Hardy J - Search Results

1

Web-based assessment of Parkinson's prodromal markers identifies GBA variants.

Noyce AJ, Mencacci NE, Schrag A, Bestwick JP, Giovannoni G, Lees AJ, Hardy J. Noyce AJ, et al. Among authors: hardy j. Mov Disord. 2015 Jun;30(7):1002-3. doi: 10.1002/mds.26249. Epub 2015 May 13. Mov Disord. 2015. PMID: 25970725 No abstract available.

2

The tau locus is not significantly associated with pathologically confirmed sporadic Parkinson's disease.

de Silva R, Hardy J, Crook J, Khan N, Graham EA, Morris CM, Wood NW, Lees AJ. de Silva R, et al. Among authors: hardy j. Neurosci Lett. 2002 Sep 20;330(2):201-3. doi: 10.1016/s0304-3940(02)00742-5. Neurosci Lett. 2002. PMID: 12231446

3

The structure of the tau haplotype in controls and in progressive supranuclear palsy.

Pittman AM, Myers AJ, Duckworth J, Bryden L, Hanson M, Abou-Sleiman P, Wood NW, Hardy J, Lees A, de Silva R. Pittman AM, et al. Among authors: hardy j. Hum Mol Genet. 2004 Jun 15;13(12):1267-74. doi: 10.1093/hmg/ddh138. Epub 2004 Apr 28. Hum Mol Genet. 2004. PMID: 15115761

4

Genome-wide analysis of the parkinsonism-dementia complex of Guam.

Morris HR, Steele JC, Crook R, Wavrant-De Vrièze F, Onstead-Cardinale L, Gwinn-Hardy K, Wood NW, Farrer M, Lees AJ, McGeer PL, Siddique T, Hardy J, Perez-Tur J. Morris HR, et al. Among authors: hardy j. Arch Neurol. 2004 Dec;61(12):1889-97. doi: 10.1001/archneur.61.12.1889. Arch Neurol. 2004. PMID: 15596609

5

Parkinson's disease: a broken nosology.

Hardy J, Lees AJ. Hardy J, et al. Mov Disord. 2005 Aug;20 Suppl 12:S2-4. doi: 10.1002/mds.20532. Mov Disord. 2005. PMID: 16092073

6

Novel GCH1 mutation in a Brazilian family with dopa-responsive dystonia.

Camargos ST, Cardoso F, Momeni P, Gianetti JG, Lees A, Hardy J, Singleton A. Camargos ST, et al. Among authors: hardy j. Mov Disord. 2008 Jan 30;23(2):299-302. doi: 10.1002/mds.21842. Mov Disord. 2008. PMID: 18044725

7

Complicated recessive dystonia parkinsonism syndromes.

Schneider SA, Bhatia KP, Hardy J. Schneider SA, et al. Among authors: hardy j. Mov Disord. 2009 Mar 15;24(4):490-9. doi: 10.1002/mds.22314. Mov Disord. 2009. PMID: 19185014 Review.

8

Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations.

Camargos ST, Dornas LO, Momeni P, Lees A, Hardy J, Singleton A, Cardoso F. Camargos ST, et al. Among authors: hardy j. Mov Disord. 2009 Apr 15;24(5):662-6. doi: 10.1002/mds.22365. Mov Disord. 2009. PMID: 19205068 Free PMC article.

9

Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease.

Neumann J, Bras J, Deas E, O'Sullivan SS, Parkkinen L, Lachmann RH, Li A, Holton J, Guerreiro R, Paudel R, Segarane B, Singleton A, Lees A, Hardy J, Houlden H, Revesz T, Wood NW. Neumann J, et al. Among authors: hardy j. Brain. 2009 Jul;132(Pt 7):1783-94. doi: 10.1093/brain/awp044. Epub 2009 Mar 13. Brain. 2009. PMID: 19286695 Free PMC article.

10

The genetics of Parkinson's syndromes: a critical review.

Hardy J, Lewis P, Revesz T, Lees A, Paisan-Ruiz C. Hardy J, et al. Curr Opin Genet Dev. 2009 Jun;19(3):254-65. doi: 10.1016/j.gde.2009.03.008. Epub 2009 May 4. Curr Opin Genet Dev. 2009. PMID: 19419854 Review.

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