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Methods in Enzymology|October 25, 2024
Subcellular fractionation by differential centrifugation for mitochondrial studiesConny Steiert, Jon V Busto, Laura Melchionda, et al.
EMBO Molecular Medicine|September 8, 2018
Mutations in <i>TIMM50</i> compromise cell survival in OxPhos-dependent metabolic conditionsAurelio Reyes, Laura Melchionda, Alberto Burlina, et al.
Biomed Research International|August 29, 2013
Rotenone upregulates alpha-synuclein and myocyte enhancer factor 2D independently from lysosomal degradation inhibitionGessica Sala, Alessandro Arosio, Giovanni Stefanoni, et al.
Frontiers in Genetics|December 3, 2014
A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesionsLaura Melchionda, Nadirah S Damseh, Bassam Y Abu Libdeh, et al.
Brain Research|December 24, 2013
Reduced expression of the chaperone-mediated autophagy carrier hsc70 protein in lymphomonocytes of patients with Parkinson's diseaseGessica Sala, Giovanni Stefanoni, Alessandro Arosio, et al.
JIMD Reports|March 17, 2015
Mitochondrial Complex III Deficiency Caused by TTC19 Defects: Report of a Novel Mutation and Review of LiteratureAnna Ardissone, Tiziana Granata, Andrea Legati, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|September 16, 2011
A panel of macroautophagy markers in lymphomonocytes of patients with amyotrophic lateral sclerosisGessica Sala, Lucio Tremolizzo, Laura Melchionda, et al.
Neurology|September 13, 2013
SURF1 deficiency causes demyelinating Charcot-Marie-Tooth diseaseAndoni Echaniz-Laguna, Daniele Ghezzi, Maïté Chassagne, et al.
American Journal of Human Genetics|May 22, 2012
Mutations of the mitochondrial-tRNA modifier MTO1 cause hypertrophic cardiomyopathy and lactic acidosisDaniele Ghezzi, Enrico Baruffini, Tobias B Haack, et al.
American Journal of Human Genetics|June 23, 2015
RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial EncephalomyopathyAurelio Reyes, Laura Melchionda, Alessia Nasca, et al.
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