Davis MB - Search Results

1

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. Among authors: davis mb. Neuroscience. 1996 Jun;72(4):877-9. doi: 10.1016/0306-4522(96)00091-7. Neuroscience. 1996. PMID: 8735215

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. Among authors: davis mb. 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

Tyrosine hydroxylase polymorphism in familial and sporadic Parkinson's disease.

Planté-Bordeneuve V, Davis MB, Maraganore DM, Marsden CD, Harding AE. Planté-Bordeneuve V, et al. Among authors: davis mb. Mov Disord. 1994 May;9(3):337-9. doi: 10.1002/mds.870090312. Mov Disord. 1994. PMID: 7913740

4

Mutation analysis in patients with possible but apparently sporadic Huntington's disease.

Davis MB, Bateman D, Quinn NP, Marsden CD, Harding AE. Davis MB, et al. Lancet. 1994 Sep 10;344(8924):714-7. doi: 10.1016/s0140-6736(94)92208-x. Lancet. 1994. PMID: 7915776

5

Debrisoquine hydroxylase gene polymorphism in familial Parkinson's disease.

Planté-Bordeneuve V, Davis MB, Maraganore DM, Marsden CD, Harding AE. Planté-Bordeneuve V, et al. Among authors: davis mb. J Neurol Neurosurg Psychiatry. 1994 Aug;57(8):911-3. doi: 10.1136/jnnp.57.8.911. J Neurol Neurosurg Psychiatry. 1994. PMID: 8057112 Free PMC article.

6

Identification and sizing of the GAA trinucleotide repeat expansion of Friedreich's ataxia in 56 patients. Clinical and genetic correlates.

Lamont PJ, Davis MB, Wood NW. Lamont PJ, et al. Among authors: davis mb. Brain. 1997 Apr;120 ( Pt 4):673-80. doi: 10.1093/brain/120.4.673. Brain. 1997. PMID: 9153129

7

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: davis mb. Mov Disord. 1998 Mar;13(2):339-40. doi: 10.1002/mds.870130223. Mov Disord. 1998. PMID: 9539351

8

Genetics of Parkinsonism: a review.

Vaughan JR, Davis MB, Wood NW. Vaughan JR, et al. Among authors: davis mb. Ann Hum Genet. 2001 Mar;65(Pt 2):111-26. doi: 10.1017/S0003480001008557. Ann Hum Genet. 2001. PMID: 11427172 Review.

9

Cortical myoclonus in Huntington's disease.

Thompson PD, Bhatia KP, Brown P, Davis MB, Pires M, Quinn NP, Luthert P, Honovar M, O'Brien MD, Marsden CD, et al. Thompson PD, et al. Among authors: davis mb. Mov Disord. 1994 Nov;9(6):633-41. doi: 10.1002/mds.870090609. Mov Disord. 1994. PMID: 7845404

10

Evidence against an X-linked visual loss susceptibility locus in Leber hereditary optic neuropathy.

Chalmers RM, Davis MB, Sweeney MG, Wood NW, Harding AE. Chalmers RM, et al. Among authors: davis mb. Am J Hum Genet. 1996 Jul;59(1):103-8. Am J Hum Genet. 1996. PMID: 8659512 Free PMC article.

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