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

بواسطة Illés, Anett, Balicza, Péter, Molnár, Viktor, Bencsik, Renáta, Szilvási, István, Molnar, Maria Judit
الحاوية / القاعدة BMC Neurol (2019)

Voice of young neurologists around the world

بواسطة Rakusa, Martin, Struhal, Walter, Gak, Sofia, Tanprawate, Surat, Balicza, Peter, Khawaja, Ayaz M., Schneider, Logan D.
الحاوية / القاعدة Neurology (2016)

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

بواسطة Balicza, Peter, Terebessy, Andras, Grosz, Zoltan, Varga, Noemi Agnes, Gal, Aniko, Fekete, Balint Andras, Molnar, Maria Judit
الحاوية / القاعدة EPMA J (2018)

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

بواسطة Toth-Bencsik, Renata, Balicza, Peter, Varga, Edina Timea, Lengyel, Andras, Rudas, Gabor, Gal, Aniko, Molnar, Maria Judit
الحاوية / القاعدة Front Genet (2021)

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

بواسطة Balicza, Péter, Grosz, Zoltán, Molnár, Viktor, Illés, Anett, Csabán, Dora, Gézsi, Andras, Dézsi, Lívia, Zádori, Dénes, Vécsei, László, Molnár, Mária Judit
الحاوية / القاعدة 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...

بواسطة Illés, Anett, Csabán, Dóra, Grosz, Zoltán, Balicza, Péter, Gézsi, András, Molnár, Viktor, Bencsik, Renáta, Gál, Anikó, Klivényi, Péter, Molnar, Maria Judit
الحاوية / القاعدة Front Genet (2019)

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

بواسطة Varga, Noémi Ágnes, Pentelényi, Klára, Balicza, Péter, Gézsi, András, Reményi, Viktória, Hársfalvi, Vivien, Bencsik, Renáta, Illés, Anett, Prekop, Csilla, Molnár, Mária Judit
الحاوية / القاعدة Behav Brain Funct (2018)

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

بواسطة Balicza, Péter, Varga, Noémi Ágnes, Bolgár, Bence, Pentelényi, Klára, Bencsik, Renáta, Gál, Anikó, Gézsi, András, Prekop, Csilla, Molnár, Viktor, Molnár, Mária Judit
الحاوية / القاعدة Front Genet (2019)

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

بواسطة Balicza, Peter, Bencsik, Renata, Lengyel, Andras, Gal, Aniko, Grosz, Zoltan, Csaban, Dora, Rudas, Gabor, Danics, Krisztina, Kovacs, Gabor G., Molnar, Maria Judit
الحاوية / القاعدة Neurol Genet (2020)

Wernicke–Korsakoff syndrome associated with mtDNA disease

بواسطة Jimoh, Idris Janos, Sebe, Barbara, Balicza, Peter, Fedor, Mariann, Pataky, Ilona, Rudas, Gabor, Gal, Aniko, Inczedy-Farkas, Gabriella, Nemeth, Gyorgy, Molnar, Maria Judit
الحاوية / القاعدة Ther Adv Neurol Disord (2020)

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

بواسطة 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
الحاوية / القاعدة 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

بواسطة 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
الحاوية / القاعدة Parkinsons Dis (2018)