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Valerio Carelli

Showing results (141-150 of 371) with videos related to

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Brain Communications|April 18, 2025
Elevated circulating cell-free mitochondrial DNA level in cerebrospinal fluid of narcolepsy type 1Monica Moresco, Concetta Valentina Tropeano, Martina Romagnoli, et al.
Transactions of the American Ophthalmological Society|January 28, 2003
A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathyAlfredo A Sadun, Valerio Carelli, Solange R Salomao, et al.
International Journal of Environmental Research and Public Health|June 10, 2022
Multishell Diffusion MR Tractography Yields Morphological and Microstructural Information of the Anterior Optic Pathway: A Proof-of-Concept Study in Patients with Leber's Hereditary Optic NeuropathyDavid Neil Manners, Laura Ludovica Gramegna, Chiara La Morgia, et al.
Archives of Neurology|March 14, 2012
Effect of EPI-743 on the clinical course of the mitochondrial disease Leber hereditary optic neuropathyAlfredo A Sadun, Carlos Filipe Chicani, Fred N Ross-Cisneros, et al.
Plos One|December 21, 2013
A novel null homozygous mutation confirms CACNA2D2 as a gene mutated in epileptic encephalopathyTommaso Pippucci, Antonia Parmeggiani, Flavia Palombo, et al.
Archives of Neurology|February 15, 2002
Biochemical-clinical correlation in patients with different loads of the mitochondrial DNA T8993G mutationValerio Carelli, Alessandra Baracca, Silvia Barogi, et al.
Clinical & Experimental Ophthalmology|May 24, 2018
Peripapillary vessel density changes in Leber's hereditary optic neuropathy: a new biomarkerNicole Balducci, Maria Lucia Cascavilla, Antonio Ciardella, et al.
Molecular Vision|December 24, 2008
Phosphorylated neurofilament heavy chain is a marker of neurodegeneration in Leber hereditary optic neuropathy (LHON)John Guy, Gerry Shaw, Fred N Ross-Cisneros, et al.
Eye (London, England)|February 7, 2023
Choroidal vascularity index in hereditary optic neuropathiesMarco Battista, Maria Lucia Cascavilla, Enrico Borrelli, et al.
Neurogenetics|April 16, 2024
Two more families supporting the existence of monogenic spinocerebellar ataxia 48Flavia Palombo, Alessandro Vaisfeld, Valentina Concetta Tropeano, et al.
Pageof 38

Showing results (141-150 of 371) with videos related to

Sort By:
Pageof 38
Brain Communications|April 18, 2025
Elevated circulating cell-free mitochondrial DNA level in cerebrospinal fluid of narcolepsy type 1Monica Moresco, Concetta Valentina Tropeano, Martina Romagnoli, et al.
Transactions of the American Ophthalmological Society|January 28, 2003
A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathyAlfredo A Sadun, Valerio Carelli, Solange R Salomao, et al.
International Journal of Environmental Research and Public Health|June 10, 2022
Multishell Diffusion MR Tractography Yields Morphological and Microstructural Information of the Anterior Optic Pathway: A Proof-of-Concept Study in Patients with Leber's Hereditary Optic NeuropathyDavid Neil Manners, Laura Ludovica Gramegna, Chiara La Morgia, et al.
Archives of Neurology|March 14, 2012
Effect of EPI-743 on the clinical course of the mitochondrial disease Leber hereditary optic neuropathyAlfredo A Sadun, Carlos Filipe Chicani, Fred N Ross-Cisneros, et al.
Plos One|December 21, 2013
A novel null homozygous mutation confirms CACNA2D2 as a gene mutated in epileptic encephalopathyTommaso Pippucci, Antonia Parmeggiani, Flavia Palombo, et al.
Archives of Neurology|February 15, 2002
Biochemical-clinical correlation in patients with different loads of the mitochondrial DNA T8993G mutationValerio Carelli, Alessandra Baracca, Silvia Barogi, et al.
Clinical & Experimental Ophthalmology|May 24, 2018
Peripapillary vessel density changes in Leber's hereditary optic neuropathy: a new biomarkerNicole Balducci, Maria Lucia Cascavilla, Antonio Ciardella, et al.
Molecular Vision|December 24, 2008
Phosphorylated neurofilament heavy chain is a marker of neurodegeneration in Leber hereditary optic neuropathy (LHON)John Guy, Gerry Shaw, Fred N Ross-Cisneros, et al.
Eye (London, England)|February 7, 2023
Choroidal vascularity index in hereditary optic neuropathiesMarco Battista, Maria Lucia Cascavilla, Enrico Borrelli, et al.
Neurogenetics|April 16, 2024
Two more families supporting the existence of monogenic spinocerebellar ataxia 48Flavia Palombo, Alessandro Vaisfeld, Valentina Concetta Tropeano, et al.
Pageof 38