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Daniele Ghezzi

Showing results (71-80 of 143) with videos related to

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Nature Genetics|February 1, 2011
Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and fliesDaniele Ghezzi, Paola Arzuffi, Mauro Zordan, et al.
Nature Genetics|May 26, 2009
SDHAF1, encoding a LYR complex-II specific assembly factor, is mutated in SDH-defective infantile leukoencephalopathyDaniele Ghezzi, Paola Goffrini, Graziella Uziel, et al.
Neurology|September 13, 2013
SURF1 deficiency causes demyelinating Charcot-Marie-Tooth diseaseAndoni Echaniz-Laguna, Daniele Ghezzi, Maïté Chassagne, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 27, 2025
Altered Dopamine Metabolism and Response to Treatment with Levodopa/Carbidopa in MCT8 DeficiencyFabio Bruschi, Ylenia Vaia, Clara E Antonello, et al.
Biomaterials Advances|March 6, 2024
Ionized jet deposition of silver nanostructured coatings: Assessment of chemico-physical and biological behavior for application in orthopedicsGabriela Graziani, Daniele Ghezzi, Marco Boi, et al.
Journal of Medical Genetics|October 29, 2017
A novel de novo dominant mutation in <i>ISCU</i> associated with mitochondrial myopathyAndrea Legati, Aurelio Reyes, Camilla Ceccatelli Berti, et al.
American Journal of Human Genetics|May 22, 2012
Mutations of the mitochondrial-tRNA modifier MTO1 cause hypertrophic cardiomyopathy and lactic acidosisDaniele Ghezzi, Enrico Baruffini, Tobias B Haack, et al.
American Journal of Human Genetics|June 23, 2015
RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial EncephalomyopathyAurelio Reyes, Laura Melchionda, Alessia Nasca, et al.
EMBO Molecular Medicine|December 16, 2018
APOPT1/COA8 assists COX assembly and is oppositely regulated by UPS and ROSAlba Signes, Raffaele Cerutti, Anna S Dickson, et al.
Nature Communications|April 9, 2021
Exploiting pyocyanin to treat mitochondrial disease due to respiratory complex III dysfunctionRoberta Peruzzo, Samantha Corrà, Roberto Costa, et al.
Pageof 15

Showing results (71-80 of 143) with videos related to

Sort By:
Pageof 15
Nature Genetics|February 1, 2011
Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and fliesDaniele Ghezzi, Paola Arzuffi, Mauro Zordan, et al.
Nature Genetics|May 26, 2009
SDHAF1, encoding a LYR complex-II specific assembly factor, is mutated in SDH-defective infantile leukoencephalopathyDaniele Ghezzi, Paola Goffrini, Graziella Uziel, et al.
Neurology|September 13, 2013
SURF1 deficiency causes demyelinating Charcot-Marie-Tooth diseaseAndoni Echaniz-Laguna, Daniele Ghezzi, Maïté Chassagne, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 27, 2025
Altered Dopamine Metabolism and Response to Treatment with Levodopa/Carbidopa in MCT8 DeficiencyFabio Bruschi, Ylenia Vaia, Clara E Antonello, et al.
Biomaterials Advances|March 6, 2024
Ionized jet deposition of silver nanostructured coatings: Assessment of chemico-physical and biological behavior for application in orthopedicsGabriela Graziani, Daniele Ghezzi, Marco Boi, et al.
Journal of Medical Genetics|October 29, 2017
A novel de novo dominant mutation in <i>ISCU</i> associated with mitochondrial myopathyAndrea Legati, Aurelio Reyes, Camilla Ceccatelli Berti, et al.
American Journal of Human Genetics|May 22, 2012
Mutations of the mitochondrial-tRNA modifier MTO1 cause hypertrophic cardiomyopathy and lactic acidosisDaniele Ghezzi, Enrico Baruffini, Tobias B Haack, et al.
American Journal of Human Genetics|June 23, 2015
RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial EncephalomyopathyAurelio Reyes, Laura Melchionda, Alessia Nasca, et al.
EMBO Molecular Medicine|December 16, 2018
APOPT1/COA8 assists COX assembly and is oppositely regulated by UPS and ROSAlba Signes, Raffaele Cerutti, Anna S Dickson, et al.
Nature Communications|April 9, 2021
Exploiting pyocyanin to treat mitochondrial disease due to respiratory complex III dysfunctionRoberta Peruzzo, Samantha Corrà, Roberto Costa, et al.
Pageof 15