Follow
Tünde Miklós
Tünde Miklós
András Jósa Szabolcs-Szatmár-Bereg County Hospital and University Teaching Hospital, Nyíregyháza
Verified email at szszbmk.hu
Title
Cited by
Cited by
Year
Factor XIII levels and factor XIII B subunit polymorphisms in patients with venous thromboembolism
ZA Mezei, É Katona, J Kállai, Z Bereczky, L Somodi, É Molnár, B Kovács, ...
Thrombosis research 158, 93-97, 2017
142017
Regulation of plasma factor XIII levels in healthy individuals; a major impact by subunit B intron K c. 1952+ 144 C> G polymorphism
ZA Mezei, É Katona, J Kállai, Z Bereczky, É Molnár, B Kovács, É Ajzner, ...
Thrombosis research 148, 101-106, 2016
122016
Age and origin of the founder antithrombin Budapest 3 (p. Leu131Phe) mutation; its high prevalence in the Roma population and its association with cardiovascular diseases
Z Bereczky, R Gindele, S Fiatal, M Speker, T Miklós, L Balogh, Z Mezei, ...
Frontiers in Cardiovascular Medicine 7, 617711, 2021
92021
Effect of α2-plasmin inhibitor heterogeneity on the risk of venous thromboembolism
B Baráth, R Bogáti, T Miklós, J Kállai, ZA Mezei, Z Bereczky, L Muszbek, ...
Thrombosis Research 203, 110-116, 2021
22021
Óriás thrombocyták myelodysplasiás szindrómában és krónikus myeloid leukémia blastos fázisában
J Jakó, T Miklós, I Fábián
Hematológia–Transzfuziológia 51 (2), 96-101, 2018
12018
PB1210 Incorporation of a2-Plasmin Inhibitor into Plasma Clots of Patients with Venous Thrombosis
É Katona, B Baráth, R Gindele, T Miklós, Z Bereczky
Research and Practice in Thrombosis and Haemostasis 7, 101033, 2023
2023
The association between EPCR gene p. Ser219Gly polymorphism and venous thromboembolism risk: a case–control study, meta-analysis, and a reproducibility study
D Pituk, T Miklós, Á Schlammadinger, K Rázsó, Z Bereczky
Frontiers in Cardiovascular Medicine 10, 2023
2023
Conclusions: ATBp3, a 400-year-old founder mutation is prevalent in Roma population and its Roma origin can reasonably be assumed. By the demonstration of the presence
Z Bereczky, R Gindele, S Fiatal, M Speker, T Miklós, L Balogh, Z Mezei, ...
The Serpin Family in the Cardiovascular System, 2022
2022
C0290: Diagnostic Considerations Based on the Experience of Genetic Analysis in Protein S Deficiency in the Hungarian Population with High Frequency of FV Leiden Mutation
T Miklós, Z Oláh, Á Schlammadinger, P Ilonczai, G Pfliegler, Z Boda, ...
Thrombosis Research, S81, 2014
2014
Effects of SERPINC1, PROC, PROS1 and EPCR Polymorphisms on the Risk of Venous Thromboembolism and Myocardial Infarction in Young Individuals
T Miklós, G Balla, L Balogh, Z Boda, Z Szabó, É Molnár, R Gindele, ...
The system can't perform the operation now. Try again later.
Articles 1–10