Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Valerio Carelli

Showing results (111-120 of 371) with videos related to

Pageof 38
Sort By:
Recenti Progressi in Medicina|October 2, 2025
Sara Mazzucato, Piervito Lopriore, Francesco Daddoveri, et al.
Journal of Molecular Medicine (Berlin, Germany)|August 28, 2020
Expanding and validating the biomarkers for mitochondrial diseasesAlessandra Maresca, Valentina Del Dotto, Martina Romagnoli, et al.
Cephalalgia : an International Journal of Headache|July 27, 2010
High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS familiesSabina Cevoli, Francesco Pallotti, Chiara La Morgia, et al.
Mitochondrion|April 17, 2017
Melanopsin-expressing retinal ganglion cells are resistant to cell injury, but not alwaysBirgitte Georg, Anna Ghelli, Carla Giordano, et al.
Chronobiology International|April 1, 2014
Nocturnal melatonin regulation in post-traumatic vegetative state: a possible role for melatonin supplementation?Pietro Guaraldi, Elisa Sancisi, Chiara La Morgia, et al.
The British Journal of Ophthalmology|April 22, 2026
Efficacy of lenadogene nolparvovec gene therapy versus idebenone in Leber hereditary optic neuropathy due to the m.11778G>A <i>MT-ND4</i> variant: two matching adjusted indirect comparisonsPatrick Yu-Wai-Man, Nancy J Newman, Valerio Carelli, et al.
Annals of Clinical and Translational Neurology|April 4, 2020
Idebenone increases chance of stabilization/recovery of visual acuity in OPA1-dominant optic atrophyMartina Romagnoli, Chiara La Morgia, Michele Carbonelli, et al.
Annals of Neurology|October 29, 2002
Rescue of a mitochondrial deficiency causing Leber Hereditary Optic NeuropathyJohn Guy, Xiaoping Qi, Francesco Pallotti, et al.
Plos One|May 9, 2014
A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneckFrancesco Pallotti, Giorgio Binelli, Raffaella Fabbri, et al.
Investigative Ophthalmology & Visual Science|September 28, 2013
Retinal function and neural conduction along the visual pathways in affected and unaffected carriers with Leber's hereditary optic neuropathyLucia Ziccardi, Federico Sadun, Anna Maria De Negri, et al.
Pageof 38

Showing results (111-120 of 371) with videos related to

Sort By:
Pageof 38
Recenti Progressi in Medicina|October 2, 2025
Sara Mazzucato, Piervito Lopriore, Francesco Daddoveri, et al.
Journal of Molecular Medicine (Berlin, Germany)|August 28, 2020
Expanding and validating the biomarkers for mitochondrial diseasesAlessandra Maresca, Valentina Del Dotto, Martina Romagnoli, et al.
Cephalalgia : an International Journal of Headache|July 27, 2010
High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS familiesSabina Cevoli, Francesco Pallotti, Chiara La Morgia, et al.
Mitochondrion|April 17, 2017
Melanopsin-expressing retinal ganglion cells are resistant to cell injury, but not alwaysBirgitte Georg, Anna Ghelli, Carla Giordano, et al.
Chronobiology International|April 1, 2014
Nocturnal melatonin regulation in post-traumatic vegetative state: a possible role for melatonin supplementation?Pietro Guaraldi, Elisa Sancisi, Chiara La Morgia, et al.
The British Journal of Ophthalmology|April 22, 2026
Efficacy of lenadogene nolparvovec gene therapy versus idebenone in Leber hereditary optic neuropathy due to the m.11778G>A <i>MT-ND4</i> variant: two matching adjusted indirect comparisonsPatrick Yu-Wai-Man, Nancy J Newman, Valerio Carelli, et al.
Annals of Clinical and Translational Neurology|April 4, 2020
Idebenone increases chance of stabilization/recovery of visual acuity in OPA1-dominant optic atrophyMartina Romagnoli, Chiara La Morgia, Michele Carbonelli, et al.
Annals of Neurology|October 29, 2002
Rescue of a mitochondrial deficiency causing Leber Hereditary Optic NeuropathyJohn Guy, Xiaoping Qi, Francesco Pallotti, et al.
Plos One|May 9, 2014
A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneckFrancesco Pallotti, Giorgio Binelli, Raffaella Fabbri, et al.
Investigative Ophthalmology & Visual Science|September 28, 2013
Retinal function and neural conduction along the visual pathways in affected and unaffected carriers with Leber's hereditary optic neuropathyLucia Ziccardi, Federico Sadun, Anna Maria De Negri, et al.
Pageof 38