Predictiting valproate toxicity in patients with mitochondrial disorders

por Remenyi, Viktoria, Kekesi, Anna, Pentelenyi, Klara, Gal, Aniko, Hársfalvi, Vivien, Molnar, Maria Judit
Publicado 2014

The Role of the Rare Variants in the Genes Encoding the Alpha-Ketoglutarate Dehydrogenase in Alzheimer’s Disease

por Csaban, Dora, Pentelenyi, Klara, Toth-Bencsik, Renata, Illes, Anett, Grosz, Zoltan, Gezsi, Andras, Molnar, Maria Judit
Publicado 2021

Broadening the phenotype of the TWNK gene associated Perrault syndrome

por Fekete, Bálint, Pentelényi, Klára, Rudas, Gabor, Gál, Anikó, Grosz, Zoltán, Illés, Anett, Idris, Jimoh, Csukly, Gabor, Domonkos, Andor, Molnar, Maria Judit
Publicado 2019

Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion

por Varga, Noémi Ágnes, Pentelényi, Klára, Balicza, Péter, Gézsi, András, Reményi, Viktória, Hársfalvi, Vivien, Bencsik, Renáta, Illés, Anett, Prekop, Csilla, Molnár, Mária Judit
Publicado 2018

Comprehensive Analysis of Rare Variants of 101 Autism-Linked Genes in a Hungarian Cohort of Autism Spectrum Disorder Patients

por Balicza, Péter, Varga, Noémi Ágnes, Bolgár, Bence, Pentelényi, Klára, Bencsik, Renáta, Gál, Anikó, Gézsi, András, Prekop, Csilla, Molnár, Viktor, Molnár, Mária Judit
Publicado 2019

Genetic landscape of early-onset dementia in Hungary

por Csaban, Dora, Illes, Anett, Renata, Toth-Bencsik, Balicza, Peter, Pentelenyi, Klara, Molnar, Viktor, Gezsi, Andras, Grosz, Zoltan, Gal, Aniko, Kovacs, Tibor, Klivenyi, Peter, Molnar, Maria Judit
Publicado 2022