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Valerio Carelli

Showing results (211-220 of 332) with videos related to

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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 24, 2016
ITA-MNGIE: an Italian regional and national survey for mitochondrial neuro-gastro-intestinal encephalomyopathyRoberto D'Angelo, Rita Rinaldi, Valerio Carelli, et al.
Plos One|June 6, 2015
Macular Microcysts in Mitochondrial Optic Neuropathies: Prevalence and Retinal Layer Thickness MeasurementsMichele Carbonelli, Chiara La Morgia, Giacomo Savini, et al.
American Journal of Ophthalmology|July 31, 2003
Extensive investigation of a large Brazilian pedigree of 11778/haplogroup J Leber hereditary optic neuropathyAlfredo A Sadun, Valerio Carelli, Solange R Salomao, et al.
Annals of Clinical and Translational Neurology|January 21, 2021
Epilepsy in MT-ATP6 - related mils/NARP: correlation of elettroclinical features with heteroplasmyLaura Licchetta, Lorenzo Ferri, Chiara La Morgia, et al.
Cancer Research|August 20, 2011
A mutation threshold distinguishes the antitumorigenic effects of the mitochondrial gene MTND1, an oncojanus functionGiuseppe Gasparre, Ivana Kurelac, Mariantonietta Capristo, et al.
Genetics in Medicine Open|December 13, 2024
Clinical study of ferredoxin-reductase-related mitochondriopathy: Genotype-phenotype correlation and proposal of ancestry-based carrier screening in the Mexican populationTeresa Campbell, Jesse Slone, Hallie Metzger, et al.
International Journal of Molecular Sciences|February 13, 2025
Adult Leigh Syndrome Associated with the m.15635T>C Mitochondrial DNA Variant Affecting the Cytochrome <i>b</i> (<i>MT-CYB</i>) GeneConcetta Valentina Tropeano, Chiara La Morgia, Alessandro Achilli, et al.
Ophthalmic Genetics|March 26, 2008
Evidence for a novel x-linked modifier locus for leber hereditary optic neuropathySuma P Shankar, John H Fingert, Valerio Carelli, et al.
Cell Metabolism|April 17, 2018
Rewiring of Glutamine Metabolism Is a Bioenergetic Adaptation of Human Cells with Mitochondrial DNA MutationsQiuying Chen, Kathryne Kirk, Yevgeniya I Shurubor, et al.
Molecular Genetics and Metabolism|December 17, 2021
Molecular biomarkers correlate with brain grey and white matter changes in patients with mitochondrial m.3243A > G mutationStefania Evangelisti, Laura Ludovica Gramegna, Chiara La Morgia, et al.
Pageof 34

Showing results (211-220 of 332) with videos related to

Sort By:
Pageof 34
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 24, 2016
ITA-MNGIE: an Italian regional and national survey for mitochondrial neuro-gastro-intestinal encephalomyopathyRoberto D'Angelo, Rita Rinaldi, Valerio Carelli, et al.
Plos One|June 6, 2015
Macular Microcysts in Mitochondrial Optic Neuropathies: Prevalence and Retinal Layer Thickness MeasurementsMichele Carbonelli, Chiara La Morgia, Giacomo Savini, et al.
American Journal of Ophthalmology|July 31, 2003
Extensive investigation of a large Brazilian pedigree of 11778/haplogroup J Leber hereditary optic neuropathyAlfredo A Sadun, Valerio Carelli, Solange R Salomao, et al.
Annals of Clinical and Translational Neurology|January 21, 2021
Epilepsy in MT-ATP6 - related mils/NARP: correlation of elettroclinical features with heteroplasmyLaura Licchetta, Lorenzo Ferri, Chiara La Morgia, et al.
Cancer Research|August 20, 2011
A mutation threshold distinguishes the antitumorigenic effects of the mitochondrial gene MTND1, an oncojanus functionGiuseppe Gasparre, Ivana Kurelac, Mariantonietta Capristo, et al.
Genetics in Medicine Open|December 13, 2024
Clinical study of ferredoxin-reductase-related mitochondriopathy: Genotype-phenotype correlation and proposal of ancestry-based carrier screening in the Mexican populationTeresa Campbell, Jesse Slone, Hallie Metzger, et al.
International Journal of Molecular Sciences|February 13, 2025
Adult Leigh Syndrome Associated with the m.15635T>C Mitochondrial DNA Variant Affecting the Cytochrome <i>b</i> (<i>MT-CYB</i>) GeneConcetta Valentina Tropeano, Chiara La Morgia, Alessandro Achilli, et al.
Ophthalmic Genetics|March 26, 2008
Evidence for a novel x-linked modifier locus for leber hereditary optic neuropathySuma P Shankar, John H Fingert, Valerio Carelli, et al.
Cell Metabolism|April 17, 2018
Rewiring of Glutamine Metabolism Is a Bioenergetic Adaptation of Human Cells with Mitochondrial DNA MutationsQiuying Chen, Kathryne Kirk, Yevgeniya I Shurubor, et al.
Molecular Genetics and Metabolism|December 17, 2021
Molecular biomarkers correlate with brain grey and white matter changes in patients with mitochondrial m.3243A > G mutationStefania Evangelisti, Laura Ludovica Gramegna, Chiara La Morgia, et al.
Pageof 34