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Francesco Nicita

Showing results (1-10 of 120) with videos related to

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International Journal of Molecular Sciences|October 8, 2020
Microtubule Dysfunction: A Common Feature of Neurodegenerative DiseasesAntonella Sferra, Francesco Nicita, Enrico Bertini
Expert Review of Neurotherapeutics|November 17, 2015
The possible use of the L-type calcium channel antagonist verapamil in drug-resistant epilepsyFrancesco Nicita, Alberto Spalice, Umberto Raucci, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 25, 2011
Fiber tractography assessment in double cortex syndromePaola Iannetti, Francesco Nicita, Alberto Spalice, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 9, 2019
SLC2A1 mutations are a rare cause of pediatric-onset hereditary spastic paraplegiaFrancesco Nicita, Tommaso Schirinzi, Fabrizia Stregapede, et al.
Seizure|October 12, 2013
Efficacy of verapamil as an adjunctive treatment in children with drug-resistant epilepsy: a pilot studyFrancesco Nicita, Alberto Spalice, Laura Papetti, et al.
Clinical Neurology and Neurosurgery|January 5, 2023
Leukoencephalopathy with spot-like calcifications caused by recessive COL4A2 variantsFrancesco Nicita, Chiara Aiello, Alessia Carboni, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 15, 2010
Tension-type headache in paediatric agePasquale Parisi, Laura Papetti, Alberto Spalice, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 6, 2009
Neuronal migration disorders: clinical, neuroradiologic and genetics aspectsAlberto Spalice, Pasquale Parisi, Francesco Nicita, et al.
Vascular|May 30, 2024
Efficacy of retrograde revascularization in diabetic patients with chronic limb-threatening ischemia after a failed antegrade approachMarco Nezzo, Marco Meloni, Alessandro Carini, et al.
Neurology. Genetics|March 7, 2022
Novel <i>SEPSECS</i> Pathogenic Variants Featuring Unusual Phenotype of Complex Movement Disorder With Thin Corpus Callosum: A Case ReportFrancesco Nicita, Lorena Travaglini, Francesco Bombelli, et al.
Pageof 12

Showing results (1-10 of 120) with videos related to

Sort By:
Pageof 12
International Journal of Molecular Sciences|October 8, 2020
Microtubule Dysfunction: A Common Feature of Neurodegenerative DiseasesAntonella Sferra, Francesco Nicita, Enrico Bertini
Expert Review of Neurotherapeutics|November 17, 2015
The possible use of the L-type calcium channel antagonist verapamil in drug-resistant epilepsyFrancesco Nicita, Alberto Spalice, Umberto Raucci, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 25, 2011
Fiber tractography assessment in double cortex syndromePaola Iannetti, Francesco Nicita, Alberto Spalice, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 9, 2019
SLC2A1 mutations are a rare cause of pediatric-onset hereditary spastic paraplegiaFrancesco Nicita, Tommaso Schirinzi, Fabrizia Stregapede, et al.
Seizure|October 12, 2013
Efficacy of verapamil as an adjunctive treatment in children with drug-resistant epilepsy: a pilot studyFrancesco Nicita, Alberto Spalice, Laura Papetti, et al.
Clinical Neurology and Neurosurgery|January 5, 2023
Leukoencephalopathy with spot-like calcifications caused by recessive COL4A2 variantsFrancesco Nicita, Chiara Aiello, Alessia Carboni, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 15, 2010
Tension-type headache in paediatric agePasquale Parisi, Laura Papetti, Alberto Spalice, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 6, 2009
Neuronal migration disorders: clinical, neuroradiologic and genetics aspectsAlberto Spalice, Pasquale Parisi, Francesco Nicita, et al.
Vascular|May 30, 2024
Efficacy of retrograde revascularization in diabetic patients with chronic limb-threatening ischemia after a failed antegrade approachMarco Nezzo, Marco Meloni, Alessandro Carini, et al.
Neurology. Genetics|March 7, 2022
Novel <i>SEPSECS</i> Pathogenic Variants Featuring Unusual Phenotype of Complex Movement Disorder With Thin Corpus Callosum: A Case ReportFrancesco Nicita, Lorena Travaglini, Francesco Bombelli, et al.
Pageof 12