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Neuropediatrics|September 10, 1999
Neuroaxonal dystrophy with dystonia and pallidal involvementA Simonati, C Trevisan, A Salviati, et al.Neurochemical Research|January 1, 1987
Effect of aging on the rate of axonal transport of choline-phosphoglyceridesM Brunetti, A Miscena, A Salviati, et al.The Biochemical Journal|October 24, 2000
Novel consensus sequence for the Golgi apparatus casein kinase, revealed using proline-rich protein-1 (PRP1)-derived peptide substratesA M Brunati, O Marin, A Bisinella, et al.Acta Neurologica Belgica|May 1, 1983
Amyotrophy in Shy-Drager syndromeP Montagna, P Martinelli, N Rizzuto, et al.The Journal of Physiology|December 1, 1996
Effects of long-term conduction block on membrane properties of reinnervated and normally innervated rat skeletal muscleE Pasino, M Buffelli, O Arancio, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|July 18, 2008
A case of Fabry disease with central nervous system (CNS) demyelinating lesions: a double trouble?P Invernizzi, M A Bonometti, E Turri, et al.Human Gene Therapy|October 6, 1998
Transduced fibroblasts and metachromatic leukodystrophy lymphocytes transfer arylsulfatase A to myelinating glia and deficient cells in vitroA Sangalli, C Taveggia, A Salviati, et al.Italian Journal of Neurological Sciences|October 1, 1982
BAEP and autopsy findings in Wallenberg syndromeA Amantini, G Arnetoli, L Rossi, et al.Journal of Neuroimmunology|November 7, 2000
Myelin oligodendrocyte glycoprotein (MOG) polymorphisms and adrenoleukodystrophyM Gomez-Lira, M G Marzari, G Uziel, et al.Molecular and Cellular Probes|March 17, 1998
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A geneC Perusi, M Gomez-Lira, M Mottes, et al.Pageof 3