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Functional Neurology|January 5, 2002
Sleep complaints in periodic paralyses: a web surveyG Buzzi, B Mostacci, E Sancisi, et al.
European Journal of Medical Genetics|September 12, 2015
A novel mutation af Cln3 associated with delayed-classic juvenile ceroid lipofuscinois and autophagic vacuolar myopathyL Licchetta, F Bisulli, M Fietz, et al.
Seizure|January 16, 2021
Epilepsy with auditory features: Contribution of known genes in 112 patientsF Bisulli, C Rinaldi, T Pippucci, et al.
Brain and Language|May 1, 2026
Post-Ictal aphasia in focal Epilepsy: Speech-language pathologist Perspectives and insightsL Ferri, V Tontini, V Linguerri, et al.
Neurology|January 25, 2008
Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonusC La Morgia, A Achilli, L Iommarini, et al.
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