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Gabriella Silvestri

Showing results (1-10 of 124) with videos related to

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Journal of the Neurological Sciences|April 29, 2019
Letter of response to "Myotonic dystrophy type 1, individualised respiratory care rather than standart prognostication"Salvatore Rossi, Gabriella Silvestri
Frontiers in Neurology|October 26, 2020
Editorial: Myotonic Dystrophies: Developments in Research From Bench to BedsideGabriella Silvestri, Federica Montagnese
International Journal of Molecular Sciences|February 11, 2023
Fluid Biomarkers of Central Nervous System (CNS) Involvement in Myotonic Dystrophy Type 1 (DM1)Salvatore Rossi, Gabriella Silvestri
JAMA Ophthalmology|September 8, 2018
Clarification on Uveal Melanoma Associated With Myotonic DystrophyGabriella Silvestri, Salvatore Rossi, Alessia Perna
Archives of Neurology|December 12, 2012
Autosomal recessive spastic ataxia of Charlevoix-Saguenay in the time of next-generation sequencingGabriella Silvestri, Marcella Masciullo, Filippo M Santorelli
Telemedicine Journal and E-Health : the Official Journal of the American Telemedicine Association|January 6, 2009
New wearable system for step-counting telemonitoring and telerehabilitation based on the Codivilla springDaniele Giansanti, Ylenia Tiberi, Gabriella Silvestri, et al.
Telemedicine Journal and E-Health : the Official Journal of the American Telemedicine Association|February 10, 2009
Toward the integration of novel wearable step-counters in gait telerehabilitation after strokeDaniele Giansanti, Ylenia Tiberi, Gabriella Silvestri, et al.
Neurology|April 25, 2018
Reader response: High frequency of gastrointestinal manifestations in myotonic dystrophy type 1 and type 2Gabriella Silvestri, Daria Maccora, Alessia Perna, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 27, 2020
Myotonic dystrophy type 1 cosegregating with autosomal dominant polycystic kidney disease type 2Tommaso Nicoletti, Pietro Chiurazzi, Marco Castori, et al.
Neurology|September 17, 2014
Teaching NeuroImages: Autosomal dominant leukodystrophy in a sporadic caseValerio Brunetti, Michela Ada Noris Ferilli, Viviana Nociti, et al.
Pageof 13

Showing results (1-10 of 124) with videos related to

Sort By:
Pageof 13
Journal of the Neurological Sciences|April 29, 2019
Letter of response to "Myotonic dystrophy type 1, individualised respiratory care rather than standart prognostication"Salvatore Rossi, Gabriella Silvestri
Frontiers in Neurology|October 26, 2020
Editorial: Myotonic Dystrophies: Developments in Research From Bench to BedsideGabriella Silvestri, Federica Montagnese
International Journal of Molecular Sciences|February 11, 2023
Fluid Biomarkers of Central Nervous System (CNS) Involvement in Myotonic Dystrophy Type 1 (DM1)Salvatore Rossi, Gabriella Silvestri
JAMA Ophthalmology|September 8, 2018
Clarification on Uveal Melanoma Associated With Myotonic DystrophyGabriella Silvestri, Salvatore Rossi, Alessia Perna
Archives of Neurology|December 12, 2012
Autosomal recessive spastic ataxia of Charlevoix-Saguenay in the time of next-generation sequencingGabriella Silvestri, Marcella Masciullo, Filippo M Santorelli
Telemedicine Journal and E-Health : the Official Journal of the American Telemedicine Association|January 6, 2009
New wearable system for step-counting telemonitoring and telerehabilitation based on the Codivilla springDaniele Giansanti, Ylenia Tiberi, Gabriella Silvestri, et al.
Telemedicine Journal and E-Health : the Official Journal of the American Telemedicine Association|February 10, 2009
Toward the integration of novel wearable step-counters in gait telerehabilitation after strokeDaniele Giansanti, Ylenia Tiberi, Gabriella Silvestri, et al.
Neurology|April 25, 2018
Reader response: High frequency of gastrointestinal manifestations in myotonic dystrophy type 1 and type 2Gabriella Silvestri, Daria Maccora, Alessia Perna, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 27, 2020
Myotonic dystrophy type 1 cosegregating with autosomal dominant polycystic kidney disease type 2Tommaso Nicoletti, Pietro Chiurazzi, Marco Castori, et al.
Neurology|September 17, 2014
Teaching NeuroImages: Autosomal dominant leukodystrophy in a sporadic caseValerio Brunetti, Michela Ada Noris Ferilli, Viviana Nociti, et al.
Pageof 13