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Stem Cell Research
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March 29, 2024
Generation of iPSCs from identical twin, one affected by LHON and one unaffected, both carrying a combination of two mitochondrial variants: m.14484 T>C and m.10680G>A
Camille Peron, Andrea Cavaliere, Chiara Fasano, et al.
Bioscience Reports
|
May 5, 2007
Mitochondrial optic neuropathies: how two genomes may kill the same cell type?
Valerio Carelli, Chiara La Morgia, Luisa Iommarini, et al.
Brain : a Journal of Neurology
|
January 8, 2015
OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation
Rosamaria Santarelli, Roberta Rossi, Pietro Scimemi, et al.
Annals of Neurology
|
October 27, 2004
The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy
Maria Lucia Valentino, Piero Barboni, Anna Ghelli, et al.
Annals of Clinical and Translational Neurology
|
September 4, 2019
Novel mutations in DNA2 associated with myopathy and mtDNA instability
Dario Ronchi, Changwei Liu, Leonardo Caporali, et al.
Scientific Reports
|
September 2, 2022
Identification and analysis of deletion breakpoints in four Mohr-Tranebjærg syndrome (MTS) patients
Nanna Dahl Rendtorff, Helena Gásdal Karstensen, Marianne Lodahl, et al.
Cell Reports
|
June 7, 2018
Infant and Adult Gut Microbiome and Metabolome in Rural Bassa and Urban Settlers from Nigeria
Funmilola A Ayeni, Elena Biagi, Simone Rampelli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 4, 2011
Brain diffusion-weighted imaging in Friedreich's ataxia
Giovanni Rizzo, Caterina Tonon, Maria Lucia Valentino, et al.
Brain : a Journal of Neurology
|
October 15, 2010
Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy
Carla Giordano, Monica Montopoli, Elena Perli, et al.
Brain : a Journal of Neurology
|
January 29, 2008
OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion
Claudia Zanna, Anna Ghelli, Anna Maria Porcelli, et al.
Page
of 34
Search research articles
Search
Showing results (161-170 of 332) with videos related to
Sort By:
Page
of 34
Stem Cell Research
|
March 29, 2024
Generation of iPSCs from identical twin, one affected by LHON and one unaffected, both carrying a combination of two mitochondrial variants: m.14484 T>C and m.10680G>A
Camille Peron, Andrea Cavaliere, Chiara Fasano, et al.
Bioscience Reports
|
May 5, 2007
Mitochondrial optic neuropathies: how two genomes may kill the same cell type?
Valerio Carelli, Chiara La Morgia, Luisa Iommarini, et al.
Brain : a Journal of Neurology
|
January 8, 2015
OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation
Rosamaria Santarelli, Roberta Rossi, Pietro Scimemi, et al.
Annals of Neurology
|
October 27, 2004
The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy
Maria Lucia Valentino, Piero Barboni, Anna Ghelli, et al.
Annals of Clinical and Translational Neurology
|
September 4, 2019
Novel mutations in DNA2 associated with myopathy and mtDNA instability
Dario Ronchi, Changwei Liu, Leonardo Caporali, et al.
Scientific Reports
|
September 2, 2022
Identification and analysis of deletion breakpoints in four Mohr-Tranebjærg syndrome (MTS) patients
Nanna Dahl Rendtorff, Helena Gásdal Karstensen, Marianne Lodahl, et al.
Cell Reports
|
June 7, 2018
Infant and Adult Gut Microbiome and Metabolome in Rural Bassa and Urban Settlers from Nigeria
Funmilola A Ayeni, Elena Biagi, Simone Rampelli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 4, 2011
Brain diffusion-weighted imaging in Friedreich's ataxia
Giovanni Rizzo, Caterina Tonon, Maria Lucia Valentino, et al.
Brain : a Journal of Neurology
|
October 15, 2010
Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy
Carla Giordano, Monica Montopoli, Elena Perli, et al.
Brain : a Journal of Neurology
|
January 29, 2008
OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion
Claudia Zanna, Anna Ghelli, Anna Maria Porcelli, et al.
Page
of 34