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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 11, 2012
Effects of cerebrolysin administration on oxidative stress-induced apoptosis in lymphocytes from CADASIL patientsPatrizia Formichi, Elena Radi, Carla Battisti, et al.Journal of Cellular Physiology|June 25, 2011
Human peripheral blood lymphocytes and fibroblasts as Notch3 expression modelsGiuseppe Di Maio, Patrizia Formichi, Elena Radi, et al.Journal of Cellular Physiology|February 5, 2020
HTRA1 expression profile and activity on TGF-β signaling in HTRA1 mutation carriersAlessandro Fasano, Patrizia Formichi, Ilaria Taglia, et al.Journal of Cellular Physiology|January 31, 2009
Apoptosis in CADASIL: an in vitro study of lymphocytes and fibroblasts from a cohort of Italian patientsPatrizia Formichi, Elena Radi, Carla Battisti, et al.Journal of Cellular Physiology|March 24, 2017
Primary cilium alterations and expression changes of Patched1 proteins in niemann-pick type C diseasePatrizia Formichi, Carla Battisti, Maria M De Santi, et al.Journal of the Neurological Sciences|August 20, 2016
Oxidative stress-induced apoptosis in peripheral blood lymphocytes from patients with POLG-related disordersPatrizia Formichi, Elena Radi, Chiara Branca, et al.Journal of Neurology|February 18, 2014
Hereditary diffuse leukoencephalopathy with axonal spheroids: three patients with stroke-like presentation carrying new mutations in the CSF1R geneCarla Battisti, Ilaria Di Donato, Silvia Bianchi, et al.Cells|February 23, 2024
Novel Biomarkers for Limb Girdle Muscular Dystrophy (LGMD)Sara Aguti, Gian Nicola Gallus, Silvia Bianchi, et al.Journal of Cellular Physiology|April 27, 2007
Psychosine-induced apoptosis and cytokine activation in immune peripheral cells of Krabbe patientsPatrizia Formichi, Elena Radi, Carla Battisti, et al.Journal of the Neurological Sciences|March 23, 2015
Analysis of opa1 isoforms expression and apoptosis regulation in autosomal dominant optic atrophy (ADOA) patients with mutations in the opa1 genePatrizia Formichi, Elena Radi, Eleonora Giorgi, et al.Pageof 3