Hardy J - Search Results

1

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.

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

Testing times for the "amyloid cascade hypothesis".

Hardy J. Hardy J. Neurobiol Aging. 2002 Nov-Dec;23(6):1073-4. doi: 10.1016/s0197-4580(02)00042-8. Neurobiol Aging. 2002. PMID: 12470803 No abstract available.

4

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

5

The uncertain anatomy of Alzheimer's disease.

Hardy J. Hardy J. Neurobiol Aging. 2004 Jul;25(6):719-20; discussion 743-6. doi: 10.1016/j.neurobiolaging.2003.12.012. Neurobiol Aging. 2004. PMID: 15165693 No abstract available.

6

The tau H2 haplotype is almost exclusively Caucasian in origin.

Evans W, Fung HC, Steele J, Eerola J, Tienari P, Pittman A, Silva Rd, Myers A, Vrieze FW, Singleton A, Hardy J. Evans W, et al. Among authors: hardy j. Neurosci Lett. 2004 Oct 21;369(3):183-5. doi: 10.1016/j.neulet.2004.05.119. Neurosci Lett. 2004. PMID: 15464261

7

Defining the ends of Parkin exon 4 deletions in two different families with Parkinson's disease.

Clarimon J, Johnson J, Dogu O, Horta W, Khan N, Lees AJ, Hardy J, Singleton A. Clarimon J, et al. Among authors: hardy j. Am J Med Genet B Neuropsychiatr Genet. 2005 Feb 5;133B(1):120-3. doi: 10.1002/ajmg.b.30119. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15635662

8

The architecture of the tau haplotype block in different ethnicities.

Fung HC, Evans J, Evans W, Duckworth J, Pittman A, de Silva R, Myers A, Hardy J. Fung HC, et al. Among authors: hardy j. Neurosci Lett. 2005 Mar 29;377(2):81-4. doi: 10.1016/j.neulet.2004.11.072. Epub 2004 Dec 22. Neurosci Lett. 2005. PMID: 15740841

9

Mutation analysis of patients with neuronal intermediate filament inclusion disease (NIFID).

Momeni P, Cairns NJ, Perry RH, Bigio EH, Gearing M, Singleton AB, Hardy J. Momeni P, et al. Among authors: hardy j. Neurobiol Aging. 2006 May;27(5):778.e1-778.e6. doi: 10.1016/j.neurobiolaging.2005.03.030. Epub 2005 Jul 7. Neurobiol Aging. 2006. PMID: 16005115

10

Taiwanese cases of SCA2 are derived from a single founder.

Momeni P, Lu CS, Chou YH, Chang HC, Chen RS, Chen CC, Hsu JT, Singleton A, Hardy J. Momeni P, et al. Among authors: hardy j. Mov Disord. 2005 Dec;20(12):1633-6. doi: 10.1002/mds.20638. Mov Disord. 2005. PMID: 16078202

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