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Neurobiology of Aging|April 10, 2007
Association of a NOS1 promoter repeat with Alzheimer's diseaseDaniela Galimberti, Elio Scarpini, Eliana Venturelli, et al.Biochimica Et Biophysica Acta|August 6, 2014
Glycogen storage disease type III: A novel Agl knockout mouse modelSerena Pagliarani, Sabrina Lucchiari, Gianna Ulzi, et al.Journal of Child Neurology|July 28, 2009
Muscular dystrophy: central nervous system alpha-dystroglycan glycosylation defects and brain malformationGigliola Fagiolari, Anna Cappellini, Rachele Cagliani, et al.Frontiers in Neurology|August 29, 2019
Ophthalmoplegia Due to Miller Fisher Syndrome in a Patient With Myasthenia GravisRoberta Brusa, Irene Faravelli, Delia Gagliardi, et al.Brain : a Journal of Neurology|May 4, 2006
The first ALS2 missense mutation associated with JPLS reveals new aspects of alsin biological functionChris Panzeri, Clara De Palma, Andrea Martinuzzi, et al.Plos One|May 22, 2008
Correlation of circulating CD133+ progenitor subclasses with a mild phenotype in Duchenne muscular dystrophy patientsChiara Marchesi, Marzia Belicchi, Mirella Meregalli, et al.Pediatric Neurology|October 18, 2011
Neurocognitive profiles in Duchenne muscular dystrophy and gene mutation siteMaria Grazia D'Angelo, Maria Luisa Lorusso, Federica Civati, et al.Brain & Development|November 5, 2013
Novel SETX variants in a patient with ataxia, neuropathy, and oculomotor apraxia are associated with normal sensitivity to oxidative DNA damaging agentsChiara Vantaggiato, Orazio Cantoni, Andrea Guidarelli, et al.Biomaterials|April 20, 2010
Ex vivo expansion of human circulating myogenic progenitors on cluster-assembled nanostructured TiO2Marzia Belicchi, Silvia Erratico, Paola Razini, et al.Pediatric Research|February 7, 2004
A new mitochondrial DNA mutation in ND3 gene causing severe Leigh syndrome with early lethalityMarco Crimi, Alexandros Papadimitriou, Sara Galbiati, et al.Pageof 34