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Neuropediatrics|May 1, 1988
Cerebro-ocular dysplasia and muscular dystrophy: report of two casesA Federico, M T Dotti, A Malandrini, et al.
Brain & Development|December 29, 1998
Ultrastructural study of enteric ganglia in three patients with Rett syndromeA Malandrini, G Hayek, M Villanova, et al.
Acta Neuropathologica|December 1, 1996
An unusual type of primary cerebral hemihypotrophy with signs of dysfunctional neuronal migrationA Malandrini, F Lo Russo, M Villanova, et al.
Acta Neurologica|June 1, 1994
Primary antiphospholipid syndrome: two case reports, one with histological examination of skin, peripheral nerve and muscleM Macucci, M T Dotti, S Battistini, et al.
Genomics|March 2, 1999
Identification and characterization of a highly conserved protein absent in the Alport syndrome (A), mental retardation (M), midface hypoplasia (M), and elliptocytosis (E) contiguous gene deletion syndrome (AMME)F Vitelli, M Piccini, F Caroli, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|August 30, 2000
Visual electrophysiological responses in subjects with cerebral autosomal arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)V Parisi, F Pierelli, A Malandrini, et al.
Neurology|June 25, 2003
Early visual function impairment in CADASILV Parisi, F Pierelli, F Fattapposta, et al.
Journal of the Neurological Sciences|April 1, 1996
Autosomal dominant limb girdle myopathy with ragged-red fibers and cardiomyopathy. A pedigree study by in vivo 31P-MR spectroscopy indicating a multisystem mitochondrial defectG M Fabrizi, R Lodi, M D'Ettorre, et al.
Brain & Development|January 1, 1996
Palatal myoclonus and unusual MRI findings in a patient with membranous lipodystrophyA Malandrini, C Scarpini, S Palmeri, et al.
Journal of Submicroscopic Cytology and Pathology|July 1, 1993
Ultrastructural sperm abnormalities and cerebellar atrophy: does a correlation exist? Report of two cases without endocrine hypogonadismA Malandrini, M Villanova, P Piomboni, et al.
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