Gwinn-Hardy K - Search Results

1

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

2

Genetic classification of primary neurodegenerative disease.

Hardy J, Gwinn-Hardy K. Hardy J, et al. Science. 1998 Nov 6;282(5391):1075-9. doi: 10.1126/science.282.5391.1075. Science. 1998. PMID: 9804538 Review.

3

The genetics of disorders with synuclein pathology and parkinsonism.

Farrer M, Gwinn-Hardy K, Hutton M, Hardy J. Farrer M, et al. Hum Mol Genet. 1999;8(10):1901-5. doi: 10.1093/hmg/8.10.1901. Hum Mol Genet. 1999. PMID: 10469843 Review.

4

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

5

Neurodegenerative disease: a different view of diagnosis.

Hardy J, Gwinn-Hardy K. Hardy J, et al. Mol Med Today. 1999 Dec;5(12):514-7. doi: 10.1016/s1357-4310(99)01604-4. Mol Med Today. 1999. PMID: 10562716

6

A family with a tau P301L mutation presenting with parkinsonism.

Walker RH, Friedman J, Wiener J, Hobler R, Gwinn-Hardy K, Adam A, DeWolfe J, Gibbs R, Baker M, Farrer M, Hutton M, Hardy J. Walker RH, et al. Parkinsonism Relat Disord. 2002 Dec;9(2):121-3. doi: 10.1016/s1353-8020(02)00003-2. Parkinsonism Relat Disord. 2002. PMID: 12473404

7

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

8

No pathogenic mutations in the persyn gene in Parkinson's disease.

Lincoln S, Gwinn-Hardy K, Goudreau J, Chartier-Harlin MC, Baker M, Mouroux V, Richard F, Destée A, Becquet E, Amouyel P, Lynch T, Hardy J, Farrer M. Lincoln S, et al. Neurosci Lett. 1999 Jan 4;259(1):65-6. doi: 10.1016/s0304-3940(98)00901-x. Neurosci Lett. 1999. PMID: 10027558

9

Low frequency of pathogenic mutations in the ubiquitin carboxy-terminal hydrolase gene in familial Parkinson's disease.

Lincoln S, Vaughan J, Wood N, Baker M, Adamson J, Gwinn-Hardy K, Lynch T, Hardy J, Farrer M. Lincoln S, et al. Neuroreport. 1999 Feb 5;10(2):427-9. doi: 10.1097/00001756-199902050-00040. Neuroreport. 1999. PMID: 10203348

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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