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Barbara Garavaglia

Showing results (41-50 of 129) with videos related to

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Tremor and Other Hyperkinetic Movements (New York, N.Y.)|April 15, 2024
Myoclonus and Dystonia as Recurrent Presenting Features in Patients with the SCA21-Associated <i>TMEM240</i> p.Pro170Leu VariantUgo Sorrentino, Luigi M Romito, Barbara Garavaglia, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|August 28, 2010
Neurophysiological evaluation of motor corticospinal pathways by TMS in idiopathic early-onset Parkinson's diseaseAnna Perretti, Anna De Rosa, Lucia Marcantonio, et al.
Developmental Medicine and Child Neurology|May 26, 2017
Phenotype and natural history of variant late infantile ceroid-lipofuscinosis 5Alessandro Simonati, Ruth E Williams, Nardo Nardocci, et al.
American Journal of Medical Genetics. Part A|August 24, 2016
Clinical findings in a patient with FARS2 mutations and early-infantile-encephalopathy with epilepsyFederico Raviglione, Giorgio Conte, Daniele Ghezzi, et al.
Movement Disorders Clinical Practice|February 13, 2019
Substantia Nigra Swelling and Dentate Nucleus T2 Hyperintensity May Be Early Magnetic Resonance Imaging Signs of β-Propeller Protein-Associated NeurodegenerationCamilla Russo, Anna Ardissone, Elena Freri, et al.
BMC Neurology|April 2, 2020
Idiopathic brain calcification in a patient with hereditary hemochromatosisStefania Scarlini, Francesco Cavallieri, Massimo Fiorini, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 3, 2014
A family with paroxysmal nonkinesigenic dyskinesias (PNKD): evidence of mitochondrial dysfunctionDaniele Ghezzi, Carlotta Canavese, Gordana Kovacevic, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 31, 2017
SLC19A3 related disorder: Treatment implication and clinical outcome of 2 new patientsDavide Tonduti, Federica Invernizzi, Celeste Panteghini, et al.
Plos One|March 31, 2017
Assessment of the retinal posterior pole in dominant optic atrophy by spectral-domain optical coherence tomography and microperimetryMassimo Cesareo, Elena Ciuffoletti, Alessio Martucci, et al.
Neurogenetics|August 13, 2021
Novel deep intronic mutation in PLA2G6 causing early-onset Parkinson's disease with brain iron accumulation through pseudo-exon activationChiara Cavestro, Celeste Panteghini, Chiara Reale, et al.
Pageof 13

Showing results (41-50 of 129) with videos related to

Sort By:
Pageof 13
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|April 15, 2024
Myoclonus and Dystonia as Recurrent Presenting Features in Patients with the SCA21-Associated <i>TMEM240</i> p.Pro170Leu VariantUgo Sorrentino, Luigi M Romito, Barbara Garavaglia, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|August 28, 2010
Neurophysiological evaluation of motor corticospinal pathways by TMS in idiopathic early-onset Parkinson's diseaseAnna Perretti, Anna De Rosa, Lucia Marcantonio, et al.
Developmental Medicine and Child Neurology|May 26, 2017
Phenotype and natural history of variant late infantile ceroid-lipofuscinosis 5Alessandro Simonati, Ruth E Williams, Nardo Nardocci, et al.
American Journal of Medical Genetics. Part A|August 24, 2016
Clinical findings in a patient with FARS2 mutations and early-infantile-encephalopathy with epilepsyFederico Raviglione, Giorgio Conte, Daniele Ghezzi, et al.
Movement Disorders Clinical Practice|February 13, 2019
Substantia Nigra Swelling and Dentate Nucleus T2 Hyperintensity May Be Early Magnetic Resonance Imaging Signs of β-Propeller Protein-Associated NeurodegenerationCamilla Russo, Anna Ardissone, Elena Freri, et al.
BMC Neurology|April 2, 2020
Idiopathic brain calcification in a patient with hereditary hemochromatosisStefania Scarlini, Francesco Cavallieri, Massimo Fiorini, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 3, 2014
A family with paroxysmal nonkinesigenic dyskinesias (PNKD): evidence of mitochondrial dysfunctionDaniele Ghezzi, Carlotta Canavese, Gordana Kovacevic, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 31, 2017
SLC19A3 related disorder: Treatment implication and clinical outcome of 2 new patientsDavide Tonduti, Federica Invernizzi, Celeste Panteghini, et al.
Plos One|March 31, 2017
Assessment of the retinal posterior pole in dominant optic atrophy by spectral-domain optical coherence tomography and microperimetryMassimo Cesareo, Elena Ciuffoletti, Alessio Martucci, et al.
Neurogenetics|August 13, 2021
Novel deep intronic mutation in PLA2G6 causing early-onset Parkinson's disease with brain iron accumulation through pseudo-exon activationChiara Cavestro, Celeste Panteghini, Chiara Reale, et al.
Pageof 13