Eye-tracking-aided characterization of saccades and antisaccades in SYNE1 ataxia patients: a pilot study
Szpisjak, Laszlo, Szaraz, Gabor, Salamon, Andras, Nemeth, Viola L, Szepfalusi, Noemi, Veres, Gabor, Kincses, Balint, Maroti, Zoltan, Kalmar, Tibor, Rydzanicz, Malgorzata, Ploski, Rafal, Klivenyi, Peter, Zadori, Denes
Published in BMC neuroscience (01.02.2021)
Published in BMC neuroscience (01.02.2021)
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Correction to: Eye-tracking-aided characterization of saccades and antisaccades in SYNE1 ataxia patients: a pilot study
Szpisjak, Laszlo, Szaraz, Gabor, Salamon, Andras, Nemeth, Viola L, Szepfalusi, Noemi, Veres, Gabor, Kincses, Balint, Maroti, Zoltan, Kalmar, Tibor, Rydzanicz, Malgorzata, Ploski, Rafal, Klivenyi, Peter, Zadori, Denes
Published in BMC neuroscience (10.03.2021)
Published in BMC neuroscience (10.03.2021)
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Predominant neurological phenotype in a Hungarian family with two novel mutations in the XPA gene—case series
Zádori, Dénes, Szpisjak, László, Németh, István Balázs, Reisz, Zita, Kovacs, Gabor G., Szépfalusi, Noémi, Németh, Viola Luca, Maróti, Zoltán, Tóth-Molnár, Edit, Oláh, Judit, Vécsei, László, Klivényi, Péter, Kalmár, Tibor
Published in Neurological sciences (01.01.2020)
Published in Neurological sciences (01.01.2020)
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Neurocognitive Characterization of an SCA28 Family Caused by a Novel AFG3L2 Gene Mutation
Szpisjak, Laszlo, Nemeth, Viola L., Szepfalusi, Noemi, Zadori, Denes, Maroti, Zoltan, Kalmar, Tibor, Vecsei, Laszlo, Klivenyi, Peter
Published in Cerebellum (London, England) (01.12.2017)
Published in Cerebellum (London, England) (01.12.2017)
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Hereditary and non-hereditary etiologies associated with extensive brain calcification: case series
Salamon, András, Zádori, Dénes, Ujfalusi, Anikó, Szpisjak, László, Lukács, Melinda, Bihari, Brigitta, Szépfalusi, Noémi, Németh, Viola Luca, Maróti, Zoltán, Horváth, Emese, Balogh, István, Bereczki, Csaba, Klivényi, Péter, Kalmár, Tibor
Published in Metabolic brain disease (01.10.2021)
Published in Metabolic brain disease (01.10.2021)
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Novel heterozygous STUB1 gene mutation causes SCA48 in a Hungarian patient
Klivényi, Péter, Szpisjak, László, Salamon, András, Németh, Viola Luca, Szépfalusi, Noémi, Maróti, Zoltán, Kalmár, Tibor, Zimmermann, Aliz, Zádori, Dénes
Published in Ideggyógyászati szemle (30.01.2023)
Published in Ideggyógyászati szemle (30.01.2023)
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Journal Article
Eye-tracking-aided Characterization of Saccades and Antisaccades in SYNE1 Ataxia Patients – A Pilot Study
Szpisjak, Laszlo, Szaraz, Gabor, Salamon, Andras, Nemeth, Viola L, Szepfalusi, Noemi, Veres, Gabor, Balint Kincses, Maroti, Zoltan, Kalmar, Tibor, Rydzanicz, Malgorzata, Ploski, Rafal, Klivenyi, Peter, Zádori, Dénes
Published in BMC Neuroscience (14.10.2020)
Published in BMC Neuroscience (14.10.2020)
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The Report of p.Val717Phe Mutation in the APP Gene in a Hungarian Family With Alzheimer Disease: A Phenomenological Study
Zádori, Dénes, Füvesi, Judit, Timár, Erzsébet, Horváth, Emese, Bencsik, Renáta, Szépfalusi, Noémi, Must, Anita, Vécsei, László, Molnár, Mária Judit, Klivényi, Péter
Published in Alzheimer disease and associated disorders (01.10.2017)
Published in Alzheimer disease and associated disorders (01.10.2017)
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Multiplex ischaemiás stroke Osler-Rendu-Weber-kórban
Salamon, András, Faragó, Péter, Németh, Viola Luca, Szépfalusi, Noémi, Horváth, Emese, Vass, Andrea, Bereczky, Zsuzsanna, Tajti, János, Vécsei, László, Klivényi, Péter, Zádori, Dénes
Published in Ideggyógyászati szemle (2019)
Published in Ideggyógyászati szemle (2019)
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Multiple ischemic stroke in Osler-Rendu-Weber disease
Salamon, András, Faragó, Péter, Németh, Viola Luca, Szépfalusi, Noémi, Horváth, Emese, Vass, Andrea, Bereczky, Zsuzsanna, Tajti, János, Vécsei, László, Klivényi, Péter, Zádori, Dénes
Published in Ideggyogyaszati szemle (30.01.2019)
Published in Ideggyogyaszati szemle (30.01.2019)
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