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Fabio Pizza

Showing results (201-210 of 227) with videos related to

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Sleep Medicine|April 9, 2014
Polysomnographic and neurometabolic features may mark preclinical autosomal dominant cerebellar ataxia, deafness, and narcolepsy due to a mutation in the DNA (cytosine-5-)-methyltransferase gene, DNMT1Keivan Kaveh Moghadam, Fabio Pizza, Caterina Tonon, et al.
European Journal of Neurology|April 22, 2025
The Many Faces of REM Sleep Behavior Disorder. Providing Evidence for a New LexiconDario Arnaldi, Pietro Mattioli, Beatrice Orso, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|March 5, 2021
Narcolepsy type 1 features across the life span: age impact on clinical and polysomnographic phenotypeAlthea Lividini, Fabio Pizza, Marco Filardi, et al.
Sleep Medicine|September 26, 2025
Excessive daytime sleepiness and sex-related differences in the clinical presentation of obstructive sleep apnea in Italian patientsGiuseppe Insalaco, Alberto Braghiroli, Francesca Buzzi, et al.
Viruses|August 28, 2021
Efficacy of Unsupervised Self-Collected Mid-Turbinate FLOQSwabs for the Diagnosis of Coronavirus Disease 2019 (COVID-19)Egildo Luca D'Andrea, Alessia Maria Cossu, Marianna Scrima, et al.
The European Respiratory Journal|June 2, 2018
Challenges and perspectives in obstructive sleep apnoea: Report by an <i>ad hoc</i> working group of the Sleep Disordered Breathing Group of the European Respiratory Society and the European Sleep Research SocietyWinfried Randerath, Claudio L Bassetti, Maria R Bonsignore, et al.
Brain : a Journal of Neurology|April 15, 2014
Narcolepsy is a common phenotype in HSAN IE and ADCA-DNKeivan Kaveh Moghadam, Fabio Pizza, Chiara La Morgia, et al.
Sleep Medicine|June 12, 2025
Hypersomnolence in focus: a white paper of the 6th Think Tank World Sleep ForumAlessandro Silvani, Claudio Bassetti, Matteo Bradicich, et al.
Plos One|August 11, 2012
Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathyAlessandro Achilli, Luisa Iommarini, Anna Olivieri, et al.
Human Molecular Genetics|January 28, 2020
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolismAlessandra Maresca, Valentina Del Dotto, Mariantonietta Capristo, et al.
Pageof 23

Showing results (201-210 of 227) with videos related to

Sort By:
Pageof 23
Sleep Medicine|April 9, 2014
Polysomnographic and neurometabolic features may mark preclinical autosomal dominant cerebellar ataxia, deafness, and narcolepsy due to a mutation in the DNA (cytosine-5-)-methyltransferase gene, DNMT1Keivan Kaveh Moghadam, Fabio Pizza, Caterina Tonon, et al.
European Journal of Neurology|April 22, 2025
The Many Faces of REM Sleep Behavior Disorder. Providing Evidence for a New LexiconDario Arnaldi, Pietro Mattioli, Beatrice Orso, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|March 5, 2021
Narcolepsy type 1 features across the life span: age impact on clinical and polysomnographic phenotypeAlthea Lividini, Fabio Pizza, Marco Filardi, et al.
Sleep Medicine|September 26, 2025
Excessive daytime sleepiness and sex-related differences in the clinical presentation of obstructive sleep apnea in Italian patientsGiuseppe Insalaco, Alberto Braghiroli, Francesca Buzzi, et al.
Viruses|August 28, 2021
Efficacy of Unsupervised Self-Collected Mid-Turbinate FLOQSwabs for the Diagnosis of Coronavirus Disease 2019 (COVID-19)Egildo Luca D'Andrea, Alessia Maria Cossu, Marianna Scrima, et al.
The European Respiratory Journal|June 2, 2018
Challenges and perspectives in obstructive sleep apnoea: Report by an <i>ad hoc</i> working group of the Sleep Disordered Breathing Group of the European Respiratory Society and the European Sleep Research SocietyWinfried Randerath, Claudio L Bassetti, Maria R Bonsignore, et al.
Brain : a Journal of Neurology|April 15, 2014
Narcolepsy is a common phenotype in HSAN IE and ADCA-DNKeivan Kaveh Moghadam, Fabio Pizza, Chiara La Morgia, et al.
Sleep Medicine|June 12, 2025
Hypersomnolence in focus: a white paper of the 6th Think Tank World Sleep ForumAlessandro Silvani, Claudio Bassetti, Matteo Bradicich, et al.
Plos One|August 11, 2012
Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathyAlessandro Achilli, Luisa Iommarini, Anna Olivieri, et al.
Human Molecular Genetics|January 28, 2020
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolismAlessandra Maresca, Valentina Del Dotto, Mariantonietta Capristo, et al.
Pageof 23