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 no BMC Neurol (2019)

Voice of young neurologists around the world

Por Rakusa, Martin, Struhal, Walter, Gak, Sofia, Tanprawate, Surat, Balicza, Peter, Khawaja, Ayaz M., Schneider, Logan D.
Publicado no Neurology (2016)

Implementation of personalized medicine in Central-Eastern Europe: pitfalls and potentials based on citizen’s attitude

Por Balicza, Peter, Terebessy, Andras, Grosz, Zoltan, Varga, Noemi Agnes, Gal, Aniko, Fekete, Balint Andras, Molnar, Maria Judit
Publicado no EPMA J (2018)

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 no Front Genet (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 no Front Genet (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 no Behav Brain Funct (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 no Front Genet (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 no Neurol Genet (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 no Ther Adv Neurol Disord (2020)

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 no EMBO Mol Med (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 no Parkinsons Dis (2018)