Lorena Di Pietro

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

Erin L. Heinzen, Kathryn J. Swoboda, Yuki Hitomi et al. · Nature Genetics · 2012 · 417 citations · Full text

Rare Diseases, Mendelian Disorder, Genetic Disorder +8

Potential therapeutic targets for ALS: MIR206, MIR208b and MIR499 are modulated during disease progression in the skeletal muscle of patients

Lorena Di Pietro, Mirko Baranzini, Maria Grazia Berardinelli et al. · Scientific Reports · 2017 · 53 citations · Full text

Schizophrenia and Human Self-Domestication: An Evolutionary Linguistics Approach

Antonio Benítez‐Burraco, Lorena Di Pietro, Marta Barba et al. · Brain Behavior and Evolution · 2017 · 49 citations

Reduction and shaping of graphene-oxide by laser-printing for controlled bone tissue regeneration and bacterial killing

Valentina Palmieri, Marta Barba, Lorena Di Pietro et al. · 2D Materials · 2017 · 45 citations · Full text

Tissue Engineering, Engineering, Biomaterials Design +21

Clinical and molecular cross-sectional study of a cohort of adult type III spinal muscular atrophy patients: clues from a biomarker study

Francesco Danilo Tiziano, Rosa Lomastro, Lorena Di Pietro et al. · European Journal of Human Genetics · 2012 · 41 citations · Full text

Genetic Epidemiology, Molecular Cross-sectional Study, Biomarkers +9