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Movement Disorders (revue) - Curation (Ncbi)

Index « Keywords » - entrée « Cytochrome P-450 CYP2D6 (genetics) »
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Cytochrome P-450 CYP2D6 (blood) < Cytochrome P-450 CYP2D6 (genetics) < Cytochrome P-450 CYP2D6 (metabolism)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 9.
Ident.Authors (with country if any)Title
000004 (1999) N. Sabbagh [France] ; A. Brice ; D. Marez ; A. Dürr ; M. Legrand ; J M Lo Guidice ; A. Destée ; Yves Agid [France] ; F. BrolyCYP2D6 polymorphism and Parkinson's disease susceptibility.
000078 (1999) O. Joost [États-Unis] ; C A Taylor ; C A Thomas ; L A Cupples ; M H Saint-Hilaire ; R G Feldman ; C T Baldwin ; R H MyersAbsence of effect of seven functional mutations in the CYP2D6 gene in Parkinson's disease.
000310 (2000) D M Maraganore [États-Unis] ; M J Farrer ; J A Hardy ; S K Mcdonnell ; D J Schaid ; W A RoccaCase-control study of debrisoquine 4-hydroxylase, N-acetyltransferase 2, and apolipoprotein E gene polymorphisms in Parkinson's disease.
000473 (2001) B S Harhangi [Pays-Bas] ; B A Oostra ; P. Heutink ; C M Van Duijn ; A. Hofman ; M M BretelerCYP2D6 polymorphism in Parkinson's disease: the Rotterdam Study.
003958 (2013) Raja Mehanna [États-Unis] ; Christine Hunter ; Anthony Davidson ; Joohi Jimenez-Shahed ; Joseph Jankovic [États-Unis]Analysis of CYP2D6 genotype and response to tetrabenazine.
004D70 (1997) S. Kösel [Allemagne] ; R. Egensperger ; N M Schnopp ; M B GraeberThe 'common deletion' is not increased in parkinsonian substantia nigra as shown by competitive polymerase chain reaction.
004F03 (1998) A G Riedl [Royaume-Uni] ; P M Watts ; P. Jenner ; C D MarsdenP450 enzymes and Parkinson's disease: the story so far.
004F69 (1998) C P Pang [Hong Kong] ; J. Zhang ; J. Woo ; D. Chan ; L K Law ; S F Tong ; T. Kwok ; R. KayRarity of debrisoquine hydroxylase gene polymorphism in Chinese patients with Parkinson's disease.
005043 (1998) D G Le Couteur ; S J MccannP450 enzymes and Parkinson's disease.

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