Farrer MJ - Search Results

1

Clinical heterogeneity of the LRRK2 G2019S mutation.

Papapetropoulos S, Singer C, Ross OA, Toft M, Johnson JL, Farrer MJ, Mash DC. Papapetropoulos S, et al. Among authors: farrer mj. Arch Neurol. 2006 Sep;63(9):1242-6. doi: 10.1001/archneur.63.9.1242. Arch Neurol. 2006. PMID: 16966501

2

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

3

Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese.

Gwinn-Hardy K, Chen JY, Liu HC, Liu TY, Boss M, Seltzer W, Adam A, Singleton A, Koroshetz W, Waters C, Hardy J, Farrer M. Gwinn-Hardy K, et al. Neurology. 2000 Sep 26;55(6):800-5. doi: 10.1212/wnl.55.6.800. Neurology. 2000. PMID: 10993999

4

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

5

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.

6

Parkin-proven disease: common founders but divergent phenotypes.

Lincoln S, Wiley J, Lynch T, Langston JW, Chen R, Lang A, Rogaeva E, Sa DS, Munhoz RP, Harris J, Marder K, Klein C, Bisceglio G, Hussey J, West A, Hulihan M, Hardy J, Farrer M. Lincoln S, et al. Neurology. 2003 May 27;60(10):1605-10. doi: 10.1212/01.wnl.0000064289.49410.a9. Neurology. 2003. PMID: 12771249

7

Compound heterozygous PANK2 mutations confirm HARP and Hallervorden-Spatz syndromes are allelic.

Houlden H, Lincoln S, Farrer M, Cleland PG, Hardy J, Orrell RW. Houlden H, et al. Neurology. 2003 Nov 25;61(10):1423-6. doi: 10.1212/01.wnl.0000094120.09977.92. Neurology. 2003. PMID: 14638969

8

DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein function.

Lockhart PJ, Lincoln S, Hulihan M, Kachergus J, Wilkes K, Bisceglio G, Mash DC, Farrer MJ. Lockhart PJ, et al. Among authors: farrer mj. J Med Genet. 2004 Mar;41(3):e22. doi: 10.1136/jmg.2003.011106. J Med Genet. 2004. PMID: 14985393 Free PMC article. No abstract available.

9

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

10

Clinical findings in a large family with a parkin ex3delta40 mutation.

Munhoz RP, Sa DS, Rogaeva E, Salehi-Rad S, Sato C, Medeiros H, Farrer M, Lang AE. Munhoz RP, et al. Arch Neurol. 2004 May;61(5):701-4. doi: 10.1001/archneur.61.5.701. Arch Neurol. 2004. PMID: 15148147

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