Lorella Valletta

Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism–dystonia

Karin Tuschl, Esther Meyer, Leonardo E. Valdivia et al. · Nature Communications · 2016 · 312 citations · Full text

Exome Sequence Reveals Mutations in CoA Synthase as a Cause of Neurodegeneration with Brain Iron Accumulation

Sabrina Dusi, Lorella Valletta, Tobias B. Haack et al. · The American Journal of Human Genetics · 2013 · 200 citations · Full text

Methylation of <i>O</i>6-Methylguanine DNA Methyltransferase and Loss of Heterozygosity on 19q and/or 17p Are Overlapping Features of Secondary Glioblastomas with Prolonged Survival

Marica Eoli, Francesca Menghi, Maria Grazia Bruzzone et al. · Clinical Cancer Research · 2007 · 159 citations

Mutations of <i>ANT1</i> , <i>Twinkle</i> , and <i>POLG1</i> in sporadic progressive external ophthalmoplegia (PEO)

A. Agostino, Lorella Valletta, Patrick F. Chinnery et al. · Neurology · 2003 · 152 citations

Biology, Ocular Disease, Mendelian Disorder +13

Effective immuno-targeting of the IDH1 mutation R132H in a murine model of intracranial glioma

Serena Pellegatta, Lorella Valletta, Cristina Corbetta et al. · Acta Neuropathologica Communications · 2015 · 117 citations · Full text