Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Laszlo Szpisjak"'
Autor:
Balint Dancso, Pal Barzo, Peter Klivenyi, Denes Zadori, Laszlo Szpisjak, Adam Varga, Norbert Szappanos, David Kis
Publikováno v:
Brain and Spine, Vol 3, Iss , Pp 102287- (2023)
Externí odkaz:
https://doaj.org/article/075343e845f5422ab74633512f4bb1a3
Autor:
Laszlo Szpisjak, Gabor Szaraz, Andras Salamon, Viola L. Nemeth, Noemi Szepfalusi, Gabor Veres, Balint Kincses, Zoltan Maroti, Tibor Kalmar, Malgorzata Rydzanicz, Rafal Ploski, Peter Klivenyi, Denes Zadori
Publikováno v:
BMC Neuroscience, Vol 22, Iss 1, Pp 1-12 (2021)
Abstract Background SYNE1 ataxia is an autosomal recessive hereditary condition, the main characteristic features of which are gait and limb ataxia and cerebellar dysarthria. Reports have revealed that the clinical phenotype of SYNE1 ataxia is more c
Externí odkaz:
https://doaj.org/article/7219bee1626749fd9fb16ed95e835d5f
Autor:
Laszlo Szpisjak, Gabor Szaraz, Andras Salamon, Viola L. Nemeth, Noemi Szepfalusi, Gabor Veres, Balint Kincses, Zoltan Maroti, Tibor Kalmar, Malgorzata Rydzanicz, Rafal Ploski, Peter Klivenyi, Denes Zadori
Publikováno v:
BMC Neuroscience, Vol 22, Iss 1, Pp 1-2 (2021)
An amendment to this paper has been published and can be accessed via the original article.
Externí odkaz:
https://doaj.org/article/480c31bd256d425f8d4295e06a101ea7
Akademický článek
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Autor:
András Salamon, Zsófia Flóra Nagy, Margit Pál, Máté Szabó, Ádám Csősz, László Szpisjak, Gabriella Gárdián, Dénes Zádori, Márta Széll, Péter Klivényi
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 13, p 10745 (2023)
Dystonia is a rare movement disorder which is characterized by sustained or intermittent muscle contractions causing abnormal and often repetitive movements, postures, or both. The two most common forms of adult-onset focal dystonia are cervical dyst
Externí odkaz:
https://doaj.org/article/f1360e3d86b747e69da2e0de596fc67e
Autor:
Fanni Annamária Boros, László Szpisjak, Renáta Bozó, Evelyn Kelemen, Dénes Zádori, András Salamon, Judit Danis, Tibor Kalmár, Zoltán Maróti, Mária Judit Molnár, Péter Klivényi, Márta Széll, Éva Ádám
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 3, p 2617 (2023)
Spinocerebellar ataxia (SCA) 40 is an extremely rare subtype of the phenotypically and genetically diverse autosomal dominant ataxias caused by mutations of the CCDC88C gene. Most reported cases of SCA40 are characterized by late-onset cerebellar ata
Externí odkaz:
https://doaj.org/article/ecbd44b5778e4e0581cb4815948338e9
Autor:
Ádám Annus, Lilla Ágnes Juhász, Elza Szabó, Ferenc Rárosi, László Szpisjak, László Vécsei, Péter Klivényi
Publikováno v:
Heliyon, Vol 6, Iss 11, Pp e05305- (2020)
Introduction: There are conflicting results in the literature regarding the connection between thrombophilias and ischaemic stroke. However, most of the clinical studies have not differentiated between various ischaemic stroke subtypes. Our aim was t
Externí odkaz:
https://doaj.org/article/586feac7768d45bc9040494d486dd2b3