Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Gábor, Mogyorósy"'
Autor:
Petra Varga, András Balajthy, Erika Biró, Bernadett Bíró, Zsolt Reiger, Edit Szikszay, Gábor Mogyorósy, Rita Káposzta, Tamás Szabó
Publikováno v:
BMC Pediatrics, Vol 23, Iss 1, Pp 1-11 (2023)
Abstract Background The aim of this study was to investigate the clinical and laboratory parameters that can predict the severity of Multisystem Inflammatory Syndrome in Children (MIS-C) at admission. Methods We conducted a single-center, partly retr
Externí odkaz:
https://doaj.org/article/df11cc8cdf0c4d3b9c3c6ef2eb38a714
Autor:
Istvan Balogh, Gábor Mogyorósy, Orsolya Nagy, Katalin Szakszon, Anikó Ujfalusi, Dóra Nagy, Brigitta Orsolya Biró, Bálint Nagy
Publikováno v:
Journal of Biotechnology. 299:86-95
Congenital heart diseases (CHDs) are the most common birth defects among life births, which could be presented as isolated or syndromic with other congenital malformations. The etiology of CHD largely unknown, genetic and environmental factors contri
Autor:
Viktória Kamarási, Gábor Mogyorósy
Publikováno v:
Orvosi Hetilap. 156:1523-1531
There is no proven effective treatment for many diseases today that proves to be one of the greatest problems of health care. Therefore, different therapeutic decisions are made in connection with the same disease by hospitals. There is a growing nee
Publikováno v:
Gyermekgyógyászat; 2021, Vol. 72 Issue 4, p293-298, 6p
Autor:
Eliana Fanous, Gábor Mogyorósy
A best evidence topic in cardiac surgery was written according to a structured protocol. The question addressed was 'Does the use of beta-blockers significantly prevent and treat the occurrence of cyanotic spells in preoperative infants with tetralog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::087d8432a1139f9656225338d46b31ed
Publikováno v:
Orvosi Hetilap. 149:2261-2268
A szerzők közleményükben beszámolnak a Pediatric Quality of Life Inventory™ (PedsQL™) gyermekkori egészségfüggő életminőség-mérő kérdőív kardiológiai moduljának magyarországi validálási folyamatáról. Háttér: A PedsQL™
Autor:
Ferenc Garzuly, Katalin Hahn, Beáta Tóth, László Vécsei, Gábor Mogyorósy, Eva Kristof, Melinda Erdős, Éva Rákóczi, Krisztina Bencsik, László Maródi, Sándor Görögh, János Grubits, Csilla Trinn
Publikováno v:
Orvosi Hetilap. 148:1087-1094
Fabry disease is a rare, progressive lysosomal storage disorder caused by mutation in the GAL gene and an impaired function of the alpha-galactosidase A enzyme. The enzymatic defect results in the progressive accumulation of glycosphingolipids in end
Autor:
Viktória, Kamarási, Gábor, Mogyorósy
Publikováno v:
Orvosi hetilap. 156(38)
There is no proven effective treatment for many diseases today that proves to be one of the greatest problems of health care. Therefore, different therapeutic decisions are made in connection with the same disease by hospitals. There is a growing nee
Autor:
László Tóth, Andrea Berkes, Gábor Mogyorósy, Enikő Felszeghy, György Balla, Ilma Rita Korponay-Szabó, Tamás Kovács
Publikováno v:
Interventional medicineapplied science. 6(4)
Introduction: Although long-term outcome studies in large pediatric myocarditis/cardiomyopathy populations have been reported in literature, none of them focused on comorbidities. Methods: All children and adolescents (age
Autor:
Katalin, Szakszon, Anikó, Ujfalusi, Erzsébet, Balogh, Gábor, Mogyorósy, Enikő, Felszeghy, Judit, Szilvássy, Edit, Horkay, Ervin, Berényi, Gabriella, Merő, Alida C, Knegt
Publikováno v:
Orvosi hetilap. 155(9)
The association of short stature, microcephaly, congenital cardiac anomaly and intellectual deficit should always raise the suspicion of chromosomal etiology. If G-banded karyotyping fails to detect large chromosomal aberrations, array comparative ge