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Brain, Behavior, and Immunity|December 3, 2014
Global changes in DNA methylation in Alzheimer's disease peripheral blood mononuclear cellsAndrea Di Francesco, Beatrice Arosio, Anastasia Falconi, et al.
Optometry and Vision Science : Official Publication of the American Academy of Optometry|June 14, 2014
Changes in macular function after ozurdex for retinal vein occlusionGiuseppe Querques, Maria Lucia Cascavilla, Edoardo Cavallero, et al.
EJNMMI Research|August 31, 2018
The kinetics of 18F-FDG in lung cancer: compartmental models and voxel analysisErica Silvestri, Valentina Scolozzi, Gaia Rizzo, et al.
Materials (Basel, Switzerland)|December 9, 2023
Recent Advances in the Use of Green Corrosion Inhibitors to Prevent Chloride-Induced Corrosion in Reinforced ConcreteLuca Casanova, Federica Ceriani, Elena Messinese, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
Cystic fibrosis presenting as metabolic alkalosis in a boy with the rare D579G mutationDonatello Salvatore, Rossella Tomaiuolo, Rosaria Abate, et al.
The Journal of Biological Chemistry|April 29, 2005
A novel peroxisome proliferator-activated receptor gamma isoform with dominant negative activity generated by alternative splicingLina Sabatino, Amelia Casamassimi, Gianfranco Peluso, et al.
The Journal of Surgical Research|May 3, 2006
Isolation of mesenchymal stem cells from human vermiform appendixPaolo De Coppi, Michela Pozzobon, Martina Piccoli, et al.
Mutation Research. Genetic Toxicology and Environmental Mutagenesis|October 8, 2017
No evidence of DNA damage by co-exposure to extremely low frequency magnetic fields and aluminum on neuroblastoma cell linesMilena Villarini, Angela Gambelunghe, Daniela Giustarini, et al.
Plos One|February 12, 2014
The neurogenic effects of exogenous neuropeptide Y: early molecular events and long-lasting effects in the hippocampus of trimethyltin-treated ratsValentina Corvino, Elisa Marchese, Maria Vittoria Podda, et al.
American Journal of Medical Genetics. Part A|February 5, 2003
X-linked recessive chondrodysplasia punctata: spectrum of arylsulfatase E gene mutations and expanded clinical variabilityNicola Brunetti-Pierri, Maria Vittoria Andreucci, Rosaria Tuzzi, et al.
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