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Nature Genetics|September 1, 1993
Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 geneK Hayasaka, M Himoro, W Sato, et al.The American Journal of Pathology|February 1, 1997
Beta-amyloid protein-containing inclusions in skeletal muscle of apolipoprotein-E-deficient miceT A Robertson, N S Dutton, R N Martins, et al.Annals of Neurology|April 1, 1994
Novel amyloid precursor protein gene mutation (codon 665Asp) in a patient with late-onset Alzheimer's diseaseM L Peacock, D L Murman, A A Sima, et al.Archives of Neurology|August 1, 1991
Diagnostic criteria for multiple sclerosis research involving multiply affected familiesD E Goodkin, T H Doolittle, S S Hauser, et al.Journal of Neuroscience Research|December 1, 1990
Isolation and localization of a slow troponin (TnT) gene on chromosome 19 by subtraction hybridization of a cDNA muscle library using myotonic dystrophy muscle cDNAF Samson, J E Lee, W Y Hung, et al.Neurology|May 12, 2004
Genes influencing Parkinson disease onset: replication of PARK3 and identification of novel lociN Pankratz, S K Uniacke, C A Halter, et al.Annals of Neurology|May 1, 1995
Cognitive scores in carriers of Huntington's disease gene compared to noncarriersT Foroud, E Siemers, D Kleindorfer, et al.Neuroscience|December 13, 2000
Susceptibility of transgenic mice expressing human apolipoprotein E to closed head injury: the allele E3 is neuroprotective whereas E4 increases fatalitiesT Sabo, L Lomnitski, A Nyska, et al.The Journal of Clinical Investigation|May 1, 1995
Modulation of skeletal muscle sodium channels by human myotonin protein kinaseJ P Mounsey, P Xu, J E John, et al.American Journal of Medical Genetics|January 1, 1980
Evidence of genetic variation for alpha-N-acetyl-D-glucosaminidase in black and white populations: a new polymorphismJ M Vance, M A Pericak-Vance, R C Elston, et al.Pageof 37