ZEVIANI, MASSIMO

ZEVIANI, MASSIMO  

Dipartimento di Neuroscienze - DNS  

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Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
155th ENMC workshop: Polymerase gamma and disorders of mitochondrial DNA synthesis, 21-23 September 2007, Naarden, The Netherlands 2008 Zeviani M. + NEUROMUSCULAR DISORDERS - -
A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA. 1989 RIZZUTO, ROSARIOZEVIANI M + SCIENCE - -
A single cell complementation class is common to several cases of Cytochrome c Oxidase defective Leigh's syndrome 1997 SANDONA', DORIANNAZEVIANI M. + HUMAN MOLECULAR GENETICS - -
The A467T and W748S POLG substitutions are a rare cause of adult-onset ataxia in Europe [1] 2007 Zeviani M. + BRAIN - -
AAV-mediated liver-specific MPV17 expression restores mtdna levels and prevents diet-induced liver failure 2014 Viscomi C.Zeviani M. + MOLECULAR THERAPY - -
AAV9-based gene therapy partially ameliorates the clinical phenotype of a mouse model of Leigh syndrome 2017 Zeviani M.Viscomi C. + GENE THERAPY - -
Accelerated cardiomyopathy in maternally inherited diabetes and deafness 2004 Zeviani, M + INTERNATIONAL JOURNAL OF CLINICAL PHARMACOLOGY RESEARCH - -
Additive effects of POLG1 and ANT1 mutations in a complex encephalomyopathy 2008 Zeviani M. + NEUROMUSCULAR DISORDERS - -
Adult-onset Alexander disease, associated with a mutation in an alternative GFAP transcript, may be phenotypically modulated by a non-neutral HDAC6 variant 2013 Liu X.Ceccherini I.D'Adamo P.Zhang J.Ghezzi D.Zeviani M. + ORPHANET JOURNAL OF RARE DISEASES - -
Adult-onset leukodystrophies from respiratory chain disorders: Do they exist? 2013 Salerno F.Zeviani M. + JOURNAL OF NEUROLOGY - -
Altered sulfide (H2S) metabolism in ethylmalonic encephalopathy 2013 Zeviani M. + COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY - -
Analysis of the trinucleotide CAG repeat from the human mitochondrial DNA polymerase gene in healthy and diseased individuals 1999 Zeviani M. + EUROPEAN JOURNAL OF HUMAN GENETICS - -
APOPT1/COA8 assists COX assembly and is oppositely regulated by UPS and ROS 2019 Viscomi C.Zeviani M. + EMBO MOLECULAR MEDICINE - -
APOPT1/COA8 assists COX assembly and is oppositely regulated by UPS and ROS 2019 Cerutti, RaffaeleViscomi, CarloFernandez-Vizarra, ErikaZeviani, Massimo + EMBO MOLECULAR MEDICINE - -
Assembly of the oxidative phosphorylation system in humans: What we have learned by studying its defects 2009 Zeviani M. + BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH - -
Assembly of the oxidative phosphorylation system in humans: what we have learned by studying its defects 2009 Fernández-Vizarra, ErikaZeviani, Massimo + BIOCHIMICA ET BIOPHYSICA ACTA - -
Ataxia in mitochondrial disorders 2012 Zeviani M. + HANDBOOK OF CLINICAL NEUROLOGY - -
ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy 2020 Tagliavini F.Carbonelli M.Maresca A.Zeviani M.Ghezzi D. + ANNALS OF NEUROLOGY - -
An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region 1989 Zeviani M.Bertini E. + NATURE - -
An autosomal locus predisposing to deletions of mitochondrial DNA 1995 Zeviani M. + NATURE GENETICS - -