Farrer MJ - Search Results

1

Autosomal dominant parkinsonism associated with variable synuclein and tau pathology.

Wszolek ZK, Pfeiffer RF, Tsuboi Y, Uitti RJ, McComb RD, Stoessl AJ, Strongosky AJ, Zimprich A, Müller-Myhsok B, Farrer MJ, Gasser T, Calne DB, Dickson DW. Wszolek ZK, et al. Among authors: farrer mj. Neurology. 2004 May 11;62(9):1619-22. doi: 10.1212/01.wnl.0000125015.06989.db. Neurology. 2004. PMID: 15136696

2

Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21-22.

Baker M, Kwok JB, Kucera S, Crook R, Farrer M, Houlden H, Isaacs A, Lincoln S, Onstead L, Hardy J, Wittenberg L, Dodd P, Webb S, Hayward N, Tannenberg T, Andreadis A, Hallupp M, Schofield P, Dark F, Hutton M. Baker M, et al. Ann Neurol. 1997 Nov;42(5):794-8. doi: 10.1002/ana.410420516. Ann Neurol. 1997. PMID: 9392579

3

Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD).

Vaughan JR, Farrer MJ, Wszolek ZK, Gasser T, Durr A, Agid Y, Bonifati V, DeMichele G, Volpe G, Lincoln S, Breteler M, Meco G, Brice A, Marsden CD, Hardy J, Wood NW. Vaughan JR, et al. Among authors: farrer mj. Hum Mol Genet. 1998 Apr;7(4):751-3. doi: 10.1093/hmg/7.4.751. Hum Mol Genet. 1998. PMID: 9499430

4

Low frequency of alpha-synuclein mutations in familial Parkinson's disease.

Farrer M, Wavrant-De Vrieze F, Crook R, Boles L, Perez-Tur J, Hardy J, Johnson WG, Steele J, Maraganore D, Gwinn K, Lynch T. Farrer M, et al. Ann Neurol. 1998 Mar;43(3):394-7. doi: 10.1002/ana.410430320. Ann Neurol. 1998. PMID: 9506559

5

Exclusion of genetic linkage to 4q21-23 and 17q21 in a family with Lewy body parkinsonism.

Hardy J, Pérez-Tur J, Baker M, Farrer M, Crook R, Hutton M, Johnson WG, Gwinn K, Muenter M, Rocca WA, Maraganore D. Hardy J, et al. Am J Med Genet. 1998 Mar 28;81(2):166-71. Am J Med Genet. 1998. PMID: 9613857

6

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

7

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.

8

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.

9

Case-control study of the ubiquitin carboxy-terminal hydrolase L1 gene in Parkinson's disease.

Maraganore DM, Farrer MJ, Hardy JA, Lincoln SJ, McDonnell SK, Rocca WA. Maraganore DM, et al. Among authors: farrer mj. Neurology. 1999 Nov 10;53(8):1858-60. doi: 10.1212/wnl.53.8.1858. Neurology. 1999. PMID: 10563640

10

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

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