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Fabrizio Rinaldi

Showing results (21-30 of 45) with videos related to

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Neuro-Degenerative Diseases|August 8, 2016
Exploring Olfactory Function and Its Relation with Behavioral and Cognitive Impairment in Amyotrophic Lateral Sclerosis Patients: A Cross-Sectional StudyAndrea Pilotto, Federica Rossi, Fabrizio Rinaldi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 30, 2011
Immigration and neurological diseases: a longitudinal study in an acute neurological careFabrizio Rinaldi, Paolo Liberini, Renata Rao, et al.
Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging|June 12, 2013
MR neurography in diagnosing nondiabetic lumbosacral radiculoplexus neuropathyMassimiliano Filosto, Elisa Pari, Mariasofia Cotelli, et al.
CNS Drugs|July 7, 2021
Exploring the Evidence for Broad-Spectrum Effectiveness of Perampanel: A Systematic Review of Clinical Data in Generalised SeizuresEugen Trinka, Simona Lattanzi, Kate Carpenter, et al.
Acta Dermato-Venereologica|May 27, 2021
Sunlight-induced Painful Skin (Sun Pain): A New Differential Diagnosis in PhotodermatologyPiergiacomo Calzavara-Pinton, Marina Venturini, Chiara Rovati, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|January 9, 2014
Non-muscle involvement in late-onset glycogenosis IIMassimiliano Filosto, Alice Todeschini, Maria Sofia Cotelli, et al.
Case Reports in Neurology|February 17, 2015
Very late-onset friedreich ataxia with laryngeal dystoniaSilvia Rota, Eleonora Marchina, Alice Todeschini, et al.
The Neurologist|November 2, 2012
Clinical spectrum and evolution of monoclonal gammopathy-associated neuropathy: an observational studyMassimiliano Filosto, Mariasofia Cotelli, Alice Todeschini, et al.
Journal of Translational Medicine|May 22, 2010
Overexpression of microRNA-206 in the skeletal muscle from myotonic dystrophy type 1 patientsStefano Gambardella, Fabrizio Rinaldi, Saverio M Lepore, et al.
Genetic Testing|August 1, 2008
Screening of EDA1 gene in X-linked anhidrotic ectodermal dysplasia using DHPLC: identification of 14 novel mutations in Italian patientsChiara Conte, Stefano Gambardella, Cristina Bulli, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
Neuro-Degenerative Diseases|August 8, 2016
Exploring Olfactory Function and Its Relation with Behavioral and Cognitive Impairment in Amyotrophic Lateral Sclerosis Patients: A Cross-Sectional StudyAndrea Pilotto, Federica Rossi, Fabrizio Rinaldi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 30, 2011
Immigration and neurological diseases: a longitudinal study in an acute neurological careFabrizio Rinaldi, Paolo Liberini, Renata Rao, et al.
Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging|June 12, 2013
MR neurography in diagnosing nondiabetic lumbosacral radiculoplexus neuropathyMassimiliano Filosto, Elisa Pari, Mariasofia Cotelli, et al.
CNS Drugs|July 7, 2021
Exploring the Evidence for Broad-Spectrum Effectiveness of Perampanel: A Systematic Review of Clinical Data in Generalised SeizuresEugen Trinka, Simona Lattanzi, Kate Carpenter, et al.
Acta Dermato-Venereologica|May 27, 2021
Sunlight-induced Painful Skin (Sun Pain): A New Differential Diagnosis in PhotodermatologyPiergiacomo Calzavara-Pinton, Marina Venturini, Chiara Rovati, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|January 9, 2014
Non-muscle involvement in late-onset glycogenosis IIMassimiliano Filosto, Alice Todeschini, Maria Sofia Cotelli, et al.
Case Reports in Neurology|February 17, 2015
Very late-onset friedreich ataxia with laryngeal dystoniaSilvia Rota, Eleonora Marchina, Alice Todeschini, et al.
The Neurologist|November 2, 2012
Clinical spectrum and evolution of monoclonal gammopathy-associated neuropathy: an observational studyMassimiliano Filosto, Mariasofia Cotelli, Alice Todeschini, et al.
Journal of Translational Medicine|May 22, 2010
Overexpression of microRNA-206 in the skeletal muscle from myotonic dystrophy type 1 patientsStefano Gambardella, Fabrizio Rinaldi, Saverio M Lepore, et al.
Genetic Testing|August 1, 2008
Screening of EDA1 gene in X-linked anhidrotic ectodermal dysplasia using DHPLC: identification of 14 novel mutations in Italian patientsChiara Conte, Stefano Gambardella, Cristina Bulli, et al.
Pageof 5