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Neurobiology of Aging|November 6, 2016
A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlationsCinzia Coppola, Dario Saracino, Gianfranco Puoti, et al.
Brain Pathology (Zurich, Switzerland)|December 21, 2016
Alzheimer neuropathology without frontotemporal lobar degeneration hallmarks (TAR DNA-binding protein 43 inclusions) in missense progranulin mutation Cys139ArgVeronica Redaelli, Giacomina Rossi, Emanuela Maderna, et al.
Neurobiology of Aging|December 15, 2015
Missense mutations in progranulin gene associated with frontotemporal lobar degeneration: study of pathogenetic featuresCeleste M Karch, Lubov Ezerskiy, Veronica Redaelli, et al.
Journal of Alzheimer'S Disease : JAD|September 26, 2013
C9ORF72 hexanucleotide repeat number in frontotemporal lobar degeneration: a genotype-phenotype correlation studyLuisa Benussi, Giacomina Rossi, Michela Glionna, et al.
Neuro-Degenerative Diseases|November 30, 2011
Optimal plasma progranulin cutoff value for predicting null progranulin mutations in neurodegenerative diseases: a multicenter Italian studyRoberta Ghidoni, Elena Stoppani, Giacomina Rossi, et al.
Biochemical Pharmacology|September 1, 2011
Amiodarone impairs trafficking through late endosomes inducing a Niemann-Pick C-like phenotypeElena Piccoli, Matteo Nadai, Carla Mucignat Caretta, et al.
Frontiers in Pharmacology|December 18, 2018
Pathophysiology of NSAID-Associated Intestinal Lesions in the Rat: Luminal Bacteria and Mucosal Inflammation as Targets for PreventionRocchina Colucci, Carolina Pellegrini, Matteo Fornai, et al.
Plos One|February 25, 2012
Infectivity in skeletal muscle of cattle with atypical bovine spongiform encephalopathySilvia Suardi, Chiara Vimercati, Cristina Casalone, et al.
Neurobiology of Aging|September 11, 2013
Different mutations at V363 MAPT codon are associated with atypical clinical phenotypes and show unusual structural and functional featuresGiacomina Rossi, Antonio Bastone, Elena Piccoli, et al.
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