Davis MB - Search Results

1

A Yorkshire family with adult-onset cranio-cervical primary torsion dystonia.

Münchau A, Valente EM, Davis MB, Stinton V, Wood NW, Quinn NP, Bhatia KP. Münchau A, et al. Among authors: davis mb. Mov Disord. 2000 Sep;15(5):954-9. doi: 10.1002/1531-8257(200009)15:5<954::aid-mds1028>3.0.co;2-i. Mov Disord. 2000. PMID: 11009204

2

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

3

A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16.

Valente EM, Spacey SD, Wali GM, Bhatia KP, Dixon PH, Wood NW, Davis MB. Valente EM, et al. Among authors: davis mb. Brain. 2000 Oct;123 ( Pt 10):2040-5. doi: 10.1093/brain/123.10.2040. Brain. 2000. PMID: 11004121

4

DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13--36.32 in an Italian family with cranial-cervical or upper limb onset.

Valente EM, Bentivoglio AR, Cassetta E, Dixon PH, Davis MB, Ferraris A, Ialongo T, Frontali M, Wood NW, Albanese A. Valente EM, et al. Among authors: davis mb. Ann Neurol. 2001 Mar;49(3):362-6. Ann Neurol. 2001. PMID: 11261511

5

Identification of a novel primary torsion dystonia locus (DYT13) on chromosome 1p36 in an Italian family with cranial-cervical or upper limb onset.

Valente EM, Bentivoglio AR, Cassetta E, Dixon PH, Davis MB, Ferraris A, Ialongo T, Frontali M, Wood NW, Albanese A. Valente EM, et al. Among authors: davis mb. Neurol Sci. 2001 Feb;22(1):95-6. doi: 10.1007/s100720170063. Neurol Sci. 2001. PMID: 11487218

6

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.

7

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

8

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.

9

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

10

Paroxysmal dystonic choreoathetosis. Genetic linkage studies in a British family.

Jarman PR, Davis MB, Hodgson SV, Marsden CD, Wood NW. Jarman PR, et al. Among authors: davis mb. Brain. 1997 Dec;120 ( Pt 12):2125-30. doi: 10.1093/brain/120.12.2125. Brain. 1997. PMID: 9448567

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