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pro vyhledávání: '"Vili Paanila"'
Autor:
Jelena Hyppönen, Vili Paanila, Marja Äikiä, Päivi Koskenkorva, Mervi Könönen, Ritva Vanninen, Esa Mervaala, Reetta Kälviäinen, Juhana Hakumäki
Publikováno v:
NeuroImage: Clinical, Vol 39, Iss , Pp 103459- (2023)
Purpose: Progressive myoclonic epilepsy, type 1A (EPM1, Unverricht-Lundborg disease), is a rare neurodegenerative autosomal recessive disorder characterized by stimulus-sensitive and action myoclonus and tonic-clonic epileptic seizures. Patients deve
Externí odkaz:
https://doaj.org/article/d92125e4969e427595c550d69288e584