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Antonio Toscano

Showing results (71-80 of 223) with videos related to

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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 22, 2022
Sleep and sleep-modifying factors in chronic migraine patients during the COVID-19 lockdownCarmelo Tiberio Currò, Antonio Ciacciarelli, Chiara Vitale, et al.
Journal of Inherited Metabolic Disease|February 3, 2016
Intracranial arterial abnormalities in patients with late onset Pompe disease (LOPD)Federica Montagnese, Francesca Granata, Olimpia Musumeci, et al.
Journal of Neurology|November 8, 2007
Evidence of cardiovascular autonomic impairment in mitochondrial disordersRita Di Leo, Olimpia Musumeci, Cesare de Gregorio, et al.
Lung|July 11, 2013
Enzyme replacement therapy improves respiratory outcomes in patients with late-onset type II glycogenosis and high ventilator dependencyAndrea Vianello, Claudio Semplicini, Luciana Paladini, et al.
BMC Neurology|July 10, 2026
Brain health awareness among solid organ transplant candidates and recipients: a single centre surveyVincenzina Lo Re, Emanuele Lo Gerfo, Monica Rizzo, et al.
Journal of Neuromuscular Diseases|November 19, 2016
Transthyretin-Related Familial Amyloid Polyneuropathy (TTR-FAP): A Single-Center Experience in Sicily, an Italian Endemic AreaAnna Mazzeo, Massimo Russo, Gianluca Di Bella, et al.
Neuromuscular Disorders : NMD|July 16, 2002
Multifocal motor neuropathy and asymptomatic Hashimoto's thyroiditis: first report of an associationAntonio Toscano, Carmelo Rodolico, Salvatore Benvenga, et al.
Neuromuscular Disorders : NMD|May 24, 2005
Asymptomatic hyperCKemia in a case of Danon disease due to a missense mutation in Lamp-2 geneOlimpia Musumeci, Carmelo Rodolico, Ichizo Nishino, et al.
Neuromuscular Disorders : NMD|July 27, 2007
Identification of the infant-type R631C mutation in patients with the benign muscular form of CPT2 deficiencyOlimpia Musumeci, Mohammed Aguennouz, Giacomo Pietro Comi, et al.
Neuromuscular Disorders : NMD|December 3, 2011
Clinical features and new molecular findings in muscle phosphofructokinase deficiency (GSD type VII)Olimpia Musumeci, Claudio Bruno, Tiziana Mongini, et al.
Pageof 23

Showing results (71-80 of 223) with videos related to

Sort By:
Pageof 23
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 22, 2022
Sleep and sleep-modifying factors in chronic migraine patients during the COVID-19 lockdownCarmelo Tiberio Currò, Antonio Ciacciarelli, Chiara Vitale, et al.
Journal of Inherited Metabolic Disease|February 3, 2016
Intracranial arterial abnormalities in patients with late onset Pompe disease (LOPD)Federica Montagnese, Francesca Granata, Olimpia Musumeci, et al.
Journal of Neurology|November 8, 2007
Evidence of cardiovascular autonomic impairment in mitochondrial disordersRita Di Leo, Olimpia Musumeci, Cesare de Gregorio, et al.
Lung|July 11, 2013
Enzyme replacement therapy improves respiratory outcomes in patients with late-onset type II glycogenosis and high ventilator dependencyAndrea Vianello, Claudio Semplicini, Luciana Paladini, et al.
BMC Neurology|July 10, 2026
Brain health awareness among solid organ transplant candidates and recipients: a single centre surveyVincenzina Lo Re, Emanuele Lo Gerfo, Monica Rizzo, et al.
Journal of Neuromuscular Diseases|November 19, 2016
Transthyretin-Related Familial Amyloid Polyneuropathy (TTR-FAP): A Single-Center Experience in Sicily, an Italian Endemic AreaAnna Mazzeo, Massimo Russo, Gianluca Di Bella, et al.
Neuromuscular Disorders : NMD|July 16, 2002
Multifocal motor neuropathy and asymptomatic Hashimoto's thyroiditis: first report of an associationAntonio Toscano, Carmelo Rodolico, Salvatore Benvenga, et al.
Neuromuscular Disorders : NMD|May 24, 2005
Asymptomatic hyperCKemia in a case of Danon disease due to a missense mutation in Lamp-2 geneOlimpia Musumeci, Carmelo Rodolico, Ichizo Nishino, et al.
Neuromuscular Disorders : NMD|July 27, 2007
Identification of the infant-type R631C mutation in patients with the benign muscular form of CPT2 deficiencyOlimpia Musumeci, Mohammed Aguennouz, Giacomo Pietro Comi, et al.
Neuromuscular Disorders : NMD|December 3, 2011
Clinical features and new molecular findings in muscle phosphofructokinase deficiency (GSD type VII)Olimpia Musumeci, Claudio Bruno, Tiziana Mongini, et al.
Pageof 23