Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Csaba Bognar"'
Autor:
Orsolya Kiss, Mate Babity, Attila Kovacs, Judit Skopal, Hajnalka Vago, Balint Karoly Lakatos, Csaba Bognar, Reka Rakoczi, Mark Zamodics, Lorinc Frivaldszky, Anna Menyhart-Hetenyi, Zsofia Dohy, Csilla Czimbalmos, Liliana Szabo, Bela Merkely
Publikováno v:
PLoS ONE, Vol 16, Iss 4, p e0249923 (2021)
The significance of cardiology screening of referees is not well established. Cardiovascular risk factors and diseases were examined in asymptomatic Hungarian elite handball referees undergoing extended screening: personal/family history, physical ex
Externí odkaz:
https://doaj.org/article/6140973a01ca4227a3d8aa411179d973
Autor:
Jan Radvanszky, Michaela Hyblova, Eva Radvanska, Peter Spalek, Alica Valachova, Gabriela Magyarova, Csaba Bognar, Emil Polak, Tomas Szemes, Ludevit Kadasi
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 17, p 3934 (2021)
Myotonic dystrophy type 2 (DM2) is caused by expansion of a (CCTG)n repeat in the cellular retroviral nucleic acid-binding protein (CNBP) gene. The sequence of the repeat is most commonly interrupted and is stably inherited in the general population.
Externí odkaz:
https://doaj.org/article/804b2b7a80e843c6ad12778391bd07ee
Autor:
David Petretei, Csaba Bognar, Gergely Csaba Babinszky, Gergő Szabó, Csaba Bence Farkas, Márta Jäckel, Gábor Dudás
Publikováno v:
Orvosi Hetilap. 161:713-722
Absztrakt: A 2019. év végén, elsőként a kínai Vuhan városában megjelenő, SARS-CoV-2 béta-koronavírus okozta járványt 2020. március 11-én világjárvánnyá minősítette az Egészségügyi Világszervezet. Magyarországon 2020. márciu
Autor:
Daniela Kluckova, Andrea Soltysova, Ludevit Kadasi, Andrej Gnip, Veronika Medova, Andrej Ficek, Tomas Foltan, Csaba Bognar, Miriam Kolnikova, Lucia Svecova
Publikováno v:
Epilepsy research. 176
CDKL5 deficiency disorder (CDD) is an independent clinical entity associated with early-onset encephalopathy, which is often considered the type of epileptic encephalopathy with CDKL5 mutation also found in children diagnosed with early-onset seizure
Autor:
Csaba Bognar, Lukáš Šebest, Klaudia Kyselicová, Radoslav Beňuš, Adam Frtús, Marian Baldovic, Ľudevít Kádaši
Publikováno v:
American Journal of Physical Anthropology. 165:536-553
Objectives In the sixth century AD, Avars came to Central Europe from middle Eurasian steppes and founded a strong Empire called the Avar Khagante (568-799/803 AD) in the Pannonian basin. During the existence of this empire, they undertook many milit
Autor:
Peter Spalek, Alica Valachova, Eva Radvanska, Ludevit Kadasi, Emil Polak, Tomáš Szemes, Jan Radvanszky, Gabriela Magyarova, Csaba Bognar, Michaela Hyblova
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 3934, p 3934 (2021)
Journal of Clinical Medicine
Volume 10
Issue 17
Journal of Clinical Medicine
Volume 10
Issue 17
Myotonic dystrophy type 2 (DM2) is caused by expansion of a (CCTG)n repeat in the cellular retroviral nucleic acid-binding protein (CNBP) gene. The sequence of the repeat is most commonly interrupted and is stably inherited in the general population.
Akademický článek
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Autor:
Ľudevít Kádaši, Michal Šarkan, Klaudia Kyselicová, Csaba Bognar, Radoslav Beňuš, Marian Baldovic, Lukáš Šebest
Publikováno v:
Biologia. 71:613-619
DNA was extracted using a Silica Bead Extraction kit from bone samples taken from a Slavonic-Avar individual found at the archaeological site of Cifer-Pac. The analysed skeletal remains from the grave number 62/79 belong to a young adult male (20–3
Publikováno v:
General physiology and biophysics. 32(1)
Parkinson disease (PD) is a chronic neurodegenerative movement disorder characterized by selective loss of nigrostriatal dopaminergic neurons and formation of Lewy bodies. Clinical manifestations include motor impairments involving tremor, bradykines
Autor:
Lucia Svecova, Ludevit Kadasi, P. Sýkora, Tomas Foltan, Csaba Bognar, Miriam Kolnikova, D. Ilenèíková
Publikováno v:
European Journal of Paediatric Neurology. 19:S148
Objective The phenotypic consequences of mutations in gene CDKL5 are: early onset epileptic encephalopathy, severe developmental delay, deceleration of head growth, impaired communication and often hand stereotypies. Epilepsy is typically manifested