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Movement Disorders (revue) - Merge (PascalFrancis)

Index « FA11s1.i » - entrée « HARDING (A. E.) »
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HARDIMAN (Oria) < HARDING (A. E.) < HARDING (Sandra J.)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 18.
Ident.Authors (with country if any)Title
002D81 (1988) V. P. Misra ; M. Baraitser ; A. E. HardingGenetic prediction in Huntington's disease: what are the limitations imposed by pedigree structure?
002D92 (1989) R. Stell ; A. M. Bronstein ; G. T. Plant ; A. E. HardingAtaxia telangiectasia: a reappraisal of the ocular motor features and their value in the diagnosis of atypical cases
002E25 (1988) N. A. Fletcher ; R. Stell ; A. E. Harding ; C. D. MarsdenDegenerative cerebellar ataxia and focal dystonia
002E32 (1988) R. J. Coleman ; S. A. Robb ; B. D. Lake ; E. M. Brett ; A. E. HardingThe diverse neurological features of Niemann-Pick disease type C: a report of two cases
002E44 (1989) A. E. HardingViewpoints on the Ramsay Hunt syndrome. III: Ramsay Hunt syndrome, Unverricht-Lundborg disease, or what?
002E73 (1990) D. Truong ; A. E. Harding ; F. Scaravilli ; S. J. M. Smith ; J. A. Morgan-Hughes ; C. D. MarsdenMovement disorders in mitochondrial myopathies: a study of nine cases with two autopsy studies
002E80 (1990) A. H. V. Schapira ; I. J. Holt ; M. Sweeney ; A. E. Harding ; P. Jenner ; C. D. MarsdenMitochondrial DNA analysis in Parkinson's disease
002F31 (1991) D. M. Maraganore ; A. E. Harding ; C. D. MarsdenA clinical and genetic study of familial Parkinson's disease
003037 (1991) N. A. Fletcher ; A. E. Harding ; C. D. MarsdenA case-control study of idiopathic torsion dystonia
003038 (1991) N. A. Fletcher ; A. E. Harding ; C. D. MarsdenIntrafamilial correlation in idiopathic torsion dystonia
003136 (1993) D. Conway ; P. G. Bain ; T. T. Warner ; M. B. Davis ; L. J. Findley ; P. D. Thompson ; C. D. Marsden ; A. E. HardingLinkage analysis with chromosome 9 markers in hereditary essential tremor
003210 (1994) T. T. Warner ; G. G. Lennox ; I. Janota ; A. E. HardingAutosomal-dominant dentatorubropallidoluysian atrophy in the United Kingdom
003211 (1994) J. O. Rinne ; S. E. Daniel ; F. Scaravilli ; M. Pires ; A. E. Harding ; C. D. MarsdenThe neuropathological features of neuroacanthocytosis
003220 (1994) V. Plante-Bordeneuve ; M. B. Davis ; D. M. Maraganore ; C. D. Marsden ; A. E. HardingTyrosine hydroxylase polymorphism in familial and sporadic Parkinson's disease
003260 (1994) P. D. Thompson ; K. P. Bhatia ; P. Brown ; M. B. Davis ; M. Pires ; N. P. Quinn ; P. Luthert ; M. Honovar ; M. D. P'Brien ; C. D. Marsden ; A. E. HardingCortical myoclonus in Huntington's disease
003325 (1995) V. Plante-Bordeneuve ; O. Bandmann ; G. Wenning ; N. P. Quinn ; S. E. Daniel ; A. E. HardingCYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy
003408 (1996) S. D. Taylor-Robinson ; R. A. Weeks ; D. J. Bryant ; J. Sargentoni ; C. D. Marcus ; A. E. Harding ; D. J. BrooksProton magnetic resonance spectroscopy in Huntington's disease : Evidence in favour of the glutamate excitotoxic theory ?
003534 (1997) G. K. Wenning ; E. Kraft ; R. Beck ; C. J. Fowler ; C. J. Mathias ; N. P. Quinn ; A. E. HardingCerebellar presentation of multiple system atrophy

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