Ivano Di Meo
Fondazione IRCCS Istituto Neurologico Carlo Besta
23 papers found
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SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder
Download from doi.orgSURF1 knockout cloned pigs: Early onset of a severe lethal phenotype
Download from doi.orgClinical, biochemical, and genetic features associated with VARS2 -related mitochondrial disease
Download from api.wiley.comTranscription Factor EB Controls Metabolic Flexibility during Exercise
Download from doi.orgCoenzyme Q deficiency causes impairment of the sulfide oxidation pathway
Download from doi.orgLiver transplant in ethylmalonic encephalopathy: a new treatment for an otherwise fatal disease
Download from doi.orgEffective AAV-mediated gene therapy in a mouse model of ethylmalonic encephalopathy
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