Showing results (71-80 of 102) with videos related to

Sort By:
Pageof 11
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.
Neurology|July 26, 2006
Peripheral neuropathy in vanishing white matter disease with a novel EIF2B5 mutationA Federico, O Scali, M L Stromillo, 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