Manuela Grazina

Mitochondrial dysfunction in autism spectrum disorders: a population-based study

Guiomar Oliveira, Luísa Diogo, Manuela Grazina et al. · Developmental Medicine & Child Neurology · 2005 · 269 citations

Neurodevelopmental Disorders, Nutrition, Typical Autism +13

Brief Report: High Frequency of Biochemical Markers for Mitochondrial Dysfunction in Autism: No Association with the Mitochondrial Aspartate/Glutamate Carrier SLC25A12 Gene

Catarina Correia, Ana M. Coutinho, Luísa Diogo et al. · Journal of Autism and Developmental Disorders · 2006 · 113 citations

Biochemical Markers, Molecular Neuroscience, Mitochondrial Function +8

Mitochondrial metabolism in Parkinson's disease impairs quality control autophagy by hampering microtubule-dependent traffic

Daniela M. Arduíno, A. Raquel Esteves, Luísa Cortes et al. · Human Molecular Genetics · 2012 · 83 citations · Full text

Mitophagy, Molecular Biology, Cytoskeleton +26

Secondary coenzyme Q 10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disorders

Dèlia Yubero, Raquel Montero, Miguel A. Martı́n et al. · Mitochondrion · 2016 · 77 citations

Biochemistry, Natural Sciences, Inherited Metabolic Disease +8

High frequency and founder effect of the CYP3A4*20 loss-of-function allele in the Spanish population classifies CYP3A4 as a polymorphic enzyme

María Apellániz-Ruiz, Lucía Inglada‐Pérez, M.E.G. Naranjo et al. · The Pharmacogenomics Journal · 2014 · 65 citations · Full text

Biology, Allelic Variant, Genetics +8