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Journal of the Neurological Sciences|July 1, 1991
Neuroaxonal dystrophy in neuronal storage disorders: evidence for major GABAergic neuron involvementS U Walkley, H J Baker, M C Rattazzi, et al.The Journal of Comparative Neurology|September 29, 1999
Ferret pyramidal cell dendritogenesis: changes in morphology and ganglioside expression during cortical developmentM Zervas, S U WalkleyBrain Research|July 29, 1985
Altered patterns of evoked synaptic activity in cortical pyramidal neurons in feline ganglioside storage diseaseA B Karabelas, S U WalkleyMolecular Genetics and Metabolism|April 7, 1999
Ovine ceroid lipofuscinosis (OCL6): postulated mechanism of neurodegenerationR D Jolly, S U WalkleyBrain Research|December 17, 1984
Locoweed-induced neuronal storage disease characterized by meganeurite formationS U Walkley, L F JamesVeterinary Pathology|December 13, 1997
Lysosomal storage diseases of animals: an essay in comparative pathologyR D Jolly, S U WalkleyBrain Research. Developmental Brain Research|May 31, 1996
Elevated GM2 ganglioside is associated with dendritic proliferation in normal developing neocortexL A Goodman, S U WalkleyBrain Research|May 1, 1985
Ectopic dendritogenesis occurs on cortical pyramidal neurons in swainsonine-induced feline alpha-mannosidosisS U Walkley, D A SiegelBrain Research|September 24, 1986
Ferric ion-ferrocyanide staining in ganglioside storage disease establishes that meganeurites are of axon hillock origin and distinct from axonal spheroidsS U Walkley, A L PierokJournal of Neurochemistry|May 1, 1994
Growth of ectopic dendrites on cortical pyramidal neurons in neuronal storage diseases correlates with abnormal accumulation of GM2 gangliosideD A Siegel, S U WalkleyPageof 11