Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Noémi Ágnes Varga"'
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:
Peter Balicza, Anikó Gál, Zoltán Grosz, András Terebessy, Bálint Fekete, Noémi Ágnes Varga, Mária Judit Molnár
Publikováno v:
EPMA Journal. 9:103-112
OBJECTIVE: Next-generation sequencing is increasingly utilized worldwide as a research and diagnostic tool and is anticipated to be implemented into everyday clinical practice. Since Central-Eastern European attitude toward genetic testing, especiall
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::705448b1f7ecf1d9403728ece5919260
https://doi.org/10.1007/s13167-017-0125-3
https://doi.org/10.1007/s13167-017-0125-3
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
Autor:
Peter Balicza, Andras Gezsi, Mariann Fedor, Judit C. Sagi, Aniko Gal, Noemi Agnes Varga, Maria Judit Molnar
Publikováno v:
Frontiers in Psychiatry, Vol 14 (2024)
We present a male patient carrying a pathogenic MECP2 p. Arg179Trp variant with predominant negative psychiatric features and multilevel evidence of mitochondrial dysfunction who responded to the cariprazine treatment. He had delayed speech developme
Externí odkaz:
https://doaj.org/article/dbee1aee261740828aabf8ee2e9df22f
Autor:
Krisztian Buza, Noémi Ágnes Varga
Publikováno v:
Applied Artificial Intelligence. 30:541-555
Parkinson’s disease is a worldwide, frequent, neurodegenerative disorder with increasing incidence. Speech disturbance appears during the progression of the disease. The Unified Parkinson’s Disease Rating Scale UPDRS is a gold-standard tool for d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51c8ae7317ef6ea25150b958cb1f2175
https://doi.org/10.1080/08839514.2016.1193716
https://doi.org/10.1080/08839514.2016.1193716
Autor:
István Balás, Norbert Kovács, Péter Barsi, Gertrúd Tamás, Noémi Ágnes Varga, Loránd Erőss, Mária Judit Molnár
Publikováno v:
Neurologia i neurochirurgia polska. 50(4)
We present the case of a 66-year-old man who has been treated for essential tremor since the age of 58. He developed mild cerebellar gait ataxia seven years after tremor onset. Moderate, global brain atrophy was identified on MRI scans. At the age of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f829e208aba70b6f491362ff4d3463c9
https://pubmed.ncbi.nlm.nih.gov/27375149
https://pubmed.ncbi.nlm.nih.gov/27375149