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Grazia Devigili

Showing results (41-50 of 80) with videos related to

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Pain|May 14, 2014
Paroxysmal itch caused by gain-of-function Nav1.7 mutationGrazia Devigili, Roberto Eleopra, Tiziana Pierro, et al.
Neuromuscular Disorders : NMD|February 21, 2017
Two novel cases of compound heterozygous mutations in mitofusin2: Finding out the inheritanceAlessandro Geroldi, Patrizia Lastella, Margherita Patruno, et al.
Neuro-Degenerative Diseases|March 21, 2019
Role of MAPT in Pure Motor Neuron Disease: Report of a Recurrent Mutation in Italian PatientsPaola Origone, Alessandro Geroldi, Merit Lamp, et al.
Neurology|July 2, 2017
A new potential biomarker for dementia with Lewy bodies: Skin nerve α-synuclein depositsVincenzo Donadio, Alex Incensi, Giovanni Rizzo, et al.
Neuromuscular Disorders : NMD|November 28, 2017
Identification and characterization of the novel m.8305C>T MTTK and m.4440G>A MTTM gene mutations causing mitochondrial myopathiesMauro Scarpelli, Lidia Carreño-Gago, Anna Russignan, et al.
Neurology|May 15, 2015
Side and time variability of intraepidermal nerve fiber densityGiuseppe Lauria, Patrizia Dacci, Raffaella Lombardi, et al.
Brain : a Journal of Neurology|May 13, 2022
Phosphorylated α-synuclein in skin Schwann cells: a new biomarker for multiple system atrophyVincenzo Donadio, Alex Incensi, Giovanni Rizzo, et al.
Neurobiology of Aging|March 12, 2018
Twenty years of molecular analyses in amyotrophic lateral sclerosis: genetic landscape of Italian patientsMerit Lamp, Paola Origone, Alessandro Geroldi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 9, 2021
Short- and long-term motor outcome of STN-DBS in Parkinson's Disease: focus on sex differencesNico Golfrè Andreasi, Luigi Michele Romito, Roberta Telese, et al.
Orphanet Journal of Rare Diseases|June 8, 2020
Exercise training alone or in combination with high-protein diet in patients with late onset Pompe disease: results of a cross over studyAnnalisa Sechi, Lucrezia Zuccarelli, Bruno Grassi, et al.
Pageof 8

Showing results (41-50 of 80) with videos related to

Sort By:
Pageof 8
Pain|May 14, 2014
Paroxysmal itch caused by gain-of-function Nav1.7 mutationGrazia Devigili, Roberto Eleopra, Tiziana Pierro, et al.
Neuromuscular Disorders : NMD|February 21, 2017
Two novel cases of compound heterozygous mutations in mitofusin2: Finding out the inheritanceAlessandro Geroldi, Patrizia Lastella, Margherita Patruno, et al.
Neuro-Degenerative Diseases|March 21, 2019
Role of MAPT in Pure Motor Neuron Disease: Report of a Recurrent Mutation in Italian PatientsPaola Origone, Alessandro Geroldi, Merit Lamp, et al.
Neurology|July 2, 2017
A new potential biomarker for dementia with Lewy bodies: Skin nerve α-synuclein depositsVincenzo Donadio, Alex Incensi, Giovanni Rizzo, et al.
Neuromuscular Disorders : NMD|November 28, 2017
Identification and characterization of the novel m.8305C>T MTTK and m.4440G>A MTTM gene mutations causing mitochondrial myopathiesMauro Scarpelli, Lidia Carreño-Gago, Anna Russignan, et al.
Neurology|May 15, 2015
Side and time variability of intraepidermal nerve fiber densityGiuseppe Lauria, Patrizia Dacci, Raffaella Lombardi, et al.
Brain : a Journal of Neurology|May 13, 2022
Phosphorylated α-synuclein in skin Schwann cells: a new biomarker for multiple system atrophyVincenzo Donadio, Alex Incensi, Giovanni Rizzo, et al.
Neurobiology of Aging|March 12, 2018
Twenty years of molecular analyses in amyotrophic lateral sclerosis: genetic landscape of Italian patientsMerit Lamp, Paola Origone, Alessandro Geroldi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 9, 2021
Short- and long-term motor outcome of STN-DBS in Parkinson's Disease: focus on sex differencesNico Golfrè Andreasi, Luigi Michele Romito, Roberta Telese, et al.
Orphanet Journal of Rare Diseases|June 8, 2020
Exercise training alone or in combination with high-protein diet in patients with late onset Pompe disease: results of a cross over studyAnnalisa Sechi, Lucrezia Zuccarelli, Bruno Grassi, et al.
Pageof 8