Gwinn-Hardy K - Search Results

1

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

2

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

3

No pathogenic mutations in the beta-synuclein gene in Parkinson's disease.

Lincoln S, Crook R, Chartier-Harlin MC, Gwinn-Hardy K, Baker M, Mouroux V, Richard F, Becquet E, Amouyel P, Destée A, Hardy J, Farrer M. Lincoln S, et al. Neurosci Lett. 1999 Jul 9;269(2):107-9. doi: 10.1016/s0304-3940(99)00420-6. Neurosci Lett. 1999. PMID: 10430516

4

Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's disease.

Toft M, Mata IF, Ross OA, Kachergus J, Hulihan MM, Haugarvoll K, Stone JT, Blazquez M, Gibson JM, Aasly JO, White LR, Lynch T, Adler CH, Gwinn-Hardy K, Farrer MJ. Toft M, et al. Mov Disord. 2007 Feb 15;22(3):389-92. doi: 10.1002/mds.21217. Mov Disord. 2007. PMID: 17216639

5

A kindred with Parkinson's disease not showing genetic linkage to established loci.

Gwinn-Hardy KA, Crook R, Lincoln S, Adler CH, Caviness JN, Hardy J, Farrer M. Gwinn-Hardy KA, et al. Neurology. 2000 Jan 25;54(2):504-7. doi: 10.1212/wnl.54.2.504. Neurology. 2000. PMID: 10668726

6

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.

7

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

8

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.

9

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

10

Spinocerebellar ataxia type 3 phenotypically resembling parkinson disease in a black family.

Gwinn-Hardy K, Singleton A, O'Suilleabhain P, Boss M, Nicholl D, Adam A, Hussey J, Critchley P, Hardy J, Farrer M. Gwinn-Hardy K, et al. Arch Neurol. 2001 Feb;58(2):296-9. doi: 10.1001/archneur.58.2.296. Arch Neurol. 2001. PMID: 11176969

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