Sweeney MG - Search Results

1

The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates.

Giunti P, Sabbadini G, Sweeney MG, Davis MB, Veneziano L, Mantuano E, Federico A, Plasmati R, Frontali M, Wood NW. Giunti P, et al. Among authors: sweeney mg. Brain. 1998 Mar;121 ( Pt 3):459-67. doi: 10.1093/brain/121.3.459. Brain. 1998. PMID: 9549522

2

Detection of the Machado-Joseph disease/spinocerebellar ataxia three trinucleotide repeat expansion in families with autosomal dominant motor disorders, including the Drew family of Walworth.

Giunti P, Sweeney MG, Harding AE. Giunti P, et al. Among authors: sweeney mg. Brain. 1995 Oct;118 ( Pt 5):1077-85. doi: 10.1093/brain/118.5.1077. Brain. 1995. PMID: 7496771

3

The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias.

Giunti P, Sweeney MG, Spadaro M, Jodice C, Novelletto A, Malaspina P, Frontali M, Harding AE. Giunti P, et al. Among authors: sweeney mg. Brain. 1994 Aug;117 ( Pt 4):645-9. doi: 10.1093/brain/117.4.645. Brain. 1994. PMID: 7922453 Free article.

4

Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degeneration.

Bandmann O, Sweeney MG, Daniel SE, Wenning GK, Quinn N, Marsden CD, Wood NW. Bandmann O, et al. Among authors: sweeney mg. Neurology. 1997 Dec;49(6):1598-604. doi: 10.1212/wnl.49.6.1598. Neurology. 1997. PMID: 9409353

5

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

6

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.

7

Genetic screening of Greek patients with Huntington’s disease phenocopies identifies an SCA8 expansion.

Koutsis G, Karadima G, Pandraud A, Sweeney MG, Paudel R, Houlden H, Wood NW, Panas M. Koutsis G, et al. Among authors: sweeney mg. J Neurol. 2012 Sep;259(9):1874-8. doi: 10.1007/s00415-012-6430-9. J Neurol. 2012. PMID: 22297462

8

Progression of nigrostriatal dysfunction in a parkin kindred: an [18F]dopa PET and clinical study.

Khan NL, Brooks DJ, Pavese N, Sweeney MG, Wood NW, Lees AJ, Piccini P. Khan NL, et al. Among authors: sweeney mg. Brain. 2002 Oct;125(Pt 10):2248-56. doi: 10.1093/brain/awf237. Brain. 2002. PMID: 12244082

9

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

10

Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data.

Khan NL, Jain S, Lynch JM, Pavese N, Abou-Sleiman P, Holton JL, Healy DG, Gilks WP, Sweeney MG, Ganguly M, Gibbons V, Gandhi S, Vaughan J, Eunson LH, Katzenschlager R, Gayton J, Lennox G, Revesz T, Nicholl D, Bhatia KP, Quinn N, Brooks D, Lees AJ, Davis MB, Piccini P, Singleton AB, Wood NW. Khan NL, et al. Among authors: sweeney mg. Brain. 2005 Dec;128(Pt 12):2786-96. doi: 10.1093/brain/awh667. Epub 2005 Nov 4. Brain. 2005. PMID: 16272164

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