Hardy J - Search Results

1

Analysis of the genetic variability in Parkinson's disease from Southern Spain.

Bandrés-Ciga S, Mencacci NE, Durán R, Barrero FJ, Escamilla-Sevilla F, Morgan S, Hehir J, Vives F, Hardy J, Pittman AM. Bandrés-Ciga S, et al. Among authors: hardy j. Neurobiol Aging. 2016 Jan;37:210.e1-210.e5. doi: 10.1016/j.neurobiolaging.2015.09.020. Epub 2015 Oct 8. Neurobiol Aging. 2016. PMID: 26518746

2

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

3

Clinical and pathological features of an Alzheimer's disease patient with the MAPT Delta K280 mutation.

Momeni P, Pittman A, Lashley T, Vandrovcova J, Malzer E, Luk C, Hulette C, Lees A, Revesz T, Hardy J, de Silva R. Momeni P, et al. Among authors: hardy j. Neurobiol Aging. 2009 Mar;30(3):388-93. doi: 10.1016/j.neurobiolaging.2007.07.013. Epub 2007 Aug 27. Neurobiol Aging. 2009. PMID: 17723255 Free PMC article.

4

Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2.

Bras J, Guerreiro R, Ribeiro M, Morgadinho A, Januario C, Dias M, Calado A, Semedo C, Oliveira C, Hardy J, Singleton A. Bras J, et al. Among authors: hardy j. BMC Neurol. 2008 Jan 22;8:1. doi: 10.1186/1471-2377-8-1. BMC Neurol. 2008. PMID: 18211709 Free PMC article.

5

Analysis of Nigerians with apparently sporadic Parkinson disease for mutations in LRRK2, PRKN and ATXN3.

Okubadejo N, Britton A, Crews C, Akinyemi R, Hardy J, Singleton A, Bras J. Okubadejo N, et al. Among authors: hardy j. PLoS One. 2008;3(10):e3421. doi: 10.1371/journal.pone.0003421. Epub 2008 Oct 17. PLoS One. 2008. PMID: 18927607 Free PMC article.

6

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.

7

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.

8

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.

9

Parkinson's disease.

Lees AJ, Hardy J, Revesz T. Lees AJ, et al. Among authors: hardy j. Lancet. 2009 Jun 13;373(9680):2055-66. doi: 10.1016/S0140-6736(09)60492-X. Lancet. 2009. PMID: 19524782 Review.

10

Widespread Lewy body and tau accumulation in childhood and adult onset dystonia-parkinsonism cases with PLA2G6 mutations.

Paisán-Ruiz C, Li A, Schneider SA, Holton JL, Johnson R, Kidd D, Chataway J, Bhatia KP, Lees AJ, Hardy J, Revesz T, Houlden H. Paisán-Ruiz C, et al. Among authors: hardy j. Neurobiol Aging. 2012 Apr;33(4):814-23. doi: 10.1016/j.neurobiolaging.2010.05.009. Epub 2010 Jul 21. Neurobiol Aging. 2012. PMID: 20619503 Free PMC article.

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