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Daniela Bernardo

Showing results (1-10 of 17) with videos related to

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Acta Neurologica Belgica|July 12, 2013
Subacute combined degenerationMarco Luigetti, Emanuele Pravatà, Daniela Bernardo, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|June 12, 2018
Small fibre neuropathy in mitochondrial diseases explored with sudoscanMarco Luigetti, Guido Primiano, Cristina Cuccagna, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|September 9, 2018
Progressive axonal polyneuropathy in a mitochondrial disorder: an uncommon association with familial amyloid neuropathyMarco Luigetti, Guido Primiano, Giulia Bisogni, et al.
Journal of Neurology|August 14, 2012
Neurological involvement during legionellosis, look beyond the lungDonato Sauchelli, Gennaro De Pascale, Giancarlo Scoppettuolo, et al.
Clinical Neurology and Neurosurgery|June 7, 2016
Erratum to "Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience" [Clin. Neurol. Neurosurg. 144 (2016) 67-71]Marco Luigetti, Gian Maria Fabrizi, Giulia Bisogni, et al.
Clinical Neurology and Neurosurgery|March 19, 2016
Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experienceMarco Luigetti, Gian Maria Fabrizi, Giulia Bisogni, et al.
Journal of Neurology|January 7, 2015
"Myo-cardiomyopathy" is commonly associated with the A8344G "MERRF" mutationMichela Catteruccia, Donato Sauchelli, Giacomo Della Marca, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 25, 2022
Analysis of <i>STMN2</i> CA repeats in italian ALS patients shows no associationPaolo Niccolò Doronzio, Serena Lattante, Giuseppe Marangi, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 2, 2021
Thr124Met myelin protein zero mutation mimicking motor neuron diseaseGiulia Bisogni, Angela Romano, Amelia Conte, et al.
Epilepsy & Behavior : E&B|February 5, 2023
Treatment of benzodiazepine-refractory status epilepticus: A retrospective, cohort studyEleonora Rollo, Marina Romozzi, Fedele Dono, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Acta Neurologica Belgica|July 12, 2013
Subacute combined degenerationMarco Luigetti, Emanuele Pravatà, Daniela Bernardo, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|June 12, 2018
Small fibre neuropathy in mitochondrial diseases explored with sudoscanMarco Luigetti, Guido Primiano, Cristina Cuccagna, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|September 9, 2018
Progressive axonal polyneuropathy in a mitochondrial disorder: an uncommon association with familial amyloid neuropathyMarco Luigetti, Guido Primiano, Giulia Bisogni, et al.
Journal of Neurology|August 14, 2012
Neurological involvement during legionellosis, look beyond the lungDonato Sauchelli, Gennaro De Pascale, Giancarlo Scoppettuolo, et al.
Clinical Neurology and Neurosurgery|June 7, 2016
Erratum to "Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience" [Clin. Neurol. Neurosurg. 144 (2016) 67-71]Marco Luigetti, Gian Maria Fabrizi, Giulia Bisogni, et al.
Clinical Neurology and Neurosurgery|March 19, 2016
Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experienceMarco Luigetti, Gian Maria Fabrizi, Giulia Bisogni, et al.
Journal of Neurology|January 7, 2015
"Myo-cardiomyopathy" is commonly associated with the A8344G "MERRF" mutationMichela Catteruccia, Donato Sauchelli, Giacomo Della Marca, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 25, 2022
Analysis of <i>STMN2</i> CA repeats in italian ALS patients shows no associationPaolo Niccolò Doronzio, Serena Lattante, Giuseppe Marangi, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 2, 2021
Thr124Met myelin protein zero mutation mimicking motor neuron diseaseGiulia Bisogni, Angela Romano, Amelia Conte, et al.
Epilepsy & Behavior : E&B|February 5, 2023
Treatment of benzodiazepine-refractory status epilepticus: A retrospective, cohort studyEleonora Rollo, Marina Romozzi, Fedele Dono, et al.
Pageof 2