Davis MB - Search Results

1

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

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

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

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

Linkage analysis with chromosome 9 markers in hereditary essential tremor.

Conway D, Bain PG, Warner TT, Davis MB, Findley LJ, Thompson PD, Marsden CD, Harding AE. Conway D, et al. Among authors: davis mb. Mov Disord. 1993 Jul;8(3):374-6. doi: 10.1002/mds.870080324. Mov Disord. 1993. PMID: 8341306

7

Evidence against an X-linked locus close to DXS7 determining visual loss susceptibility in British and Italian families with Leber hereditary optic neuropathy.

Sweeney MG, Davis MB, Lashwood A, Brockington M, Toscano A, Harding AE. Sweeney MG, et al. Among authors: davis mb. Am J Hum Genet. 1992 Oct;51(4):741-8. Am J Hum Genet. 1992. PMID: 1415219 Free PMC article.

8

Transthyretin gene analysis in European patients with suspected familial amyloid polyneuropathy.

Reilly MM, Adams D, Booth DR, Davis MB, Said G, Laubriat-Bianchin M, Pepys MB, Thomas PK, Harding AE. Reilly MM, et al. Among authors: davis mb. Brain. 1995 Aug;118 ( Pt 4):849-56. doi: 10.1093/brain/118.4.849. Brain. 1995. PMID: 7655883

9

Loss of heterozygosity for DNA polymorphisms mapping to chromosomes 10 and 17 and prognosis in patients with gliomas.

Jones CE, Davis MB, Darling JL, Geddes JF, Thomas DG, Harding AE. Jones CE, et al. Among authors: davis mb. J Neurol Neurosurg Psychiatry. 1995 Feb;58(2):218-21. doi: 10.1136/jnnp.58.2.218. J Neurol Neurosurg Psychiatry. 1995. PMID: 7876855 Free PMC article.

10

Evidence for locus heterogeneity in autosomal dominant torsion dystonia.

Ahmad F, Davis MB, Waddy HM, Oley CA, Marsden CD, Harding AE. Ahmad F, et al. Among authors: davis mb. Genomics. 1993 Jan;15(1):9-12. doi: 10.1006/geno.1993.1003. Genomics. 1993. PMID: 8432555

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