Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Csilla Prekop"'
Autor:
Noémi Ágnes Varga, Klára Pentelényi, Péter Balicza, András Gézsi, Viktória Reményi, Vivien Hársfalvi, Renáta Bencsik, Anett Illés, Csilla Prekop, Mária Judit Molnár
Publikováno v:
Behavioral and Brain Functions, Vol 14, Iss 1, Pp 1-14 (2018)
Abstract Background The etiology of autism spectrum disorders (ASD) is very heterogeneous. Mitochondrial dysfunction has been described in ASD; however, primary mitochondrial disease has been genetically proven in a small subset of patients. The main
Externí odkaz:
https://doaj.org/article/652b60e4f28447cc84307c54a3ca3ccb
Autor:
Péter Balicza, Noémi Ágnes Varga, Bence Bolgár, Klára Pentelényi, Renáta Bencsik, Anikó Gál, András Gézsi, Csilla Prekop, Viktor Molnár, Mária Judit Molnár
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
BackgroundAutism spectrum disorder (ASD) is genetically and phenotypically heterogeneous. Former genetic studies suggested that both common and rare genetic variants play a role in the etiology. In this study, we aimed to analyze rare variants detect
Externí odkaz:
https://doaj.org/article/53ba25c4f3e045d2a718d6c5730e49b7
Autor:
András Gézsi, Viktoria Remenyi, Noémi Ágnes Varga, Klára Pentelényi, Peter Balicza, Anett Illés, Renáta Bencsik, Vivien Hársfalvi, Csilla Prekop, Mária Judit Molnár
Publikováno v:
Behavioral and Brain Functions, Vol 14, Iss 1, Pp 1-14 (2018)
Behavioral and Brain Functions : BBF
Behavioral and Brain Functions : BBF
Background The etiology of autism spectrum disorders (ASD) is very heterogeneous. Mitochondrial dysfunction has been described in ASD; however, primary mitochondrial disease has been genetically proven in a small subset of patients. The main goal of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8844ec6be88d0e4877c9d5d513451c5c
http://link.springer.com/article/10.1186/s12993-018-0135-x
http://link.springer.com/article/10.1186/s12993-018-0135-x
Autor:
Bence Bolgár, Peter Balicza, Noémi Ágnes Varga, Anikó Gál, Viktor Molnár, Csilla Prekop, Klára Pentelényi, Renáta Bencsik, András Gézsi, Mária Judit Molnár
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, Vol 10 (2019)
Frontiers in Genetics, Vol 10 (2019)
Background Autism spectrum disorder (ASD) is genetically and phenotypically heterogeneous. Former genetic studies suggested that both common and rare genetic variants play a role in the etiology. In this study, we aimed to analyze rare variants detec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5cb3f5907918581de0ee769baf4b281
https://pubmed.ncbi.nlm.nih.gov/31134136
https://pubmed.ncbi.nlm.nih.gov/31134136
Publikováno v:
Neuropsychopharmacologia Hungarica : a Magyar Pszichofarmakologiai Egyesulet lapja = official journal of the Hungarian Association of Psychopharmacology. 11(3)
The aim of the current study is to provide a short overview on autism, attention deficit hyperactivity disorder (ADHD) and Tourette syndrome. According to international data, the prevalence of autism is 2-60/10000 and the symptoms persist during the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7da7592a30935326a4eac262cd8ee8e9
https://pubmed.ncbi.nlm.nih.gov/20128394
https://pubmed.ncbi.nlm.nih.gov/20128394
Autor:
Csilla Prekop, Andrea Bíró, Péter Halász, Zsolt I. Lázár, András P. Keszei, Júlia Gádoros, Zsanett Tarnok, Miklos Gyori, Róbert Bódizs, Alpar S. Lazar, Krisztina Stefanik
Publikováno v:
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. 121(11)
Objective: To investigate whether sleep macrostructure and EEG power spectral density and coherence during NREM sleep are different in Asperger syndrome (AS) compared to typically developing children and adolescents. Methods: Standard all night EEG s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::daba9e824f6a2139baac92e0a0a729f7
https://pubmed.ncbi.nlm.nih.gov/20434395
https://pubmed.ncbi.nlm.nih.gov/20434395