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Neurology|July 4, 2008
Natural history of young-adult amyotrophic lateral sclerosisM Sabatelli, F Madia, A Conte, et al.Journal of the Neurological Sciences|August 16, 2011
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlationA Del Grande, A Conte, S Lattante, et al.Journal of the Neurological Sciences|September 28, 2010
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotypeM Luigetti, G M Fabrizi, F Madia, et al.Journal of the Neurological Sciences|January 7, 2010
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiencyM Luigetti, A Pizzuti, S Bartoletti, et al.Journal of the Neurological Sciences|February 13, 2010
Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemiaM Luigetti, G Frisullo, L Laurenti, et al.Neurology|October 13, 2006
Cryptic chromosome deletions involving SCN1A in severe myoclonic epilepsy of infancyF Madia, P Striano, E Gennaro, et al.Neuromuscular Disorders : NMD|June 14, 2002
Peripheral neuropathy with hypomyelinating features in adult-onset Krabbe's diseaseM Sabatelli, L Quaranta, F Madia, et al.European Review for Medical and Pharmacological Sciences|April 30, 2021
SARS-CoV-2 was already circulating in Italy, in early December 2019L Gragnani, M Monti, S A Santini, et al.American Journal of Human Genetics|April 28, 2001
Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneityM Malacarne, E Gennaro, F Madia, et al.Neurology|June 25, 2003
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancyR Nabbout, E Gennaro, B Dalla Bernardina, et al.Pageof 3