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

Valerio Carelli

Showing results (101-110 of 371) with videos related to

Pageof 38
Sort By:
Neuro-Ophthalmology (Aeolus Press)|September 22, 2025
A Case of Late-Onset Leber's Hereditary Optic Neuropathy in Association with Heteroplasmic m.11778G>A/ND4 MutationGiacomo Portaro, Francesco Cavallieri, Giulia Amore, et al.
Mitochondrion|July 19, 2017
Incomplete penetrance in mitochondrial optic neuropathiesLeonardo Caporali, Alessandra Maresca, Mariantonietta Capristo, et al.
The Journal of Biological Chemistry|December 3, 2008
Respiratory complex I dysfunction due to mitochondrial DNA mutations shifts the voltage threshold for opening of the permeability transition pore toward resting levelsAnna Maria Porcelli, Alessia Angelin, Anna Ghelli, et al.
Annals of Neurology|July 12, 2002
Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathyMaria Lucia Valentino, Patrizia Avoni, Piero Barboni, et al.
Ophthalmology|March 2, 2019
Functional Changes of Retinal Ganglion Cells and Visual Pathways in Patients with Chronic Leber's Hereditary Optic Neuropathy during One Year of Follow-upVincenzo Parisi, Lucia Ziccardi, Federico Sadun, et al.
Brain : a Journal of Neurology|February 25, 2005
Isolation of transcriptomal changes attributable to LHON mutations and the cybridization processSteven R Danielson, Valerio Carelli, Guolin Tan, et al.
Annals of Clinical and Translational Neurology|December 7, 2020
Missense PDSS1 mutations in CoenzymeQ10 synthesis cause optic atrophy and sensorineural deafnessFrancesca Nardecchia, Agnese De Giorgi, Flavia Palombo, et al.
Journal of Neuroscience Research|July 11, 2008
Antioxidants partially restore glutamate transport defect in leber hereditary optic neuropathy cybridsGessica Sala, Federica Trombin, Simone Beretta, et al.
Biochimica Et Biophysica Acta|July 30, 2004
Bioenergetics shapes cellular death pathways in Leber's hereditary optic neuropathy: a model of mitochondrial neurodegenerationValerio Carelli, Michela Rugolo, Gianluca Sgarbi, et al.
Sleep Medicine|December 22, 2009
Sleep-related periodic respiration with central sleep apnea in Leber Hereditary Optic Neuropathy (LHON)Roberto Vetrugno, Maria Lucia Valentino, Chiara La Morgia, et al.
Pageof 38

Showing results (101-110 of 371) with videos related to

Sort By:
Pageof 38
Neuro-Ophthalmology (Aeolus Press)|September 22, 2025
A Case of Late-Onset Leber's Hereditary Optic Neuropathy in Association with Heteroplasmic m.11778G>A/ND4 MutationGiacomo Portaro, Francesco Cavallieri, Giulia Amore, et al.
Mitochondrion|July 19, 2017
Incomplete penetrance in mitochondrial optic neuropathiesLeonardo Caporali, Alessandra Maresca, Mariantonietta Capristo, et al.
The Journal of Biological Chemistry|December 3, 2008
Respiratory complex I dysfunction due to mitochondrial DNA mutations shifts the voltage threshold for opening of the permeability transition pore toward resting levelsAnna Maria Porcelli, Alessia Angelin, Anna Ghelli, et al.
Annals of Neurology|July 12, 2002
Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathyMaria Lucia Valentino, Patrizia Avoni, Piero Barboni, et al.
Ophthalmology|March 2, 2019
Functional Changes of Retinal Ganglion Cells and Visual Pathways in Patients with Chronic Leber's Hereditary Optic Neuropathy during One Year of Follow-upVincenzo Parisi, Lucia Ziccardi, Federico Sadun, et al.
Brain : a Journal of Neurology|February 25, 2005
Isolation of transcriptomal changes attributable to LHON mutations and the cybridization processSteven R Danielson, Valerio Carelli, Guolin Tan, et al.
Annals of Clinical and Translational Neurology|December 7, 2020
Missense PDSS1 mutations in CoenzymeQ10 synthesis cause optic atrophy and sensorineural deafnessFrancesca Nardecchia, Agnese De Giorgi, Flavia Palombo, et al.
Journal of Neuroscience Research|July 11, 2008
Antioxidants partially restore glutamate transport defect in leber hereditary optic neuropathy cybridsGessica Sala, Federica Trombin, Simone Beretta, et al.
Biochimica Et Biophysica Acta|July 30, 2004
Bioenergetics shapes cellular death pathways in Leber's hereditary optic neuropathy: a model of mitochondrial neurodegenerationValerio Carelli, Michela Rugolo, Gianluca Sgarbi, et al.
Sleep Medicine|December 22, 2009
Sleep-related periodic respiration with central sleep apnea in Leber Hereditary Optic Neuropathy (LHON)Roberto Vetrugno, Maria Lucia Valentino, Chiara La Morgia, et al.
Pageof 38