Gwinn-Hardy K - Search Results

1

Neuropathology of two members of a German-American kindred (Family C) with late onset parkinsonism.

Wszolek ZK, Gwinn-Hardy K, Wszolek EK, Muenter MD, Pfeiffer RF, Rodnitzky RL, Uitti RJ, McComb RD, Gasser T, Dickson DW. Wszolek ZK, et al. Acta Neuropathol. 2002 Apr;103(4):344-50. doi: 10.1007/s00401-001-0474-8. Epub 2001 Dec 8. Acta Neuropathol. 2002. PMID: 11904753

2

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. Acta Neuropathol. 2000 Jun;99(6):663-72. doi: 10.1007/s004010051177. Acta Neuropathol. 2000. PMID: 10867800

3

Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications.

Farrer M, Kachergus J, Forno L, Lincoln S, Wang DS, Hulihan M, Maraganore D, Gwinn-Hardy K, Wszolek Z, Dickson D, Langston JW. Farrer M, et al. Ann Neurol. 2004 Feb;55(2):174-9. doi: 10.1002/ana.10846. Ann Neurol. 2004. PMID: 14755720

4

Electrophysiological observations in hereditary parkinsonism-dementia with Lewy body pathology.

Caviness JN, Gwinn-Hardy K, Adler CH, Muenter MD. Caviness JN, et al. Mov Disord. 2000 Jan;15(1):140-5. doi: 10.1002/1531-8257(200001)15:1<140::aid-mds1022>3.0.co;2-5. Mov Disord. 2000. PMID: 10634254

5

A chromosome 4p haplotype segregating with Parkinson's disease and postural tremor.

Farrer M, Gwinn-Hardy K, Muenter M, DeVrieze FW, Crook R, Perez-Tur J, Lincoln S, Maraganore D, Adler C, Newman S, MacElwee K, McCarthy P, Miller C, Waters C, Hardy J. Farrer M, et al. Hum Mol Genet. 1999 Jan;8(1):81-5. doi: 10.1093/hmg/8.1.81. Hum Mol Genet. 1999. PMID: 9887334

6

Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein.

Lewis J, McGowan E, Rockwood J, Melrose H, Nacharaju P, Van Slegtenhorst M, Gwinn-Hardy K, Paul Murphy M, Baker M, Yu X, Duff K, Hardy J, Corral A, Lin WL, Yen SH, Dickson DW, Davies P, Hutton M. Lewis J, et al. Nat Genet. 2000 Aug;25(4):402-5. doi: 10.1038/78078. Nat Genet. 2000. PMID: 10932182

7

DLB and PDD boundary issues: diagnosis, treatment, molecular pathology, and biomarkers.

Lippa CF, Duda JE, Grossman M, Hurtig HI, Aarsland D, Boeve BF, Brooks DJ, Dickson DW, Dubois B, Emre M, Fahn S, Farmer JM, Galasko D, Galvin JE, Goetz CG, Growdon JH, Gwinn-Hardy KA, Hardy J, Heutink P, Iwatsubo T, Kosaka K, Lee VM, Leverenz JB, Masliah E, McKeith IG, Nussbaum RL, Olanow CW, Ravina BM, Singleton AB, Tanner CM, Trojanowski JQ, Wszolek ZK; DLB/PDD Working Group. Lippa CF, et al. Neurology. 2007 Mar 13;68(11):812-9. doi: 10.1212/01.wnl.0000256715.13907.d3. Neurology. 2007. PMID: 17353469 Review.

8

Accurate determination of ataxin-2 polyglutamine expansion in patients with intermediate-range repeats.

Hussey J, Lockhart PJ, Seltzer W, Wszolek ZK, Payami H, Hanson M, Gwinn-Hardy K, Farrer M. Hussey J, et al. Genet Test. 2002 Fall;6(3):217-20. doi: 10.1089/109065702761403397. Genet Test. 2002. PMID: 12490063

9

L-dopa slows the progression of familial parkinsonism.

Gwinn-Hardy K, Evidente VG, Waters C, Muenter MD, Hardy J. Gwinn-Hardy K, et al. Lancet. 1999 May 29;353(9167):1850-1. doi: 10.1016/S0140-6736(99)01398-7. Lancet. 1999. PMID: 10359414 No abstract available.

10

Lewy bodies and parkinsonism in families with parkin mutations.

Farrer M, Chan P, Chen R, Tan L, Lincoln S, Hernandez D, Forno L, Gwinn-Hardy K, Petrucelli L, Hussey J, Singleton A, Tanner C, Hardy J, Langston JW. Farrer M, et al. Ann Neurol. 2001 Sep;50(3):293-300. doi: 10.1002/ana.1132. Ann Neurol. 2001. PMID: 11558785

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