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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 Bedside
Gabriella 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 Dystrophy
Gabriella Silvestri, Salvatore Rossi, Alessia Perna
Archives of Neurology
|
December 12, 2012
Autosomal recessive spastic ataxia of Charlevoix-Saguenay in the time of next-generation sequencing
Gabriella 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 spring
Daniele 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 stroke
Daniele 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 2
Gabriella 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 2
Tommaso Nicoletti, Pietro Chiurazzi, Marco Castori, et al.
Neurology
|
September 17, 2014
Teaching NeuroImages: Autosomal dominant leukodystrophy in a sporadic case
Valerio Brunetti, Michela Ada Noris Ferilli, Viviana Nociti, et al.
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of 13
Search research articles
Search
Showing results (1-10 of 124) with videos related to
Sort By:
Page
of 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 Bedside
Gabriella 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 Dystrophy
Gabriella Silvestri, Salvatore Rossi, Alessia Perna
Archives of Neurology
|
December 12, 2012
Autosomal recessive spastic ataxia of Charlevoix-Saguenay in the time of next-generation sequencing
Gabriella 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 spring
Daniele 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 stroke
Daniele 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 2
Gabriella 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 2
Tommaso Nicoletti, Pietro Chiurazzi, Marco Castori, et al.
Neurology
|
September 17, 2014
Teaching NeuroImages: Autosomal dominant leukodystrophy in a sporadic case
Valerio Brunetti, Michela Ada Noris Ferilli, Viviana Nociti, et al.
Page
of 13