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Davide Pareyson

Showing results (61-70 of 231) with videos related to

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Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 1, 2020
Severe worsening of adult-onset Alexander disease after minor head trauma: Report of two patients and review of the literatureChiara Benzoni, Domenico Aquino, Daniela Di Bella, et al.
Journal of the Neurological Sciences|October 15, 2010
Mitochondrial dementia: a sporadic case of progressive cognitive and behavioral decline with hearing loss due to the rare m.3291T>C MELAS mutationEttore Salsano, Anna Rita Giovagnoli, Lucia Morandi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 1, 2008
The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndromeGiacomina Rossi, Cecilia Marelli, Laura Farina, et al.
Journal of the Peripheral Nervous System : JPNS|August 27, 2015
Mutational mechanisms in MFN2-related neuropathy: compound heterozygosity for recessive and semidominant mutationsGiuseppe Piscosquito, Paola Saveri, Stefania Magri, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 23, 2016
Validation of the Italian version of the SBMA Functional Rating Scale as outcome measureGiorgia Querin, Elisa DaRe, Ilaria Martinelli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 18, 2007
Rapid progression of late onset axonal Charcot-Marie-Tooth disease associated with a novel MPZ mutation in the extracellular domainMatilde Laurà, Micaela Milani, Michela Morbin, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 3, 2017
Posterior column ataxia with retinitis pigmentosa coexisting with sensory-autonomic neuropathy and leukemia due to the homozygous p.Pro221Ser FLVCR1 mutationMarco Castori, Silvia Morlino, Martin Ungelenk, et al.
Journal of the Peripheral Nervous System : JPNS|May 28, 2014
X-linked Charcot-Marie-Tooth type 1: stroke-like presentation of a novel GJB1 mutationAnna Sagnelli, Giuseppe Piscosquito, Luisa Chiapparini, et al.
Human Mutation|October 22, 2015
Alternative Splicing in the Human PMP22 Gene: Implications in CMT1A NeuropathyDavide Visigalli, Patrizio Castagnola, Giovanna Capodivento, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 4, 2026
Primary oculoleptomeningeal transthyretin amyloidosis with subarachnoid hemorrhages, visual loss, and heart and skin amyloid depositsAlessandro Francia, Daniele Mattavelli, Massimiliano Braga, et al.
Pageof 24

Showing results (61-70 of 231) with videos related to

Sort By:
Pageof 24
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 1, 2020
Severe worsening of adult-onset Alexander disease after minor head trauma: Report of two patients and review of the literatureChiara Benzoni, Domenico Aquino, Daniela Di Bella, et al.
Journal of the Neurological Sciences|October 15, 2010
Mitochondrial dementia: a sporadic case of progressive cognitive and behavioral decline with hearing loss due to the rare m.3291T>C MELAS mutationEttore Salsano, Anna Rita Giovagnoli, Lucia Morandi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 1, 2008
The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndromeGiacomina Rossi, Cecilia Marelli, Laura Farina, et al.
Journal of the Peripheral Nervous System : JPNS|August 27, 2015
Mutational mechanisms in MFN2-related neuropathy: compound heterozygosity for recessive and semidominant mutationsGiuseppe Piscosquito, Paola Saveri, Stefania Magri, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 23, 2016
Validation of the Italian version of the SBMA Functional Rating Scale as outcome measureGiorgia Querin, Elisa DaRe, Ilaria Martinelli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 18, 2007
Rapid progression of late onset axonal Charcot-Marie-Tooth disease associated with a novel MPZ mutation in the extracellular domainMatilde Laurà, Micaela Milani, Michela Morbin, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 3, 2017
Posterior column ataxia with retinitis pigmentosa coexisting with sensory-autonomic neuropathy and leukemia due to the homozygous p.Pro221Ser FLVCR1 mutationMarco Castori, Silvia Morlino, Martin Ungelenk, et al.
Journal of the Peripheral Nervous System : JPNS|May 28, 2014
X-linked Charcot-Marie-Tooth type 1: stroke-like presentation of a novel GJB1 mutationAnna Sagnelli, Giuseppe Piscosquito, Luisa Chiapparini, et al.
Human Mutation|October 22, 2015
Alternative Splicing in the Human PMP22 Gene: Implications in CMT1A NeuropathyDavide Visigalli, Patrizio Castagnola, Giovanna Capodivento, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 4, 2026
Primary oculoleptomeningeal transthyretin amyloidosis with subarachnoid hemorrhages, visual loss, and heart and skin amyloid depositsAlessandro Francia, Daniele Mattavelli, Massimiliano Braga, et al.
Pageof 24