Lees AJ - Search Results

1

Parkin disease in a Brazilian kindred: Manifesting heterozygotes and clinical follow-up over 10 years.

Khan NL, Horta W, Eunson L, Graham E, Johnson JO, Chang S, Davis M, Singleton A, Wood NW, Lees AJ. Khan NL, et al. Among authors: lees aj. Mov Disord. 2005 Apr;20(4):479-484. doi: 10.1002/mds.20335. Mov Disord. 2005. PMID: 15641013

2

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: lees aj. 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

3

Parkinsonism and nigrostriatal dysfunction are associated with spinocerebellar ataxia type 6 (SCA6).

Khan NL, Giunti P, Sweeney MG, Scherfler C, Brien MO, Piccini P, Wood NW, Lees AJ. Khan NL, et al. Among authors: lees aj. Mov Disord. 2005 Sep;20(9):1115-9. doi: 10.1002/mds.20564. Mov Disord. 2005. PMID: 15954136

4

Nigral degeneration and striatal dopaminergic dysfunction in idiopathic and Parkin-linked Parkinson's disease.

Hu MT, Scherfler C, Khan NL, Hajnal JV, Lees AJ, Quinn N, Wood NW, Brooks DJ. Hu MT, et al. Among authors: lees aj. Mov Disord. 2006 Mar;21(3):299-305. doi: 10.1002/mds.20702. Mov Disord. 2006. PMID: 16211589

5

Nigrostriatal dysfunction in homozygous and heterozygous parkin gene carriers: an 18F-dopa PET progression study.

Pavese N, Khan NL, Scherfler C, Cohen L, Brooks DJ, Wood NW, Bhatia KP, Quinn NP, Lees AJ, Piccini P. Pavese N, et al. Among authors: lees aj. Mov Disord. 2009 Nov 15;24(15):2260-6. doi: 10.1002/mds.22817. Mov Disord. 2009. PMID: 19845000

6

An intragenic duplication in guanosine triphosphate cyclohydrolase-1 gene in a dopa-responsive dystonia family.

Ling H, Polke JM, Sweeney MG, Haworth A, Sandford CA, Heales SJ, Wood NW, Davis MB, Lees AJ. Ling H, et al. Among authors: lees aj. Mov Disord. 2011 Apr;26(5):905-9. doi: 10.1002/mds.23593. Epub 2011 Feb 1. Mov Disord. 2011. PMID: 21287604

7

Parkin disease: a phenotypic study of a large case series.

Khan NL, Graham E, Critchley P, Schrag AE, Wood NW, Lees AJ, Bhatia KP, Quinn N. Khan NL, et al. Among authors: lees aj. Brain. 2003 Jun;126(Pt 6):1279-92. doi: 10.1093/brain/awg142. Brain. 2003. PMID: 12764051

8

Neurofibrillary tangle parkinsonian disorders--tau pathology and tau genetics.

Morris HR, Lees AJ, Wood NW. Morris HR, et al. Among authors: lees aj. Mov Disord. 1999 Sep;14(5):731-6. doi: 10.1002/1531-8257(199909)14:5<731::aid-mds1004>3.0.co;2-j. Mov Disord. 1999. PMID: 10495033 Review.

9

The glucocerobrosidase E326K variant predisposes to Parkinson's disease, but does not cause Gaucher's disease.

Duran R, Mencacci NE, Angeli AV, Shoai M, Deas E, Houlden H, Mehta A, Hughes D, Cox TM, Deegan P, Schapira AH, Lees AJ, Limousin P, Jarman PR, Bhatia KP, Wood NW, Hardy J, Foltynie T. Duran R, et al. Among authors: lees aj. Mov Disord. 2013 Feb;28(2):232-236. doi: 10.1002/mds.25248. Epub 2012 Dec 5. Mov Disord. 2013. PMID: 23225227 Free PMC article.

10

UCHL-1 gene in multiple system atrophy: a haplotype tagging approach.

Healy DG, Abou-Sleiman PM, Quinn N, Ahmadi KR, Ozawa T, Kamm C, Wullner U, Oertel WH, Burk K, Dupont E, Pellecchia MT, Tolosa E, Gasser T, Holton JL, Revesz T, Goldstein DB, Lees AJ, Wood NW; European MSA Study Group. Healy DG, et al. Among authors: lees aj. Mov Disord. 2005 Oct;20(10):1338-43. doi: 10.1002/mds.20575. Mov Disord. 2005. PMID: 16007636

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