deficiencies: A large cohort study from a single diagnostic center

Réka Gindele, Anna Selmeczi, Zsolt Oláh et al. · Thrombosis Research · 2017 · 26 citations · Full text

Medicine, Hematology, Internal Medicine +15

High penetrance of inferior vena cava system atresia in severe thrombophilia caused by homozygous antithrombin Budapest 3 variant: Description of a new syndrome

María Eugenia de la Morena‐Barrio, Réka Gindele, Carlos Bravo‐Pérez et al. · American Journal of Hematology · 2021 · 17 citations · Full text

Medicine, Genetics, Hematology +13