Dynamic interaction of genetic risk factors and cocaine abuse in the background of Parkinsonism – a case report

por Illés, Anett, Balicza, Péter, Molnár, Viktor, Bencsik, Renáta, Szilvási, István, Molnar, Maria Judit
Publicado 2019

New Insights of Phospholipase A2 Associated Neurodegeneration Phenotype Based on the Long-Term Follow-Up of a Large Hungarian Family

por Toth-Bencsik, Renata, Balicza, Peter, Varga, Edina Timea, Lengyel, Andras, Rudas, Gabor, Gal, Aniko, Molnar, Maria Judit
Publicado 2021

NKX2-1 New Mutation Associated With Myoclonus, Dystonia, and Pituitary Involvement

por Balicza, Péter, Grosz, Zoltán, Molnár, Viktor, Illés, Anett, Csabán, Dora, Gézsi, Andras, Dézsi, Lívia, Zádori, Dénes, Vécsei, László, Molnár, Mária Judit
Publicado 2018

The Role of Genetic Testing in the Clinical Practice and Research of Early-Onset Parkinsonian Disorders in a Hungarian Cohort: Increasing Challenge in Genetic Counselling, Improvin...

por Illés, Anett, Csabán, Dóra, Grosz, Zoltán, Balicza, Péter, Gézsi, András, Molnár, Viktor, Bencsik, Renáta, Gál, Anikó, Klivényi, Péter, 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

Novel dominant MPAN family with a complex genetic architecture as a basis for phenotypic variability

por Balicza, Peter, Bencsik, Renata, Lengyel, Andras, Gal, Aniko, Grosz, Zoltan, Csaban, Dora, Rudas, Gabor, Danics, Krisztina, Kovacs, Gabor G., Molnar, Maria Judit
Publicado 2020

Wernicke–Korsakoff syndrome associated with mtDNA disease

por Jimoh, Idris Janos, Sebe, Barbara, Balicza, Peter, Fedor, Mariann, Pataky, Ilona, Rudas, Gabor, Gal, Aniko, Inczedy-Farkas, Gabriella, Nemeth, Gyorgy, Molnar, Maria Judit
Publicado 2020

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

MSTO1 is a cytoplasmic pro‐mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans

por Gal, Aniko, Balicza, Peter, Weaver, David, Naghdi, Shamim, Joseph, Suresh K, Várnai, Péter, Gyuris, Tibor, Horváth, Attila, Nagy, Laszlo, Seifert, Erin L, Molnar, Maria Judit, Hajnóczky, György
Publicado 2023

MSTO1 is a cytoplasmic pro‐mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans

por Gal, Aniko, Balicza, Peter, Weaver, David, Naghdi, Shamim, Joseph, Suresh K, Várnai, Péter, Gyuris, Tibor, Horváth, Attila, Nagy, Laszlo, Seifert, Erin L, Molnar, Maria Judit, Hajnóczky, György
Publicado 2017

The rs13388259 Intergenic Polymorphism in the Genomic Context of the BCYRN1 Gene Is Associated with Parkinson's Disease in the Hungarian Population

por Márki, Sándor, Göblös, Anikó, Szlávicz, Eszter, Török, Nóra, Balicza, Péter, Bereznai, Benjamin, Takáts, Annamária, Engelhardt, József, Klivényi, Péter, Vécsei, László, Molnár, Mária Judit, Nagy, Nikoletta, Széll, Márta
Publicado 2018