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Caterina Garone

Showing results (1-10 of 54) with videos related to

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European Journal of Human Genetics : EJHG|October 3, 2023
Mitochondrial Cytochrome C deficiency can show the first disease signs in the prenatal stageCaterina Garone
Developmental Disabilities Research Reviews|September 7, 2010
Historical perspective on mitochondrial medicineSalvatore DiMauro, Caterina Garone
Biochemical Society Transactions|October 11, 2018
Towards a therapy for mitochondrial disease: an updateCaterina Garone, Carlo Viscomi
Life (Basel, Switzerland)|March 25, 2022
From the Structural and (Dys)Function of ATP Synthase to Deficiency in Age-Related DiseasesCaterina Garone, Andrea Pietra, Salvatore Nesci
Current Rheumatology Reports|August 3, 2010
Metabolic myopathiesSalvatore DiMauro, Caterina Garone, Ali Naini
Brain : a Journal of Neurology|September 22, 2011
Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathyCaterina Garone, Saba Tadesse, Michio Hirano
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 25, 2025
Gene therapy and mRNA drugs approach for mitochondrial OXPHOS deficienciesCaterina Garone, Silvia Sabeni, Sara Carli
Biochimica Et Biophysica Acta|January 26, 2012
CoQ(10) deficiencies and MNGIE: two treatable mitochondrial disordersMichio Hirano, Caterina Garone, Catarina M Quinzii
Journal of Child Neurology|July 11, 2007
No kinetic interaction between levetiracetam and cyclosporine: a case reportEmilio Franzoni, Jasenka Sarajlija, Caterina Garone, et al.
Frontiers in Genetics|January 11, 2019
Mitochondrial Neurogastrointestinal Encephalomyopathy: Into the Fourth Decade, What We Have Learned So FarDario Pacitti, Michelle Levene, Caterina Garone, et al.
Pageof 6

Showing results (1-10 of 54) with videos related to

Sort By:
Pageof 6
European Journal of Human Genetics : EJHG|October 3, 2023
Mitochondrial Cytochrome C deficiency can show the first disease signs in the prenatal stageCaterina Garone
Developmental Disabilities Research Reviews|September 7, 2010
Historical perspective on mitochondrial medicineSalvatore DiMauro, Caterina Garone
Biochemical Society Transactions|October 11, 2018
Towards a therapy for mitochondrial disease: an updateCaterina Garone, Carlo Viscomi
Life (Basel, Switzerland)|March 25, 2022
From the Structural and (Dys)Function of ATP Synthase to Deficiency in Age-Related DiseasesCaterina Garone, Andrea Pietra, Salvatore Nesci
Current Rheumatology Reports|August 3, 2010
Metabolic myopathiesSalvatore DiMauro, Caterina Garone, Ali Naini
Brain : a Journal of Neurology|September 22, 2011
Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathyCaterina Garone, Saba Tadesse, Michio Hirano
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 25, 2025
Gene therapy and mRNA drugs approach for mitochondrial OXPHOS deficienciesCaterina Garone, Silvia Sabeni, Sara Carli
Biochimica Et Biophysica Acta|January 26, 2012
CoQ(10) deficiencies and MNGIE: two treatable mitochondrial disordersMichio Hirano, Caterina Garone, Catarina M Quinzii
Journal of Child Neurology|July 11, 2007
No kinetic interaction between levetiracetam and cyclosporine: a case reportEmilio Franzoni, Jasenka Sarajlija, Caterina Garone, et al.
Frontiers in Genetics|January 11, 2019
Mitochondrial Neurogastrointestinal Encephalomyopathy: Into the Fourth Decade, What We Have Learned So FarDario Pacitti, Michelle Levene, Caterina Garone, et al.
Pageof 6