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Valerio Carelli

Showing results (241-250 of 332) with videos related to

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Mitochondrion|June 11, 2013
Optic nerve histopathology in a case of Wolfram Syndrome: a mitochondrial pattern of axonal lossFred N Ross-Cisneros, Billy X Pan, Ruwan A Silva, et al.
JAMA Ophthalmology|December 19, 2024
Five-Year Outcomes of Lenadogene Nolparvovec Gene Therapy in Leber Hereditary Optic NeuropathyPatrick Yu-Wai-Man, Nancy J Newman, Valérie Biousse, et al.
Frontiers in Neurology|February 15, 2021
Impaired Ganglion Cell Function Objectively Assessed by the Photopic Negative Response in Affected and Asymptomatic Members From Brazilian Families With Leber's Hereditary Optic NeuropathyGabriel Izan Santos Botelho, Solange Rios Salomão, Célia Harumi Tengan, et al.
Journal of Neurology|February 3, 2019
Muscle pain in mitochondrial diseases: a picture from the Italian networkMassimiliano Filosto, Stefano Cotti Piccinelli, Costanza Lamperti, et al.
Investigative Ophthalmology & Visual Science|June 6, 2013
The pupil light reflex in Leber's hereditary optic neuropathy: evidence for preservation of melanopsin-expressing retinal ganglion cellsAna Laura A Moura, Balázs V Nagy, Chiara La Morgia, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|August 20, 2021
Long-Term Follow-Up After Unilateral Intravitreal Gene Therapy for Leber Hereditary Optic Neuropathy: The RESTORE StudyValérie Biousse, Nancy J Newman, Patrick Yu-Wai-Man, et al.
American Journal of Human Genetics|March 15, 2006
Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigreesValerio Carelli, Alessandro Achilli, Maria Lucia Valentino, et al.
Neurology. Genetics|November 19, 2020
Primary mitochondrial myopathy: Clinical features and outcome measures in 118 cases from ItalyVincenzo Montano, Francesco Gruosso, Valerio Carelli, et al.
Mitochondrion|August 14, 2021
The m.3890G>A/MT-ND1 mtDNA rare pathogenic variant: Expanding clinical and MRI phenotypesVeria Vacchiano, Leonardo Caporali, Chiara La Morgia, et al.
Frontiers in Genetics|November 24, 2022
Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorderLeonardo Caporali, Claudio Fiorini, Flavia Palombo, et al.
Pageof 34

Showing results (241-250 of 332) with videos related to

Sort By:
Pageof 34
Mitochondrion|June 11, 2013
Optic nerve histopathology in a case of Wolfram Syndrome: a mitochondrial pattern of axonal lossFred N Ross-Cisneros, Billy X Pan, Ruwan A Silva, et al.
JAMA Ophthalmology|December 19, 2024
Five-Year Outcomes of Lenadogene Nolparvovec Gene Therapy in Leber Hereditary Optic NeuropathyPatrick Yu-Wai-Man, Nancy J Newman, Valérie Biousse, et al.
Frontiers in Neurology|February 15, 2021
Impaired Ganglion Cell Function Objectively Assessed by the Photopic Negative Response in Affected and Asymptomatic Members From Brazilian Families With Leber's Hereditary Optic NeuropathyGabriel Izan Santos Botelho, Solange Rios Salomão, Célia Harumi Tengan, et al.
Journal of Neurology|February 3, 2019
Muscle pain in mitochondrial diseases: a picture from the Italian networkMassimiliano Filosto, Stefano Cotti Piccinelli, Costanza Lamperti, et al.
Investigative Ophthalmology & Visual Science|June 6, 2013
The pupil light reflex in Leber's hereditary optic neuropathy: evidence for preservation of melanopsin-expressing retinal ganglion cellsAna Laura A Moura, Balázs V Nagy, Chiara La Morgia, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|August 20, 2021
Long-Term Follow-Up After Unilateral Intravitreal Gene Therapy for Leber Hereditary Optic Neuropathy: The RESTORE StudyValérie Biousse, Nancy J Newman, Patrick Yu-Wai-Man, et al.
American Journal of Human Genetics|March 15, 2006
Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigreesValerio Carelli, Alessandro Achilli, Maria Lucia Valentino, et al.
Neurology. Genetics|November 19, 2020
Primary mitochondrial myopathy: Clinical features and outcome measures in 118 cases from ItalyVincenzo Montano, Francesco Gruosso, Valerio Carelli, et al.
Mitochondrion|August 14, 2021
The m.3890G>A/MT-ND1 mtDNA rare pathogenic variant: Expanding clinical and MRI phenotypesVeria Vacchiano, Leonardo Caporali, Chiara La Morgia, et al.
Frontiers in Genetics|November 24, 2022
Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorderLeonardo Caporali, Claudio Fiorini, Flavia Palombo, et al.
Pageof 34