Bandmann O - Search Results

1

Detailed genotyping demonstrates association between the slow acetylator genotype for N-acetyltransferase 2 (NAT2) and familial Parkinson's disease.

Bandmann O, Vaughan JR, Holmans P, Marsden CD, Wood NW. Bandmann O, et al. Mov Disord. 2000 Jan;15(1):30-5. doi: 10.1002/1531-8257(200001)15:1<30::aid-mds1007>3.0.co;2-v. Mov Disord. 2000. PMID: 10634239

2

Sequence of the superoxide dismutase 1 (SOD 1) gene in familial Parkinson's disease.

Bandmann O, Davis MB, Marsden CD, Harding AE. Bandmann O, et al. J Neurol Neurosurg Psychiatry. 1995 Jul;59(1):90-1. doi: 10.1136/jnnp.59.1.90. J Neurol Neurosurg Psychiatry. 1995. PMID: 7608718 Free PMC article.

3

CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy.

Planté-Bordeneuve V, Bandmann O, Wenning G, Quinn NP, Daniel SE, Harding AE. Planté-Bordeneuve V, et al. Among authors: bandmann o. Mov Disord. 1995 May;10(3):277-8. doi: 10.1002/mds.870100307. Mov Disord. 1995. PMID: 7651442

4

The human homologue of the weaver mouse gene in familial and sporadic Parkinson's disease.

Bandmann O, Davis MB, Marsden CD, Wood NW. Bandmann O, et al. Neuroscience. 1996 Jun;72(4):877-9. doi: 10.1016/0306-4522(96)00091-7. Neuroscience. 1996. PMID: 8735215

5

Dopa-responsive dystonia in British patients: new mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneity.

Bandmann O, Nygaard TG, Surtees R, Marsden CD, Wood NW, Harding AE. Bandmann O, et al. Hum Mol Genet. 1996 Mar;5(3):403-6. doi: 10.1093/hmg/5.3.403. Hum Mol Genet. 1996. PMID: 8852666

6

The GTP-cyclohydrolase I gene in atypical parkinsonian patients: a clinico-genetic study.

Bandmann O, Daniel S, Marsden CD, Wood NW, Harding AE. Bandmann O, et al. J Neurol Sci. 1996 Sep 15;141(1-2):27-32. doi: 10.1016/0022-510x(96)00098-6. J Neurol Sci. 1996. PMID: 8880688

7

Mitochondrial DNA polymorphisms in pathologically proven Parkinson's disease.

Bandmann O, Sweeney MG, Daniel SE, Marsden CD, Wood NW. Bandmann O, et al. J Neurol. 1997 Apr;244(4):262-5. doi: 10.1007/s004150050082. J Neurol. 1997. PMID: 9112596

8

GTP cyclohydrolase I mutations in patients with dystonia responsive to anticholinergic drugs.

Jarman PR, Bandmann O, Marsden CD, Wood NW. Jarman PR, et al. Among authors: bandmann o. J Neurol Neurosurg Psychiatry. 1997 Sep;63(3):304-8. doi: 10.1136/jnnp.63.3.304. J Neurol Neurosurg Psychiatry. 1997. PMID: 9328244 Free PMC article.

9

Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease.

Bandmann O, Vaughan J, Holmans P, Marsden CD, Wood NW. Bandmann O, et al. Lancet. 1997 Oct 18;350(9085):1136-9. doi: 10.1016/s0140-6736(97)03495-8. Lancet. 1997. PMID: 9343502

10

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. Neurology. 1997 Dec;49(6):1598-604. doi: 10.1212/wnl.49.6.1598. Neurology. 1997. PMID: 9409353

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