Hardev Sangha < Harding < Hari K. Bhat

Facettes :

List of bibliographic references indexed by Harding

Number of relevant bibliographic references: 9.

Ident.	Authors (with country if any)	Title
005925 (1995)	V. Planté-Bordeneuve [Royaume-Uni] ; O. Bandmann [Royaume-Uni] ; G. Wenning [Royaume-Uni] ; N. P. Quinn [Royaume-Uni] ; S. E. Daniel [Royaume-Uni] ; Harding [Royaume-Uni]	CYP2D6‐debrisoquine hydroxylase gene polymorphism in multiple system atrophy
005A74 (1994)	V. Planté-Bordeneuve [Royaume-Uni] ; M. B. Davis [Royaume-Uni] ; D. M. Maraganore [Royaume-Uni] ; C. D. Marsden [Royaume-Uni] ; Harding [Royaume-Uni]	Tyrosine hydroxylase polymorphism in familial and sporadic Parkinson's disease
005B94 (1994)	P. D. Thompson [Royaume-Uni] ; K. P. Bhatia [Royaume-Uni] ; P. Brown [Royaume-Uni] ; M. B. Davis [Royaume-Uni] ; M. Pires [Royaume-Uni] ; N. P. Quinn [Royaume-Uni] ; P. Luthert [Royaume-Uni] ; M. Honovar [Royaume-Uni] ; M. D. O'Brien [Royaume-Uni] ; C. D. Marsden [Royaume-Uni] ; Harding [Royaume-Uni]	Cortical myoclonus in huntington's disease
005C15 (1994)	T. T. Warner ; G. G. Lennox ; I. Janota [Royaume-Uni] ; Harding	Autosomal‐dominant dentatorubropallidoluysian atrophy in the United Kingdom
005D74 (1993)	D. Conway [Royaume-Uni] ; P. G. Bain [Royaume-Uni] ; T. T. Warner [Royaume-Uni] ; M. B. Davis [Royaume-Uni] ; L. J. Findley [Royaume-Uni] ; P. D. Thompson [Royaume-Uni] ; C. D. Marsden [Royaume-Uni] ; Harding [Royaume-Uni]	Linkage analysis with chromosome 9 markers in hereditary essential tremor
006298 (1990)	Truong [Royaume-Uni, États-Unis] ; Harding [Royaume-Uni] ; F. Scaravilli [Royaume-Uni] ; S. J. M. Smith [Royaume-Uni] ; J. A. Morgan-Hughes [Royaume-Uni] ; C. D. Marsden [Royaume-Uni]	Movement disorders in mitochondrial myopathies. A study of nine cases with two autopsy studies
006434 (1989)	Harding [Royaume-Uni]	Ramsay Hunt syndrome, Unverricht‐Lundborg disease, or what?
006526 (1988)	R. J. Coleman [Royaume-Uni] ; S. A. Robb [Royaume-Uni] ; B. D. Lake [Royaume-Uni] ; E. M. Brett [Royaume-Uni] ; Harding [Royaume-Uni]	The diverse neurological features of Niemann‐Pick disease type C: A report of two cases
006546 (1988)	V. Peter Misra [Royaume-Uni] ; Michael Baraitser [Royaume-Uni] ; Harding [Royaume-Uni]	Genetic prediction in Huntington's disease: What are the limitations imposed by pedigree structure

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