Bandmann O - Search Results

1

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

2

The master energy homeostasis regulator PGC-1α exhibits an mRNA nuclear export function.

Mihaylov SR, Castelli LM, Lin YH, Gül A, Soni N, Hastings C, Flynn HR, Păun O, Dickman MJ, Snijders AP, Goldstone R, Bandmann O, Shelkovnikova TA, Mortiboys H, Ultanir SK, Hautbergue GM. Mihaylov SR, et al. Among authors: bandmann o. Nat Commun. 2023 Sep 7;14(1):5496. doi: 10.1038/s41467-023-41304-8. Nat Commun. 2023. PMID: 37679383 Free PMC article.

3

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.

4

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

5

Apo E genotypes in multiple sclerosis, Parkinson's disease, schwannomas and late-onset Alzheimer's disease.

Rubinsztein DC, Hanlon CS, Irving RM, Goodburn S, Evans DG, Kellar-Wood H, Xuereb JH, Bandmann O, Harding AE. Rubinsztein DC, et al. Among authors: bandmann o. Mol Cell Probes. 1994 Dec;8(6):519-25. doi: 10.1006/mcpr.1994.1073. Mol Cell Probes. 1994. PMID: 7700274

6

Arg296 to Cys296 polymorphism in exon 6 of cytochrome P-450-2D6 (CYP2D6) is not associated with multiple system atrophy.

Bandmann O, Wenning GK, Quinn NP, Harding AE. Bandmann O, et al. J Neurol Neurosurg Psychiatry. 1995 Nov;59(5):557. doi: 10.1136/jnnp.59.5.557. J Neurol Neurosurg Psychiatry. 1995. PMID: 8530951 Free PMC article. No abstract available.

7

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

8

Debrisoquine hydroxylase polymorphism in Leber's hereditary optic neuropathy.

Chalmers RM, Bandmann O, Harding AE. Chalmers RM, et al. Among authors: bandmann o. J Neurol Neurosurg Psychiatry. 1996 May;60(5):588. doi: 10.1136/jnnp.60.5.588. J Neurol Neurosurg Psychiatry. 1996. PMID: 8778272 Free PMC article. No abstract available.

9

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

10

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

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