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Archives of Neurology|October 1, 1994
A molecular genetic study of intracerebral hemorrhageC Graffagnino, M H Herbstreith, A D Roses, et al.Archives of Neurology|August 1, 1975
Phenytoin and membrane fluidity in myotonic dystrophyA D Roses, A Butterfield, S H Appel, et al.American Journal of Medical Genetics|January 1, 1983
Age-of-onset heterogeneity in Huntington disease familiesM A Pericak-Vance, R C Elston, P M Conneally, et al.Annals of the New York Academy of Sciences|June 21, 1993
Nicotinic neuronal acetylcholine receptor alpha-3 subunit transcription in normal and myasthenic thymusM Mihovilovic, C Hulette, J Mittelstaedt, et al.Neurology|January 1, 1988
Clinical and genetic investigation in autosomal dominant limb-girdle muscular dystrophyJ M Gilchrist, M Pericak-Vance, L Silverman, et al.Circulation|December 1, 1979
The natural history of conduction system disease in myotonic muscular dystrophy as determined by serial electrophysiologic studiesE N Prystowsky, E L Pritchett, A D Roses, et al.Neurobiology of Disease|December 22, 1999
Apolipoprotein E expression by neurons surviving excitotoxic stressU Boschert, E Merlo-Pich, G Higgins, et al.Proceedings of the National Academy of Sciences of the United States of America|March 1, 1974
Electron spin resonance studies of erythrocytes from patients with myotonic muscular dystrophyD A Butterfield, D B Chesnut, A D Roses, et al.Neurobiology of Disease|December 16, 1998
Uptake and internalization of exogenous apolipoprotein E3 by cultured human central nervous system neuronsK R Williams, A M Saunders, A D Roses, et al.Proceedings of the National Academy of Sciences of the United States of America|December 1, 1989
Pelizaeus-Merzbacher disease: tight linkage to proteolipid protein gene exon variantJ A Trofatter, S R Dlouhy, W DeMyer, et al.Pageof 37