Phenothiazines < Phenotype < Phenylcarbamates

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 26.
[20-40] [0 - 20][0 - 26]

Ident.	Authors (with country if any)	Title
001314 (2000)	M G Murer [France] ; G. Dziewczapolski ; P. Salin ; M. Vila ; K Y Tseng ; M. Ruberg ; M. Rubinstein ; M A Kelly ; D K Grandy ; M J Low ; E. Hirsch ; R. Raisman-Vozari ; O. Gershanik	The indirect basal ganglia pathway in dopamine D(2) receptor-deficient mice.
001367 (1999)	N. Abbas [France] ; C B Lücking ; S. Ricard ; A. Dürr ; V. Bonifati ; G. De Michele ; S. Bouley ; J R Vaughan ; T. Gasser ; R. Marconi ; E. Broussolle ; C. Brefel-Courbon ; B S Harhangi ; B A Oostra ; E. Fabrizio ; G A Böhme ; L. Pradier ; N W Wood ; A. Filla ; G. Meco ; P. Denefle ; Y. Agid ; A. Brice	A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
001375 (1999)	N. Sabbagh [France] ; A. Brice ; D. Marez ; A. Dürr ; M. Legrand ; J M Lo Guidice ; A. Destée ; Y. Agid ; F. Broly	CYP2D6 polymorphism and Parkinson's disease susceptibility.
001529 (1996)	A. Dürr [France] ; A. Brice	Genetics of movement disorders.
001531 (1996)	G. Lucotte [France] ; J C Turpin ; N. Gérard ; S. Panserat ; R. Krishnamoorthy	Mutation frequencies of the cytochrome CYP2D6 gene in Parkinson disease patients and in families.
001654 (1994)	F. Tison ; C. Coutelle ; P. Henry ; A. Cassaigne	Glutathion S-transferase (class mu) phenotype in Parkinson's disease.

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