Sweeney MG - Search Results

1

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: sweeney mg. Mov Disord. 2005 Nov;20(11):1521-3. doi: 10.1002/mds.20529. Mov Disord. 2005. PMID: 16037935

2

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: sweeney mg. Mov Disord. 2005 Sep;20(9):1115-9. doi: 10.1002/mds.20564. Mov Disord. 2005. PMID: 15954136

3

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: sweeney mg. Mov Disord. 2008 Apr 15;23(5):716-20. doi: 10.1002/mds.21915. Mov Disord. 2008. PMID: 18181206

4

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: sweeney mg. Mov Disord. 2010 Oct 15;25(13):2176-82. doi: 10.1002/mds.23223. Mov Disord. 2010. PMID: 20669319

5

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: sweeney mg. Mov Disord. 2011 Apr;26(5):905-9. doi: 10.1002/mds.23593. Epub 2011 Feb 1. Mov Disord. 2011. PMID: 21287604

6

Generalized chorea in two patients harboring the Friedreich's ataxia gene trinucleotide repeat expansion.

Hanna MG, Davis MB, Sweeney MG, Noursadeghi M, Ellis CJ, Elliot P, Wood NW, Marsden CD. Hanna MG, et al. Among authors: sweeney mg. Mov Disord. 1998 Mar;13(2):339-40. doi: 10.1002/mds.870130223. Mov Disord. 1998. PMID: 9539351

7

The role of interruptions in polyQ in the pathology of SCA1.

Menon RP, Nethisinghe S, Faggiano S, Vannocci T, Rezaei H, Pemble S, Sweeney MG, Wood NW, Davis MB, Pastore A, Giunti P. Menon RP, et al. Among authors: sweeney mg. PLoS Genet. 2013;9(7):e1003648. doi: 10.1371/journal.pgen.1003648. Epub 2013 Jul 25. PLoS Genet. 2013. PMID: 23935513 Free PMC article.

8

C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies.

Hensman Moss DJ, Poulter M, Beck J, Hehir J, Polke JM, Campbell T, Adamson G, Mudanohwo E, McColgan P, Haworth A, Wild EJ, Sweeney MG, Houlden H, Mead S, Tabrizi SJ. Hensman Moss DJ, et al. Among authors: sweeney mg. Neurology. 2014 Jan 28;82(4):292-9. doi: 10.1212/WNL.0000000000000061. Epub 2013 Dec 20. Neurology. 2014. PMID: 24363131 Free PMC article.

9

Phenotypic homogeneity of the Huntington disease-like presentation in a SCA17 family.

Schneider SA, van de Warrenburg BP, Hughes TD, Davis M, Sweeney M, Wood N, Quinn NP, Bhatia KP. Schneider SA, et al. Neurology. 2006 Nov 14;67(9):1701-3. doi: 10.1212/01.wnl.0000242740.01273.00. Neurology. 2006. PMID: 17101913

10

Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India.

Sinha KK, Worth PF, Jha DK, Sinha S, Stinton VJ, Davis MB, Wood NW, Sweeney MG, Bhatia KP. Sinha KK, et al. Among authors: sweeney mg. J Neurol Neurosurg Psychiatry. 2004 Mar;75(3):448-52. doi: 10.1136/jnnp.2002.004895. J Neurol Neurosurg Psychiatry. 2004. PMID: 14966163 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

113 results

Search Page