Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Bálint, MIKES"'
Autor:
Eszter Trojnar, Mihály Józsi, Zsóka Szabó, Marienn Réti, Péter Farkas, Kata Kelen, George S. Reusz, Attila J. Szabó, Nóra Garam, Bálint Mikes, György Sinkovits, Blanka Mező, Dorottya Csuka, Zoltán Prohászka
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Pentraxin-3 (PTX3) and C-reactive protein (CRP) have been shown to regulate complement activation in vitro, but their role has not been investigated in complement consumption in vivo. Thrombotic microangiopathies (TMA) are often accompanied by comple
Externí odkaz:
https://doaj.org/article/2c55557813bf4ca7b39e7ede92db00de
Publikováno v:
Hypertonia és Nephrologia. 26:77-85
Az X-hez kötött hypophosphataemia (XLH) a foszfátanyagcsere veleszületett zavara. Patogenezise összetett, kórfolyamata a foszfáthomeosztázis, illetve a csontanyagcsere összehangolt szabályozási zavarához kötött. Összefoglalónkban átt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15519d2bf313f64cb0e8b73b4ee9d7dd
https://doi.org/10.33668/hn.26.009
https://doi.org/10.33668/hn.26.009
Autor:
Tamás Kaucsár, Bálint Mikes, Kata Kelen, Eszter Jávorszky, Ildikó Szatmári, Deján Dobi, Kinga Nyikuly, Ildikó Várkonyi, Erika Maka, Antal Dezsőfi-Gottl, István Máttyus, Csaba Lódi, Kálmán Tory, Péter Sallay, J. Attila Szabó, György Reusz
Publikováno v:
Hypertonia és Nephrologia. 26:276-281
A primer hyperoxaluria ritka anyagcsere-betegség. A glioxilát anyagcserezavara miatt nagy mennyiségű oxalát keletkezik, amely – mivel rosszul oldódik – a szövetekben oxalátkicsapódáshoz, oxalosishoz vezet. Az oxalosis elsőként a vesé
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6a2c0d5fcd11500c505d6b01484de26
https://doi.org/10.33668/hn.26.030
https://doi.org/10.33668/hn.26.030
Autor:
Bálint, MIKES, Zsófia, CSIZEK, Orsolya, HORVÁTH, Tamás, KAUCSÁR, Magdolna, KARDOS, Attila József, SZABÓ, György Sándor, REUSZ
Publikováno v:
Hypertonia és Nephrologia; 2023, Vol. 27 Issue 4, p185-191, 7p
Autor:
Bálint Mikes, György Sinkovits, Ágnes Szilágyi, Dorottya Csuka, Eszter Trojnár, Zoltán Prohászka
Publikováno v:
memo - Magazine of European Medical Oncology. 11:227-234
Thrombotic microangiopathies (TMAs) are rare but life-threatening disorders characterized by microvascular hemolytic anemia and acute thrombocytopenia with or without organ damage. The term TMA covers various subgroups of diseases, the pathogenesis o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40014511eb89fa30627c95aaa017eae5
https://doi.org/10.1007/s12254-017-0380-y
https://doi.org/10.1007/s12254-017-0380-y
Publikováno v:
Hypertonia és Nephrologia; 2022, Vol. 26 Issue 2, p77-85, 9p
Autor:
Marienn Réti, Gáspár Radványi, Péter Farkas, Bálint Mikes, Judit Demeter, György Sinkovits, Zoltán Prohászka, Dorottya Csuka, Katalin Rázsó
Publikováno v:
Thrombosis and Haemostasis. 115:1034-1043
SummaryThrombotic thrombocytopenic purpura (TTP) is characterised by the deficiency of the von Willebrand factor (VWF) cleaving protease (ADAMTS-13). Although several observations indicate an important role of endothelial activation in the pathogenes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9714fefa9158812585296332a7e9b051
https://doi.org/10.1160/th15-07-0564
https://doi.org/10.1160/th15-07-0564
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:
Eszter Trojnár, Zoltán Prohászka, Mihály Józsi, Dorottya Csuka, György Sinkovits, Blanka Mező, Nóra Garam, Zsóka Szabó, Bálint Mikes
Publikováno v:
Molecular Immunology. 102:222-223
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0129b1008282ec98569c6b060c4146e
https://doi.org/10.1016/j.molimm.2018.06.233
https://doi.org/10.1016/j.molimm.2018.06.233
Autor:
Bálint Mikes, Attila Szabo, Jonatan Leffler, György Reusz, Myriam Martin, György Sinkovits, Katarzyna Ciacma, Anna M. Blom, Kata Kelen, Marienn Réti, Zoltán Prohászka, Péter Farkas
Publikováno v:
Journal of innate immunity. 9(1)
Background: Neutrophil extracellular traps (NETs) can stimulate thrombosis, and their degradation is decreased in several autoimmune disorders. It was recently reported that some patients with haemolytic uraemic syndrome (HUS) also fail to degrade NE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97aee1736a0ae7e7194c35e95ab397fc
https://pubmed.ncbi.nlm.nih.gov/27784011
https://pubmed.ncbi.nlm.nih.gov/27784011