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Archives of Neurology|April 17, 2008
Cryptogenic epileptic syndromes related to SCN1A: twelve novel mutations identifiedClaudio Zucca, Francesca Redaelli, Roberta Epifanio, et al.Neurobiology of Aging|July 28, 2009
No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohortRoberto Del Bo, Stefania Corti, Domenico Santoro, et al.Journal of Alzheimer'S Disease : JAD|September 6, 2011
Cerebrospinal fluid biomarkers in Progranulin mutations carriersMiryam Carecchio, Chiara Fenoglio, Francesca Cortini, et al.Human Mutation|February 20, 2013
Long-standing balancing selection in the THBS4 gene: influence on sex-specific brain expression and gray matter volumes in Alzheimer diseaseRachele Cagliani, Franca R Guerini, Raquel Rubio-Acero, et al.Neuroscience Letters|July 31, 2010
Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration?Eliana Venturelli, Chiara Villa, Chiara Fenoglio, et al.Journal of Alzheimer'S Disease : JAD|January 12, 2010
FUS/TLS genetic variability in sporadic frontotemporal lobar degenerationClaudia Cantoni, Chiara Fenoglio, Francesca Cortini, et al.Journal of Alzheimer'S Disease : JAD|July 24, 2009
Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's diseaseChiara Fenoglio, Daniela Galimberti, Francesca Cortini, et al.Human Mutation|January 18, 2008
A clinical, genetic, and biochemical characterization of SPG7 mutations in a large cohort of patients with hereditary spastic paraplegiaAlessia Arnoldi, Alessandra Tonelli, Francesca Crippa, et al.Parkinsonism & Related Disorders|April 8, 2020
SLC25A46 mutations in patients with Parkinson's Disease and optic atrophyGiacomo Bitetto, Maria Chiara Malaguti, Roberto Ceravolo, et al.Journal of Alzheimer'S Disease : JAD|May 23, 2012
Genetics and expression analysis of the specificity protein 4 gene (SP4) in patients with Alzheimer's disease and frontotemporal lobar degenerationChiara Villa, Laura Ghezzi, Chiara Fenoglio, et al.Pageof 34