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

Daniele Ghezzi

Showing results (11-20 of 153) with videos related to

Pageof 16
Sort By:
Molecular Genetics and Metabolism Reports|March 1, 2016
Mitochondrial leukoencephalopathy and complex II deficiency associated with a recessive <i>SDHB</i> mutation with reduced penetranceAnna Ardissone, Federica Invernizzi, Alessia Nasca, et al.
Journal of Child Neurology|April 25, 2015
Cerebrospinal Fluid Monoamine Metabolite Analysis in Pediatric Movement DisordersDavide Tonduti, Giovanna Zorzi, Daniele Ghezzi, et al.
Frontiers in Pediatrics|December 17, 2025
Amino acid supplementation in mitochondrial aminoacyl-tRNA synthetase defects: two case reports of tyrosine supplementation in <i>YARS2</i>-associated disease and a review of the literatureGiulia Ferrera, Giorgia Segre, Eleonora Lamantea, et al.
EMBO Molecular Medicine|September 8, 2018
Mutations in <i>TIMM50</i> compromise cell survival in OxPhos-dependent metabolic conditionsAurelio Reyes, Laura Melchionda, Alberto Burlina, et al.
The Journal of Molecular Diagnostics : JMD|March 30, 2021
Current and New Next-Generation Sequencing Approaches to Study Mitochondrial DNAAndrea Legati, Nadia Zanetti, Alessia Nasca, et al.
European Journal of Neurology|April 11, 2023
Phenotyping mitochondrial DNA-related diseases in childhood: A cohort study of 150 patientsAnna Ardissone, Giulia Ferrera, Costanza Lamperti, et al.
Human Mutation|December 10, 2021
Response to: Phenotypic heterogeneity of Leigh syndrome due to NDUFA12 variants is multicausalAlessandra Torraco, Reza Maroofian, Agnès Rötig, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 14, 2007
Myoclonus-dystonia syndrome: clinical presentation, disease course, and genetic features in 11 familiesNardo Nardocci, Giovanna Zorzi, Chiara Barzaghi, et al.
Antibiotics (Basel, Switzerland)|January 21, 2023
Antibacterial and Antibiofilm Activity of Nanostructured Copper Films Prepared by Ionized Jet DepositionDaniele Ghezzi, Enrico Sassoni, Marco Boi, et al.
Scientific Reports|December 31, 2025
Taxonomy and functional profile of microbial communities across the depths of the Alpine Cenote Abyss ice caveStefano Fedi, Daniele Ghezzi, Andrea Firrincieli, et al.
Pageof 16

Showing results (11-20 of 153) with videos related to

Sort By:
Pageof 16
Molecular Genetics and Metabolism Reports|March 1, 2016
Mitochondrial leukoencephalopathy and complex II deficiency associated with a recessive <i>SDHB</i> mutation with reduced penetranceAnna Ardissone, Federica Invernizzi, Alessia Nasca, et al.
Journal of Child Neurology|April 25, 2015
Cerebrospinal Fluid Monoamine Metabolite Analysis in Pediatric Movement DisordersDavide Tonduti, Giovanna Zorzi, Daniele Ghezzi, et al.
Frontiers in Pediatrics|December 17, 2025
Amino acid supplementation in mitochondrial aminoacyl-tRNA synthetase defects: two case reports of tyrosine supplementation in <i>YARS2</i>-associated disease and a review of the literatureGiulia Ferrera, Giorgia Segre, Eleonora Lamantea, et al.
EMBO Molecular Medicine|September 8, 2018
Mutations in <i>TIMM50</i> compromise cell survival in OxPhos-dependent metabolic conditionsAurelio Reyes, Laura Melchionda, Alberto Burlina, et al.
The Journal of Molecular Diagnostics : JMD|March 30, 2021
Current and New Next-Generation Sequencing Approaches to Study Mitochondrial DNAAndrea Legati, Nadia Zanetti, Alessia Nasca, et al.
European Journal of Neurology|April 11, 2023
Phenotyping mitochondrial DNA-related diseases in childhood: A cohort study of 150 patientsAnna Ardissone, Giulia Ferrera, Costanza Lamperti, et al.
Human Mutation|December 10, 2021
Response to: Phenotypic heterogeneity of Leigh syndrome due to NDUFA12 variants is multicausalAlessandra Torraco, Reza Maroofian, Agnès Rötig, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 14, 2007
Myoclonus-dystonia syndrome: clinical presentation, disease course, and genetic features in 11 familiesNardo Nardocci, Giovanna Zorzi, Chiara Barzaghi, et al.
Antibiotics (Basel, Switzerland)|January 21, 2023
Antibacterial and Antibiofilm Activity of Nanostructured Copper Films Prepared by Ionized Jet DepositionDaniele Ghezzi, Enrico Sassoni, Marco Boi, et al.
Scientific Reports|December 31, 2025
Taxonomy and functional profile of microbial communities across the depths of the Alpine Cenote Abyss ice caveStefano Fedi, Daniele Ghezzi, Andrea Firrincieli, et al.
Pageof 16