Piero Barboni

Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484.

Antonio Torroni, M. Petrozzi, Leila D'Urbano et al. · PubMed · 1997 · 417 citations

Melanopsin retinal ganglion cell loss in <scp>A</scp>lzheimer disease

Chiara La Morgia, Fred N. Ross‐Cisneros, Yosef Koronyo et al. · Annals of Neurology · 2015 · 384 citations · Full text

Efficient mitochondrial biogenesis drives incomplete penetrance in Leber’s hereditary optic neuropathy

Carla Giordano, Luisa Iommarini, Luca Giordano et al. · Brain · 2013 · 281 citations · Full text

Biology, Neurodegenerative Diseases, Molecular Neuroscience +14

Use of a Support Vector Machine for Keratoconus and Subclinical Keratoconus Detection by Topographic and Tomographic Data

María Clara Arbelaez, Francesco Versaci, Gabriele Vestri et al. · Ophthalmology · 2012 · 254 citations

Support Vector Machine, Image Analysis, Engineering +10

Retinal nerve fiber layer evaluation by optical coherence tomography in Leber's hereditary optic neuropathy

Piero Barboni, Giacomo Savini, Maria Lucia Valentino et al. · Ophthalmology · 2004 · 247 citations

Ocular Disease, Retina, Ophthalmology +7