A. E. Harding And NotAngleterre
List of bibliographic references
Number of relevant bibliographic references: 10.| Ident. | Authors (with country if any) | Title |
|---|---|---|
| 005A26 | V. Plante-Bordeneuve [Royaume-Uni] ; O. Bandmann ; G. Wenning ; N. P. Quinn ; S. E. Daniel ; A. E. Harding | CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy |
| 005C40 | V. Plante-Bordeneuve [Royaume-Uni] ; M. B. Davis ; D. M. Maraganore ; C. D. Marsden ; A. E. Harding | Tyrosine hydroxylase polymorphism in familial and sporadic Parkinson's disease |
| 006229 | N. A. Fletcher [Royaume-Uni] ; A. E. Harding ; C. D. Marsden | Intrafamilial correlation in idiopathic torsion dystonia |
| 006247 | D. M. Maraganore ; A. E. Harding ; C. D. Marsden | A clinical and genetic study of familial Parkinson's disease |
| 006248 | N. A. Fletcher [Royaume-Uni] ; A. E. Harding ; C. D. Marsden | A case-control study of idiopathic torsion dystonia |
| 006372 | D. Truong ; A. E. Harding ; F. Scaravilli ; S. J. M. Smith ; J. A. Morgan-Hughes ; C. D. Marsden | Movement disorders in mitochondrial myopathies: a study of nine cases with two autopsy studies |
| 006374 | A. H. V. Schapira ; I. J. Holt ; M. Sweeney ; A. E. Harding ; P. Jenner ; C. D. Marsden | Mitochondrial DNA analysis in Parkinson's disease |
| 006488 | A. E. Harding | Viewpoints on the Ramsay Hunt syndrome. III: Ramsay Hunt syndrome, Unverricht-Lundborg disease, or what? |
| 006512 | R. Stell ; A. M. Bronstein ; G. T. Plant ; A. E. Harding | Ataxia telangiectasia: a reappraisal of the ocular motor features and their value in the diagnosis of atypical cases |
| 006585 | N. A. Fletcher ; R. Stell ; A. E. Harding ; C. D. Marsden | Degenerative cerebellar ataxia and focal dystonia |
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