Davis MB - Search Results

1

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.

2

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

3

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.

4

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

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

Transthyretin gene mutations in British and French patients with amyloid neuropathy.

Bhatia K, Reilly M, Adams D, Davis MB, Hawkes CH, Thomas PK, Said G, Harding AE. Bhatia K, et al. Among authors: davis mb. J Neurol Neurosurg Psychiatry. 1993 Jun;56(6):694-7. doi: 10.1136/jnnp.56.6.694. J Neurol Neurosurg Psychiatry. 1993. PMID: 8509786 Free PMC article.

7

Haplotype analysis of French, British and other European patients with familial amyloid polyneuropathy (met 30 and tyr 77).

Reilly MM, Adams D, Davis MB, Said G, Harding AE. Reilly MM, et al. Among authors: davis mb. J Neurol. 1995 Oct;242(10):664-8. doi: 10.1007/BF00866917. J Neurol. 1995. PMID: 8568528

8

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

9

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.

10

Prenatal diagnosis of mitochondrial DNA8993 T----G disease.

Harding AE, Holt IJ, Sweeney MG, Brockington M, Davis MB. Harding AE, et al. Among authors: davis mb. Am J Hum Genet. 1992 Mar;50(3):629-33. Am J Hum Genet. 1992. PMID: 1539598 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

287 results

Search Page

Filters