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Valerio Carelli

Showing results (191-200 of 332) with videos related to

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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.
Investigative Ophthalmology & Visual Science|April 27, 2007
Male prevalence of acquired color vision defects in asymptomatic carriers of Leber's hereditary optic neuropathyDora Fix Ventura, Mirella Gualtieri, André G F Oliveira, et al.
International Journal of Molecular Sciences|August 12, 2022
Anatomical Laser Microdissection of the Ileum Reveals mtDNA Depletion Recovery in A Mitochondrial Neuro-Gastrointestinal Encephalomyopathy (MNGIE) Patient Receiving Liver TransplantElisa Boschetti, Leonardo Caporali, Roberto D'Angelo, et al.
BMC Neurology|July 12, 2022
Absence of lenadogene nolparvovec DNA in a brain tumor biopsy from a patient in the REVERSE clinical study, a case reportNancy J Newman, Matthew Schniederjan, Pia R Mendoza, et al.
Journal of Lipid Research|May 19, 2024
Lipidomics reveals the reshaping of the mitochondrial phospholipid profile in cells lacking OPA1 and mitofusinsAndrea Castellaneta, Ilario Losito, Vito Porcelli, et al.
Investigative Ophthalmology & Visual Science|August 16, 2012
Neuron-specific enolase is elevated in asymptomatic carriers of Leber's hereditary optic neuropathyKenneth M Yee, Fred N Ross-Cisneros, Jeong Goo Lee, et al.
Journal of Neuroimmunology|December 7, 2007
Differential cerebro spinal fluid proteome investigation of Leber hereditary optic neuropathy (LHON) and multiple sclerosisSimona D'Aguanno, Alessandra Barassi, Santina Lupisella, et al.
Scientific Reports|November 18, 2016
Changes in Choroidal Thickness follow the RNFL Changes in Leber's Hereditary Optic NeuropathyEnrico Borrelli, Giacinto Triolo, Maria Lucia Cascavilla, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|October 9, 2018
Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell modelsValentina Del Dotto, Mario Fogazza, Francesco Musiani, 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.
Pageof 34

Showing results (191-200 of 332) with videos related to

Sort By:
Pageof 34
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.
Investigative Ophthalmology & Visual Science|April 27, 2007
Male prevalence of acquired color vision defects in asymptomatic carriers of Leber's hereditary optic neuropathyDora Fix Ventura, Mirella Gualtieri, André G F Oliveira, et al.
International Journal of Molecular Sciences|August 12, 2022
Anatomical Laser Microdissection of the Ileum Reveals mtDNA Depletion Recovery in A Mitochondrial Neuro-Gastrointestinal Encephalomyopathy (MNGIE) Patient Receiving Liver TransplantElisa Boschetti, Leonardo Caporali, Roberto D'Angelo, et al.
BMC Neurology|July 12, 2022
Absence of lenadogene nolparvovec DNA in a brain tumor biopsy from a patient in the REVERSE clinical study, a case reportNancy J Newman, Matthew Schniederjan, Pia R Mendoza, et al.
Journal of Lipid Research|May 19, 2024
Lipidomics reveals the reshaping of the mitochondrial phospholipid profile in cells lacking OPA1 and mitofusinsAndrea Castellaneta, Ilario Losito, Vito Porcelli, et al.
Investigative Ophthalmology & Visual Science|August 16, 2012
Neuron-specific enolase is elevated in asymptomatic carriers of Leber's hereditary optic neuropathyKenneth M Yee, Fred N Ross-Cisneros, Jeong Goo Lee, et al.
Journal of Neuroimmunology|December 7, 2007
Differential cerebro spinal fluid proteome investigation of Leber hereditary optic neuropathy (LHON) and multiple sclerosisSimona D'Aguanno, Alessandra Barassi, Santina Lupisella, et al.
Scientific Reports|November 18, 2016
Changes in Choroidal Thickness follow the RNFL Changes in Leber's Hereditary Optic NeuropathyEnrico Borrelli, Giacinto Triolo, Maria Lucia Cascavilla, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|October 9, 2018
Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell modelsValentina Del Dotto, Mario Fogazza, Francesco Musiani, 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.
Pageof 34