-
1
-
-
0020680904
-
Chronic parkinsonism in humans due to a product of meperidine-analog synthesis
-
Langston JW, Ballard P, Tetrud JW, Irwin I. Chronic parkinsonism in humans due to a product of meperidine-analog synthesis. Science 1983;219:979-980.
-
(1983)
Science
, vol.219
, pp. 979-980
-
-
Langston, J.W.1
Ballard, P.2
Tetrud, J.W.3
Irwin, I.4
-
2
-
-
0031979752
-
Hypothesis: The role of dopaminergic transporters in selective vulnerability of cells in Parkinson's disease
-
Uhl GR. Hypothesis: the role of dopaminergic transporters in selective vulnerability of cells in Parkinson's disease. Ann Neurol 1998;43:555-560.
-
(1998)
Ann. Neurol.
, vol.43
, pp. 555-560
-
-
Uhl, G.R.1
-
3
-
-
0030921878
-
Association of a polymorphism in the dopamine-transporter gene with Parkinson's disease
-
Le Couteur DG, Leighton PW, McCann SJ, Pond SM. Association of a polymorphism in the dopamine-transporter gene with Parkinson's disease. Mov Disord 1997;12:760-763.
-
(1997)
Mov. Disord.
, vol.12
, pp. 760-763
-
-
Le Couteur, D.G.1
Leighton, P.W.2
McCann, S.J.3
Pond, S.M.4
-
4
-
-
0029588602
-
Polymorphisms of dopamine receptor and transporter genes and Parkinson's disease
-
Higuchi S, Muramatsu T, Arai H, Hayashida M, Sasaki H, Trojanowski JQ. Polymorphisms of dopamine receptor and transporter genes and Parkinson's disease. J Neural Transm 1995;10:107-113.
-
(1995)
J. Neural. Transm.
, vol.10
, pp. 107-113
-
-
Higuchi, S.1
Muramatsu, T.2
Arai, H.3
Hayashida, M.4
Sasaki, H.5
Trojanowski, J.Q.6
-
5
-
-
0033407580
-
Variations in the monoamine oxidase B (MAOB) gene are associated with Parkinson's disease
-
Mellick GD, Buchanan DD, McCann SJ, et al. Variations in the monoamine oxidase B (MAOB) gene are associated with Parkinson's disease. Mov Disord 1999;14:219-224.
-
(1999)
Mov. Disord.
, vol.14
, pp. 219-224
-
-
Mellick, G.D.1
Buchanan, D.D.2
McCann, S.J.3
-
6
-
-
0033837202
-
Variability and validity of polymorphism association studies in Parkinson's disease
-
Tan EK, Khajavi M, Thornby JI, Nagamitsu S, Jankovic J, Ashizawa T. Variability and validity of polymorphism association studies in Parkinson's disease. Neurology 2000;55:533-538.
-
(2000)
Neurology
, vol.55
, pp. 533-538
-
-
Tan, E.K.1
Khajavi, M.2
Thornby, J.I.3
Nagamitsu, S.4
Jankovic, J.5
Ashizawa, T.6
-
8
-
-
0031015324
-
High and low activity alleles of catechol-O-methyltransferase gene: Ethnic difference and possible association with Parkinson's disease
-
Kunugi H. Nanko S, Ueki A, et al. High and low activity alleles of catechol-O-methyltransferase gene: ethnic difference and possible association with Parkinson's disease. Neurosci Lett 1997;221:202-204.
-
(1997)
Neurosci. Lett.
, vol.221
, pp. 202-204
-
-
Kunugi, H.1
Nanko, S.2
Ueki, A.3
-
9
-
-
0031436062
-
Catechol-O-methyltransferase genotype and susceptibility to Parkinson's disease in Japan
-
Yoritaka A, Hattori N, Yoshino H, Mizuno Y. Catechol-O-methyltransferase genotype and susceptibility to Parkinson's disease in Japan. J Neural Transm 1997;104:1313-1317.
-
(1997)
J. Neural. Transm.
, vol.104
, pp. 1313-1317
-
-
Yoritaka, A.1
Hattori, N.2
Yoshino, H.3
Mizuno, Y.4
-
10
-
-
0033544368
-
Case-control study of the ubiquitin carboxyterminal hydrolase L1 gene in Parkinson's disease
-
Maraganore DM, Farrer MJ, Hardy JA, Lincoln SJ, McDonnell SK, Rocca WA. Case-control study of the ubiquitin carboxyterminal hydrolase L1 gene in Parkinson's disease. Neurology 1999;53:1858-1860.
-
(1999)
Neurology
, vol.53
, pp. 1858-1860
-
-
Maraganore, D.M.1
Farrer, M.J.2
Hardy, J.A.3
Lincoln, S.J.4
McDonnell, S.K.5
Rocca, W.A.6
-
11
-
-
0033941972
-
Case-control study of debrisoquine 4-hydroxylase, N-acetyltransferase 2, and apolipoprotein E gene polymorphisms in Parkinson's disease
-
Maraganore DM, Fatter MJ, Hardy JA, McDonnell SK, Schaid DJ, Rocca WA. Case-control study of debrisoquine 4-hydroxylase, N-acetyltransferase 2, and apolipoprotein E gene polymorphisms in Parkinson's disease. Mov Disord 2000;15:714-719.
-
(2000)
Mov. Disord.
, vol.15
, pp. 714-719
-
-
Maraganore, D.M.1
Fatter, M.J.2
Hardy, J.A.3
McDonnell, S.K.4
Schaid, D.J.5
Rocca, W.A.6
-
12
-
-
0034760406
-
Case-control study of the extended tau gene haplotype in Parkinson's disease
-
Maraganore DM, Hernandez DG, Singleton AB, et al. Case-control study of the extended tau gene haplotype in Parkinson's disease. Ann Neurol 2001;50:658-661.
-
(2001)
Ann. Neurol.
, vol.50
, pp. 658-661
-
-
Maraganore, D.M.1
Hernandez, D.G.2
Singleton, A.B.3
-
13
-
-
0032946784
-
Incidence and distribution of parkinsonism in Olmsted County, Minnesota, 1976-1990
-
Bower JH, Maraganore DM, McDonnell SK, Rocca WA. Incidence and distribution of parkinsonism in Olmsted County, Minnesota, 1976-1990. Neurology 1999;52:1214-1220.
-
(1999)
Neurology
, vol.52
, pp. 1214-1220
-
-
Bower, J.H.1
Maraganore, D.M.2
McDonnell, S.K.3
Rocca, W.A.4
-
14
-
-
0033819269
-
Influence of strict, intermediate, and broad diagnostic criteria on the age- and sex-specific incidence of Parkinson's disease
-
Bower JH, Maraganore DM, McDonnell SK, Rocca WA. Influence of strict, intermediate, and broad diagnostic criteria on the age- and sex-specific incidence of Parkinson's disease. Mov Disord 2000; 15:819-825.
-
(2000)
Mov. Disord.
, vol.15
, pp. 819-825
-
-
Bower, J.H.1
Maraganore, D.M.2
McDonnell, S.K.3
Rocca, W.A.4
-
15
-
-
0027156835
-
A 40-nucleotide repeat polymorphism in the human dopamine transporter gene
-
Sano A, Kondoh K, Kakimoto Y, Kondo I. A 40-nucleotide repeat polymorphism in the human dopamine transporter gene. Hum Genet 1993;91:405-406.
-
(1993)
Hum. Genet.
, vol.91
, pp. 405-406
-
-
Sano, A.1
Kondoh, K.2
Kakimoto, Y.3
Kondo, I.4
-
16
-
-
0008899828
-
No association between Parkinson's disease and low-activity alleles of catechol O-methyltransferase
-
Hoda F, Nicholl D, Bennett P, et al. No association between Parkinson's disease and low-activity alleles of catechol O-methyltransferase. Biochem Biophys Res Commun 1996;228:780-784.
-
(1996)
Biochem. Biophys. Res. Commun.
, vol.228
, pp. 780-784
-
-
Hoda, F.1
Nicholl, D.2
Bennett, P.3
-
18
-
-
0024095149
-
Gm3;5,13,14 and type 2 diabetes mellitus: An association in American Indians with genetic admixture
-
Knowler WC, Williams RC, Pettitt DJ, Steinberg AG. Gm3;5,13,14 and type 2 diabetes mellitus: an association in American Indians with genetic admixture. Am J Hum Genet 1988;43:520-526.
-
(1988)
Am. J. Hum. Genet.
, vol.43
, pp. 520-526
-
-
Knowler, W.C.1
Williams, R.C.2
Pettitt, D.J.3
Steinberg, A.G.4
-
19
-
-
0004235298
-
-
American Psychiatric Association. 4th ed. DSM-IV. Washington, DC: American Psychiatric Association
-
American Psychiatric Association. Diagnostic and statistical manual of mental disorders. 4th ed. DSM-IV. Washington, DC: American Psychiatric Association; 1994.
-
(1994)
Diagnostic and Statistical Manual of Mental Disorders
-
-
-
20
-
-
0027078061
-
Human dopamine transporter gene (DAT1) maps to chromosome 5p15.3 and displays a VNTR
-
Vandenbergh DJ, Persico AM, Hawkins AL, et al. Human dopamine transporter gene (DAT1) maps to chromosome 5p15.3 and displays a VNTR. Genomics 1992;14:1104-1106.
-
(1992)
Genomics
, vol.14
, pp. 1104-1106
-
-
Vandenbergh, D.J.1
Persico, A.M.2
Hawkins, A.L.3
-
21
-
-
0034142232
-
Genotype influences in vivo dopamine transporter availability in human striatum
-
Heinz A, Goldman D, Jones DW, et al. Genotype influences in vivo dopamine transporter availability in human striatum. Neuropsychopharmacology 2000;22:133-139.
-
(2000)
Neuropsychopharmacology
, vol.22
, pp. 133-139
-
-
Heinz, A.1
Goldman, D.2
Jones, D.W.3
-
22
-
-
0032965756
-
Variable number tandem repeat dopamine transporter gene polymorphism and Parkinson's disease: No association found
-
Mercier G, Turpin JC, Lucotte G. Variable number tandem repeat dopamine transporter gene polymorphism and Parkinson's disease: no association found. J Neurol 1999;246:45-47.
-
(1999)
J. Neurol.
, vol.246
, pp. 45-47
-
-
Mercier, G.1
Turpin, J.C.2
Lucotte, G.3
-
23
-
-
0031467513
-
The dopamine transporter gene and Parkinson's disease in a Chinese population
-
Leighton PW, Le Couteur DG, Pang CCP, et al. The dopamine transporter gene and Parkinson's disease in a Chinese population. Neurology 1997;49:1577-1579.
-
(1997)
Neurology
, vol.49
, pp. 1577-1579
-
-
Leighton, P.W.1
Le Couteur, D.G.2
Pang, C.C.P.3
-
24
-
-
0032740464
-
A study of five candidate genes in Parkinson's disease and related neurodegenerative disorders
-
Nicholl DJ, Bennett P, Hiller L, et al. A study of five candidate genes in Parkinson's disease and related neurodegenerative disorders. Neurology 1999:53:1415-1421.
-
(1999)
Neurology
, vol.53
, pp. 1415-1421
-
-
Nicholl, D.J.1
Bennett, P.2
Hiller, L.3
-
25
-
-
2542507783
-
Evaluation of four candidate genes encoding proteins of the dopamine pathway in familial and sporadic Parkinson's disease: Evidence for association of a DRD2 allele
-
Planté-Bordeneuve V, Taussig D, Thomas F, et al. Evaluation of four candidate genes encoding proteins of the dopamine pathway in familial and sporadic Parkinson's disease: evidence for association of a DRD2 allele. Neurology 1997;48:1589-1593.
-
(1997)
Neurology
, vol.48
, pp. 1589-1593
-
-
Planté-Bordeneuve, V.1
Taussig, D.2
Thomas, F.3
-
28
-
-
0021276089
-
Metabolism of the neurotoxic tertiary amine, MPTP, by brain mormamine oxidase
-
Chiba K, Trevor A, Castagnoli N Jr. Metabolism of the neurotoxic tertiary amine, MPTP, by brain mormamine oxidase. Biochem Biophys Res Common 1984;120:574-578.
-
(1984)
Biochem. Biophys. Res. Common.
, vol.120
, pp. 574-578
-
-
Chiba, K.1
Trevor, A.2
Castagnoli N., Jr.3
-
29
-
-
0034022516
-
The monoamine oxidase B gene GT repeat polymorphism and Parkinson's disease in a Chinese population
-
Mellick GD, Buchanan DD, Silburn PA, et al. The monoamine oxidase B gene GT repeat polymorphism and Parkinson's disease in a Chinese population. J Neurol 2000;247:52-55.
-
(2000)
J. Neurol.
, vol.247
, pp. 52-55
-
-
Mellick, G.D.1
Buchanan, D.D.2
Silburn, P.A.3
-
30
-
-
0033608187
-
Parkinson's disease in twins. An etiological study
-
Tanner CM, Ottman R, Goldman SM, et al. Parkinson's disease in twins. An etiological study. JAMA 1999;281:341-346.
-
(1999)
JAMA
, vol.281
, pp. 341-346
-
-
Tanner, C.M.1
Ottman, R.2
Goldman, S.M.3
-
31
-
-
0026034792
-
Human catechol-O-methyltransferase: Cloning and expression of the membrane associated form
-
Bertocci B, Miggiano V, Da Prada M, Dembic Z, Lahm H-W, Malherbe P. Human catechol-O-methyltransferase: cloning and expression of the membrane associated form. Proc Natl Acad Sci U S A 1991;88:1416-1420.
-
(1991)
Proc. Natl. Acad. Sci. U S A
, vol.88
, pp. 1416-1420
-
-
Bertocci, B.1
Miggiano, V.2
Da Prada, M.3
Dembic, Z.4
Lahm, H.-W.5
Malherbe, P.6
-
33
-
-
0028918413
-
Kinetics of human soluble and membrane-bound catechol O-methyltransferase: A revised mechanism and description of the thermolabile variant of the enzyme
-
Lotta T, Vidgren J, Tilgmann C, et al. Kinetics of human soluble and membrane-bound catechol O-methyltransferase: a revised mechanism and description of the thermolabile variant of the enzyme. Biochemistry 1995;34:4202-4210.
-
(1995)
Biochemistry
, vol.34
, pp. 4202-4210
-
-
Lotta, T.1
Vidgren, J.2
Tilgmann, C.3
-
34
-
-
0030611325
-
1947 polymorphism in catechol-O-methyltransferase (COMT) gene in Parkinson's disease
-
1947 polymorphism in catechol-O-methyltransferase (COMT) gene in Parkinson's disease. Mov Disord 1997;12:426-427.
-
(1997)
Mov. Disord.
, vol.12
, pp. 426-427
-
-
Xie, T.1
Ho, S.L.2
Li, L.S.W.3
Ma, O.C.K.4
-
35
-
-
0035852840
-
The COMT L allele modifies the association between MAOB polymorphism and PD in Taiwanese
-
Wu RM, Cheng CW, Chen KH. et al. The COMT L allele modifies the association between MAOB polymorphism and PD in Taiwanese. Neurology 2001;56:375-382.
-
(2001)
Neurology
, vol.56
, pp. 375-382
-
-
Wu, R.M.1
Cheng, C.W.2
Chen, K.H.3
-
36
-
-
0033680875
-
Use of classification trees for association studies
-
Zhang H, Bonney G. Use of classification trees for association studies. Genet Epidemiol 2000;19:323-332.
-
(2000)
Genet. Epidemiol.
, vol.19
, pp. 323-332
-
-
Zhang, H.1
Bonney, G.2
-
37
-
-
0033060947
-
Characterization and implications of estrogenic down-regulation of human catechol-O-methyltransferase gene transcription
-
Xie T, Ho S-L, Ramsden D. Characterization and implications of estrogenic down-regulation of human catechol-O-methyltransferase gene transcription. Mol Pharmacol 1999;56:31-38.
-
(1999)
Mol. Pharmacol.
, vol.56
, pp. 31-38
-
-
Xie, T.1
Ho, S.-L.2
Ramsden, D.3
-
38
-
-
0018736142
-
Bias in analytic research
-
Sackett DL. Bias in analytic research. J Chronic Dis 1979;32:51-63.
-
(1979)
J. Chronic. Dis.
, vol.32
, pp. 51-63
-
-
Sackett, D.L.1
-
39
-
-
0003550725
-
Fundamentals of genetic epidemiology
-
New York: Oxford University Press
-
Khoury MJ, Beaty TH, Cohen BH. Fundamentals of genetic epidemiology. New York: Oxford University Press; 1993.
-
(1993)
-
-
Khoury, M.J.1
Beaty, T.H.2
Cohen, B.H.3
-
40
-
-
0032542897
-
What's wrong with Bonferroni adjustments
-
Perneger TV. What's wrong with Bonferroni adjustments. BMJ 1998;316:1236-1238.
-
(1998)
BMJ
, vol.316
, pp. 1236-1238
-
-
Perneger, T.V.1
|