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Valerio Carelli

Showing results (91-100 of 371) with videos related to

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Frontiers in Neurology|September 2, 2025
Late-onset Leber's hereditary optic neuropathy and antiandrogens for prostate cancer: is there a causative link?Giulia Amore, Michele Carbonelli, Diego D'Angeli, et al.
Biochimica Et Biophysica Acta|October 16, 2002
Respiratory function in cybrid cell lines carrying European mtDNA haplogroups: implications for Leber's hereditary optic neuropathyValerio Carelli, Lodovica Vergani, Barbara Bernazzi, et al.
Archives of Neurology|May 11, 2005
Severe impairment of complex I-driven adenosine triphosphate synthesis in leber hereditary optic neuropathy cybridsAlessandra Baracca, Giancarlo Solaini, Gianluca Sgarbi, et al.
Mitochondrion|March 15, 2011
Variation in MAPT is not a contributing factor to the incomplete penetrance in LHONGavin Hudson, Patrick Yu-Wai-Man, Philip G Griffiths, et al.
Brain : a Journal of Neurology|March 27, 2016
Reply: Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunctionRosamaria Santarelli, Elona Cama, Pietro Scimemi, et al.
Brain : a Journal of Neurology|September 3, 2004
Leber hereditary optic neuropathy mtDNA mutations disrupt glutamate transport in cybrid cell linesSimone Beretta, Laura Mattavelli, Gessica Sala, et al.
Neurology. Genetics|August 11, 2022
A Second Case With the V374A <i>KCND3</i> Pathogenic Variant in an Italian Patient With Early-Onset Spinocerebellar AtaxiaFlavia Palombo, Chiara La Morgia, Claudio Fiorini, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|March 26, 2004
Ocular findings in mitochondrial neurogastrointestinal encephalomyopathy: a case reportPiero Barboni, Giacomo Savini, Giuseppe Plazzi, et al.
Scientific Reports|March 11, 2022
The relevance of migraine in the clinical spectrum of mitochondrial disordersAlberto Terrin, Luca Bello, Maria Lucia Valentino, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|January 21, 2020
Cataplexy and ataxia: red flags for the diagnosis of DNA methyltransferase 1 mutationEmanuela Postiglione, Elena Antelmi, Fabio Pizza, et al.
Pageof 38

Showing results (91-100 of 371) with videos related to

Sort By:
Pageof 38
Frontiers in Neurology|September 2, 2025
Late-onset Leber's hereditary optic neuropathy and antiandrogens for prostate cancer: is there a causative link?Giulia Amore, Michele Carbonelli, Diego D'Angeli, et al.
Biochimica Et Biophysica Acta|October 16, 2002
Respiratory function in cybrid cell lines carrying European mtDNA haplogroups: implications for Leber's hereditary optic neuropathyValerio Carelli, Lodovica Vergani, Barbara Bernazzi, et al.
Archives of Neurology|May 11, 2005
Severe impairment of complex I-driven adenosine triphosphate synthesis in leber hereditary optic neuropathy cybridsAlessandra Baracca, Giancarlo Solaini, Gianluca Sgarbi, et al.
Mitochondrion|March 15, 2011
Variation in MAPT is not a contributing factor to the incomplete penetrance in LHONGavin Hudson, Patrick Yu-Wai-Man, Philip G Griffiths, et al.
Brain : a Journal of Neurology|March 27, 2016
Reply: Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunctionRosamaria Santarelli, Elona Cama, Pietro Scimemi, et al.
Brain : a Journal of Neurology|September 3, 2004
Leber hereditary optic neuropathy mtDNA mutations disrupt glutamate transport in cybrid cell linesSimone Beretta, Laura Mattavelli, Gessica Sala, et al.
Neurology. Genetics|August 11, 2022
A Second Case With the V374A <i>KCND3</i> Pathogenic Variant in an Italian Patient With Early-Onset Spinocerebellar AtaxiaFlavia Palombo, Chiara La Morgia, Claudio Fiorini, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|March 26, 2004
Ocular findings in mitochondrial neurogastrointestinal encephalomyopathy: a case reportPiero Barboni, Giacomo Savini, Giuseppe Plazzi, et al.
Scientific Reports|March 11, 2022
The relevance of migraine in the clinical spectrum of mitochondrial disordersAlberto Terrin, Luca Bello, Maria Lucia Valentino, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|January 21, 2020
Cataplexy and ataxia: red flags for the diagnosis of DNA methyltransferase 1 mutationEmanuela Postiglione, Elena Antelmi, Fabio Pizza, et al.
Pageof 38