Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Giovanni Rizzo

Showing results (121-130 of 131) with videos related to

Pageof 14
Sort By:
Frontiers in Neuroscience|July 2, 2019
L-Dopa Modulation of Brain Connectivity in Parkinson's Disease Patients: A Pilot EEG-fMRI StudyStefania Evangelisti, Francesca Pittau, Claudia Testa, et al.
Journal of Neurology|March 26, 2021
Targeted sequencing panels in Italian ALS patients support different etiologies in the ALS/FTD continuumAnna Bartoletti-Stella, Veria Vacchiano, Silvia De Pasqua, et al.
Journal of Clinical Medicine|August 13, 2020
Diagnostic and Prognostic Value of Conventional Brain MRI in the Clinical Work-Up of Patients with Amyotrophic Lateral SclerosisGiovanni Rizzo, Anna Federica Marliani, Stella Battaglia, et al.
Cancer Research|January 17, 2016
DNA Hypomethylation and Histone Variant macroH2A1 Synergistically Attenuate Chemotherapy-Induced Senescence to Promote Hepatocellular Carcinoma ProgressionMichela Borghesan, Caterina Fusilli, Francesca Rappa, et al.
European Journal of Neurology|February 23, 2021
Insomnia disorder: clinical and research challenges for the 21st centuryLuigi Ferini-Strambi, Reto Auer, Bjørn Bjorvatn, et al.
American Journal of Ophthalmology|June 8, 2014
Early macular retinal ganglion cell loss in dominant optic atrophy: genotype-phenotype correlationPiero Barboni, Giacomo Savini, Maria Lucia Cascavilla, et al.
Biochimica Et Biophysica Acta|December 19, 2012
Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesionsLeonardo Caporali, Anna Maria Ghelli, Luisa Iommarini, et al.
Human Mutation|May 28, 2014
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intoleranceValeria Carossa, Anna Ghelli, Concetta Valentina Tropeano, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|February 20, 2026
Low Prevalence and Inconsistency of LRP4-IgG Detection in Suspected Myasthenia Gravis: A Multicenter CBA ComparisonIlaria Gligora, Pietro Businaro, Lucrezia Serra, et al.
Annals of Neurology|March 31, 2015
Syndromic parkinsonism and dementia associated with OPA1 missense mutationsValerio Carelli, Olimpia Musumeci, Leonardo Caporali, et al.
Pageof 14

Showing results (121-130 of 131) with videos related to

Sort By:
Pageof 14
Frontiers in Neuroscience|July 2, 2019
L-Dopa Modulation of Brain Connectivity in Parkinson's Disease Patients: A Pilot EEG-fMRI StudyStefania Evangelisti, Francesca Pittau, Claudia Testa, et al.
Journal of Neurology|March 26, 2021
Targeted sequencing panels in Italian ALS patients support different etiologies in the ALS/FTD continuumAnna Bartoletti-Stella, Veria Vacchiano, Silvia De Pasqua, et al.
Journal of Clinical Medicine|August 13, 2020
Diagnostic and Prognostic Value of Conventional Brain MRI in the Clinical Work-Up of Patients with Amyotrophic Lateral SclerosisGiovanni Rizzo, Anna Federica Marliani, Stella Battaglia, et al.
Cancer Research|January 17, 2016
DNA Hypomethylation and Histone Variant macroH2A1 Synergistically Attenuate Chemotherapy-Induced Senescence to Promote Hepatocellular Carcinoma ProgressionMichela Borghesan, Caterina Fusilli, Francesca Rappa, et al.
European Journal of Neurology|February 23, 2021
Insomnia disorder: clinical and research challenges for the 21st centuryLuigi Ferini-Strambi, Reto Auer, Bjørn Bjorvatn, et al.
American Journal of Ophthalmology|June 8, 2014
Early macular retinal ganglion cell loss in dominant optic atrophy: genotype-phenotype correlationPiero Barboni, Giacomo Savini, Maria Lucia Cascavilla, et al.
Biochimica Et Biophysica Acta|December 19, 2012
Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesionsLeonardo Caporali, Anna Maria Ghelli, Luisa Iommarini, et al.
Human Mutation|May 28, 2014
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intoleranceValeria Carossa, Anna Ghelli, Concetta Valentina Tropeano, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|February 20, 2026
Low Prevalence and Inconsistency of LRP4-IgG Detection in Suspected Myasthenia Gravis: A Multicenter CBA ComparisonIlaria Gligora, Pietro Businaro, Lucrezia Serra, et al.
Annals of Neurology|March 31, 2015
Syndromic parkinsonism and dementia associated with OPA1 missense mutationsValerio Carelli, Olimpia Musumeci, Leonardo Caporali, et al.
Pageof 14