Purificación Gutiérrez Ríos

Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions

Dario Ronchi, Caterina Garone, Andrea Bordoni et al. · Brain · 2012 · 97 citations · Full text

Mitochondrial Myopathy, Mendelian Disorder, Mitochondrial Function +14

Progressive External Ophthalmoplegia and Vision and Hearing Loss in a Patient With Mutations in POLG2 and OPA1

Silvio Ferraris, Susanna Clark, Emanuela Garelli et al. · Archives of Neurology · 2008 · 56 citations · Full text

A Novel Mutation in the Mitochondrial DNA Cytochrome <i>b</i> Gene (<i>MTCYB) </i> in a Patient With Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes Syndrome

Valentina Emmanuele, Evangelia Sotiriou, Purificación Gutiérrez Ríos et al. · Journal of Child Neurology · 2012 · 47 citations

<i>TK2</i> mutation presenting as indolent myopathy

Carmen Paradas, Purificación Gutiérrez Ríos, Eloy Rivas et al. · Neurology · 2013 · 30 citations · Full text

Mitochondrial Myopathy, Indolent Myopathy, Mtdna Depletion +12