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Journal of Neurology|March 15, 2011
Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-upFrancesca Magri, Alessandra Govoni, Maria Grazia D'Angelo, et al.
Plos One|April 15, 2016
Clinical and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot StudyAndrea Martinuzzi, Domenico Montanaro, Marinela Vavla, et al.
Rejuvenation Research|May 10, 2011
Role of hnRNP-A1 and miR-590-3p in neuronal death: genetics and expression analysis in patients with Alzheimer disease and frontotemporal lobar degenerationChiara Villa, Chiara Fenoglio, Milena De Riz, et al.
American Journal of Human Genetics|January 29, 2013
Mutations in DNA2 link progressive myopathy to mitochondrial DNA instabilityDario Ronchi, Alessio Di Fonzo, Weiqiang Lin, et al.
Neurology|May 9, 2014
Lower motor neuron disease with respiratory failure caused by a novel MAPT mutationAlessio Di Fonzo, Dario Ronchi, Francesca Gallia, et al.
Archives of Neurology|May 10, 2006
Eight novel mutations in SPG4 in a large sample of patients with hereditary spastic paraplegiaFrancesca Crippa, Chris Panzeri, Andrea Martinuzzi, et al.
Biopreservation and Biobanking|May 23, 2014
Pediatric biobanking: a pilot qualitative survey of practices, rules, and researcher opinions in ten European countriesElena Salvaterra, Roberto Giorda, Maria T Bassi, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|September 27, 2018
Mitochondrial dysfunction in fibroblasts of Multiple System AtrophyGiacomo Monzio Compagnoni, Giulio Kleiner, Andreina Bordoni, et al.
Neurobiology of Aging|July 11, 2016
Mutational analysis of COQ2 in patients with MSA in ItalyDario Ronchi, Ernesto Di Biase, Giulia Franco, et al.
Eneurologicalsci|January 25, 2021
Posterior reversible encephalopathy syndrome and COVID-19: A series of 6 cases from Lombardy, ItalyAntonio Colombo, Filippo Martinelli Boneschi, Sandro Beretta, et al.
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