Zimmerman TR - Search Results

1

Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneity.

Piccardo P, Dlouhy SR, Lievens PM, Young K, Bird TD, Nochlin D, Dickson DW, Vinters HV, Zimmerman TR, Mackenzie IR, Kish SJ, Ang LC, De Carli C, Pocchiari M, Brown P, Gibbs CJ Jr, Gajdusek DC, Bugiani O, Ironside J, Tagliavini F, Ghetti B. Piccardo P, et al. Among authors: zimmerman tr. J Neuropathol Exp Neurol. 1998 Oct;57(10):979-88. doi: 10.1097/00005072-199810000-00010. J Neuropathol Exp Neurol. 1998. PMID: 9786248

2

Gerstmann-Sträussler-Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patients.

Young K, Jones CK, Piccardo P, Lazzarini A, Golbe LI, Zimmerman TR Jr, Dickson DW, McLachlan DC, St George-Hyslop P, Lennox A, et al. Young K, et al. Among authors: zimmerman tr jr. Neurology. 1995 Jun;45(6):1127-34. doi: 10.1212/wnl.45.6.1127. Neurology. 1995. PMID: 7783876

3

Pathology of PD in monozygotic twins with a 20-year discordance interval.

Dickson D, Farrer M, Lincoln S, Mason RP, Zimmerman TR Jr, Golbe LI, Hardy J. Dickson D, et al. Among authors: zimmerman tr jr. Neurology. 2001 Apr 10;56(7):981-2. doi: 10.1212/wnl.56.7.981. Neurology. 2001. PMID: 11294946 No abstract available.

4

Widespread alterations of alpha-synuclein in multiple system atrophy.

Dickson DW, Liu W, Hardy J, Farrer M, Mehta N, Uitti R, Mark M, Zimmerman T, Golbe L, Sage J, Sima A, D'Amato C, Albin R, Gilman S, Yen SH. Dickson DW, et al. Am J Pathol. 1999 Oct;155(4):1241-51. doi: 10.1016/s0002-9440(10)65226-1. Am J Pathol. 1999. PMID: 10514406 Free PMC article.

5

A clinical genetic study of Parkinson's disease: evidence for dominant transmission.

Lazzarini AM, Myers RH, Zimmerman TR Jr, Mark MH, Golbe LI, Sage JI, Johnson WG, Duvoisin RC. Lazzarini AM, et al. Among authors: zimmerman tr jr. Neurology. 1994 Mar;44(3 Pt 1):499-506. doi: 10.1212/wnl.44.3_part_1.499. Neurology. 1994. PMID: 8145922

6

A 17th-century founder gives rise to a large north American pedigree of autosomal dominant spinocerebellar ataxia not linked to the SCA1 locus on chromosome 6.

Lazzarini A, Zimmerman TR Jr, Johnson WG, Duvoisin RC. Lazzarini A, et al. Among authors: zimmerman tr jr. Neurology. 1992 Nov;42(11):2118-24. doi: 10.1212/wnl.42.11.2118. Neurology. 1992. PMID: 1436521

7

Follow-up study of risk factors in progressive supranuclear palsy.

Golbe LI, Rubin RS, Cody RP, Belsh JM, Duvoisin RC, Grosmann C, Lepore FE, Mark MH, Sachdeo RC, Sage JI, Zimmerman TR Jr. Golbe LI, et al. Among authors: zimmerman tr jr. Neurology. 1996 Jul;47(1):148-54. doi: 10.1212/wnl.47.1.148. Neurology. 1996. PMID: 8710069

8

Parkinson's disease in twins studied with 18F-dopa and positron emission tomography.

Burn DJ, Mark MH, Playford ED, Maraganore DM, Zimmerman TR Jr, Duvoisin RC, Harding AE, Marsden CD, Brooks DJ. Burn DJ, et al. Among authors: zimmerman tr jr. Neurology. 1992 Oct;42(10):1894-900. doi: 10.1212/wnl.42.10.1894. Neurology. 1992. PMID: 1407569

9

Comparison of combination pergolide and levodopa to levodopa alone after 63 months of treatment.

Zimmerman T, Sage JI. Zimmerman T, et al. Clin Neuropharmacol. 1991 Apr;14(2):165-9. doi: 10.1097/00002826-199104000-00006. Clin Neuropharmacol. 1991. PMID: 2015613

10

Ten years' experience with enteral levodopa infusions for motor fluctuations in Parkinson's disease.

Syed N, Murphy J, Zimmerman T Jr, Mark MH, Sage JI. Syed N, et al. Mov Disord. 1998 Mar;13(2):336-8. doi: 10.1002/mds.870130222. Mov Disord. 1998. PMID: 9539350

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