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Brain : a Journal of Neurology|December 1, 1985
Clinical and neuropathological criteria for the diagnosis and staging of diabetic polyneuropathyP J Dyck, J L Karnes, J Daube, et al.Mayo Clinic Proceedings|July 1, 1983
Linkage evidence for genetic heterogeneity among kinships with hereditary motor and sensory neuropathy, type IP J Dyck, J Ott, S B Moore, et al.Journal of Child Psychology and Psychiatry, and Allied Disciplines|July 1, 2004
Is the discrepancy criterion for defining developmental disorders valid?Murray J Dyck, David Hay, Mike Anderson, et al.American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|July 25, 2008
Decreasing intramuscular phosphagen content simultaneously increases plasma membrane FAT/CD36 and GLUT4 transporter abundanceKristin E Pandke, Kerry L Mullen, Laelie A Snook, et al.Archives of Neurology|May 18, 2000
Hereditary motor and sensory neuropathy type 2C is genetically distinct from types 2B and 2DM Nagamatsu, R B Jenkins, D J Schaid, et al.Mayo Clinic Proceedings|September 1, 1983
Evaluation of skin vasomotor reflexes by using laser Doppler velocimetryP A Low, C Neumann, P J Dyck, et al.Journal of Neuropathology and Experimental Neurology|March 1, 1986
Axonal caliber and neurofilaments are proportionately decreased in galactose neuropathyH Nukada, P J Dyck, P A Low, et al.Nursing Forum|June 27, 2018
Social capital, health, health behavior, and utilization of healthcare services among older adults: A conceptual frameworkSheryl A Emmering, Kim Schafer Astroth, Wendy M Woith, et al.Metabolism Open|March 28, 2022
The effects of diet and chronic exercise on skeletal muscle ghrelin responseAndrew J Lovell, Evan M Hoecht, Barbora Hucik, et al.Advances in Experimental Medicine and Biology|January 1, 1985
Diabetic neuropathyP J Dyck, A Windebank, H Yasuda, et al.Pageof 56