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Movement Disorders (revue) - Checkpoint (Ncbi)

Index « Auteurs » - entrée « A E Harding »
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A E Di Rosa < A E Harding < A E Holley  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 17.
Ident.Authors (with country if any)Title
001D26 (1991) N A Fletcher [Royaume-Uni] ; A E Harding ; C D MarsdenA case-control study of idiopathic torsion dystonia.
001D27 (1991) N A Fletcher [Royaume-Uni] ; A E Harding ; C D MarsdenIntrafamilial correlation in idiopathic torsion dystonia.
002540 (1991) D M Maraganore [Royaume-Uni] ; A E Harding ; C D MarsdenA clinical and genetic study of familial Parkinson's disease.
002840 (1990) A H Schapira [Royaume-Uni] ; I J Holt ; M. Sweeney ; A E Harding ; P. Jenner ; C D MarsdenMitochondrial DNA analysis in Parkinson's disease.
003940 (1990) D D Truong [Royaume-Uni] ; A E Harding ; F. Scaravilli ; S J Smith ; J A Morgan-Hughes ; C D MarsdenMovement disorders in mitochondrial myopathies. A study of nine cases with two autopsy studies.
004031 (1989) A E Harding [Royaume-Uni]Ramsay Hunt syndrome, Unverricht-Lundborg disease, or what?
004550 (1989) R. Stell [Royaume-Uni] ; 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.
004580 (1988) V P Misra [Royaume-Uni] ; M. Baraitser ; A E HardingGenetic prediction in Huntington's disease: what are the limitations imposed by pedigree structure?
004596 (1988) R J Coleman [Royaume-Uni] ; 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.
004613 (1988) N A Fletcher [Royaume-Uni] ; R. Stell ; A E Harding ; C D MarsdenDegenerative cerebellar ataxia and focal dystonia.
004721 (1995) V. Planté-Bordeneuve [Royaume-Uni] ; O. Bandmann ; G. Wenning ; N P Quinn ; S E Daniel ; A E HardingCYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy.
004813 (1994) V. Planté-Bordeneuve [Royaume-Uni] ; M B Davis ; D M Maraganore ; C D Marsden ; A E HardingTyrosine hydroxylase polymorphism in familial and sporadic Parkinson's disease.
004846 (1994) T T Warner [Royaume-Uni] ; G G Lennox ; I. Janota ; A E HardingAutosomal-dominant dentatorubropallidoluysian atrophy in the United Kingdom.
004847 (1994) J O Rinne [Royaume-Uni] ; S E Daniel ; F. Scaravilli ; M. Pires ; A E Harding ; C D MarsdenThe neuropathological features of neuroacanthocytosis.
004970 (1993) D. Conway [Royaume-Uni] ; 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.
004A77 (1996) S D Taylor-Robinson [Royaume-Uni] ; 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.
004C62 (1997) G K Wenning [Royaume-Uni] ; 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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