Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Ágota Schlammadinger"'
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
BackgroundThe rs867186 single-nucleotide polymorphism in the PROCR gene (g.6936A > G, c.4600A > G) results in a serine-to-glycine substitution at codon 219 of endothelial protein C receptor (EPCR). We performed a case–control study followed by an u
Externí odkaz:
https://doaj.org/article/1bc46de5d2ed4689835874f95989861e
Autor:
Réka Gindele, Adrienne Kerényi, Judit Kállai, György Pfliegler, Ágota Schlammadinger, István Szegedi, Tamás Major, Zsuzsanna Szabó, Zsuzsa Bagoly, Csongor Kiss, János Kappelmayer, Zsuzsanna Bereczky
Publikováno v:
Life, Vol 11, Iss 3, p 202 (2021)
Diagnosis of rare bleeding disorders is challenging and there are several differential diagnostics issues. Next-generation sequencing (NGS) is a useful tool to overcome these problems. The aim of this study was to demonstrate the usefulness of molecu
Externí odkaz:
https://doaj.org/article/701e79842d7344f49c5b1ac8c1499b3c
Publikováno v:
Lege Artis Medicine (LAM); apr2024, Vol. 34 Issue 4, p219-225, 7p
Autor:
Maria S Infante, Réka Gindele, Zsolt Oláh, Marianna Speker, Isabel Zuazu, Carlos Bravo-Pérez, Péter Ilonczai, Laura Entrena, José María Navarro García, Asunción Mora-Casado, María Eugenia de la Morena-Barrio, Antonia Miñano, José Padilla, Ágota Schlammadinger, Vicente Vicente, Belén de la Morena-Barrio, Zsuzsanna Bereczky, Javier Corral, Juan J Rodríguez-Sevilla, Rosa Cifuentes-Riquelme
Publikováno v:
American Journal of Hematology. 96:1363-1373
Atresia of inferior vena cava (IVC) is a rare congenital malformation associated with high risk of venous thrombosis that still has unknown etiology, although intrauterine IVC thrombosis has been suggested to be involved. The identification of IVC at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50742fe85bdd01f647bd2ec0234b6bca
https://doi.org/10.1002/ajh.26304
https://doi.org/10.1002/ajh.26304
Autor:
Ferenc Magyari, Ágota Schlammadinger, Judit Bedekovics, Zsuzsanna Bereczky, Bertalan Kracskó, Árpád Illés
Publikováno v:
Hematology. 26:301-304
Acquired von Willebrand syndrome (AVWS) is a rare, frequently underdiagnosed and underestimated bleeding disorder. Careful personal and family history and late-onset mucocutaneous bleeding could help clarify the etiology of bleeding deficiency.An 82-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb1204900dc747af36ecbed08dfc8c12
https://doi.org/10.1080/16078454.2021.1892322
https://doi.org/10.1080/16078454.2021.1892322
Autor:
György Pfliegler, Ágota Schlammadinger, Zsuzsanna Bereczky, Réka Gindele, Erzsébet Marján, Ágnes Nagy, Anna Selmeczi, László Muszbek, Zsolt Oláh, László Nemes, Hajna Losonczy, Gábor Balogh, István Komáromi, Zoltán Boda, Péter Ilonczai, Katalin Rázsó, Mirjana Kovac, Gorana Mitic
Publikováno v:
Thrombosis Research. 160:119-128
Introduction Inherited antithrombin (AT) deficiency is a heterogeneous disease. Due to low prevalence, only a few studies are available concerning genotype-phenotype associations. The aim was to describe the clinical, laboratory and genetic character
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c53b80fa5a214159456d39e0dc89c01c
https://doi.org/10.1016/j.thromres.2017.10.023
https://doi.org/10.1016/j.thromres.2017.10.023
Autor:
Ágota Schlammadinger, Zsolt Oláh, Péter Ilonczai, Anita Árokszállási, Zsuzsanna Bereczky, Zoltán Boda, Katalin Rázsó
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 29(3)
In acquired haemophilia A (AHA), risk for recurrent bleeding exists until the inhibitor is detectable. Thus, patients with persisting inhibitor may benefit from prophylaxis with activated prothrombin complex concentrate (aPCC). Potential thromboembol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2891061a0d019e8b331b4b518bf36e3
https://pubmed.ncbi.nlm.nih.gov/29474202
https://pubmed.ncbi.nlm.nih.gov/29474202
Akademický článek
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Autor:
Judit Demeter, György Sinkovits, Ágota Schlammadinger, Katalin Rázsó, Gyula Domján, Dorottya Csuka, Marienn Réti, Péter Farkas, Bálint Mikes, Zoltán Prohászka
Publikováno v:
Thrombosis Research. 133:616-621
Introduction Genetic and autoimmune risk factors contribute to the development of thrombotic thrombocytopenic purpura (TTP) but triggers are needed to bring about acute disease. The aim of the study was to investigate the association of neutrophil ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b59fb53fa59e7fff4602a09cda9aae3c
https://doi.org/10.1016/j.thromres.2014.01.034
https://doi.org/10.1016/j.thromres.2014.01.034
Autor:
Helga Bárdos, László Muszbek, Anna Selmeczi, Péter Ilonczai, Ágota Schlammadinger, Zsuzsanna Bereczky, Zsolt Oláh, Attila Fekete, Kitti Bernadett Kovács, Róza Ádány, Zoltán Boda, Réka Gindele, Katalin Rázsó, István Komáromi
Publikováno v:
Thrombosis research. 158
Introduction Hereditary antithrombin (AT) deficiency is a rare thrombophilic disorder with heterogeneous genetic background and various clinical presentations. In this study we identified a novel AT mutation. Genotype-phenotype correlations, molecula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fc72bac7fb7d1d19cc8c06f1aa738ea
https://pubmed.ncbi.nlm.nih.gov/28783511
https://pubmed.ncbi.nlm.nih.gov/28783511