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Page 1
Familial progressive subcortical gliosis.
Lanska DJ, Currier RD, Cohen M, Gambetti P, Smith EE, Bebin J, Jackson JF, Whitehouse PJ, Markesbery WR. Lanska DJ, et al. Among authors: currier rd. Neurology. 1994 Sep;44(9):1633-43. doi: 10.1212/wnl.44.9.1633. Neurology. 1994. PMID: 7936288
Whether or not predictive tests?
Currier RD, Schut LJ, Jackson JF. Currier RD, et al. Neurology. 1981 Mar;31(3):362. doi: 10.1212/wnl.31.3.362. Neurology. 1981. PMID: 7193832 No abstract available.
A medullary syndrome characterized by wild arm ataxia.
Jaster JH, Smith TW, Gleckman AM, Currier RD, Bebin J. Jaster JH, et al. Among authors: currier rd. Neurology. 2000 Jul 25;55(2):321. doi: 10.1212/wnl.55.2.321. Neurology. 2000. PMID: 10908923 No abstract available.
Facioscapulohumeral dystrophy associated with multiple sclerosis.
Mishra SK, Currier RD, Smith EE, Malhotra C, Bebin J, Hudson JM. Mishra SK, et al. Among authors: currier rd. Arch Neurol. 1984 May;41(5):570-1. doi: 10.1001/archneur.1984.04050170120032. Arch Neurol. 1984. PMID: 6721727 No abstract available.
Genetic linkage and spinocerebellar ataxia.
Jackson JF, Whittington JE, Currier RD, Terasaki PI, Morton NE, Keats BJ. Jackson JF, et al. Among authors: currier rd. Adv Neurol. 1978;21:315-8. Adv Neurol. 1978. PMID: 735928 No abstract available.
Dominant spinocerebellar ataxia: genetic counseling.
Jackson JF, Currier RD, Morton NE. Jackson JF, et al. Among authors: currier rd. J Neurogenet. 1983 Sep;1(1):87-90. doi: 10.3109/01677068309107074. J Neurogenet. 1983. PMID: 6681442
89 results