Broadening the phenotype of the TWNK gene associated Perrault syndrome von Fekete, Bálint, Pentelényi, Klára, Rudas, Gabor, Gál, Anikó, Grosz, Zoltán, Illés, Anett, Idris, Jimoh, Csukly, Gabor, Domonkos, Andor, Molnar, Maria Judit

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Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion von Varga, Noémi Ágnes, Pentelényi, Klára, Balicza, Péter, Gézsi, András, Reményi, Viktória, Hársfalvi, Vivien, Bencsik, Renáta, Illés, Anett, Prekop, Csilla, Molnár, Mária Judit

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Whole mitochondrial genome diversity in two Hungarian populations von Malyarchuk, Boris, Derenko, Miroslava, Denisova, Galina, Litvinov, Andrey, Rogalla, Urszula, Skonieczna, Katarzyna, Grzybowski, Tomasz, Pentelényi, Klára, Guba, Zsuzsanna, Zeke, Tamás, Molnár, Mária Judit

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Comprehensive Analysis of Rare Variants of 101 Autism-Linked Genes in a Hungarian Cohort of Autism Spectrum Disorder Patients von Balicza, Péter, Varga, Noémi Ágnes, Bolgár, Bence, Pentelényi, Klára, Bencsik, Renáta, Gál, Anikó, Gézsi, András, Prekop, Csilla, Molnár, Viktor, Molnár, Mária Judit

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Targeted next generation sequencing of a panel of autism-related genes identifies an EHMT1 mutation in a Kleefstra syndrome patient with autism and normal intellectual performance von Bock, István, Németh, Krisztina, Pentelényi, Klára, Balicza, Péter, Balázs, Anna, Molnár, Mária Judit, Román, Viktor, Nagy, József, Lévay, György, Kobolák, Julianna, Dinnyés, András

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The Role of the Rare Variants in the Genes Encoding the Alpha-Ketoglutarate Dehydrogenase in Alzheimer's Disease von Csaban, Dora, Pentelenyi, Klara, Toth-Bencsik, Renata, Illes, Anett, Grosz, Zoltan, Gezsi, Andras, Molnar, Maria Judit

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Coexisting huntingtin and SCA8 repeat expansion: Case report of a severe complex neurodegenerative syndrome von Bereznai, Benjamin, Lovas, Gábor, Pentelenyi, Klára, Rudas, Gábor, Molnar, Mária Judit

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Bcl-2 or bcl-XL gene therapy increases neural plasticity proteins nestin and c-fos expression in PC12 cells von Gal, Aniko, Pentelenyi, Klara, Remenyi, Viktoria, Wappler, Edina A., Safrany, Geza, Skopal, Judit, Nagy, Zoltan

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Genetic landscape of early-onset dementia in Hungary von 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

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Genetic Background of the Hereditary Spastic Paraplegia Phenotypes in Hungary (P5.049) von Molnar, Maria, Balicza, Peter, Grosz, Zoltan, Gonzalez, Michael, Bencsik, Renata, Pentelenyi, Klara, Gal, Aniko, Varga, Edina, Klivenyi, Peter, Zuchner, Stephan

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Genetic background of the hereditary spastic paraplegia phenotypes in Hungary — An analysis of 58 probands von Balicza, Peter, Grosz, Zoltan, Gonzalez, Michael A, Bencsik, Renata, Pentelenyi, Klara, Gal, Aniko, Varga, Edina, Klivenyi, Peter, Koller, Julia, Züchner, Stephan, Molnar, Judit Maria

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Analysis of mtDNA A3243G mutation frequency in Hungary von Gal, Aniko, Komlosi, Katalin, Maasz, Anita, Pentelenyi, Klara, Remenyi, Viktoria, Ovary, Csaba, Valikovics, Attila, Dioszeghy, Peter, Bereczki, Daniel, Melegh, Bela, Molnár, Maria Judit

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Predictiting valproate toxicity in patients with mitochondrial disorders von Remenyi, Viktoria, Kekesi, Anna, Pentelenyi, Klara, Gal, Aniko, Hársfalvi, Vivien, Molnar, Maria Judit

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MOESM1 of Broadening the phenotype of the TWNK gene associated Perrault syndrome von Fekete, Bálint, Pentelényi, Klára, Gabor Rudas, Gál, Anikó, Grosz, Zoltán, Illés, Anett, Jimoh Idris, Gabor Csukly, Domonkos, Andor, Molnar, Maria

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MOESM1 of Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion von Varga, Noémi, Pentelényi, Klára, Balicza, Péter, Gézsi, András, Reményi, Viktória, Hársfalvi, Vivien, Bencsik, Renáta, Illés, Anett, Prekop, Csilla, Molnár, Mária

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Factors predisposing to autism von dr. Molnar Maria Judit, Pentelenyi Klara, dr. Balicza Peter, dr. Varga Noemi Agnes

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