Tudóstér: Gindele Réka publikációi

Kállai, J., Gindele, R., Pénzes-Daku, K., Balogh, G., Kissné Bogáti, R., Bécsi, B., Katona, É., Oláh, Z., Ilonczai, P., Boda, Z., Róna-Tas, Á., Nemes, L., Marton, I., Bereczky, Z.: Clinical and Molecular Characterization of Nine Novel Antithrombin Mutations.
Int. J. Mol. Sci. 25 (5), 1-19, 2024.

Bereczky, Z., Gindele, R., Fiatal, S., Speker, M., Miklós, T., Balogh, L., Mezei, Z., Szabó, Z., Ádány, R.: 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.
Front. Cardiovasc. Med. 7 1-15, 2021.

Major, T., Bereczky, Z., Gindele, R., Balogh, G., Rácz, B., Bora, L., Kézsmárki, Z., Brúgós, B., Pfliegler, G.: Current Status of Clinical and Genetic Screening of Hereditary Hemorrhagic Telangiectasia Families in Hungary.
J Clin Med. 10 (17), 1-17, 2021.

Major, T., Gindele, R., Balogh, G., Bárdossy, P., Bereczky, Z.: Founder Effects in Hereditary Hemorrhagic Telangiectasia.
J Clin Med. 10 (8), 1-20, 2021.

Morena-Barrio, M., Gindele, R., Bravo-Pérez, C., Ilonczai, P., Zuazu, I., Speker, M., Oláh, Z., Rodríguez-Sevilla, J., Entrena, L., Infante, M., Morena-Barrio, B., García, J., Schlammadinger, Á., Cifuentes-Riquelme, R., Mora, -., Miñano, A., Padilla, J., Vicente, V., Corral, J., Bereczky, Z.: High penetrance of inferior vena cava system atresia in severe thrombophilia caused by homozygous antithrombin Budapest 3 variant: description of a new syndrome.
Am. J. Hematol. 96 (11), 1363-1373, 2021.

Gindele, R., Pénzes-Daku, K., Balogh, G., Kállai, J., Kissné Bogáti, R., Bécsi, B., Erdődi, F., Katona, É., Bereczky, Z.: Investigation of the Differences in Antithrombin to Heparin Binding among Antithrombin Budapest 3, Basel, and Padua Mutations by Biochemical and In Silico Methods.
Biomolecules. 11 (4), 1-18, 2021.

Gindele, R., Kerényi, A., Kállai, J., Pfliegler, G., Schlammadinger, Á., Szegedi, I., Major, T., Szabó, Z., Bagoly, Z., Kiss, C., Kappelmayer, J., Bereczky, Z.: Resolving Differential Diagnostic Problems in von Willebrand Disease, in Fibrinogen Disorders, in Prekallikrein Deficiency and in Hereditary Hemorrhagic Telangiectasia by Next-Generation Sequencing.
Life (Basel). 11 (3), 1-23, 2021.

Reményi, G., Bereczky, Z., Gindele, R., Ujfalusi, A., Illés, Á., Udvardy, M.: rs779805 Von Hippel-Lindau Gene Polymorphism Induced/Related Polycythemia Entity, Clinical Features, Cancer Association, and Familiar Characteristics.
Pathol. Oncol. Res. 27 1-6, 2021.

Major, T., Csobay-Novák, C., Gindele, R., Szabó, Z., Bora, L., Jóni, N., Rácz, T., Karosi, T., Bereczky, Z.: Pitfalls of delaying the diagnosis of hereditary haemorrhagic telangiectasia.
J. Int. Med. Res. 48 (2), 1-7, 2020.

Major, T., Gindele, R., Szabó, Z., Kis, Z., Bora, L., Jóni, N., Bárdossy, P., Rácz, T., Bereczky, Z.: The Stratified Population Screening of Hereditary Hemorrhagic Telangiectasia.
Pathol. Oncol. Res. 26 (4), 2783-2788, 2020.

Major, T., Gindele, R., Szabó, Z., Jóni, N., Kis, Z., Bora, L., Bárdossy, P., Rácz, T., Karosi, T., Bereczky, Z.: A herediter haemorrhagiás teleangiectasia (Osler-Weber-Rendu-kór) genetikai diagnosztikája.
Orv. hetil. 160 (18), 710-719, 2019.

Katona, É., Kissné Bogáti, R., Miklós, T., Gindele, R., Speker, M., Fedoriska, V., Orosz, A., Mezei, Z., Bereczky, Z.: ALPHA-2 Plasmin Inhibitor Activity and Antigen Levels and p.Arg6Trp Polymorphism in Patients with Venous Thromboembolism.
Proceedings. 2 (9), 102-103, 2018.

Balogh, L., Katona, É., Mezei, Z., Kállai, J., Gindele, R., Édes, I., Muszbek, L., Papp, Z., Bereczky, Z.: Effect of factor XIII levels and polymorphisms on the risk of myocardial infarction in young patients.
Mol. Cell. Biochem. 448 (1-2), 199-209, 2018.

Miklós, T., Balla, G., Balogh, L., Boda, Z., Szabó, Z., Molnár, É., Gindele, R., Katona, É., Bereczky, Z.: Effects of Serpinc1, Proc, Pros1 and Epcr Polymorphisms on the Plasma Levels of Natural Anticoagulants in Healthy Individuals and on the Risk of Venous Thromboembolism and Myocardial Infarction.
Proceedings. 2 (9), 78, 2018.

Miklós, T., Balla, G., Balogh, L., Boda, Z., Szabó, Z., Molnár, É., Gindele, R., Katona, É., Bereczky, Z.: Effects of SERPINC1, PROC, PROS1 and EPCR Polymorphisms on the Risk of Venous Thromboembolism and Myocardial Infarction in Young Individuals.
Res Pract Thromb Haemost. 2 178, 2018.

Gindele, R., Colombo, R., Szabó, Z., Speker, M., Mezei, Z., Balogh, L., Katona, É., Bagoly, Z., Fiatal, S., Bereczky, Z.: Prevalence of Antithrombin Budapest 3 Mutation among Different Patients Groups; Investigation of the Age and Origin of Mutation Common in Hungary.
Proceedings. 2 (9), 76-77, 2018.

Katona, É., Kissné Bogáti, R., Miklós, T., Gindele, R., Speker, M., Fedoriska, V., Orosz, A., Mezei, Z., Bereczky, Z.: The Effect of Alpha-2 Plasmin Inhibitor Activity and Antigen Levels and p.Arg6Trp Polymorphism on the Risk of Venous Thromboembolism.
Res Pract Thromb Haemost. 2 324-324, 2018.

Selmeczi, A., Gindele, R., Ilonczai, P., Fekete, A., Komáromi, I., Schlammadinger, Á., Molnárné Rázsó, K., Kovács, K., Bárdos, H., Ádány, R., Muszbek, L., Bereczky, Z., Boda, Z., Oláh, Z.: Antithrombin Debrecen (p.Leu205Pro) - Clinical and molecular characterization of a novel mutation associated with severe thrombotic tendency.
Thromb. Res. 158 1-7, 2017.

Gindele, R., Selmeczi, A., Oláh, Z., Ilonczai, P., Pfliegler, G., Marján, E., Nemes, L., Nagy, Á., Losonczy, H., Mitic, G., Kovac, M., Balogh, G., Komáromi, I., Schlammadinger, Á., Molnárné Rázsó, K., Boda, Z., Muszbek, L., Bereczky, Z.: Clinical and laboratory characteristics of antithrombin deficiencies: a large cohort study from a single diagnostic center.
Thromb. Res. 160 119-128, 2017.

Bereczky, Z., Gindele, R., Speker, M., Kállai, J.: Deficiencies of the natural anticoagulants: novel clinical laboratory aspects of thrombophilia testing.
EJIFCC. 27 (2), 130-146, 2016.

Bereczky, Z., Speker, M., Gindele, R., Szabó, Z., Oláh, Z., Pfliegler, G., Kerényi, A., Boda, Z.: Diagnostic issues in antithrombin, protein C and protein S deficiency in the hungarian population: experience of a large thrombosis laboratory.
J. Throm. Haemost. 14 (Suppl.), 98, 2016.

Major, T., Gindele, R., Szabó, Z., Alef, T., Thiele, B., Bora, L., Kis, Z., Bárdossy, P., Rácz, T., Havacs, I., Bereczky, Z.: Evidence for the founder effect of a novel ACVRL1 splice-site mutation in Hungarian hereditary hemorrhagic telangiectasia families.
Clin. Genet. 90 (5), 466-467, 2016.

Gindele, R., Oláh, Z., Ilonczai, P., Speker, M., Udvari, Á., Selmeczi, A., Pfliegler, G., Marján, E., Kovács, B., Boda, Z., Muszbek, L., Bereczky, Z.: Founder effect is responsible for the p.Leu131Phe heparin-binding-site antithrombin mutation common in Hungary: phenotype analysis in a large cohort.
J. Thromb. Haemost. 14 (4), 704-715, 2016.

Mezei, Z., Bereczky, Z., Katona, É., Gindele, R., Balogh, E., Fiatal, S., Balogh, L., Czuriga, I., Ádány, R., Édes, I., Muszbek, L.: Factor XIII B Subunit Polymorphisms and the Risk of Coronary Artery Disease.
Int. J. Mol. Sci. 16 (1), 1143-1159, 2015.

Kovács, K., Pataki, I., Bárdos, H., Fekete, A., Pfliegler, G., Haramura, G., Gindele, R., Komáromi, I., Balla, G., Ádány, R., Muszbek, L., Bereczky, Z.: Molecular characterization of p.Asp77Gly and the novel p.Ala163Val and p.Ala163Glu mutations causing protein C deficiency.
Thromb. Res. 135 (4), 718-726, 2015.

Kovács, B., Bereczky, Z., Selmeczi, A., Gindele, R., Oláh, Z., Kerényi, A., Boda, Z., Muszbek, L.: Progressive chromogenic anti-factor Xa assay and its use in the classification of antithrombin deficiencies.
Clin. Chem. Lab. Med. 52 (12), 1797-1806, 2014.

Kovács, B., Bereczky, Z., Oláh, Z., Gindele, R., Kerényi, A., Selmeczi, A., Boda, Z., Muszbek, L.: The Superiority of Anti-FXa Assay Over Anti-FIIa Assay in Detecting Heparin-Binding Site Antithrombin Deficiency.
Am. J. Clin. Pathol. 140 (5), 675-679, 2013.