Showing results (11-20 of 102) with videos related to

Sort By:
Pageof 11
Journal of the Neurological Sciences|July 1, 1992
Imipramine induced lipidosis and dexamethasone effect: morphological and biochemical study in normal and chronic GM2 gangliosidosis fibroblastsS Palmeri, L Mangano, C Battisti, et al.
European Journal of Ophthalmology|December 1, 2007
Air-guided manual deep anterior lamellar keratoplasty: long-term results and confocal microscopic findingsA Balestrazzi, A Malandrini, C Traversi, et al.
Brain & Development|March 1, 1994
Association of myopathy with multiple exostoses and mental retardation: a case reportN De Stefano, M T Dotti, A Malandrini, et al.
Neuromuscular Disorders : NMD|July 17, 1999
Decreased expression of laminin beta 1 in chromosome 21-linked Bethlem myopathyL Merlini, M Villanova, P Sabatelli, et al.
Brain & Development|July 1, 1993
Mental retardation with marfanoid syndrome: presentation of a family with different phenotypical expressionM T Dotti, A Malandrini, S Bartolini, et al.
Acta Neurologica|April 1, 1993
Sensory-motor hereditary neuropathy with early onset. A case reportA Malandrini, N De Stefano, M T Dotti, et al.
Acta Neurologica Scandinavica|August 1, 1993
Axonal motor and sensory neuropathy in myotonic dystrophyM Mondelli, A Rossi, A Malandrini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 30, 2005
Typical pathological changes of CADASIL in the optic nerveA Rufa, A Malandrini, M T Dotti, et al.
Developmental Neuroscience|January 1, 1991
The clinical aspects of adult hexosaminidase deficienciesA Federico, S Palmeri, A Malandrini, et al.
Brain & Development|July 1, 1995
Myopathic involvement in two cases of Hallervorden-Spatz diseaseA Malandrini, U Bonuccelli, E Parrotta, et al.
Pageof 11