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4. Oxidative polymorphism of debrisoquine is not related to the risk of Alzheimer's disease. Benítez J; Barquero MS; Coria F; Molina JA; Jiménez-Jiménez FJ; Ladero JM J Neurol Sci; 1993 Jul; 117(1-2):8-11. PubMed ID: 8410072 [TBL] [Abstract][Full Text] [Related]
5. 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) is N-demethylated by cytochromes P450 2D6, 1A2 and 3A4--implications for susceptibility to Parkinson's disease. Coleman T; Ellis SW; Martin IJ; Lennard MS; Tucker GT J Pharmacol Exp Ther; 1996 May; 277(2):685-90. PubMed ID: 8627546 [TBL] [Abstract][Full Text] [Related]
6. Debrisoquine hydroxylation genotype in familial forms of idiopathic Parkinson's disease. Bordet R; Broly F; Destée A; Libersa C Adv Neurol; 1996; 69():97-100. PubMed ID: 8615190 [No Abstract] [Full Text] [Related]
7. The metabolism of aprindine in relation to the sparteine/debrisoquine polymorphism. Ebner T; Eichelbaum M Br J Clin Pharmacol; 1993 Apr; 35(4):426-30. PubMed ID: 8485023 [TBL] [Abstract][Full Text] [Related]
16. [Hydroxylation of debrisoquin in Parkinson's disease]. Meillard MN; Bentué-Ferrer D; Brunet-Bourgin F; Morel G; Allain H Presse Med; 1990 May; 19(20):947-9. PubMed ID: 2141131 [TBL] [Abstract][Full Text] [Related]
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18. Debrisoquine and S-mephenytoin hydroxylation polymorphisms in a Russian population living in Estonia. Marandi T; Dahl ML; Rägo L; Kiivet R; Sjöqvist F Eur J Clin Pharmacol; 1997; 53(3-4):257-60. PubMed ID: 9476041 [TBL] [Abstract][Full Text] [Related]
19. Hepatic monooxygenase activities in subjects with a genetic defect in drug oxidation. Meier PJ; Mueller HK; Dick B; Meyer UA Gastroenterology; 1983 Sep; 85(3):682-92. PubMed ID: 6603386 [TBL] [Abstract][Full Text] [Related]
20. Cytochrome P450 isozymes catalyzing 4-hydroxylation of parkinsonism-related compound 1,2,3,4-tetrahydroisoquinoline in rat liver microsomes. Suzuki T; Fujita S; Narimatsu S; Masubuchi Y; Tachibana M; Ohta S; Hirobe M FASEB J; 1992 Jan; 6(2):771-6. PubMed ID: 1537468 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]