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Heliyon|June 3, 2024
Genetic variability of <i>FOXP2</i> and its targets <i>CNTNAP2</i> and <i>PRNP</i> in frontotemporal dementia: A pilot study in a southern Italian populationPaolina Crocco, Francesco De Rango, Francesco Bruno, et al.Dementia and Geriatric Cognitive Disorders|June 24, 2004
Relation of apolipoprotein(a) size to alzheimer's disease and vascular dementiaEnzo Emanuele, Emmanouil Peros, Carmine Tomaino, et al.Plos One|October 27, 2010
Somatic point mutations in mtDNA control region are influenced by genetic background and associated with healthy aging: a GEHA studyGiuseppina Rose, Giuseppe Romeo, Serena Dato, et al.Experimental Gerontology|December 9, 2008
APOE polymorphism affects episodic memory among non demented elderly subjectsSimona De Blasi, Alberto Montesanto, Cinzia Martino, et al.Aging|November 15, 2018
Uncoupling protein 4 (<i>UCP4</i>) gene variability in neurodegenerative disorders: further evidence of association in Frontotemporal dementiaAlberto Montesanto, Paolina Crocco, Serena Dato, et al.Archives of Neurology|November 16, 2005
Circulating levels of soluble receptor for advanced glycation end products in Alzheimer disease and vascular dementiaEnzo Emanuele, Angela D'Angelo, Carmine Tomaino, et al.Journal of Alzheimer'S Disease : JAD|March 1, 2016
The Genetic Variability of UCP4 Affects the Individual Susceptibility to Late-Onset Alzheimer's Disease and Modifies the Disease's Risk in APOE-ɛ4 CarriersAlberto Montesanto, Paolina Crocco, Maria Anfossi, et al.Journal of Neurology|February 12, 2015
Influence of controlled encoding and retrieval facilitation on memory performance in patients with different profiles of mild cognitive impairmentRoberta Perri, Marco Monaco, Lucia Fadda, et al.Neuroscience Letters|March 24, 2004
Apolipoprotein(a) null phenotype is related to a delayed age at onset of Alzheimer's diseaseEnzo Emanuele, Emmanouil Peros, Carmine Tomaino, et al.Movement Disorders : Official Journal of the Movement Disorder Society|March 15, 2006
Characterization of nigrostriatal dysfunction in spinocerebellar ataxia 17Elena Salvatore, Andrea Varrone, Valeria Sansone, et al.Pageof 7