Psychiatric symptoms of patients with primary mitochondrial DNA disorders von Inczedy-Farkas, Gabriella, Remenyi, Viktoria, Gal, Aniko, Varga, Zsofia, Balla, Petra, Udvardy-Meszaros, Agnes, Bereznai, Benjamin, Molnar, Maria 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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MELAS syndrome mimicking somatoform disorder von Inczedy-Farkas, Gabriella, Remenyi, Viktoria, Meszaros, Agnes, Gal, Aniko, Blasko, Gyorgy, Bereznai, Benjamin, Molnar, Maria Judit

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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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Mitochondrial DNA Mutations and Cognition: A Case-Series Report von GABRIELLA, Inczedy-Farkas, TRAMPUSH, Joey W, FORINTOS, Dora Perczel, BEECH, Danielle, ANDREJKOVICS, Monika, VARGA, Zsofia, REMENYI, Viktoria, BEREZNAI, Benjamin, GAL, Aniko, MOLNAR, Maria Judit

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Oestrogen receptor alpha gene intronic polymorphisms and autoimmune myasthenia gravis in Caucasian women von Pal, Zsuzsanna, Gal, Anikó, Remenyi, Viktória, Tordai, Attila, 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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Rare finding in early-onset dementia: Description of a patient with a novel PSEN2 mutation harbouring pathogenic huntingtin allele von Kovacs, Tibor, Remenyi, Viktoria, Molnar, Maria Judit, Tegze, Narcisz, Miltenberger-Miltenyi, Gabriel

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P4‐139: Rare finding in early‐onset dementia: Description of a patient with a novel PSEN2 mutation harbouring pathogenic huntingtin allele von Kovacs, Tibor, Remenyi, Viktoria, Molnar, Maria Judit, Tegze, Narcisz, Miltenberger‐Miltenyi, Gabriel

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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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Interleukin-4 receptor alpha polymorphisms in autoimmune myasthenia gravis in a Caucasian population von Pál, Zsuzsanna, Varga, Zsófia, Semsei, Ágnes, Reményi, Viktória, Rózsa, Csilla, Falus, András, Illes, Zsolt, Buzás, Edit Irén, Molnar, Maria Judit

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B28 Combined replication malfunctions in huntington’s disease von Grosz, Zoltan, Szirmai, Danuta, Reményi, Viktória, Bencsik, Renáta, Molnár, Judit Mária

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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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Rewiring of RSK–PDZ Interactome by Linear Motif Phosphorylation von Gógl, Gergő, Biri-Kovács, Beáta, Durbesson, Fabien, Jane, Pau, Nomine, Yves, Kostmann, Camille, Bilics, Viktória, Simon, Márton, Reményi, Attila, Vincentelli, Renaud, Trave, Gilles, Nyitray, László

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Rewiring of RSK–PDZ Interactome by Linear Motif Phosphorylation von Gógl, Gergő, Biri-Kovács, Beáta, Durbesson, Fabien, Jane, Pau, Nomine, Yves, Kostmann, Camille, Bilics, Viktória, Simon, Márton, Reményi, Attila, Vincentelli, Renaud, Trave, Gilles, Nyitray, László

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