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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
August 5, 2022
Predictors of "brain fog" 1 year after COVID-19 disease
Viviana Cristillo, Andrea Pilotto, Stefano Cotti Piccinelli, et al.
Frontiers in Neurology
|
February 27, 2019
Advances in Quantitative Imaging of Genetic and Acquired Myopathies: Clinical Applications and Perspectives
Matteo Paoletti, Anna Pichiecchio, Stefano Cotti Piccinelli, et al.
Frontiers in Neurology
|
October 23, 2023
Hereditary transthyretin amyloidosis: a comprehensive review with a focus on peripheral neuropathy
Loris Poli, Beatrice Labella, Stefano Cotti Piccinelli, et al.
BMC Medical Informatics and Decision Making
|
February 3, 2023
Leveraging process mining for modeling progression trajectories in amyotrophic lateral sclerosis
Erica Tavazzi, Roberto Gatta, Mauro Vallati, et al.
Journal of Clinical Medicine
|
August 12, 2023
Prognostic Usefulness of Motor Unit Number Index (MUNIX) in Patients Newly Diagnosed with Amyotrophic Lateral Sclerosis
Barbara Risi, Stefano Cotti Piccinelli, Stefano Gazzina, et al.
Biomolecules
|
September 28, 2023
A Comprehensive Update on Late-Onset Pompe Disease
Beatrice Labella, Stefano Cotti Piccinelli, Barbara Risi, et al.
Aging Clinical and Experimental Research
|
January 11, 2022
Premorbid vulnerability and disease severity impact on Long-COVID cognitive impairment
Viviana Cristillo, Andrea Pilotto, Stefano Cotti Piccinelli, et al.
Journal of Clinical Medicine
|
October 31, 2018
Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE-MTDPS1)
Massimiliano Filosto, Stefano Cotti Piccinelli, Filomena Caria, et al.
Brain Sciences
|
August 26, 2023
Juvenile-Onset Recurrent Rhabdomyolysis Due to Compound Heterozygote Variants in the <i>ACADVL</i> Gene
Beatrice Labella, Gaetana Lanzi, Stefano Cotti Piccinelli, et al.
Journal of Clinical Medicine
|
December 26, 2018
A Novel Mutation in the Stalk Domain of <i>KIF5A</i> Causes a Slowly Progressive Atypical Motor Syndrome
Massimiliano Filosto, Stefano Cotti Piccinelli, Ilaria Palmieri, et al.
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Search research articles
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Showing results (1-10 of 46) with videos related to
Sort By:
Page
of 5
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
August 5, 2022
Predictors of "brain fog" 1 year after COVID-19 disease
Viviana Cristillo, Andrea Pilotto, Stefano Cotti Piccinelli, et al.
Frontiers in Neurology
|
February 27, 2019
Advances in Quantitative Imaging of Genetic and Acquired Myopathies: Clinical Applications and Perspectives
Matteo Paoletti, Anna Pichiecchio, Stefano Cotti Piccinelli, et al.
Frontiers in Neurology
|
October 23, 2023
Hereditary transthyretin amyloidosis: a comprehensive review with a focus on peripheral neuropathy
Loris Poli, Beatrice Labella, Stefano Cotti Piccinelli, et al.
BMC Medical Informatics and Decision Making
|
February 3, 2023
Leveraging process mining for modeling progression trajectories in amyotrophic lateral sclerosis
Erica Tavazzi, Roberto Gatta, Mauro Vallati, et al.
Journal of Clinical Medicine
|
August 12, 2023
Prognostic Usefulness of Motor Unit Number Index (MUNIX) in Patients Newly Diagnosed with Amyotrophic Lateral Sclerosis
Barbara Risi, Stefano Cotti Piccinelli, Stefano Gazzina, et al.
Biomolecules
|
September 28, 2023
A Comprehensive Update on Late-Onset Pompe Disease
Beatrice Labella, Stefano Cotti Piccinelli, Barbara Risi, et al.
Aging Clinical and Experimental Research
|
January 11, 2022
Premorbid vulnerability and disease severity impact on Long-COVID cognitive impairment
Viviana Cristillo, Andrea Pilotto, Stefano Cotti Piccinelli, et al.
Journal of Clinical Medicine
|
October 31, 2018
Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE-MTDPS1)
Massimiliano Filosto, Stefano Cotti Piccinelli, Filomena Caria, et al.
Brain Sciences
|
August 26, 2023
Juvenile-Onset Recurrent Rhabdomyolysis Due to Compound Heterozygote Variants in the <i>ACADVL</i> Gene
Beatrice Labella, Gaetana Lanzi, Stefano Cotti Piccinelli, et al.
Journal of Clinical Medicine
|
December 26, 2018
A Novel Mutation in the Stalk Domain of <i>KIF5A</i> Causes a Slowly Progressive Atypical Motor Syndrome
Massimiliano Filosto, Stefano Cotti Piccinelli, Ilaria Palmieri, et al.
Page
of 5