Tabrizi SJ - Search Results

1

An ITPR1 gene deletion causes spinocerebellar ataxia 15/16: a genetic, clinical and radiological description.

Novak MJ, Sweeney MG, Li A, Treacy C, Chandrashekar HS, Giunti P, Goold RG, Davis MB, Houlden H, Tabrizi SJ. Novak MJ, et al. Among authors: tabrizi sj. Mov Disord. 2010 Oct 15;25(13):2176-82. doi: 10.1002/mds.23223. Mov Disord. 2010. PMID: 20669319

2

Models of Parkinson's disease.

Orth M, Tabrizi SJ. Orth M, et al. Among authors: tabrizi sj. Mov Disord. 2003 Jul;18(7):729-37. doi: 10.1002/mds.10447. Mov Disord. 2003. PMID: 12815651 Review.

3

Somatic and germline mosaicism in sporadic early-onset Alzheimer's disease.

Beck JA, Poulter M, Campbell TA, Uphill JB, Adamson G, Geddes JF, Revesz T, Davis MB, Wood NW, Collinge J, Tabrizi SJ. Beck JA, et al. Among authors: tabrizi sj. Hum Mol Genet. 2004 Jun 15;13(12):1219-24. doi: 10.1093/hmg/ddh134. Epub 2004 Apr 28. Hum Mol Genet. 2004. PMID: 15115757

4

Spinocerebellar ataxia type 17: extension of phenotype with putaminal rim hyperintensity on magnetic resonance imaging.

Loy CT, Sweeney MG, Davis MB, Wills AJ, Sawle GV, Lees AJ, Tabrizi SJ. Loy CT, et al. Among authors: tabrizi sj. Mov Disord. 2005 Nov;20(11):1521-3. doi: 10.1002/mds.20529. Mov Disord. 2005. PMID: 16037935

5

Huntington's disease phenocopies are clinically and genetically heterogeneous.

Wild EJ, Mudanohwo EE, Sweeney MG, Schneider SA, Beck J, Bhatia KP, Rossor MN, Davis MB, Tabrizi SJ. Wild EJ, et al. Among authors: tabrizi sj. Mov Disord. 2008 Apr 15;23(5):716-20. doi: 10.1002/mds.21915. Mov Disord. 2008. PMID: 18181206

6

Whole-brain atrophy as a measure of progression in premanifest and early Huntington's disease.

Henley SM, Wild EJ, Hobbs NZ, Frost C, MacManus DG, Barker RA, Fox NC, Tabrizi SJ. Henley SM, et al. Among authors: tabrizi sj. Mov Disord. 2009 Apr 30;24(6):932-6. doi: 10.1002/mds.22485. Mov Disord. 2009. PMID: 19243073

7

Rate and acceleration of whole-brain atrophy in premanifest and early Huntington's disease.

Wild EJ, Henley SM, Hobbs NZ, Frost C, MacManus DG, Barker RA, Fox NC, Tabrizi SJ. Wild EJ, et al. Among authors: tabrizi sj. Mov Disord. 2010 May 15;25(7):888-95. doi: 10.1002/mds.22969. Mov Disord. 2010. PMID: 20461806 Free PMC article.

8

Abnormal explicit but normal implicit sequence learning in premanifest and early Huntington's disease.

Schneider SA, Wilkinson L, Bhatia KP, Henley SM, Rothwell JC, Tabrizi SJ, Jahanshahi M. Schneider SA, et al. Among authors: tabrizi sj. Mov Disord. 2010 Jul 30;25(10):1343-9. doi: 10.1002/mds.22692. Mov Disord. 2010. PMID: 20544716 Free PMC article.

9

Huntington's disease.

Novak MJ, Tabrizi SJ. Novak MJ, et al. Among authors: tabrizi sj. BMJ. 2010 Jun 30;340:c3109. doi: 10.1136/bmj.c3109. BMJ. 2010. PMID: 20591965 Review. No abstract available.

10

Rapid cell-surface prion protein conversion revealed using a novel cell system.

Goold R, Rabbanian S, Sutton L, Andre R, Arora P, Moonga J, Clarke AR, Schiavo G, Jat P, Collinge J, Tabrizi SJ. Goold R, et al. Among authors: tabrizi sj. Nat Commun. 2011;2:281. doi: 10.1038/ncomms1282. Nat Commun. 2011. PMID: 21505437 Free PMC article.

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