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Brain & Development|October 7, 1998
Neuronal intranuclear inclusion disease: neuropathologic study of a caseA Malandrini, M Villanova, S Tripodi, et al.Clinical Genetics|June 6, 2003
Neurological presentation of Ehlers-Danlos syndrome type IV in a family with parental mosaicismS Palmeri, F Mari, I Meloni, et al.Journal of Neurology, Neurosurgery, and Psychiatry|May 18, 2004
DNA end labelling (TUNEL) in a 3 year old girl with Leigh syndrome and prevalent cortical involvementP Formichi, A Malandrini, C Battisti, et al.Journal of Submicroscopic Cytology and Pathology|July 1, 1997
Immunolocalization of several laminin chains in the normal human central and peripheral nervous systemM Villanova, C Sewry, A Malandrini, et al.Clinical Genetics|September 13, 2001
PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardationA Malandrini, F Mari, S Palmeri, et al.Journal of the Neurological Sciences|June 1, 1994
Atypical McLeod syndrome manifested as X-linked chorea-acanthocytosis, neuromyopathy and dilated cardiomyopathy: report of a familyA Malandrini, G M Fabrizi, F Truschi, et al.Journal of the Neurological Sciences|April 30, 1998
Juvenile Leigh syndrome with protracted course presenting as chronic sensory motor neuropathy, ataxia, deafness and retinitis pigmentosa: a clinicopathological reportA Malandrini, S Palmeri, G M Fabrizi, et al.Neurology|July 26, 2006
Peripheral neuropathy in vanishing white matter disease with a novel EIF2B5 mutationA Federico, O Scali, M L Stromillo, et al.Neurology|May 1, 1997
Unusual clinical features and early brain MRI lesions in a family with cerebral autosomal dominant arteriopathyA Malandrini, P Carrera, G Ciacci, et al.The Journal of Rheumatology|May 17, 2000
Autonomic nervous system and smooth muscle cell involvement in systemic sclerosis: ultrastructural study of 3 casesA Malandrini, E Selvi, M Villanova, et al.Pageof 11