Harding AE - Search Results

1

[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.

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: harding ae. Brain. 1995 Aug;118 ( Pt 4):849-56. doi: 10.1093/brain/118.4.849. Brain. 1995. PMID: 7655883

3

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: harding ae. 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.

4

Molecular genetics of amyloid neuropathy in Europe.

Holt IJ, Harding AE, Middleton L, Chrysostomou G, Said G, King RH, Thomas PK. Holt IJ, et al. Among authors: harding ae. Lancet. 1989 Mar 11;1(8637):524-6. doi: 10.1016/s0140-6736(89)90068-8. Lancet. 1989. PMID: 2564060

5

Familial amyloid polyneuropathy (TTR ala 60) in north west Ireland: a clinical, genetic, and epidemiological study.

Reilly MM, Staunton H, Harding AE. Reilly MM, et al. Among authors: harding ae. J Neurol Neurosurg Psychiatry. 1995 Jul;59(1):45-9. doi: 10.1136/jnnp.59.1.45. J Neurol Neurosurg Psychiatry. 1995. PMID: 7608709 Free PMC article.

6

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

7

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

8

Molecular genetics of peripheral neuropathies.

Harding AE. Harding AE. Baillieres Clin Neurol. 1995 Nov;4(3):383-400. Baillieres Clin Neurol. 1995. PMID: 8599717 Review.

9

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. Among authors: harding ae. Lancet. 1994 Sep 10;344(8924):714-7. doi: 10.1016/s0140-6736(94)92208-x. Lancet. 1994. PMID: 7915776

10

Irish (Donegal) amyloidosis is associated with the transthyretinALA60 (Appalachian) variant.

Staunton H, Davis MB, Guiloff RJ, Nakazato M, Miyazato N, Harding AE. Staunton H, et al. Among authors: harding ae. Brain. 1991 Dec;114 ( Pt 6):2675-9. doi: 10.1093/brain/114.6.2675. Brain. 1991. PMID: 1664269

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