Dickson DW - Search Results

1

A family with Parkinsonism, essential tremor, restless legs syndrome, and depression.

Puschmann A, Pfeiffer RF, Stoessl AJ, Kuriakose R, Lash JL, Searcy JA, Strongosky AJ, Vilariño-Güell C, Farrer MJ, Ross OA, Dickson DW, Wszolek ZK. Puschmann A, et al. Among authors: dickson dw. Neurology. 2011 May 10;76(19):1623-30. doi: 10.1212/WNL.0b013e318219fb42. Neurology. 2011. PMID: 21555728 Free PMC article.

2

Autosomal dominant parkinsonism with benign course and typical Lewy-body pathology.

Golbe LI, Lazzarini AM, Schwarz KO, Mark MH, Dickson DW, Duvoisin RC. Golbe LI, et al. Among authors: dickson dw. Neurology. 1993 Nov;43(11):2222-7. doi: 10.1212/wnl.43.11.2222. Neurology. 1993. PMID: 8232933 Review.

3

Pathologic heterogeneity in clinically diagnosed corticobasal degeneration.

Boeve BF, Maraganore DM, Parisi JE, Ahlskog JE, Graff-Radford N, Caselli RJ, Dickson DW, Kokmen E, Petersen RC. Boeve BF, et al. Among authors: dickson dw. Neurology. 1999 Sep 11;53(4):795-800. doi: 10.1212/wnl.53.4.795. Neurology. 1999. PMID: 10489043

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

Distinctive neuropathology revealed by alpha-synuclein antibodies in hereditary parkinsonism and dementia linked to chromosome 4p.

Gwinn-Hardy K, Mehta ND, Farrer M, Maraganore D, Muenter M, Yen SH, Hardy J, Dickson DW. Gwinn-Hardy K, et al. Among authors: dickson dw. Acta Neuropathol. 2000 Jun;99(6):663-72. doi: 10.1007/s004010051177. Acta Neuropathol. 2000. PMID: 10867800

6

Cockayne syndrome and xeroderma pigmentosum.

Rapin I, Lindenbaum Y, Dickson DW, Kraemer KH, Robbins JH. Rapin I, et al. Among authors: dickson dw. Neurology. 2000 Nov 28;55(10):1442-9. doi: 10.1212/wnl.55.10.1442. Neurology. 2000. PMID: 11185579 Free PMC article. Review.

7

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. Neurology. 2001 Apr 10;56(7):981-2. doi: 10.1212/wnl.56.7.981. Neurology. 2001. PMID: 11294946 No abstract available.

8

Lack of nigral pathology in transgenic mice expressing human alpha-synuclein driven by the tyrosine hydroxylase promoter.

Matsuoka Y, Vila M, Lincoln S, McCormack A, Picciano M, LaFrancois J, Yu X, Dickson D, Langston WJ, McGowan E, Farrer M, Hardy J, Duff K, Przedborski S, Di Monte DA. Matsuoka Y, et al. Neurobiol Dis. 2001 Jun;8(3):535-9. doi: 10.1006/nbdi.2001.0392. Neurobiol Dis. 2001. PMID: 11442360

9

Progressive supranuclear palsy as a disease phenotype caused by the S305S tau gene mutation.

Wszolek ZK, Tsuboi Y, Uitti RJ, Reed L, Hutton ML, Dickson DW. Wszolek ZK, et al. Among authors: dickson dw. Brain. 2001 Aug;124(Pt 8):1666-70. doi: 10.1093/brain/124.8.1666. Brain. 2001. PMID: 11459757 No abstract available.

10

Lewy bodies are not increased in progressive supranuclear palsy compared with normal controls.

Tsuboi Y, Ahlskog JE, Apaydin H, Parisi JE, Dickson DW. Tsuboi Y, et al. Among authors: dickson dw. Neurology. 2001 Nov 13;57(9):1675-8. doi: 10.1212/wnl.57.9.1675. Neurology. 2001. PMID: 11706110

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