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Epileptic Disorders : International Epilepsy Journal with Videotape|September 14, 2016
Myoclonus epilepsy in mitochondrial disordersCostanza Lamperti, Massimo Zeviani
Handbook of Clinical Neurology|February 22, 2023
Currently available therapies in mitochondrial diseaseCornelia Kornblum, Costanza Lamperti, Sumit Parikh
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 7, 2025
National diagnostic gaps for TK2 Deficiency in Italy: insights from the AIM Multicenter SurveyMichelangelo Mancuso, Costanza Lamperti, Olimpia Musumeci
EMBO Molecular Medicine|July 22, 2015
Mitochondrial diseases caused by toxic compound accumulation: from etiopathology to therapeutic approachesIvano Di Meo, Costanza Lamperti, Valeria Tiranti
International Journal of Molecular Sciences|January 11, 2022
The Roles of Coenzyme Q in Disease: Direct and Indirect Involvement in Cellular FunctionsFrancesco Pallotti, Christian Bergamini, Costanza Lamperti, et al.
Pharmaceutics|November 14, 2020
Therapeutic Approaches to Treat Mitochondrial Diseases: "One-Size-Fits-All" and "Precision Medicine" StrategiesEmanuela Bottani, Costanza Lamperti, Alessandro Prigione, et al.
Neuromuscular Disorders : NMD|January 10, 2012
Partial tandem duplication of mtDNA-tRNA(Phe) impairs mtDNA translation in late-onset mitochondrial myopathyPaola Arzuffi, Costanza Lamperti, Erika Fernandez-Vizarra, et al.
EMBO Molecular Medicine|August 21, 2012
Effective AAV-mediated gene therapy in a mouse model of ethylmalonic encephalopathyIvano Di Meo, Alberto Auricchio, Costanza Lamperti, et al.
The Journal of Molecular Diagnostics : JMD|March 30, 2021
Current and New Next-Generation Sequencing Approaches to Study Mitochondrial DNAAndrea Legati, Nadia Zanetti, Alessia Nasca, et al.
European Journal of Neurology|April 11, 2023
Phenotyping mitochondrial DNA-related diseases in childhood: A cohort study of 150 patientsAnna Ardissone, Giulia Ferrera, Costanza Lamperti, et al.
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