Paola Da Pozzo

Redefining phenotypes associated with mitochondrial DNA single deletion

Michelangelo Mancuso, Daniele Orsucci, C. Angelini et al. · Journal of Neurology · 2015 · 100 citations

Biology, Mitochondrial Function, Natural Sciences +4

Alu-element insertion in an OPA1 intron sequence associated with autosomal dominant optic atrophy.

Gian Nicola Gallus, Elena Cardaioli, Alessandra Rufa et al. · PubMed · 2010 · 41 citations

Modulation of<i>nurr1</i>gene expression in mesencephalic dopaminergic neurones

Floriana Volpicelli, Carla Perrone‐Capano, Paola Da Pozzo et al. · Journal of Neurochemistry · 2004 · 31 citations · Full text

A novel mutation in the mitochondrial tRNAPro gene associated with late-onset ataxia, retinitis pigmentosa, deafness, leukoencephalopathy and complex I deficiency

Paola Da Pozzo, Elena Cardaioli, Edoardo Malfatti et al. · European Journal of Human Genetics · 2009 · 30 citations · Full text

Mendelian Disorder, Genetic Disorder, Retinitis Pigmentosa +9

Epigenetic cues in midbrain dopaminergic neuron development

Carla Perrone‐Capano, Paola Da Pozzo, Umberto di Porzio · Neuroscience & Biobehavioral Reviews · 2000 · 26 citations

Developmental Biology, Developmental Cognitive Neuroscience, Neuroanatomy +6