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Vidmer Scaioli

Showing results (21-30 of 28) with videos related to

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Epileptic Disorders : International Epilepsy Journal with Videotape|April 18, 2020
Early Parkinsonism in a Senegalese girl with Lafora diseaseFrancesca Ragona, Laura Canafoglia, Barbara Castellotti, et al.
Journal of the Neurological Sciences|December 21, 2010
Lower limb areflexia without central and peripheral conduction abnormalities is highly suggestive of Gerstmann-Sträussler-Scheinker disease Pro102LeuEttore Salsano, Roberto Fancellu, Giuseppe Di Fede, et al.
Journal of Neurology|July 26, 2014
A new mutation in GJC2 associated with subclinical leukodystrophyCharles K Abrams, Steven S Scherer, Rafael Flores-Obando, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 13, 2010
Myoclonus in Creutzfeldt-Jakob disease: polygraphic and video-electroencephalography assessment of 109 patientsSimona Binelli, Pamela Agazzi, Laura Canafoglia, et al.
Neurology|June 28, 2015
Electroclinical spectrum of the neuronal ceroid lipofuscinoses associated with CLN6 mutationsLaura Canafoglia, Isabella Gilioli, Federica Invernizzi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 2, 2008
A neurophysiological study of myoclonus in patients with DYT11 myoclonus-dystonia syndromeCecilia Marelli, Laura Canafoglia, Federica Zibordi, et al.
Journal of Neurology|May 12, 2023
Adult-onset leukodystrophy with vanishing white matter: a case series of 19 patientsChiara Benzoni, Marco Moscatelli, Laura Farina, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 7, 2019
Expanding the spectrum of genes responsible for hereditary motor neuropathiesStefano C Previtali, Edward Zhao, Dejan Lazarevic, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Epileptic Disorders : International Epilepsy Journal with Videotape|April 18, 2020
Early Parkinsonism in a Senegalese girl with Lafora diseaseFrancesca Ragona, Laura Canafoglia, Barbara Castellotti, et al.
Journal of the Neurological Sciences|December 21, 2010
Lower limb areflexia without central and peripheral conduction abnormalities is highly suggestive of Gerstmann-Sträussler-Scheinker disease Pro102LeuEttore Salsano, Roberto Fancellu, Giuseppe Di Fede, et al.
Journal of Neurology|July 26, 2014
A new mutation in GJC2 associated with subclinical leukodystrophyCharles K Abrams, Steven S Scherer, Rafael Flores-Obando, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 13, 2010
Myoclonus in Creutzfeldt-Jakob disease: polygraphic and video-electroencephalography assessment of 109 patientsSimona Binelli, Pamela Agazzi, Laura Canafoglia, et al.
Neurology|June 28, 2015
Electroclinical spectrum of the neuronal ceroid lipofuscinoses associated with CLN6 mutationsLaura Canafoglia, Isabella Gilioli, Federica Invernizzi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 2, 2008
A neurophysiological study of myoclonus in patients with DYT11 myoclonus-dystonia syndromeCecilia Marelli, Laura Canafoglia, Federica Zibordi, et al.
Journal of Neurology|May 12, 2023
Adult-onset leukodystrophy with vanishing white matter: a case series of 19 patientsChiara Benzoni, Marco Moscatelli, Laura Farina, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 7, 2019
Expanding the spectrum of genes responsible for hereditary motor neuropathiesStefano C Previtali, Edward Zhao, Dejan Lazarevic, et al.
Pageof 3