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Paolo Tacconi

Showing results (11-20 of 21) with videos related to

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Muscle & Nerve|August 19, 2007
A novel mutation in the central rod domain of lamin A/C producing a phenotype resembling the Emery-Dreifuss muscular dystrophy phenotypeMaria Antonietta Maioli, Giovanni Marrosu, Anna Mateddu, et al.
Cerebellum (London, England)|August 19, 2021
Therapeutic Use of Cerebellar Intermittent Theta Burst Stimulation (iTBS) in a Sardinian Family Affected by Spinocerebellar Ataxia 38 (SCA 38)Angela Sanna, Paolo Follesa, Paolo Tacconi, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|January 19, 2017
F-Wave Duration as a Specific and Sensitive Tool for the Diagnosis of Restless Legs Syndrome/Willis-Ekbom DiseasePatrizia Congiu, Maria Livia Fantini, Giulia Milioli, et al.
Journal of Neuromuscular Diseases|March 1, 2024
A c.1775C > T Point Mutation of Sodium Channel Alfa Subunit Gene (SCN4A) in a Three-Generation Sardinian Family with Sodium Channel MyotoniaCarmen Campanale, Paola Laghetti, Ilaria Saltarella, et al.
Neuroscience Letters|November 29, 2019
Cerebellar continuous theta burst stimulation reduces levodopa-induced dyskinesias and decreases serum BDNF levelsAngela Sanna, Paolo Follesa, Monica Puligheddu, et al.
Cerebellum (London, England)|January 14, 2026
Efficacy of Cerebellar Transcranial Direct Current Stimulation in Degenerative Ataxia. A Sham-Controlled Clinical and Quantitative AnalysisAngela Sanna, Massimiliano Pau, Micaela Porta, et al.
Cerebellum (London, England)|August 4, 2023
Comparison of Two Therapeutic Approaches of Cerebellar Transcranial Direct Current Stimulation in a Sardinian Family Affected by Spinocerebellar Ataxia 38: a Clinical and Computerized 3D Gait Analysis StudyAngela Sanna, Massimiliano Pau, Giuseppina Pilia, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 14, 2017
Charcot-Marie-Tooth disease: genetic subtypes in the Sardinian populationLorena Lorefice, Maria Rita Murru, Giancarlo Coghe, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 3, 2012
ALS/FTD phenotype in two Sardinian families carrying both C9ORF72 and TARDBP mutationsAdriano Chiò, Gabriella Restagno, Maura Brunetti, et al.
Neurogenetics|April 3, 2013
The p.A382T TARDBP gene mutation in Sardinian patients affected by Parkinson's disease and other degenerative parkinsonismsAntonino Cannas, Giuseppe Borghero, Gian Luca Floris, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Muscle & Nerve|August 19, 2007
A novel mutation in the central rod domain of lamin A/C producing a phenotype resembling the Emery-Dreifuss muscular dystrophy phenotypeMaria Antonietta Maioli, Giovanni Marrosu, Anna Mateddu, et al.
Cerebellum (London, England)|August 19, 2021
Therapeutic Use of Cerebellar Intermittent Theta Burst Stimulation (iTBS) in a Sardinian Family Affected by Spinocerebellar Ataxia 38 (SCA 38)Angela Sanna, Paolo Follesa, Paolo Tacconi, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|January 19, 2017
F-Wave Duration as a Specific and Sensitive Tool for the Diagnosis of Restless Legs Syndrome/Willis-Ekbom DiseasePatrizia Congiu, Maria Livia Fantini, Giulia Milioli, et al.
Journal of Neuromuscular Diseases|March 1, 2024
A c.1775C > T Point Mutation of Sodium Channel Alfa Subunit Gene (SCN4A) in a Three-Generation Sardinian Family with Sodium Channel MyotoniaCarmen Campanale, Paola Laghetti, Ilaria Saltarella, et al.
Neuroscience Letters|November 29, 2019
Cerebellar continuous theta burst stimulation reduces levodopa-induced dyskinesias and decreases serum BDNF levelsAngela Sanna, Paolo Follesa, Monica Puligheddu, et al.
Cerebellum (London, England)|January 14, 2026
Efficacy of Cerebellar Transcranial Direct Current Stimulation in Degenerative Ataxia. A Sham-Controlled Clinical and Quantitative AnalysisAngela Sanna, Massimiliano Pau, Micaela Porta, et al.
Cerebellum (London, England)|August 4, 2023
Comparison of Two Therapeutic Approaches of Cerebellar Transcranial Direct Current Stimulation in a Sardinian Family Affected by Spinocerebellar Ataxia 38: a Clinical and Computerized 3D Gait Analysis StudyAngela Sanna, Massimiliano Pau, Giuseppina Pilia, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 14, 2017
Charcot-Marie-Tooth disease: genetic subtypes in the Sardinian populationLorena Lorefice, Maria Rita Murru, Giancarlo Coghe, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 3, 2012
ALS/FTD phenotype in two Sardinian families carrying both C9ORF72 and TARDBP mutationsAdriano Chiò, Gabriella Restagno, Maura Brunetti, et al.
Neurogenetics|April 3, 2013
The p.A382T TARDBP gene mutation in Sardinian patients affected by Parkinson's disease and other degenerative parkinsonismsAntonino Cannas, Giuseppe Borghero, Gian Luca Floris, et al.
Pageof 3