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Journal of Neurology|March 12, 2010
Brain involvement in myotonic dystrophies: neuroimaging and neuropsychological comparative study in DM1 and DM2Vincenzo Romeo, E Pegoraro, C Ferrati, et al.Neurology|July 23, 1998
Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patientsE Pegoraro, H Marks, C A Garcia, et al.Neurology|March 23, 2007
Phenotypic clustering of lamin A/C mutations in neuromuscular patientsS Benedetti, I Menditto, M Degano, et al.Neuromuscular Disorders : NMD|June 3, 2008
POMT1 and POMT2 mutations in CMD patients: a multicentric Italian studyS Messina, M Mora, E Pegoraro, et al.Neurology|September 8, 2010
Congenital muscular dystrophies with cognitive impairment. A population studyS Messina, C Bruno, I Moroni, et al.Neurology|March 21, 2009
Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population studyE Mercuri, S Messina, C Bruno, et al.Pageof 4