Davis MB - Search Results

1

Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic study.

Nicholl DJ, Vaughan JR, Khan NL, Ho SL, Aldous DE, Lincoln S, Farrer M, Gayton JD, Davis MB, Piccini P, Daniel SE, Lennox GG, Brooks DJ, Williams AC, Wood NW. Nicholl DJ, et al. Among authors: davis mb. Brain. 2002 Jan;125(Pt 1):44-57. doi: 10.1093/brain/awf013. Brain. 2002. PMID: 11834592

2

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

3

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.

4

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

5

The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates.

Giunti P, Sabbadini G, Sweeney MG, Davis MB, Veneziano L, Mantuano E, Federico A, Plasmati R, Frontali M, Wood NW. Giunti P, et al. Among authors: davis mb. Brain. 1998 Mar;121 ( Pt 3):459-67. doi: 10.1093/brain/121.3.459. Brain. 1998. PMID: 9549522

6

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

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

8

Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3.

Worth PF, Giunti P, Gardner-Thorpe C, Dixon PH, Davis MB, Wood NW. Worth PF, et al. Among authors: davis mb. Am J Hum Genet. 1999 Aug;65(2):420-6. doi: 10.1086/302495. Am J Hum Genet. 1999. PMID: 10417284 Free PMC article.

9

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

10

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

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