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Neuroepidemiology|January 1, 1996
Motor neuron disease in the Padua district of Italy: an epidemiological studyC Briani, M Marcon, M Dam, et al.Neuromuscular Disorders : NMD|July 1, 1994
Clinical-molecular correlation in 104 mild X-linked muscular dystrophy patients: characterization of sub-clinical phenotypesC Angelini, M Fanin, E Pegoraro, et al.The Journal of Clinical Investigation|April 1, 1997
RNA metabolism in myotonic dystrophy: patient muscle shows decreased insulin receptor RNA and protein consistent with abnormal insulin resistanceA Morrone, E Pegoraro, C Angelini, et al.Muscle & Nerve|April 1, 1994
Deflazacort in Duchenne dystrophy: study of long-term effectC Angelini, E Pegoraro, E Turella, et al.Muscle & Nerve|September 1, 1996
Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: threshold effect for deletion size?M Fanin, M P Freda, L Vitiello, et al.Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|October 12, 2005
Secular trends in nosocomial candidaemia in non-neutropenic patients in an Italian tertiary hospitalR Luzzati, B Allegranzi, L Antozzi, et al.American Journal of Human Genetics|July 1, 1997
Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28E Pegoraro, J Whitaker, P Mowery-Rushton, et al.Journal of the Neurological Sciences|December 24, 2008
Emotional Lability in MND: Relationship to cognition and psychopathology and impact on caregiversA Palmieri, S Abrahams, G Sorarù, et al.Neuropediatrics|June 1, 1995
An X:autosome translocation stabilizes truncated dystrophin: implications for lack of truncated dystrophins in Duchenne muscular dystrophyA Fidzianska, A Morrone, E Pegoraro, et al.Neurology|April 22, 2009
Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypesM Fanin, A C Nascimbeni, S Aurino, et al.Pageof 8