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Maria Nolano

Showing results (71-80 of 98) with videos related to

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Annals of Clinical and Translational Neurology|December 26, 2014
Unusual Stüve-Wiedemann syndrome with complete maternal chromosome 5 isodisomyMariarosa A B Melone, Michael J Pellegrino, Maria Nolano, et al.
Cellular and Molecular Life Sciences : CMLS|April 14, 2020
Alteration of the late endocytic pathway in Charcot-Marie-Tooth type 2B diseaseRoberta Romano, Cristina Rivellini, Maria De Luca, et al.
Journal of the Peripheral Nervous System : JPNS|November 11, 2019
Insights into the pathogenesis of ATP1A1-related CMT disease using patient-specific iPSCsFiore Manganelli, Silvia Parisi, Maria Nolano, et al.
Biomedicines|October 27, 2022
Correlation between Retinal Vascularization and Disease Aggressiveness in Amyotrophic Lateral SclerosisGilda Cennamo, Daniela Montorio, Francesco Pio Ausiello, et al.
Acta Neuropathologica|June 20, 2018
Small fiber pathology parallels disease progression in Parkinson disease: a longitudinal studyMaria Nolano, Vincenzo Provitera, Annamaria Stancanelli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 23, 2023
Heterogenous electrophysiological features in early stage of hereditary transthyretin amyloidosis neuropathyStefano Tozza, Giovanni Palumbo, Daniele Severi, et al.
Journal of Neurology|December 25, 2013
Update on laser-evoked potential findings in fibromyalgia patients in light of clinical and skin biopsy featuresMarina de Tommaso, Maria Nolano, Florenzo Iannone, et al.
Neurogenetics|September 21, 2010
Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variabilityLucio Santoro, Guido J Breedveld, Fiore Manganelli, et al.
Neurology|May 20, 2014
Postganglionic sudomotor denervation in patients with multiple system atrophyVincenzo Provitera, Maria Nolano, Giuseppe Caporaso, et al.
Frontiers in Neurology|February 27, 2023
Neuropathic pain experience in symptomatic and presymptomatic subjects carrying a transthyretin gene mutationStefano Tozza, Marco Luigetti, Giovanni Antonini, et al.
Pageof 10

Showing results (71-80 of 98) with videos related to

Sort By:
Pageof 10
Annals of Clinical and Translational Neurology|December 26, 2014
Unusual Stüve-Wiedemann syndrome with complete maternal chromosome 5 isodisomyMariarosa A B Melone, Michael J Pellegrino, Maria Nolano, et al.
Cellular and Molecular Life Sciences : CMLS|April 14, 2020
Alteration of the late endocytic pathway in Charcot-Marie-Tooth type 2B diseaseRoberta Romano, Cristina Rivellini, Maria De Luca, et al.
Journal of the Peripheral Nervous System : JPNS|November 11, 2019
Insights into the pathogenesis of ATP1A1-related CMT disease using patient-specific iPSCsFiore Manganelli, Silvia Parisi, Maria Nolano, et al.
Biomedicines|October 27, 2022
Correlation between Retinal Vascularization and Disease Aggressiveness in Amyotrophic Lateral SclerosisGilda Cennamo, Daniela Montorio, Francesco Pio Ausiello, et al.
Acta Neuropathologica|June 20, 2018
Small fiber pathology parallels disease progression in Parkinson disease: a longitudinal studyMaria Nolano, Vincenzo Provitera, Annamaria Stancanelli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 23, 2023
Heterogenous electrophysiological features in early stage of hereditary transthyretin amyloidosis neuropathyStefano Tozza, Giovanni Palumbo, Daniele Severi, et al.
Journal of Neurology|December 25, 2013
Update on laser-evoked potential findings in fibromyalgia patients in light of clinical and skin biopsy featuresMarina de Tommaso, Maria Nolano, Florenzo Iannone, et al.
Neurogenetics|September 21, 2010
Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variabilityLucio Santoro, Guido J Breedveld, Fiore Manganelli, et al.
Neurology|May 20, 2014
Postganglionic sudomotor denervation in patients with multiple system atrophyVincenzo Provitera, Maria Nolano, Giuseppe Caporaso, et al.
Frontiers in Neurology|February 27, 2023
Neuropathic pain experience in symptomatic and presymptomatic subjects carrying a transthyretin gene mutationStefano Tozza, Marco Luigetti, Giovanni Antonini, et al.
Pageof 10