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Michele Carbonelli

Showing results (51-60 of 83) with videos related to

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Brain : a Journal of Neurology|February 8, 2013
Idebenone treatment in patients with OPA1-mutant dominant optic atrophyPiero Barboni, Maria Lucia Valentino, Chiara La Morgia, et al.
Frontiers in Neuroscience|August 28, 2020
Chromatic Pupillometry Findings in Alzheimer's DiseaseMartina Romagnoli, Michelangelo Stanzani Maserati, Maddalena De Matteis, et al.
Brain : a Journal of Neurology|August 23, 2014
'Behr syndrome' with OPA1 compound heterozygote mutationsValerio Carelli, Mario Sabatelli, Rosalba Carrozzo, et al.
European Journal of Ophthalmology|May 8, 2012
Retinal nerve fiber layer thickness variability in Leber hereditary optic neuropathy carriersPiero Barboni, Giacomo Savini, William J Feuer, et al.
Journal of Medical Genetics|September 21, 2023
Recessive <i>MECR</i> pathogenic variants cause an LHON-like optic neuropathyClaudio Fiorini, Andrea Degiorgi, Maria Lucia Cascavilla, et al.
American Journal of Ophthalmology|May 5, 2022
Capturing the Pattern of Transition From Carrier to Affected in Leber Hereditary Optic NeuropathyMichele Carbonelli, Chiara La Morgia, Martina Romagnoli, et al.
Archives of Neurology|September 15, 2010
Defective mitochondrial adenosine triphosphate production in skeletal muscle from patients with dominant optic atrophy due to OPA1 mutationsRaffaele Lodi, Caterina Tonon, Maria Lucia Valentino, 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.
Scientific Reports|February 9, 2022
Retinal vascular impairment in Wolfram syndrome: an optical coherence tomography angiography studyMarco Battista, Maria Lucia Cascavilla, Domenico Grosso, et al.
Frontiers in Genetics|June 20, 2022
Case Report: Optic Atrophy and Nephropathy With m.13513G>A/MT-ND5 mtDNA Pathogenic VariantValentina Barone, Chiara La Morgia, Leonardo Caporali, et al.
Pageof 9

Showing results (51-60 of 83) with videos related to

Sort By:
Pageof 9
Brain : a Journal of Neurology|February 8, 2013
Idebenone treatment in patients with OPA1-mutant dominant optic atrophyPiero Barboni, Maria Lucia Valentino, Chiara La Morgia, et al.
Frontiers in Neuroscience|August 28, 2020
Chromatic Pupillometry Findings in Alzheimer's DiseaseMartina Romagnoli, Michelangelo Stanzani Maserati, Maddalena De Matteis, et al.
Brain : a Journal of Neurology|August 23, 2014
'Behr syndrome' with OPA1 compound heterozygote mutationsValerio Carelli, Mario Sabatelli, Rosalba Carrozzo, et al.
European Journal of Ophthalmology|May 8, 2012
Retinal nerve fiber layer thickness variability in Leber hereditary optic neuropathy carriersPiero Barboni, Giacomo Savini, William J Feuer, et al.
Journal of Medical Genetics|September 21, 2023
Recessive <i>MECR</i> pathogenic variants cause an LHON-like optic neuropathyClaudio Fiorini, Andrea Degiorgi, Maria Lucia Cascavilla, et al.
American Journal of Ophthalmology|May 5, 2022
Capturing the Pattern of Transition From Carrier to Affected in Leber Hereditary Optic NeuropathyMichele Carbonelli, Chiara La Morgia, Martina Romagnoli, et al.
Archives of Neurology|September 15, 2010
Defective mitochondrial adenosine triphosphate production in skeletal muscle from patients with dominant optic atrophy due to OPA1 mutationsRaffaele Lodi, Caterina Tonon, Maria Lucia Valentino, 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.
Scientific Reports|February 9, 2022
Retinal vascular impairment in Wolfram syndrome: an optical coherence tomography angiography studyMarco Battista, Maria Lucia Cascavilla, Domenico Grosso, et al.
Frontiers in Genetics|June 20, 2022
Case Report: Optic Atrophy and Nephropathy With m.13513G>A/MT-ND5 mtDNA Pathogenic VariantValentina Barone, Chiara La Morgia, Leonardo Caporali, et al.
Pageof 9