-
1
-
-
0028964602
-
Association between the oxidative polymorphism and early onset of Parkinson's disease
-
Agundez JAG, Jimenez-Jimenez FJ, Luengo A, Bernal ML, Molina JA, Ayuso L, et al. Association between the oxidative polymorphism and early onset of Parkinson's disease. Clin Pharmacol Ther 1995; 57:291-298.
-
(1995)
Clin Pharmacol Ther
, vol.57
, pp. 291-298
-
-
Agundez, J.A.G.1
Jimenez-Jimenez, F.J.2
Luengo, A.3
Bernal, M.L.4
Molina, J.A.5
Ayuso, L.6
-
2
-
-
0025572192
-
Hydroxylation polymorphisms of debrisoquine and mephenytoin in European populations
-
Alvan G, Bechtel P, Iselius L, Gundert Remy U. Hydroxylation polymorphisms of debrisoquine and mephenytoin in European populations. Eur J Clin Pharmacol 1990; 39:533-537.
-
(1990)
Eur J Clin Pharmacol
, vol.39
, pp. 533-537
-
-
Alvan, G.1
Bechtel, P.2
Iselius, L.3
Gundert Remy, U.4
-
3
-
-
0026589459
-
Mutant debrisoquine hydroxylation genes in Parkinson's disease
-
Armstrong M, Daly AK, Cholerton S, Bateman DN, Idle JR. Mutant debrisoquine hydroxylation genes in Parkinson's disease. Lancet 1992; 339:1017-1018.
-
(1992)
Lancet
, vol.339
, pp. 1017-1018
-
-
Armstrong, M.1
Daly, A.K.2
Cholerton, S.3
Bateman, D.N.4
Idle, J.R.5
-
4
-
-
0022408175
-
Ecogenetics of Parkinson's disease: 4-hydroxylation of debrisoquine
-
Barbeau A, Roy M, Paris S, Cloutier T, Plasse L, Poirier J. Ecogenetics of Parkinson's disease: 4-hydroxylation of debrisoquine. Lancet 1985; 30:1213-1215.
-
(1985)
Lancet
, vol.30
, pp. 1213-1215
-
-
Barbeau, A.1
Roy, M.2
Paris, S.3
Cloutier, T.4
Plasse, L.5
Poirier, J.6
-
5
-
-
0025269613
-
Oxidative polymorphism of debrisoquine in Parkinson's disease
-
Benitez J, Ladero JM, Jiménez-Jiménez FJ, Martinez C, Puerto AM, Valdivielso MJ, et al. Oxidative polymorphism of debrisoquine in Parkinson's disease. J Neurol Neurosurg Psych 1990; 53:289-292.
-
(1990)
J Neurol Neurosurg Psych
, vol.53
, pp. 289-292
-
-
Benitez, J.1
Ladero, J.M.2
Jiménez-Jiménez, F.J.3
Martinez, C.4
Puerto, A.M.5
Valdivielso, M.J.6
-
6
-
-
0029685631
-
Debrisoquine hydroxylation genotype in familial forms of idiopathic Parkinson's disease
-
Bordet R, Broly F, Desteé A, Libersa C. Debrisoquine hydroxylation genotype in familial forms of idiopathic Parkinson's disease. Adv Neurol 1996; 69:97-100.
-
(1996)
Adv Neurol
, vol.69
, pp. 97-100
-
-
Bordet, R.1
Broly, F.2
Desteé, A.3
Libersa, C.4
-
7
-
-
0024359574
-
Clinical significance of the sparteine/debrisoquine oxidation polymorphism
-
Brosen K, Gram LF. Clinical significance of the sparteine/debrisoquine oxidation polymorphism. Eur J Clin Pharmacol 1989; 36:537-547.
-
(1989)
Eur J Clin Pharmacol
, vol.36
, pp. 537-547
-
-
Brosen, K.1
Gram, L.F.2
-
8
-
-
0345406830
-
Sparteine oxidation in patients with early and late-onset of Parkinson's disease
-
Chiba K, Imai H, Yoshino H, Kato J, Ishizaki T, Narabayashi H. Sparteine oxidation in patients with early and late-onset of Parkinson's disease. Clin Neurol 1993; 33:103-109.
-
(1993)
Clin Neurol
, vol.33
, pp. 103-109
-
-
Chiba, K.1
Imai, H.2
Yoshino, H.3
Kato, J.4
Ishizaki, T.5
Narabayashi, H.6
-
9
-
-
0031015828
-
The sparteine/debrisoquine (CYP2D6) oxidation polymorphism and the risk of lung cancer: A meta-analysis
-
Christensen PM, Gotzsche PC, Brosen K. The sparteine/debrisoquine (CYP2D6) oxidation polymorphism and the risk of lung cancer: a meta-analysis. Eur J Clin Pharmacol 1997; 51:389-393.
-
(1997)
Eur J Clin Pharmacol
, vol.51
, pp. 389-393
-
-
Christensen, P.M.1
Gotzsche, P.C.2
Brosen, K.3
-
10
-
-
0010506383
-
Debrisoquine metabolism in Parkinson's disease
-
Comella CL, Tanner CM, Goetz CG, Gans S, Rapp D, Fischer J. Debrisoquine metabolism in Parkinson's disease. Neurology 1987; 37(Suppl 1):261-262.
-
(1987)
Neurology
, vol.37
, Issue.SUPPL. 1
, pp. 261-262
-
-
Comella, C.L.1
Tanner, C.M.2
Goetz, C.G.3
Gans, S.4
Rapp, D.5
Fischer, J.6
-
11
-
-
0029835547
-
Genetic variability of the CYP2D6 gene is not a risk factor for sporadic Parkinson's disease
-
Diederich N, Hilger C, Goetz CG, Keipes M, Hentges F, Vieregge P, Metz H. Genetic variability of the CYP2D6 gene is not a risk factor for sporadic Parkinson's disease. Ann Neurol 1996; 40:463-465.
-
(1996)
Ann Neurol
, vol.40
, pp. 463-465
-
-
Diederich, N.1
Hilger, C.2
Goetz, C.G.3
Keipes, M.4
Hentges, F.5
Vieregge, P.6
Metz, H.7
-
12
-
-
0023568113
-
MPTP, the neurotoxin inducing Parkinson's disease, is a potent competitive inhibitor of human and nit cytochrome P450 isozymes (P450bufl, P450db1) catalyzing debrisoquine 4-hydroxylation
-
Fonne Pfister R, Bargetzi MJ, Meyer UA. MPTP, the neurotoxin inducing Parkinson's disease, is a potent competitive inhibitor of human and nit cytochrome P450 isozymes (P450bufl, P450db1) catalyzing debrisoquine 4-hydroxylation. Biochem Biophys Res Commun 1987; 148:1144-1150.
-
(1987)
Biochem Biophys Res Commun
, vol.148
, pp. 1144-1150
-
-
Fonne Pfister, R.1
Bargetzi, M.J.2
Meyer, U.A.3
-
13
-
-
0029851872
-
The CYP2D6B allele is not overrepresented in a population of German patients with idiopathic Parkinson's disease
-
Gasser T, Müller-Myhsok B, Supala A, Zimmer G, Wieditz G, Wszolek ZK, et al. The CYP2D6B allele is not overrepresented in a population of German patients with idiopathic Parkinson's disease. J Neurol Neurosurg Psych 1996; 61:518-520.
-
(1996)
J Neurol Neurosurg Psych
, vol.61
, pp. 518-520
-
-
Gasser, T.1
Müller-Myhsok, B.2
Supala, A.3
Zimmer, G.4
Wieditz, G.5
Wszolek, Z.K.6
-
14
-
-
0025307264
-
Poor hydroxylator phenotypes of debrisoquine and S-mephenytoin are not over-represented in a group of patients with Parkinson's disease
-
Gudjonsson O, Sanz E, Alvan G, Aquilonius SM, Reviriego J. Poor hydroxylator phenotypes of debrisoquine and S-mephenytoin are not over-represented in a group of patients with Parkinson's disease. Br J Clin Pharmacol 1990; 30:301-502.
-
(1990)
Br J Clin Pharmacol
, vol.30
, pp. 301-502
-
-
Gudjonsson, O.1
Sanz, E.2
Alvan, G.3
Aquilonius, S.M.4
Reviriego, J.5
-
15
-
-
0025080352
-
Genotypingof poor metabolisers of debrisoquine by allele-specific PCR amplification
-
Heim M, Meyer UA. Genotypingof poor metabolisers of debrisoquine by allele-specific PCR amplification [see comments]. Lancet 1990; 336:529-532.
-
(1990)
Lancet
, vol.336
, pp. 529-532
-
-
Heim, M.1
Meyer, U.A.2
-
16
-
-
0026101719
-
Debrisoquine oxidation in Parkinson's disease
-
Kallio J, Marttila RJ, Rinne UK, Sonninen V, Syvaelahti E, Debrisoquine oxidation in Parkinson's disease. Acta Neurol Scand 1991; 83:194-197.
-
(1991)
Acta Neurol Scand
, vol.83
, pp. 194-197
-
-
Kallio, J.1
Marttila, R.J.2
Rinne, U.K.3
Sonninen, V.4
Syvaelahti, E.5
-
17
-
-
0002255855
-
Debrisoquine/sparteine monooxygenase and other P-450s in the brain
-
Kalow W. editors. New York: Pergamon Press
-
Kalow W, Tyndale RF. Debrisoquine/sparteine monooxygenase and other P-450s in the brain. In: Kalow W. editors. Pharmacogenetics of drug metabolism. New York: Pergamon Press; 1992. pp. 649-656.
-
(1992)
Pharmacogenetics of Drug Metabolism
, pp. 649-656
-
-
Kalow, W.1
Tyndale, R.F.2
-
18
-
-
0027348840
-
Association of Xba I allele (Xba I 44 kb) of the human cytochrome P-450dbl (CYP2D6) gene in Japanese patients with idiopathic Parkinsons's disease
-
Kondo I, Kanazawa, I. Association of Xba I allele (Xba I 44 kb) of the human cytochrome P-450dbl (CYP2D6) gene in Japanese patients with idiopathic Parkinsons's disease. Adv Neurol 1993; 60:338-342.
-
(1993)
Adv Neurol
, vol.60
, pp. 338-342
-
-
Kondo, I.1
Kanazawa, I.2
-
19
-
-
0027330416
-
Variant cytochrome P455 CYP2D6 allelic frequencies in Parkinson's disease
-
Kurth MC, Kurth JH. Variant cytochrome P455 CYP2D6 allelic frequencies in Parkinson's disease. Am J Med Gen 1993; 48:166-168.
-
(1993)
Am J Med Gen
, vol.48
, pp. 166-168
-
-
Kurth, M.C.1
Kurth, J.H.2
-
20
-
-
0029686092
-
Gene-environment interaction in Parkinson's disease. The cease of CYP2D6 gene polymorphism
-
Landi MT, Ceroni M, Martignoni E, Bertazzi PA, Caporaso NE, Nappi G. Gene-environment interaction in Parkinson's disease. The cease of CYP2D6 gene polymorphism. Adv Neurol 1996; 69:61-72.
-
(1996)
Adv Neurol
, vol.69
, pp. 61-72
-
-
Landi, M.T.1
Ceroni, M.2
Martignoni, E.3
Bertazzi, P.A.4
Caporaso, N.E.5
Nappi, G.6
-
21
-
-
0026667928
-
Debrisoquine metabolism in Chinese patients with Alzheimer's and Parkinson's diseases
-
Liu TY, Chi CW, Yang JC, Cheung SC, Liu HC. Debrisoquine metabolism in Chinese patients with Alzheimer's and Parkinson's diseases. Mol Chem Neuropathol 1992; 17:31-37.
-
(1992)
Mol Chem Neuropathol
, vol.17
, pp. 31-37
-
-
Liu, T.Y.1
Chi, C.W.2
Yang, J.C.3
Cheung, S.C.4
Liu, H.C.5
-
22
-
-
0029846366
-
Mutation frequencies of the cytochrome CYP2D6 gene in Parkinson's disease patients and in families
-
Lucotte G, Turpin JC, Gerard N, Panserat S, Krishnamoorthy R. Mutation frequencies of the cytochrome CYP2D6 gene in Parkinson's disease patients and in families. Am J Med Gen 1996; 67:361-365.
-
(1996)
Am J Med Gen
, vol.67
, pp. 361-365
-
-
Lucotte, G.1
Turpin, J.C.2
Gerard, N.3
Panserat, S.4
Krishnamoorthy, R.5
-
23
-
-
0025232430
-
Parkinson's disease
-
Marsden CD, Parkinson's disease. Lancet 1990; 335:948-952.
-
(1990)
Lancet
, vol.335
, pp. 948-952
-
-
Marsden, C.D.1
-
24
-
-
0025284578
-
Etude de l'hydroxylation de la debrisoquine dans la maladie de Parkinson
-
Meillard MN, Bentue-Ferrer D, Brunet-Bourgin F, Morel G, Allain H. Etude de l'hydroxylation de la debrisoquine dans la maladie de Parkinson. Presse Med 1990; 19:947-949.
-
(1990)
Presse Med
, vol.19
, pp. 947-949
-
-
Meillard, M.N.1
Bentue-Ferrer, D.2
Brunet-Bourgin, F.3
Morel, G.4
Allain, H.5
-
25
-
-
0025136874
-
Metabolism and brain accumulation of tetrahydroisoquinoline (TIQ) a possible parkinsonism inducing substance, in an animal model of a poor debrisoquine metabolizer
-
Ohta S, Tachikawa O, Makino Y, Tasaki Y, Hirobe M. Metabolism and brain accumulation of tetrahydroisoquinoline (TIQ) a possible parkinsonism inducing substance, in an animal model of a poor debrisoquine metabolizer. Life Sci 1990; 46:599-605.
-
(1990)
Life Sci
, vol.46
, pp. 599-605
-
-
Ohta, S.1
Tachikawa, O.2
Makino, Y.3
Tasaki, Y.4
Hirobe, M.5
-
26
-
-
0023216759
-
Statistical problems in the reporting of clinical trials: A survey of three medical journals
-
Pocock SJ, Hughes MD, Lee RJ. Statistical problems in the reporting of clinical trials: a survey of three medical journals. N Engl J Med 1987; 317:426-432.
-
(1987)
N Engl J Med
, vol.317
, pp. 426-432
-
-
Pocock, S.J.1
Hughes, M.D.2
Lee, R.J.3
-
27
-
-
0023279624
-
Debrisoquine metabolism in Parkinsonian patients treated with antihistamine drugs
-
Poirier J, Roy M, Campanella G, Cloutier T, Paris S. Debrisoquine metabolism in Parkinsonian patients treated with antihistamine drugs. Lancet 1987; 2:386.
-
(1987)
Lancet
, vol.2
, pp. 386
-
-
Poirier, J.1
Roy, M.2
Campanella, G.3
Cloutier, T.4
Paris, S.5
-
28
-
-
0031013848
-
Prevalence of parkinsonism and Parkinson's disease in Europe: The Europarkinson Collaborative Study. European community concerted action on the epidemiology of Parkinson's disease
-
Rijk MC, Tzourio C, Breteler NM, Dartigues JF, Amaducci L, Lopez-Pousa S. et al. Prevalence of parkinsonism and Parkinson's disease in Europe: The Europarkinson Collaborative Study. European community concerted action on the epidemiology of Parkinson's disease. J Neurol Neurosurg Psychiatry 1997; 62:10-15.
-
(1997)
J Neurol Neurosurg Psychiatry
, vol.62
, pp. 10-15
-
-
Rijk, M.C.1
Tzourio, C.2
Breteler, N.M.3
Dartigues, J.F.4
Amaducci, L.5
Lopez-Pousa, S.6
-
29
-
-
0030056697
-
CYP2D6 allelic frequencies in young onset Parkinson's disease
-
Sandy MS, Armstrong M, Tanner CM, Daly AK, Di Monte DA. Langston JW, Idle JR. CYP2D6 allelic frequencies in young onset Parkinson's disease. Neurology 1996; 47:225-230.
-
(1996)
Neurology
, vol.47
, pp. 225-230
-
-
Sandy, M.S.1
Armstrong, M.2
Tanner, C.M.3
Daly, A.K.4
Di Monte, D.A.5
Langston, J.W.6
Idle, J.R.7
-
30
-
-
0026747176
-
Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinsons's disease
-
Smith CAD, Gough AC, Leigh PN, Summers BA, Harding AE, Maranganore DM, et al. Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinsons's disease. Lancet 1992; 339:1375-1377.
-
(1992)
Lancet
, vol.339
, pp. 1375-1377
-
-
Smith, C.A.D.1
Gough, A.C.2
Leigh, P.N.3
Summers, B.A.4
Harding, A.E.5
Maranganore, D.M.6
-
31
-
-
0026781283
-
Debrisoquine hydroxylation in Parkinson's disease
-
Steiger M. Lledo P, Quinn N, Marsden C, Turner P, Jenner PG. Debrisoquine hydroxylation in Parkinson's disease. Acta Neurol Scand 1992; 86:159-164.
-
(1992)
Acta Neurol Scand
, vol.86
, pp. 159-164
-
-
Steiger, M.1
Lledo, P.2
Quinn, N.3
Marsden, C.4
Turner, P.5
Jenner, P.G.6
-
32
-
-
0024507618
-
Degenerative neurological disease and debrisoquine-4-hydroxylation capacity
-
Steventon GB, Haefield MTH, Sturman SG, Waring RH, Williams AC, Ellingham J. Degenerative neurological disease and debrisoquine-4-hydroxylation capacity. Med Sci Res 1989; 17:163-164.
-
(1989)
Med Sci Res
, vol.17
, pp. 163-164
-
-
Steventon, G.B.1
Haefield, M.T.H.2
Sturman, S.G.3
Waring, R.H.4
Williams, A.C.5
Ellingham, J.6
-
33
-
-
0025779409
-
Neuronal cytochrome P450IID1 (debrisoquine/sparteine-type): Potent inhibition of activity by (-)-cocaine and nucleotide sequence identity to human hepatic P450 gene CYP2D6
-
Tyndale RF, Sunahara R, Inaba T, Kalow W, Gonzalez FJ, Niznik HB. Neuronal cytochrome P450IID1 (debrisoquine/sparteine-type): potent inhibition of activity by (-)-cocaine and nucleotide sequence identity to human hepatic P450 gene CYP2D6. Mol Pharmacol 1991; 40:63-68.
-
(1991)
Mol Pharmacol
, vol.40
, pp. 63-68
-
-
Tyndale, R.F.1
Sunahara, R.2
Inaba, T.3
Kalow, W.4
Gonzalez, F.J.5
Niznik, H.B.6
-
34
-
-
0027358350
-
Worldwide occurrence of Parkinson's disease: An updated review
-
Zang ZX, Roman GC. Worldwide occurrence of Parkinson's disease: an updated review. Neuropidemiology 1993; 12:195-208.
-
(1993)
Neuropidemiology
, vol.12
, pp. 195-208
-
-
Zang, Z.X.1
Roman, G.C.2
-
35
-
-
0023684586
-
Absence of hepatic cytochrome P450bufl causes genetically deficient debrisoquine oxidation in man
-
Zanger UM, Vilbois F, Hardwick JP, Meyer UA. Absence of hepatic cytochrome P450bufl causes genetically deficient debrisoquine oxidation in man. Biochemistry 1988; 27:5447-5454.
-
(1988)
Biochemistry
, vol.27
, pp. 5447-5454
-
-
Zanger, U.M.1
Vilbois, F.2
Hardwick, J.P.3
Meyer, U.A.4
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