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Neuromuscular Disorders : NMD|May 1, 1996
Muscular dystrophy, mental retardation and cardiomyopathy not associated with dystrophin deficiencyM Villanova, A Malandrini, R Biancotti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 26, 2012
Peripheral neuropathy in late-onset Krabbe disease: report of three casesA Malandrini, C D'Eramo, S Palmeri, et al.
Journal of Submicroscopic Cytology and Pathology|December 16, 1998
Association in the same patient of autosomal dominant progressive external ophthalmoplegia with multiple mtDNA deletions and X-linked ichthyosis: clinical, biochemical, histological, submicroscopic and molecular genetic studyA Federico, M T Dotti, E Cardaioli, et al.
Journal of the Neurological Sciences|September 1, 1996
Acanthocytosis, retinitis pigmentosa, pallidal degeneration. Report of two cases without serum lipid abnormalitiesA Malandrini, S Cesaretti, M Mulinari, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 9, 2005
Lung involvement in Niemann-Pick disease type C1: improvement with bronchoalveolar lavageS Palmeri, P Tarugi, F Sicurelli, et al.
Neurology|August 28, 2002
Asymptomatic cores and paracrystalline mitochondrial inclusions in CADASILA Malandrini, F Albani, S Palmeri, et al.
European Neurology|February 25, 2000
Type I sialidosis: a clinical, biochemical and neuroradiological studyS Palmeri, M Villanova, A Malandrini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 24, 2006
Leukoencephalopathy as a rare complication of hepatitis C infectionR Buccoliero, S Gambelli, F Sicurelli, et al.
Acta Neuropathologica|July 21, 1999
Detection of beta-A4 amyloid and its precursor protein in the muscle of a patient with juvenile neuronal ceroid lipofuscinosis (Spielmeyer-Vogt-Sjögren)M Villanova, C Ceuterick, M T Dotti, et al.
Journal of the Neurological Sciences|July 8, 2008
Chronic progressive external ophthalmoplegia: a new heteroplasmic tRNA(Leu(CUN)) mutation of mitochondrial DNAE Cardaioli, P Da Pozzo, E Malfatti, et al.
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