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Davide Pareyson

Showing results (51-60 of 231) with videos related to

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Neuromuscular Disorders : NMD|August 24, 2015
Spinal and bulbar muscular atrophy and Charcot-Marie-Tooth type 1A: Co-existence of two rare neuromuscular genetic diseases in the same patientAnna Sagnelli, Vidmer Scaioli, Giuseppe Piscosquito, et al.
The Neurologist|November 6, 2019
Leukoencephalopathy With Predominant Infratentorial Involvement Caused by a Novel ABCD1 Mutation: Does the Spinocerebellar Variant of Adrenoleukodystrophy Exist?Chiara Benzoni, Laura Farina, Viviana Pensato, et al.
Journal of the Peripheral Nervous System : JPNS|December 17, 2016
A novel NDRG1 mutation in a non-Romani patient with CMT4D/HMSN-LomGiuseppe Piscosquito, Stefania Magri, Paola Saveri, et al.
Muscle & Nerve|January 12, 2017
Repeatability, consistency, and accuracy of hand-held dynamometry with and without fixation for measuring ankle plantarflexion strength in healthy adolescents and adultsPhillip R Davis, Marnee J McKay, Jennifer N Baldwin, et al.
Journal of the Peripheral Nervous System : JPNS|August 26, 2006
Expression of capsaicin receptor immunoreactivity in human peripheral nervous system and in painful neuropathiesGiuseppe Lauria, Michela Morbin, Raffaella Lombardi, et al.
Journal of the Peripheral Nervous System : JPNS|October 19, 2011
Outcome measures for Charcot-Marie-Tooth disease: clinical and neurofunctional assessment in childrenEmanuela Pagliano, Isabella Moroni, Giovanni Baranello, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|March 27, 2019
Biopsy-proven primary angiitis of the central nervous system mimicking leukodystrophy: A case report and review of the literatureLuigi Caputi, Alessandra Erbetta, Gianluca Marucci, et al.
Journal of Molecular Neuroscience : MN|November 18, 2015
Clinical Trials in Spinal and Bulbar Muscular Atrophy-Past, Present, and FuturePatrick Weydt, Anna Sagnelli, Angela Rosenbohm, et al.
Muscle & Nerve|June 11, 2015
Novel loss-of-function mutation of the HINT1 gene in a patient with distal motor axonal neuropathy without neuromyotoniaFrancesca Boaretto, Mario Cacciavillani, Maria Luisa Mostacciuolo, et al.
BMJ Case Reports|June 21, 2011
A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern ItalyMaria Muglia, Giovanni Vazza, Alessandra Patitucci, et al.
Pageof 24

Showing results (51-60 of 231) with videos related to

Sort By:
Pageof 24
Neuromuscular Disorders : NMD|August 24, 2015
Spinal and bulbar muscular atrophy and Charcot-Marie-Tooth type 1A: Co-existence of two rare neuromuscular genetic diseases in the same patientAnna Sagnelli, Vidmer Scaioli, Giuseppe Piscosquito, et al.
The Neurologist|November 6, 2019
Leukoencephalopathy With Predominant Infratentorial Involvement Caused by a Novel ABCD1 Mutation: Does the Spinocerebellar Variant of Adrenoleukodystrophy Exist?Chiara Benzoni, Laura Farina, Viviana Pensato, et al.
Journal of the Peripheral Nervous System : JPNS|December 17, 2016
A novel NDRG1 mutation in a non-Romani patient with CMT4D/HMSN-LomGiuseppe Piscosquito, Stefania Magri, Paola Saveri, et al.
Muscle & Nerve|January 12, 2017
Repeatability, consistency, and accuracy of hand-held dynamometry with and without fixation for measuring ankle plantarflexion strength in healthy adolescents and adultsPhillip R Davis, Marnee J McKay, Jennifer N Baldwin, et al.
Journal of the Peripheral Nervous System : JPNS|August 26, 2006
Expression of capsaicin receptor immunoreactivity in human peripheral nervous system and in painful neuropathiesGiuseppe Lauria, Michela Morbin, Raffaella Lombardi, et al.
Journal of the Peripheral Nervous System : JPNS|October 19, 2011
Outcome measures for Charcot-Marie-Tooth disease: clinical and neurofunctional assessment in childrenEmanuela Pagliano, Isabella Moroni, Giovanni Baranello, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|March 27, 2019
Biopsy-proven primary angiitis of the central nervous system mimicking leukodystrophy: A case report and review of the literatureLuigi Caputi, Alessandra Erbetta, Gianluca Marucci, et al.
Journal of Molecular Neuroscience : MN|November 18, 2015
Clinical Trials in Spinal and Bulbar Muscular Atrophy-Past, Present, and FuturePatrick Weydt, Anna Sagnelli, Angela Rosenbohm, et al.
Muscle & Nerve|June 11, 2015
Novel loss-of-function mutation of the HINT1 gene in a patient with distal motor axonal neuropathy without neuromyotoniaFrancesca Boaretto, Mario Cacciavillani, Maria Luisa Mostacciuolo, et al.
BMJ Case Reports|June 21, 2011
A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern ItalyMaria Muglia, Giovanni Vazza, Alessandra Patitucci, et al.
Pageof 24