Gwinn-Hardy K - Search Results

1

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

2

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

3

Genetics of Parkinson's disease and parkinsonism.

Hardy J, Cai H, Cookson MR, Gwinn-Hardy K, Singleton A. Hardy J, et al. Ann Neurol. 2006 Oct;60(4):389-98. doi: 10.1002/ana.21022. Ann Neurol. 2006. PMID: 17068789 Review.

4

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

5

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

6

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

7

Parkinson's genetics: an embarrassment of riches.

Gwinn-Hardy K, Farrer M. Gwinn-Hardy K, et al. Ann Neurol. 2002 Jan;51(1):7-8. doi: 10.1002/ana.10091. Ann Neurol. 2002. PMID: 11782975 Review. No abstract available.

8

Clinical, 18F-dopa PET, and genetic analysis of an ethnic Chinese kindred with early-onset parkinsonism and parkin gene mutations.

Wu RM, Shan DE, Sun CM, Liu RS, Hwu WL, Tai CH, Hussey J, West A, Gwinn-Hardy K, Hardy J, Chen J, Farrer M, Lincoln S. Wu RM, et al. Mov Disord. 2002 Jul;17(4):670-5. doi: 10.1002/mds.10184. Mov Disord. 2002. PMID: 12210855

9

Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation.

Hague S, Rogaeva E, Hernandez D, Gulick C, Singleton A, Hanson M, Johnson J, Weiser R, Gallardo M, Ravina B, Gwinn-Hardy K, Crawley A, St George-Hyslop PH, Lang AE, Heutink P, Bonifati V, Hardy J, Singleton A. Hague S, et al. Ann Neurol. 2003 Aug;54(2):271-4. doi: 10.1002/ana.10663. Ann Neurol. 2003. PMID: 12891685

10

Parkin mutations and early-onset parkinsonism in a Taiwanese cohort.

Wu RM, Bounds R, Lincoln S, Hulihan M, Lin CH, Hwu WL, Chen J, Gwinn-Hardy K, Farrer M. Wu RM, et al. Arch Neurol. 2005 Jan;62(1):82-7. doi: 10.1001/archneur.62.1.82. Arch Neurol. 2005. PMID: 15642853

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