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Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy.
La Spada AR, Wilson EM, Lubahn DB, Harding AE, Fischbeck KH. La Spada AR, et al. Nature. 1991 Jul 4;352(6330):77-9. doi: 10.1038/352077a0. Nature. 1991. PMID: 2062380
Mitochondrial myopathies: genetic defects.
Harding AE, Holt IJ, Cooper JM, Schapira AH, Sweeney M, Clark JB, Morgan-Hughes JA. Harding AE, et al. Biochem Soc Trans. 1990 Aug;18(4):519-22. doi: 10.1042/bst0180519. Biochem Soc Trans. 1990. PMID: 2276422 Review. No abstract available.
Evidence for locus heterogeneity in autosomal dominant torsion dystonia.
Ahmad F, Davis MB, Waddy HM, Oley CA, Marsden CD, Harding AE. Ahmad F, et al. Genomics. 1993 Jan;15(1):9-12. doi: 10.1006/geno.1993.1003. Genomics. 1993. PMID: 8432555
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. Mov Disord. 1994 May;9(3):337-9. doi: 10.1002/mds.870090312. Mov Disord. 1994. PMID: 7913740
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. 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.
Linkage analysis in British and French families with idiopathic torsion dystonia.
Warner TT, Fletcher NA, Davis MB, Ahmad F, Conway D, Feve A, Rondot P, Marsden CD, Harding AE. Warner TT, et al. Brain. 1993 Jun;116 ( Pt 3):739-44. doi: 10.1093/brain/116.3.739. Brain. 1993. PMID: 8513401
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