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Sleep Medicine
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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, DNMT1
Keivan 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 Lexicon
Dario 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 phenotype
Althea 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 patients
Giuseppe 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 Society
Winfried 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-DN
Keivan 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 Forum
Alessandro 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 neuropathy
Alessandro Achilli, Luisa Iommarini, Anna Olivieri, et al.
Human Molecular Genetics
|
January 28, 2020
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism
Alessandra Maresca, Valentina Del Dotto, Mariantonietta Capristo, et al.
Page
of 23
Search research articles
Search
Showing results (201-210 of 227) with videos related to
Sort By:
Page
of 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, DNMT1
Keivan 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 Lexicon
Dario 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 phenotype
Althea 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 patients
Giuseppe 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 Society
Winfried 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-DN
Keivan 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 Forum
Alessandro 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 neuropathy
Alessandro Achilli, Luisa Iommarini, Anna Olivieri, et al.
Human Molecular Genetics
|
January 28, 2020
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism
Alessandra Maresca, Valentina Del Dotto, Mariantonietta Capristo, et al.
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of 23