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Journal Abstract Search


119 related items for PubMed ID: 8615186

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  • 2. CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy.
    Planté-Bordeneuve V, Bandmann O, Wenning G, Quinn NP, Daniel SE, Harding AE.
    Mov Disord; 1995 May; 10(3):277-8. PubMed ID: 7651442
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  • 4. Association between the oxidative polymorphism and early onset of Parkinson's disease.
    Agúndez JA, Jiménez-Jiménez FJ, Luengo A, Bernal ML, Molina JA, Ayuso L, Vázquez A, Parra J, Duarte J, Coria F.
    Clin Pharmacol Ther; 1995 Mar; 57(3):291-8. PubMed ID: 7697946
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  • 6. Genetic polymorphisms in Parkinson's disease.
    Checkoway H, Farin FM, Costa-Mallen P, Kirchner SC, Costa LG.
    Neurotoxicology; 1998 Mar; 19(4-5):635-43. PubMed ID: 9745923
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  • 9. A novel cytochrome P-450IID6 mutant gene associated with Parkinson's disease.
    Tsuneoka Y, Matsuo Y, Iwahashi K, Takeuchi H, Ichikawa Y.
    J Biochem; 1993 Aug; 114(2):263-6. PubMed ID: 7903297
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  • 10. Debrisoquine hydroxylase and Parkinson's disease.
    Kondo I, Kanazawa I.
    Adv Neurol; 1993 Aug; 60():338-42. PubMed ID: 8420147
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  • 13. P450 enzymes and Parkinson's disease: the story so far.
    Riedl AG, Watts PM, Jenner P, Marsden CD.
    Mov Disord; 1998 Mar; 13(2):212-20. PubMed ID: 9539332
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  • 16. Pharmacogenetics: Part II.
    Gibaldi M.
    Ann Pharmacother; 1992 Feb; 26(2):255-61. PubMed ID: 1554942
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  • 18. Rarity of debrisoquine hydroxylase gene polymorphism in Chinese patients with Parkinson's disease.
    Pang CP, Zhang J, Woo J, Chan D, Law LK, Tong SF, Kwok T, Kay R.
    Mov Disord; 1998 May; 13(3):529-32. PubMed ID: 9613747
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