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Items where Author is "Szepfalusi, Noémi"

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Number of items: 4.

Article

Zádori, Dénes and Szpisjak, László and Németh, István Balázs and Reisz, Zita and Kovács, Gábor Géza and Szepfalusi, Noémi and Németh, Viola Luca and Maróti, Zoltán and Tóth-Molnár, Edit and Oláh, Judit and Vécsei, László and Klivényi, Péter and Kalmár, Tibor (2019) Predominant neurological phenotype in a Hungarian family with two novel mutations in the XPA gene – case series. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. ISSN 1590-3478

Salamon, András and Faragó, Péter and Németh, Viola Luca and Szepfalusi, Noémi and Horváth, Emese and Vass, Andrea and Bereczky, Zsuzsanna and Tajti, János and Vécsei, László and Klivényi, Péter and Zádori, Dénes (2018) Multiplex ischaemiás stroke Osler-Rendu-Weber-kórban = Multiple ischemic stroke in Osler-Rendu-Weber disease. IDEGGYÓGYÁSZATI SZEMLE / CLINICAL NEUROSCIENCE. ISSN 0019-1442 (In Press)

Szpisjak, László and Németh, Viola Luca and Szepfalusi, Noémi and Zádori, Dénes and Maróti, Zoltán and Kalmár, Tibor and Vécsei, László and Klivényi, Péter (2017) Neurocognitive characterization of an SCA28 family caused by a novel AFG3L2 gene mutation. Cerebellum, 16 (5-6). pp. 979-985. ISSN 1473-4222 (Print) 1473-4230 (Online)

Zádori, Dénes and Füvesi, Judit and Timár, Erzsébet and Horváth, Emese and Bencsik, Renáta and Szepfalusi, Noémi and Must, Anita and Vécsei, László and Molnár, Mária Judit and Klivényi, Péter (2017) The Report of p.Val717Phe Mutation in the APP Gene in a Hungarian Family with Alzheimer Disease : A Phenomenological Study. ALZHEIMER DISEASE & ASSOCIATED DISORDERS, 31 (4). pp. 343-345. ISSN 0893-0341

This list was generated on Thu Mar 28 18:55:46 2024 CET.