Harding AE - Search Results

1

Evaluation of four candidate genes encoding proteins of the dopamine pathway in familial and sporadic Parkinson's disease: evidence for association of a DRD2 allele.

Planté-Bordeneuve V, Taussig D, Thomas F, Said G, Wood NW, Marsden CD, Harding AE. Planté-Bordeneuve V, et al. Among authors: harding ae. Neurology. 1997 Jun;48(6):1589-93. doi: 10.1212/wnl.48.6.1589. Neurology. 1997. PMID: 9191771

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: harding ae. 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

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: harding ae. Mov Disord. 1994 May;9(3):337-9. doi: 10.1002/mds.870090312. Mov Disord. 1994. PMID: 7913740

4

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: harding ae. 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.

5

A clinical and genetic study of familial Parkinson's disease.

Maraganore DM, Harding AE, Marsden CD. Maraganore DM, et al. Among authors: harding ae. Mov Disord. 1991;6(3):205-11. doi: 10.1002/mds.870060303. Mov Disord. 1991. PMID: 1922124

6

Nigral degeneration in neuroacanthocytosis.

Rinne JO, Daniel SE, Scaravilli F, Harding AE, Marsden CD. Rinne JO, et al. Among authors: harding ae. Neurology. 1994 Sep;44(9):1629-32. doi: 10.1212/wnl.44.9.1629. Neurology. 1994. PMID: 7936287

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: harding ae. J Neurol. 1995 Oct;242(10):664-8. doi: 10.1007/BF00866917. J Neurol. 1995. PMID: 8568528

8

[Demonstration of genetic mutation in most of the amyloid neuropathies with sporadic occurrence].

Adams D, Reilly M, Harding AE, Said G. Adams D, et al. Among authors: harding ae. Rev Neurol (Paris). 1992;148(12):736-41. Rev Neurol (Paris). 1992. PMID: 1338934 Review. French.

9

Parkinson's disease in twins studied with 18F-dopa and positron emission tomography.

Burn DJ, Mark MH, Playford ED, Maraganore DM, Zimmerman TR Jr, Duvoisin RC, Harding AE, Marsden CD, Brooks DJ. Burn DJ, et al. Among authors: harding ae. Neurology. 1992 Oct;42(10):1894-900. doi: 10.1212/wnl.42.10.1894. Neurology. 1992. PMID: 1407569

10

A genetic study of idiopathic focal dystonias.

Waddy HM, Fletcher NA, Harding AE, Marsden CD. Waddy HM, et al. Among authors: harding ae. Ann Neurol. 1991 Mar;29(3):320-4. doi: 10.1002/ana.410290315. Ann Neurol. 1991. PMID: 2042948

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