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Valerio Carelli

Showing results (31-40 of 371) with videos related to

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Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|July 9, 2005
Relative post-mortem sparing of afferent pupil fibers in a patient with 3460 Leber's hereditary optic neuropathySwaraj Bose, Navneet Dhillon, Fred N Ross-Cisneros, et al.
Nature Reviews. Genetics|November 3, 2021
Implications of mitochondrial DNA mutations in human induced pluripotent stem cellsValerio Carelli, Michio Hirano, José Antonio Enríquez, et al.
Biochimica Et Biophysica Acta. Bioenergetics|February 1, 2018
Eight human OPA1 isoforms, long and short: What are they for?Valentina Del Dotto, Mario Fogazza, Valerio Carelli, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 14, 2011
Optical coherence tomography for optic disc edemaGiacomo Savini, Piero Barboni, Michele Carbonelli, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|September 24, 2020
Visual Outcomes in Leber Hereditary Optic Neuropathy Patients With the m.11778G>A (MTND4) Mitochondrial DNA MutationNancy J Newman, Valerio Carelli, Magali Taiel, et al.
Nature Reviews. Neurology|December 10, 2014
Disturbed mitochondrial dynamics and neurodegenerative disordersFlorence Burté, Valerio Carelli, Patrick F Chinnery, et al.
The Lancet. Neurology|September 26, 2022
Understanding the molecular basis and pathogenesis of hereditary optic neuropathies: towards improved diagnosis and managementNancy J Newman, Patrick Yu-Wai-Man, Valérie Biousse, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|January 28, 2014
HPLC-UV analysis of thymidine and deoxyuridine in plasma of patients with thymidine phosphorylase deficiencySusan Mohamed, Leonardo Caporali, Roberto De Giorgio, et al.
Frontiers in Psychology|January 23, 2024
Chromatic pupillometry for evaluating melanopsin retinal ganglion cell function in Alzheimer's disease and other neurodegenerative disorders: a reviewMartina Romagnoli, Giulia Amore, Pietro Avanzini, et al.
Biochimica Et Biophysica Acta|July 30, 2004
Bioenergetics of mitochondrial diseases associated with mtDNA mutationsGiorgio Lenaz, Alessandra Baracca, Valerio Carelli, et al.
Pageof 38

Showing results (31-40 of 371) with videos related to

Sort By:
Pageof 38
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|July 9, 2005
Relative post-mortem sparing of afferent pupil fibers in a patient with 3460 Leber's hereditary optic neuropathySwaraj Bose, Navneet Dhillon, Fred N Ross-Cisneros, et al.
Nature Reviews. Genetics|November 3, 2021
Implications of mitochondrial DNA mutations in human induced pluripotent stem cellsValerio Carelli, Michio Hirano, José Antonio Enríquez, et al.
Biochimica Et Biophysica Acta. Bioenergetics|February 1, 2018
Eight human OPA1 isoforms, long and short: What are they for?Valentina Del Dotto, Mario Fogazza, Valerio Carelli, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 14, 2011
Optical coherence tomography for optic disc edemaGiacomo Savini, Piero Barboni, Michele Carbonelli, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|September 24, 2020
Visual Outcomes in Leber Hereditary Optic Neuropathy Patients With the m.11778G>A (MTND4) Mitochondrial DNA MutationNancy J Newman, Valerio Carelli, Magali Taiel, et al.
Nature Reviews. Neurology|December 10, 2014
Disturbed mitochondrial dynamics and neurodegenerative disordersFlorence Burté, Valerio Carelli, Patrick F Chinnery, et al.
The Lancet. Neurology|September 26, 2022
Understanding the molecular basis and pathogenesis of hereditary optic neuropathies: towards improved diagnosis and managementNancy J Newman, Patrick Yu-Wai-Man, Valérie Biousse, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|January 28, 2014
HPLC-UV analysis of thymidine and deoxyuridine in plasma of patients with thymidine phosphorylase deficiencySusan Mohamed, Leonardo Caporali, Roberto De Giorgio, et al.
Frontiers in Psychology|January 23, 2024
Chromatic pupillometry for evaluating melanopsin retinal ganglion cell function in Alzheimer's disease and other neurodegenerative disorders: a reviewMartina Romagnoli, Giulia Amore, Pietro Avanzini, et al.
Biochimica Et Biophysica Acta|July 30, 2004
Bioenergetics of mitochondrial diseases associated with mtDNA mutationsGiorgio Lenaz, Alessandra Baracca, Valerio Carelli, et al.
Pageof 38