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Valerio Carelli

Showing results (181-190 of 332) with videos related to

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American Journal of Ophthalmology|February 14, 2004
Ophthalmologic findings in a large pedigree of 11778/Haplogroup J Leber hereditary optic neuropathyFederico Sadun, Anna Maria De Negri, Valerio Carelli, et al.
Investigative Ophthalmology & Visual Science|January 31, 2022
Longitudinal Study of Optic Disk Perfusion and Retinal Structure in Leber's Hereditary Optic NeuropathyGiacomo Calzetti, Chiara La Morgia, Marco Cattaneo, et al.
Ophthalmology|April 27, 2010
OPA1 mutations associated with dominant optic atrophy influence optic nerve head sizePiero Barboni, Michele Carbonelli, Giacomo Savini, et al.
Biochimica Et Biophysica Acta. Bioenergetics|December 12, 2019
Fine-tuning of the respiratory complexes stability and supercomplexes assembly in cells defective of complex IIIConcetta V Tropeano, Serena J Aleo, Claudia Zanna, et al.
Frontiers in Neuroscience|August 28, 2020
Chromatic Pupillometry Findings in Alzheimer's DiseaseMartina Romagnoli, Michelangelo Stanzani Maserati, Maddalena De Matteis, et al.
Plos One|May 8, 2014
Liver as a source for thymidine phosphorylase replacement in mitochondrial neurogastrointestinal encephalomyopathyElisa Boschetti, Roberto D'Alessandro, Francesca Bianco, et al.
Gastroenterology|March 15, 2006
Mitochondrial neurogastrointestinal encephalomyopathy: evidence of mitochondrial DNA depletion in the small intestineCarla Giordano, Mariangela Sebastiani, Giuseppe Plazzi, et al.
Human Molecular Genetics|September 23, 2008
Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial diseaseRosa Pello, Miguel A Martín, Valerio Carelli, et al.
Acta Ophthalmologica|September 20, 2017
Retinal dysfunction characterizes subtypes of dominant optic atrophyMaria Lucia Cascavilla, Vincenzo Parisi, Giacinto Triolo, et al.
Human Molecular Genetics|March 24, 2020
Metabolomics hallmarks OPA1 variants correlating with their in vitro phenotype and predicting clinical severityJuan Manuel Chao de la Barca, Mario Fogazza, Michela Rugolo, et al.
Pageof 34

Showing results (181-190 of 332) with videos related to

Sort By:
Pageof 34
American Journal of Ophthalmology|February 14, 2004
Ophthalmologic findings in a large pedigree of 11778/Haplogroup J Leber hereditary optic neuropathyFederico Sadun, Anna Maria De Negri, Valerio Carelli, et al.
Investigative Ophthalmology & Visual Science|January 31, 2022
Longitudinal Study of Optic Disk Perfusion and Retinal Structure in Leber's Hereditary Optic NeuropathyGiacomo Calzetti, Chiara La Morgia, Marco Cattaneo, et al.
Ophthalmology|April 27, 2010
OPA1 mutations associated with dominant optic atrophy influence optic nerve head sizePiero Barboni, Michele Carbonelli, Giacomo Savini, et al.
Biochimica Et Biophysica Acta. Bioenergetics|December 12, 2019
Fine-tuning of the respiratory complexes stability and supercomplexes assembly in cells defective of complex IIIConcetta V Tropeano, Serena J Aleo, Claudia Zanna, et al.
Frontiers in Neuroscience|August 28, 2020
Chromatic Pupillometry Findings in Alzheimer's DiseaseMartina Romagnoli, Michelangelo Stanzani Maserati, Maddalena De Matteis, et al.
Plos One|May 8, 2014
Liver as a source for thymidine phosphorylase replacement in mitochondrial neurogastrointestinal encephalomyopathyElisa Boschetti, Roberto D'Alessandro, Francesca Bianco, et al.
Gastroenterology|March 15, 2006
Mitochondrial neurogastrointestinal encephalomyopathy: evidence of mitochondrial DNA depletion in the small intestineCarla Giordano, Mariangela Sebastiani, Giuseppe Plazzi, et al.
Human Molecular Genetics|September 23, 2008
Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial diseaseRosa Pello, Miguel A Martín, Valerio Carelli, et al.
Acta Ophthalmologica|September 20, 2017
Retinal dysfunction characterizes subtypes of dominant optic atrophyMaria Lucia Cascavilla, Vincenzo Parisi, Giacinto Triolo, et al.
Human Molecular Genetics|March 24, 2020
Metabolomics hallmarks OPA1 variants correlating with their in vitro phenotype and predicting clinical severityJuan Manuel Chao de la Barca, Mario Fogazza, Michela Rugolo, et al.
Pageof 34