Valerio Carelli
IRCCS Istituto Delle Scienze Neurologiche di Bologna
217 papers found
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Impaired complex I repair causes recessive Leber’s hereditary optic neuropathy
Download from doi.orgPrimary mitochondrial myopathy
Download from doi.orgExpanding and validating the biomarkers for mitochondrial diseases
Download from link.springer.comMitochondrial diseases in adults
UploadSSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder
Download from doi.orgMutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder
Download from www.nature.comSyndromic parkinsonism and dementia associated with OPA1 missense mutations
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