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Neurology|August 1, 1992
Striatal monoamine neurotransmitters and metabolites in dominantly inherited olivopontocerebellar atrophyS J Kish, Y Robitaille, M el-Awar, et al.Neurology|April 1, 1991
Very mild Alzheimer's disease: informant-based clinical, psychometric, and pathologic distinction from normal agingJ C Morris, D W McKeel, M Storandt, et al.Medical Hypotheses|December 21, 2004
Can a herpes simplex virus type 1 neuroinvasive score be correlated to other risk factors in Alzheimer's disease?J M Hill, B M Gebhardt, A M Azcuy, et al.Clinical Science (London, England : 1979)|March 14, 1998
Relationship of serum leptin to total and truncal body fatM S Solin, M J Ball, I Robertson, et al.Atherosclerosis|April 1, 1991
Variation at the apo AI/CIII/AIV gene complex is associated with elevated plasma levels of apo CIIIC C Shoulders, P J Harry, L Lagrost, et al.Journal of Internal Medicine|June 16, 2010
A prospective randomized, controlled trial of intravenous versus oral iron for moderate iron deficiency anaemia of pregnancyA Khalafallah, A Dennis, J Bates, et al.The Journal of Biological Chemistry|February 23, 1996
Water-soluble Abeta (N-40, N-42) oligomers in normal and Alzheimer disease brainsY M Kuo, M R Emmerling, C Vigo-Pelfrey, et al.American Journal of Human Genetics|September 1, 1993
Chromosome 14 and late-onset familial Alzheimer disease (FAD)G D Schellenberg, H Payami, E M Wijsman, et al.European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|November 7, 2016
Adhesion of Escherichia coli under flow conditions reveals potential novel effects of FimH mutationsT Feenstra, M S Thøgersen, E Wieser, et al.American Journal of Human Genetics|September 1, 1991
APP717, APP693, and PRIP gene mutations are rare in Alzheimer diseaseG D Schellenberg, L Anderson, S O'dahl, et al.Pageof 19