Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Viola L. Németh"'
Autor:
László Szpisjak, András Salamon, Viola L. Németh, Noémi Szépfalusi, Zoltán Maróti, Tibor Kalmár, Aliz Zimmermann, Dénes Zádori, Péter Klivényi
Publikováno v:
Ideggyógyászati szemle. 76:63-72
Spinocerebellar ataxia type 48 (SCA48) is an autosomal dominantly inherited disease characterized by gait and limb ataxia, cerebellar dysarthria, cognitive impairment, psychiatric abnormalities and variable types of movement disorders. To date, more
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abfdca8b4e00e3989d0a8b0901780cce
https://doi.org/10.18071/isz.76.0063
https://doi.org/10.18071/isz.76.0063
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