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Eva Trevisson

Showing results (1-10 of 86) with videos related to

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Journal of Human Genetics|April 18, 2009
Mutation analysis of COX18 in 29 patients with isolated cytochrome c oxidase deficiencySabrina Sacconi, Leonardo Salviati, Eva Trevisson
Current Opinion in Neurology|August 17, 2011
Coenzyme Q deficiency in muscleEva Trevisson, Salvatore DiMauro, Placido Navas, et al.
Essays in Biochemistry|July 22, 2018
Clinical syndromes associated with Coenzyme Q<sub>10</sub> deficiencyMaría Alcázar-Fabra, Eva Trevisson, Gloria Brea-Calvo
La Radiologia Medica|October 9, 2015
Regression of gadolinium-enhanced lesions in patients affected by neurofibromatosis type 1Marta Lucchetta, Renzo Manara, Giorgio Perilongo, et al.
Free Radical Biology & Medicine|March 7, 2021
Primary Coenzyme Q deficiencies: A literature review and online platform of clinical features to uncover genotype-phenotype correlationsMaría Alcázar-Fabra, Francisco Rodríguez-Sánchez, Eva Trevisson, et al.
Journal of Inherited Metabolic Disease|August 6, 2014
Genetic bases and clinical manifestations of coenzyme Q10 (CoQ 10) deficiencyMaria Andrea Desbats, Giada Lunardi, Mara Doimo, et al.
European Journal of Ophthalmology|June 24, 2021
Two novel compound heterozygous <i>SAG</i> mutations in an Italian patient with Oguchi disease: A genetic and multimodal retinal imaging studyElisabetta Pilotto, Eva Trevisson, Elisabetta Beatrice Nacci, et al.
International Journal of Molecular Sciences|March 10, 2022
The Splicing of the Mitochondrial Calcium Uniporter Genuine Activator MICU1 Is Driven by RBFOX2 Splicing Factor during Myogenic DifferentiationDenis Vecellio Reane, Cristina Cerqua, Sabrina Sacconi, et al.
Molecular Syndromology|August 16, 2014
Genetics of coenzyme q10 deficiencyMara Doimo, Maria A Desbats, Cristina Cerqua, et al.
Scientific Reports|April 27, 2019
Vitamin K2 cannot substitute Coenzyme Q<sub>10</sub> as electron carrier in the mitochondrial respiratory chain of mammalian cellsCristina Cerqua, Alberto Casarin, Fabien Pierrel, et al.
Pageof 9

Showing results (1-10 of 86) with videos related to

Sort By:
Pageof 9
Journal of Human Genetics|April 18, 2009
Mutation analysis of COX18 in 29 patients with isolated cytochrome c oxidase deficiencySabrina Sacconi, Leonardo Salviati, Eva Trevisson
Current Opinion in Neurology|August 17, 2011
Coenzyme Q deficiency in muscleEva Trevisson, Salvatore DiMauro, Placido Navas, et al.
Essays in Biochemistry|July 22, 2018
Clinical syndromes associated with Coenzyme Q<sub>10</sub> deficiencyMaría Alcázar-Fabra, Eva Trevisson, Gloria Brea-Calvo
La Radiologia Medica|October 9, 2015
Regression of gadolinium-enhanced lesions in patients affected by neurofibromatosis type 1Marta Lucchetta, Renzo Manara, Giorgio Perilongo, et al.
Free Radical Biology & Medicine|March 7, 2021
Primary Coenzyme Q deficiencies: A literature review and online platform of clinical features to uncover genotype-phenotype correlationsMaría Alcázar-Fabra, Francisco Rodríguez-Sánchez, Eva Trevisson, et al.
Journal of Inherited Metabolic Disease|August 6, 2014
Genetic bases and clinical manifestations of coenzyme Q10 (CoQ 10) deficiencyMaria Andrea Desbats, Giada Lunardi, Mara Doimo, et al.
European Journal of Ophthalmology|June 24, 2021
Two novel compound heterozygous <i>SAG</i> mutations in an Italian patient with Oguchi disease: A genetic and multimodal retinal imaging studyElisabetta Pilotto, Eva Trevisson, Elisabetta Beatrice Nacci, et al.
International Journal of Molecular Sciences|March 10, 2022
The Splicing of the Mitochondrial Calcium Uniporter Genuine Activator MICU1 Is Driven by RBFOX2 Splicing Factor during Myogenic DifferentiationDenis Vecellio Reane, Cristina Cerqua, Sabrina Sacconi, et al.
Molecular Syndromology|August 16, 2014
Genetics of coenzyme q10 deficiencyMara Doimo, Maria A Desbats, Cristina Cerqua, et al.
Scientific Reports|April 27, 2019
Vitamin K2 cannot substitute Coenzyme Q<sub>10</sub> as electron carrier in the mitochondrial respiratory chain of mammalian cellsCristina Cerqua, Alberto Casarin, Fabien Pierrel, et al.
Pageof 9