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 (41-50 of 143) with videos related to

Pageof 15
Sort By:
Journal of Biological Engineering|March 6, 2023
Customized biofilm device for antibiofilm and antibacterial screening of newly developed nanostructured silver and zinc coatingsDaniele Ghezzi, Marco Boi, Enrico Sassoni, et al.
Orphanet Journal of Rare Diseases|May 16, 2024
A novel MT-ATP6 variant associated with complicated ataxia in two unrelated Italian patients: case report and functional studiesDaniele Sala, Silvia Marchet, Lorenzo Nanetti, et al.
Frontiers in Neurology|March 21, 2022
Diagnostic Challenges in Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: Clinical, Morphological, and Genetic AspectsAntonino Lupica, Rosaria Oteri, Sara Volta, et al.
Journal of Materials Chemistry. B|August 28, 2024
A natural multifunction and multiscale hierarchical matrix as a drug-eluting scaffold for biomedical applicationsGabriela Graziani, Carla Triunfo, Giulia Magnabosco, et al.
Journal of Medical Genetics|September 30, 2016
COA7 (C1orf163/RESA1) mutations associated with mitochondrial leukoencephalopathy and cytochrome c oxidase deficiencyAnabel Martinez Lyons, Anna Ardissone, Aurelio Reyes, et al.
Metabolic Brain Disease|January 24, 2018
Neonatal mitochondrial leukoencephalopathy with brain and spinal involvement and high lactate: expanding the phenotype of ISCA2 gene mutationsIrene Toldo, Margherita Nosadini, Chiara Boscardin, et al.
Frontiers in Genetics|March 28, 2015
Mitochondrial dysfunction in Parkinson disease: evidence in mutant PARK2 fibroblastsMaria C Zanellati, Valentina Monti, Chiara Barzaghi, et al.
Environmental Microbiome|April 24, 2024
The microbiota characterizing huge carbonatic moonmilk structures and its correlation with preserved organic matterDaniele Ghezzi, Nicasio Tomás Jiménez-Morillo, Lisa Foschi, et al.
International Journal of Molecular Sciences|August 26, 2023
Evaluation of Mitochondrial Dysfunction and Idebenone Responsiveness in Fibroblasts from Leber's Hereditary Optic Neuropathy (LHON) SubjectsMirko Baglivo, Alessia Nasca, Eleonora Lamantea, et al.
Acta Neurologica Scandinavica|May 19, 2019
Epileptic phenotypes in children with early-onset mitochondrial diseasesSara Matricardi, Laura Canafoglia, Anna Ardissone, et al.
Pageof 15

Showing results (41-50 of 143) with videos related to

Sort By:
Pageof 15
Journal of Biological Engineering|March 6, 2023
Customized biofilm device for antibiofilm and antibacterial screening of newly developed nanostructured silver and zinc coatingsDaniele Ghezzi, Marco Boi, Enrico Sassoni, et al.
Orphanet Journal of Rare Diseases|May 16, 2024
A novel MT-ATP6 variant associated with complicated ataxia in two unrelated Italian patients: case report and functional studiesDaniele Sala, Silvia Marchet, Lorenzo Nanetti, et al.
Frontiers in Neurology|March 21, 2022
Diagnostic Challenges in Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: Clinical, Morphological, and Genetic AspectsAntonino Lupica, Rosaria Oteri, Sara Volta, et al.
Journal of Materials Chemistry. B|August 28, 2024
A natural multifunction and multiscale hierarchical matrix as a drug-eluting scaffold for biomedical applicationsGabriela Graziani, Carla Triunfo, Giulia Magnabosco, et al.
Journal of Medical Genetics|September 30, 2016
COA7 (C1orf163/RESA1) mutations associated with mitochondrial leukoencephalopathy and cytochrome c oxidase deficiencyAnabel Martinez Lyons, Anna Ardissone, Aurelio Reyes, et al.
Metabolic Brain Disease|January 24, 2018
Neonatal mitochondrial leukoencephalopathy with brain and spinal involvement and high lactate: expanding the phenotype of ISCA2 gene mutationsIrene Toldo, Margherita Nosadini, Chiara Boscardin, et al.
Frontiers in Genetics|March 28, 2015
Mitochondrial dysfunction in Parkinson disease: evidence in mutant PARK2 fibroblastsMaria C Zanellati, Valentina Monti, Chiara Barzaghi, et al.
Environmental Microbiome|April 24, 2024
The microbiota characterizing huge carbonatic moonmilk structures and its correlation with preserved organic matterDaniele Ghezzi, Nicasio Tomás Jiménez-Morillo, Lisa Foschi, et al.
International Journal of Molecular Sciences|August 26, 2023
Evaluation of Mitochondrial Dysfunction and Idebenone Responsiveness in Fibroblasts from Leber's Hereditary Optic Neuropathy (LHON) SubjectsMirko Baglivo, Alessia Nasca, Eleonora Lamantea, et al.
Acta Neurologica Scandinavica|May 19, 2019
Epileptic phenotypes in children with early-onset mitochondrial diseasesSara Matricardi, Laura Canafoglia, Anna Ardissone, et al.
Pageof 15