Davis MB - Search Results

1

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

2

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

3

Linkage analysis in British and French families with idiopathic torsion dystonia.

Warner TT, Fletcher NA, Davis MB, Ahmad F, Conway D, Feve A, Rondot P, Marsden CD, Harding AE. Warner TT, et al. Among authors: davis mb. Brain. 1993 Jun;116 ( Pt 3):739-44. doi: 10.1093/brain/116.3.739. Brain. 1993. PMID: 8513401

4

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.

5

Hereditary geniospasm: linkage to chromosome 9q13-q21 and evidence for genetic heterogeneity.

Jarman PR, Wood NW, Davis MT, Davis PV, Bhatia KP, Marsden CD, Davis MB. Jarman PR, et al. Among authors: davis mb, davis pv, davis mt. Am J Hum Genet. 1997 Oct;61(4):928-33. doi: 10.1086/514883. Am J Hum Genet. 1997. PMID: 9382105 Free PMC article.

6

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.

7

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.

8

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.

9

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

10

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

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