Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Afferent ataxia"'
Autor:
Danique Beijer, Maike F. Dohrn, Jonathan De Winter, Sarah Fazal, Andrea Cortese, Tanya Stojkovic, Gorka Fernández‐Eulate, Gauthier Remiche, Mattia Gentile, Rudy Van Coster, Claudia Dufke, Matthis Synofzik, Peter De Jonghe, Stephan Züchner, Jonathan Baets
Publikováno v:
Eur J Neurol
European journal of neurology
European journal of neurology 29(7), 2156-2161 (2022). doi:10.1111/ene.15310
European journal of neurology
European journal of neurology 29(7), 2156-2161 (2022). doi:10.1111/ene.15310
Ataxia and cough are rare features in hereditary sensory and autonomic neuropathies (HSAN), a group of diseases of mostly unknown genetic cause. Biallelic repeat expansions in RFC1 are associated with cerebellar ataxia, neuropathy, and vestibular are
Akademický článek
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Autor:
Lydia Pescollderungg, Vanessa Cecchin, Federico Mercolini, Lucio Parmeggiani, Serena Pellegrin
Publikováno v:
Journal of Pediatric Neurology. 18:190-194
Acute or subacute ataxia in young children is rare and, in most cases, the diagnosis of the underlying etiology can be challenging. An extensive number of possible causes must be considered when approaching a child with ataxia. We report the case of
Publikováno v:
Imaging of Brain Metabolism Spine and Cord Interventional Neuroradiology Free Communications ISBN: 9783642743399
Fri edreich’s ataxia is an autosomal recessive hereditary disease with onset in childhood. As a prototype of afferent ataxia in its early stages primarily the posterior column and spinal cerebellar tracks are affected and only later the cerebellum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b08f5cc9ae5de093e10700b02fa96422
https://doi.org/10.1007/978-3-642-74337-5_43
https://doi.org/10.1007/978-3-642-74337-5_43