Showing results (141-150 of 331) with videos related to
Sort By:
Pageof 34
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 25, 2005
Skeletal muscle gene expression profiling in mitochondrial disordersMarco Crimi, Andreina Bordoni, Giorgia Menozzi, et al.Neurobiology of Aging|November 26, 2005
Serum MCP-1 levels are increased in mild cognitive impairment and mild Alzheimer's diseaseDaniela Galimberti, Chiara Fenoglio, Carlo Lovati, et al.Neurobiology of Aging|January 10, 2006
Oxidative imbalance in patients with mild cognitive impairment and Alzheimer's diseaseIlaria Guidi, Daniela Galimberti, Silvia Lonati, et al.Journal of Child Neurology|November 6, 2004
Study of attentional processes in children with idiopathic epilepsy by Conners' Continuous Performance TestRenato Borgatti, Paolo Piccinelli, Rosario Montirosso, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|November 22, 2021
Cell-penetrating peptide-conjugated Morpholino rescues SMA in a symptomatic preclinical modelMargherita Bersani, Mafalda Rizzuti, Elisa Pagliari, et al.Cognitive and Behavioral Neurology : Official Journal of the Society for Behavioral and Cognitive Neurology|March 20, 2010
A cortically blind patient with preserved visual imageryStefano Zago, Stefania Corti, Anna Bersano, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 5, 2010
A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutationRomina Romaniello, Claudio Zucca, Alessandra Tonelli, et al.Human Molecular Genetics|July 24, 2010
Systemic transplantation of c-kit+ cells exerts a therapeutic effect in a model of amyotrophic lateral sclerosisStefania Corti, Monica Nizzardo, Martina Nardini, et al.Biochimica Et Biophysica Acta. Molecular Basis of Disease|August 5, 2018
Glucose-free/high-protein diet improves hepatomegaly and exercise intolerance in glycogen storage disease type III miceSerena Pagliarani, Sabrina Lucchiari, Gianna Ulzi, et al.Journal of the Neurological Sciences|February 19, 2010
The m.12316G>A mutation in the mitochondrial tRNA Leu(CUN) gene is associated with mitochondrial myopathy and respiratory impairmentDario Ronchi, Roberta Virgilio, Andreina Bordoni, et al.Pageof 34