-
1
-
-
0029791355
-
Huntington disease: New insights into the relationship between CAG expansion and disease
-
Nasir J, Goldberg Y, Hayden M. Huntington disease: new insights into the relationship between CAG expansion and disease. Hum Mol Genet 1996:5:1431-1435.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1431-1435
-
-
Nasir, J.1
Goldberg, Y.2
Hayden, M.3
-
3
-
-
2642615954
-
Über Heredofamiliarität bei Paralysis agitans
-
Kückens H. Über Heredofamiliarität bei Paralysis agitans. Klin Wochenschr 1925;4:2289-2291.
-
(1925)
Klin Wochenschr
, vol.4
, pp. 2289-2291
-
-
Kückens, H.1
-
4
-
-
0001835824
-
Paralysis agitans. A clinical genetic study
-
Mjönes H. Paralysis agitans. A clinical genetic study. Acta Neurol Scand 1949;25(suppl 54):1-195.
-
(1949)
Acta Neurol Scand
, vol.25
, Issue.SUPPL. 54
, pp. 1-195
-
-
Mjönes, H.1
-
5
-
-
0027356273
-
The genetics of Parkinson's disease
-
Duvosin R. The genetics of Parkinson's disease. Adv Neurol 1993;60:306-315.
-
(1993)
Adv Neurol
, vol.60
, pp. 306-315
-
-
Duvosin, R.1
-
6
-
-
0028060492
-
Increased risk of Parkinson's disease in parents and siblings of patients
-
Payami H, Larsen K, Bernard S, Nutt J. Increased risk of Parkinson's disease in parents and siblings of patients. Ann Neurol 1994;36:659-661.
-
(1994)
Ann Neurol
, vol.36
, pp. 659-661
-
-
Payami, H.1
Larsen, K.2
Bernard, S.3
Nutt, J.4
-
7
-
-
0030012558
-
Possible environmental, occupational and other etiologic factors for Parkinson's disease: A case control study in Germany
-
Seidler A, Hellenbrand W, Robra B-P, et al. Possible environmental, occupational and other etiologic factors for Parkinson's disease: a case control study in Germany. Neurology 1996;46:1275-1284.
-
(1996)
Neurology
, vol.46
, pp. 1275-1284
-
-
Seidler, A.1
Hellenbrand, W.2
Robra, B.-P.3
-
8
-
-
0030031344
-
Environmental and genetic risk factors in Parkinson's disease: A case-control study in southern Italy
-
De Michele G, Filla A, Volpe G, et al. Environmental and genetic risk factors in Parkinson's disease: a case-control study in southern Italy. Mov Disord 1996;11:17-23.
-
(1996)
Mov Disord
, vol.11
, pp. 17-23
-
-
De Michele, G.1
Filla, A.2
Volpe, G.3
-
9
-
-
0027256104
-
Parkinson's disease: A test of the multifactorial etiologic hypothesis
-
Semchuk K, Love E, Lee R. Parkinson's disease: a test of the multifactorial etiologic hypothesis. Neurology 1993;43:1173-1180.
-
(1993)
Neurology
, vol.43
, pp. 1173-1180
-
-
Semchuk, K.1
Love, E.2
Lee, R.3
-
10
-
-
0030056696
-
Risk of Parkinson's disease among first degree relatives: A community based study
-
Marder K, Tang M-X, Mejia H, et al. Risk of Parkinson's disease among first degree relatives: a community based study. Neurology 1996;47:155-160.
-
(1996)
Neurology
, vol.47
, pp. 155-160
-
-
Marder, K.1
Tang, M.-X.2
Mejia, H.3
-
11
-
-
0028339708
-
Parkinson's disease and brain levels of organochlorine pesticides
-
Fleming L, Mann J, Bean J, Briggle T, Sanchez-Ramos J. Parkinson's disease and brain levels of organochlorine pesticides. Ann Neurol 1994;36:100-103.
-
(1994)
Ann Neurol
, vol.36
, pp. 100-103
-
-
Fleming, L.1
Mann, J.2
Bean, J.3
Briggle, T.4
Sanchez-Ramos, J.5
-
12
-
-
0029090567
-
Parkinson's disease and the environment in early life
-
Martyn C, Osmond C. Parkinson's disease and the environment in early life. J Neurol Sci 1995;132:201-206.
-
(1995)
J Neurol Sci
, vol.132
, pp. 201-206
-
-
Martyn, C.1
Osmond, C.2
-
14
-
-
0028198309
-
Familial juvenile parkinsonism: Clinical and pathologic study in a family
-
Takahashi H, Ohama E, Suzuki S, et al. Familial juvenile parkinsonism: clinical and pathologic study in a family. Neurology 1994;44:437-441.
-
(1994)
Neurology
, vol.44
, pp. 437-441
-
-
Takahashi, H.1
Ohama, E.2
Suzuki, S.3
-
18
-
-
0020623657
-
Parkinson's disease in 65 pairs of twins and in a set of quadruplets
-
Ward C, Duvoisin R, Ince S, Nutt J, Eldridge R, Calne D. Parkinson's disease in 65 pairs of twins and in a set of quadruplets. Neurology 1983;33:815-824.
-
(1983)
Neurology
, vol.33
, pp. 815-824
-
-
Ward, C.1
Duvoisin, R.2
Ince, S.3
Nutt, J.4
Eldridge, R.5
Calne, D.6
-
19
-
-
0025128071
-
Twin studies and the genetics of Parkinson's disease - A reappraisal
-
Johnson W, Hodge S, Duvoisin R. Twin studies and the genetics of Parkinson's disease - a reappraisal. Mov Disord 1990;5:187-194.
-
(1990)
Mov Disord
, vol.5
, pp. 187-194
-
-
Johnson, W.1
Hodge, S.2
Duvoisin, R.3
-
20
-
-
0026699670
-
Parkinson's disease in twins
-
Vieregge P, Schiffke K, Friedrich H, Müller B, Ludin H. Parkinson's disease in twins. Neurology 1992;42:1453-1461.
-
(1992)
Neurology
, vol.42
, pp. 1453-1461
-
-
Vieregge, P.1
Schiffke, K.2
Friedrich, H.3
Müller, B.4
Ludin, H.5
-
21
-
-
0023898945
-
The relevance of the Lewy body in the pathogenesis of idiopathic Parkinson's disease
-
Gibb W, Lees A. The relevance of the Lewy body in the pathogenesis of idiopathic Parkinson's disease. J Neurol Neurosurg Psychiatry 1988;51:745-752.
-
(1988)
J Neurol Neurosurg Psychiatry
, vol.51
, pp. 745-752
-
-
Gibb, W.1
Lees, A.2
-
22
-
-
0026793873
-
Parkinson's disease in twins studied with 18F-dopa and positron emission tomography
-
Burn D, Mark M, Playford E, et al. Parkinson's disease in twins studied with 18F-dopa and positron emission tomography. Neurology 1992;42:1894-1900.
-
(1992)
Neurology
, vol.42
, pp. 1894-1900
-
-
Burn, D.1
Mark, M.2
Playford, E.3
-
23
-
-
0028067526
-
Discordant twins with Parkinson's disease: Positron emission tomography and early signs of impaired cognitive circuits
-
Holthoff V, Vieregge P, Kessler J, et al. Discordant twins with Parkinson's disease: positron emission tomography and early signs of impaired cognitive circuits. Ann Neurol 1994;36:176-182.
-
(1994)
Ann Neurol
, vol.36
, pp. 176-182
-
-
Holthoff, V.1
Vieregge, P.2
Kessler, J.3
-
24
-
-
0026514953
-
Accuracy of clinical diagnosis of idiopathic Parkinson's disease: A clinicopathological study
-
Hughes A, Daniel S, Kilford L, Lees A. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinicopathological study. J Neurol Neurosurg Psychiatry 1992;55:181-184.
-
(1992)
J Neurol Neurosurg Psychiatry
, vol.55
, pp. 181-184
-
-
Hughes, A.1
Daniel, S.2
Kilford, L.3
Lees, A.4
-
25
-
-
0000334724
-
A pedigree of paralysis agitans
-
Bell J, Clark A. A pedigree of paralysis agitans. Annals of Eugenics 1926;1:455-462.
-
(1926)
Annals of Eugenics
, vol.1
, pp. 455-462
-
-
Bell, J.1
Clark, A.2
-
26
-
-
0027504703
-
Autosomal dominant parkinsonism with benign course and typical Lewy-body pathology
-
Golbe L, Lazzarini A, Schwarz K, Mark M, Dickson D, Duvoisin R. Autosomal dominant parkinsonism with benign course and typical Lewy-body pathology. Neurology 1993;43:2222-2227.
-
(1993)
Neurology
, vol.43
, pp. 2222-2227
-
-
Golbe, L.1
Lazzarini, A.2
Schwarz, K.3
Mark, M.4
Dickson, D.5
Duvoisin, R.6
-
27
-
-
0029806563
-
Clinical genetic analysis of Parkinson's disease in the Contursi kindred
-
Golbe L, Di Iorio G, Sanges G, et al. Clinical genetic analysis of Parkinson's disease in the Contursi kindred. Ann Neurol 1996;40:767-775.
-
(1996)
Ann Neurol
, vol.40
, pp. 767-775
-
-
Golbe, L.1
Di Iorio, G.2
Sanges, G.3
-
28
-
-
10544234193
-
Mapping of a gene for Parkinson's disease to chromosome 4q21-23
-
Polymeropoulos M, Higgins J, Golbe L, et al. Mapping of a gene for Parkinson's disease to chromosome 4q21-23. Science 1996;274:1197-1199.
-
(1996)
Science
, vol.274
, pp. 1197-1199
-
-
Polymeropoulos, M.1
Higgins, J.2
Golbe, L.3
-
29
-
-
0031577202
-
Muller-Myhsok B, Wszolek ZK, et al. Genetic heterogeneity in familial parkinsonism: No linkage to the PD-1 locus on chromosome 4q in 11 of 13 families
-
Gasser T. Muller-Myhsok B, Wszolek ZK, et al. Genetic heterogeneity in familial parkinsonism: no linkage to the PD-1 locus on chromosome 4q in 11 of 13 families. Science 1997;277:388-389.
-
(1997)
Science
, vol.277
, pp. 388-389
-
-
Gasser, T.1
-
30
-
-
0030483182
-
Genetic factors in Alzheimer's disease: A review of recent advances
-
Levy-Lahad E, Bird T. Genetic factors in Alzheimer's disease: a review of recent advances. Ann Neurol 1996;40:829-840.
-
(1996)
Ann Neurol
, vol.40
, pp. 829-840
-
-
Levy-Lahad, E.1
Bird, T.2
-
31
-
-
0029810307
-
Genetics of amyotrophic lateral sclerosis
-
Siddique T, Deng H-X. Genetics of amyotrophic lateral sclerosis. Hum Mol Genet 1996;5:1465-1470.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1465-1470
-
-
Siddique, T.1
Deng, H.-X.2
-
32
-
-
0029049738
-
Western Nebraska family (family D) with autosomal dominant parkinsonism
-
Wszolek Z, Pfeiffer B, Fulgham J, et al. Western Nebraska family (family D) with autosomal dominant parkinsonism. Neurology 1995;45:502-505.
-
(1995)
Neurology
, vol.45
, pp. 502-505
-
-
Wszolek, Z.1
Pfeiffer, B.2
Fulgham, J.3
-
33
-
-
0028127866
-
Autosomal dominant Lewy body parkinsonism in a four-generation family
-
Waters C, Miller C. Autosomal dominant Lewy body parkinsonism in a four-generation family. Ann Neurol 1994;35:59-64.
-
(1994)
Ann Neurol
, vol.35
, pp. 59-64
-
-
Waters, C.1
Miller, C.2
-
35
-
-
0029090839
-
A Greek-American kindred with autosomal dominant, levodopa-responsive parkinsonism and anticipation
-
Markopoulou K, Wszolek ZK, Pfeiffer RF. A Greek-American kindred with autosomal dominant, levodopa-responsive parkinsonism and anticipation. Ann Neurol 1995;38:373-378.
-
(1995)
Ann Neurol
, vol.38
, pp. 373-378
-
-
Markopoulou, K.1
Wszolek, Z.K.2
Pfeiffer, R.F.3
-
36
-
-
0031049889
-
Dopaminergic function in familial Parkinson's disease: A clinical and 18F-dopa study
-
Piccini P, Morrish PK, Turjanski N, et al. Dopaminergic function in familial Parkinson's disease: a clinical and 18F-dopa study. Ann Neurol 1997;41:222-229.
-
(1997)
Ann Neurol
, vol.41
, pp. 222-229
-
-
Piccini, P.1
Morrish, P.K.2
Turjanski, N.3
-
37
-
-
0026468019
-
The identification of presymptomatic parkinsonism: Clinical and 18F-dopa positron emission tomography studies in an Irish kindred
-
Sawle GV, Wroe SJ, Lees AJ, et al. The identification of presymptomatic parkinsonism: clinical and 18F-dopa positron emission tomography studies in an Irish kindred. Ann Neurol 1992;32:609-617.
-
(1992)
Ann Neurol
, vol.32
, pp. 609-617
-
-
Sawle, G.V.1
Wroe, S.J.2
Lees, A.J.3
-
38
-
-
0027996828
-
Dynamic mutations hit double figures
-
Willems P. Dynamic mutations hit double figures. Nat Genet 1994;8:221-228.
-
(1994)
Nat Genet
, vol.8
, pp. 221-228
-
-
Willems, P.1
-
39
-
-
0028869758
-
Genetic anticipation in Parkinson's disease
-
Payami H, Bernard S, Larsen K, Kaye J, Nutt J. Genetic anticipation in Parkinson's disease. Neurology 1995;45:135-138.
-
(1995)
Neurology
, vol.45
, pp. 135-138
-
-
Payami, H.1
Bernard, S.2
Larsen, K.3
Kaye, J.4
Nutt, J.5
-
40
-
-
0029750744
-
Anticipation in familial Parkinson's disease: A reanalysis of 13 United Kingdom kindreds
-
Maraganore D, Schaid D, Rocca W, Harding AE. Anticipation in familial Parkinson's disease: a reanalysis of 13 United Kingdom kindreds. Neurology 1996;47:1512-1517.
-
(1996)
Neurology
, vol.47
, pp. 1512-1517
-
-
Maraganore, D.1
Schaid, D.2
Rocca, W.3
Harding, A.E.4
-
41
-
-
0027279516
-
Hereditärer Morbus Parkinson: Bericht über drei Familien mit autosomal-dominantem Erbgang
-
Wszolek ZK, Cordes M, Calne DB, Münter MD, Cordes I, Pfeifer RF. Hereditärer Morbus Parkinson: Bericht über drei Familien mit autosomal-dominantem Erbgang. Nervenarzt 1993;64:331-335.
-
(1993)
Nervenarzt
, vol.64
, pp. 331-335
-
-
Wszolek, Z.K.1
Cordes, M.2
Calne, D.B.3
Münter, M.D.4
Cordes, I.5
Pfeifer, R.F.6
-
42
-
-
0028787434
-
No evidence for association of familial Parkinson's disease with CAG repeat expansion
-
Carrero-Valenzuela R, Lindblad K, Payami H, et al. No evidence for association of familial Parkinson's disease with CAG repeat expansion. Neurology 1995;45:1760-1763.
-
(1995)
Neurology
, vol.45
, pp. 1760-1763
-
-
Carrero-Valenzuela, R.1
Lindblad, K.2
Payami, H.3
-
43
-
-
0028124654
-
Genetic linkage studies in autosomal dominant parkinsonism: Evaluation of seven candidate genes
-
Gasser T, Wszolek Z, Trofatter J, et al. Genetic linkage studies in autosomal dominant parkinsonism: evaluation of seven candidate genes. Ann Neurol 1994;36:387-396.
-
(1994)
Ann Neurol
, vol.36
, pp. 387-396
-
-
Gasser, T.1
Wszolek, Z.2
Trofatter, J.3
-
44
-
-
0343025316
-
Genetic linkage studies in autosomal dominant parkinsonism: Evaluation of candidate genes
-
Supala A, Wszolek Z, Trofatter J, et al. Genetic linkage studies in autosomal dominant parkinsonism: evaluation of candidate genes. Mov Disord 1994;9:32.
-
(1994)
Mov Disord
, vol.9
, pp. 32
-
-
Supala, A.1
Wszolek, Z.2
Trofatter, J.3
-
45
-
-
0027989294
-
Debrisoquine hydroxylase gene polymorphism in familial Parkinson's disease
-
Plante-Bordeneuve P, Davis M, Maraganore D, Marsden CD, Harding AE. Debrisoquine hydroxylase gene polymorphism in familial Parkinson's disease. J Neurol Neurosurg Psychiatry 1994;57:911-913.
-
(1994)
J Neurol Neurosurg Psychiatry
, vol.57
, pp. 911-913
-
-
Plante-Bordeneuve, P.1
Davis, M.2
Maraganore, D.3
Marsden, C.D.4
Harding, A.E.5
-
46
-
-
0028356805
-
Tyrosine hydroxylase gene polymorphism in familial and sporadic Parkinson's disease
-
Plante-Bordeneuve V, Davis M, Maraganore D, Marsden C, Harding A. Tyrosine hydroxylase gene polymorphism in familial and sporadic Parkinson's disease. Mov Disord 1994;9:337-339.
-
(1994)
Mov Disord
, vol.9
, pp. 337-339
-
-
Plante-Bordeneuve, V.1
Davis, M.2
Maraganore, D.3
Marsden, C.4
Harding, A.5
-
47
-
-
0027401203
-
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
-
Rosen D, Siddique T, Patterson D, et al. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature 1993;362:59-62.
-
(1993)
Nature
, vol.362
, pp. 59-62
-
-
Rosen, D.1
Siddique, T.2
Patterson, D.3
-
48
-
-
0026941070
-
Substantia nigra degeneration in motor neuron disease: A quantitative study
-
Burrow J, Blumbergs P. Substantia nigra degeneration in motor neuron disease: a quantitative study. Aust NZ J Med 1992;22:469-472.
-
(1992)
Aust NZ J Med
, vol.22
, pp. 469-472
-
-
Burrow, J.1
Blumbergs, P.2
-
49
-
-
0027358662
-
Evidence for a dopaminergic deficit in sporadic amyotrophic lateral sclerosis on positron emission scanning
-
Takahashi H, Snow B, Bhatt M, Peppard R, Eisen A, Calne D. Evidence for a dopaminergic deficit in sporadic amyotrophic lateral sclerosis on positron emission scanning. Lancet 1993;342:1016-1018.
-
(1993)
Lancet
, vol.342
, pp. 1016-1018
-
-
Takahashi, H.1
Snow, B.2
Bhatt, M.3
Peppard, R.4
Eisen, A.5
Calne, D.6
-
50
-
-
0028046648
-
Familial aggregation of amyotrophic lateral sclerosis, dementia, and Parkinson's disease: Evidence of shared genetic susceptibility
-
Majoor-Krakauer D, Ottman R, Johnson W, Rowland L. Familial aggregation of amyotrophic lateral sclerosis, dementia, and Parkinson's disease: evidence of shared genetic susceptibility. Neurology 1994;44:1872-1877.
-
(1994)
Neurology
, vol.44
, pp. 1872-1877
-
-
Majoor-Krakauer, D.1
Ottman, R.2
Johnson, W.3
Rowland, L.4
-
51
-
-
0026583465
-
Transgenic mice with increased Cu/Zn-superoxide dismutase activity are resistant to N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced neurotoxicity
-
Przedborski S, Kostic V, Jackson-Lewis V, et al. Transgenic mice with increased Cu/Zn-superoxide dismutase activity are resistant to N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced neurotoxicity. J Neurosci 1992;12:1658-1667.
-
(1992)
J Neurosci
, vol.12
, pp. 1658-1667
-
-
Przedborski, S.1
Kostic, V.2
Jackson-Lewis, V.3
-
53
-
-
0028827062
-
Absence of mutations in superoxide dismutase and catalase genes in patients with Parkinson's disease
-
Parboosingh J, Rousseau M, Rogan F, et al. Absence of mutations in superoxide dismutase and catalase genes in patients with Parkinson's disease. Arch Neurol 1995;52:1160-1163.
-
(1995)
Arch Neurol
, vol.52
, pp. 1160-1163
-
-
Parboosingh, J.1
Rousseau, M.2
Rogan, F.3
-
54
-
-
0029090063
-
Dopa-responsive parkinsonism phenotype of Machado-Joseph disease: Confirmation of 14q CAG expansion
-
Tuite P, Rogaeva E, St George-Hyslop PH, et al. Dopa-responsive parkinsonism phenotype of Machado-Joseph disease: confirmation of 14q CAG expansion. Ann Neurol 1995;38:684-687.
-
(1995)
Ann Neurol
, vol.38
, pp. 684-687
-
-
Tuite, P.1
Rogaeva, E.2
St George-Hyslop, P.H.3
-
55
-
-
0028091176
-
Indices of oxidative stress and mitochondrial function in individuals with incidental Lewy body disease
-
Dexter D, Sian J, Rose S, et al. Indices of oxidative stress and mitochondrial function in individuals with incidental Lewy body disease. Ann Neurol 1994;35:38-44.
-
(1994)
Ann Neurol
, vol.35
, pp. 38-44
-
-
Dexter, D.1
Sian, J.2
Rose, S.3
-
56
-
-
0022408175
-
Ecogenetics of Parkinson's disease: 4-hydroxylation of debrisoquine
-
Barbeau A, Cloutier T, Roy M, Plasse L, Paris S, Poirier J. Ecogenetics of Parkinson's disease: 4-hydroxylation of debrisoquine. Lancet 1985;1213-1215.
-
(1985)
Lancet
, pp. 1213-1215
-
-
Barbeau, A.1
Cloutier, T.2
Roy, M.3
Plasse, L.4
Paris, S.5
Poirier, J.6
-
58
-
-
0026101719
-
Debrisoquine oxidation in Parkinson's disease
-
Kallio J, Marttila R, Rinne U, Sonninen V, Syvälahti 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.2
Rinne, U.3
Sonninen, V.4
Syvälahti, E.5
-
59
-
-
0026781283
-
Debrisoquine hydroxylation in Parkinson's disease
-
Steiger M, Lledo P, Quinn N, Marsden D, Turner P, Jenner P. 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, D.4
Turner, P.5
Jenner, P.6
-
60
-
-
0026589459
-
Mutant debrisoquine hydroxylation genes in Parkinson's disease
-
Armstrong M, Daly A, Cholerton S, Bateman D, Idle J. 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.2
Cholerton, S.3
Bateman, D.4
Idle, J.5
-
61
-
-
0026747176
-
Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease
-
Smith C, Gough A, Leigh P, et al. Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease. Lancet 1992;339:1375-1377.
-
(1992)
Lancet
, vol.339
, pp. 1375-1377
-
-
Smith, C.1
Gough, A.2
Leigh, P.3
-
62
-
-
0027330416
-
Variant cytochrome P450 CYP2D6 allelic frequencies in Parkinson's disease
-
Kurth M, Kurth J. Variant cytochrome P450 CYP2D6 allelic frequencies in Parkinson's disease. Am J Med Genet 1993;48:166-168.
-
(1993)
Am J Med Genet
, vol.48
, pp. 166-168
-
-
Kurth, M.1
Kurth, J.2
-
63
-
-
0028964602
-
Association between the oxidative polymorphism and early onset of Parkinson's disease
-
Agundez J, Jimenez-Jimenez F, Luengo A, 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.1
Jimenez-Jimenez, F.2
Luengo, A.3
-
64
-
-
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, et al. The CYP2D6B allele is not overrepresented in a population of German patients with idiopathic Parkinson's disease. J Neurol Neurosurg Psychiatry 1996;61:518-520.
-
(1996)
J Neurol Neurosurg Psychiatry
, vol.61
, pp. 518-520
-
-
Gasser, T.1
Müller-Myhsok, B.2
Supala, A.3
-
65
-
-
0029835547
-
Genetic variability of the CYP2D6 gene is not a risk factor for sporadic Parkinson's disease
-
Diederich N, Hilger C, Goetz C, 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.3
Vieregge, P.4
Metz, H.5
-
66
-
-
0030056697
-
CYP2D6 allelic frequencies in young-onset Parkinson's disease
-
Sandy M, Armstrong M, Tanner C, et al. CYP2D6 allelic frequencies in young-onset Parkinson's disease. Neurology 1996;47:225-230.
-
(1996)
Neurology
, vol.47
, pp. 225-230
-
-
Sandy, M.1
Armstrong, M.2
Tanner, C.3
-
67
-
-
0028788093
-
Apolipoprotein E genotype in Spanish patients of Alzheimer's or Parkinson's disease
-
Ibarreta D, Gomez-Isla T, Portera-Sanchez A, Parrilla R, Ayuso M. Apolipoprotein E genotype in Spanish patients of Alzheimer's or Parkinson's disease. J Neurol Sci 1995;134:146-149.
-
(1995)
J Neurol Sci
, vol.134
, pp. 146-149
-
-
Ibarreta, D.1
Gomez-Isla, T.2
Portera-Sanchez, A.3
Parrilla, R.4
Ayuso, M.5
-
68
-
-
0028798254
-
Apolipoprotein E genotypes in Parkinson's disease with and without dementia
-
Koller W, Glatt S, Hubble J, et al. Apolipoprotein E genotypes in Parkinson's disease with and without dementia. Ann Neurol 1995;37:242-245.
-
(1995)
Ann Neurol
, vol.37
, pp. 242-245
-
-
Koller, W.1
Glatt, S.2
Hubble, J.3
-
69
-
-
0029955915
-
Frequency of the apolipoprotein E e4 allele in a case-control study of early onset Parkinson's disease
-
Whitehead A. Bertrandy S, Finnan F, Butler A, Smith G, Ben-Shlomo Y. Frequency of the apolipoprotein E e4 allele in a case-control study of early onset Parkinson's disease. J Neurol Neurosurg Psychiatry 1996;61:347-351.
-
(1996)
J Neurol Neurosurg Psychiatry
, vol.61
, pp. 347-351
-
-
Bertrandy S, W.A.1
Finnan, F.2
Butler, A.3
Smith, G.4
Ben-Shlomo, Y.5
-
71
-
-
0021182244
-
Pargyline prevents MPTP induced parkinsonism in primates
-
Langston J, Irwin I, Tetrud J, Langston E, Forno E. Pargyline prevents MPTP induced parkinsonism in primates. Science 1984;225:1480-1482.
-
(1984)
Science
, vol.225
, pp. 1480-1482
-
-
Langston, J.1
Irwin, I.2
Tetrud, J.3
Langston, E.4
Forno, E.5
-
72
-
-
0027464780
-
Association of a monoamine oxidase B allele with Parkinson's disease
-
Kurth J, Kurth M, Poduslo S, Schwankhaus J. Association of a monoamine oxidase B allele with Parkinson's disease. Ann Neurol 1993;33:368-372.
-
(1993)
Ann Neurol
, vol.33
, pp. 368-372
-
-
Kurth, J.1
Kurth, M.2
Poduslo, S.3
Schwankhaus, J.4
-
73
-
-
0028963983
-
Williams A. An allelic association study of monoamine oxidase B in Parkinson's disease
-
Ho S, Kapadi A, Ramsden D. Williams A. An allelic association study of monoamine oxidase B in Parkinson's disease. Ann Neurol 1995;37:403-405.
-
(1995)
Ann Neurol
, vol.37
, pp. 403-405
-
-
Ho, S.1
Kapadi, A.2
Ramsden, D.3
-
74
-
-
0028260282
-
Hereditary variations in monoamine oxidase as a risk factor for Parkinson's disease
-
Hotamisligil G, Girmen A, Fink J, et al. Hereditary variations in monoamine oxidase as a risk factor for Parkinson's disease. Mov Disord 1994;9:305-310.
-
(1994)
Mov Disord
, vol.9
, pp. 305-310
-
-
Hotamisligil, G.1
Girmen, A.2
Fink, J.3
-
75
-
-
0029588602
-
Polymorphisms of dopamine receptor and transporter genes and Parkinson's disease
-
Higuchi S, Muramatsu T, Arai H, Hayashida M, Sasaki H, Trojanowski J. 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.6
-
76
-
-
1642493745
-
Genetic control of number of midbrain dopaminergic neurons in inbred strains of mice: Relationship to size and neuronal density of the striatum
-
Baker H, Joh T, Reis D. Genetic control of number of midbrain dopaminergic neurons in inbred strains of mice: relationship to size and neuronal density of the striatum. Proc Natl Acad Sci USA 1980;77:4369-4373.
-
(1980)
Proc Natl Acad Sci USA
, vol.77
, pp. 4369-4373
-
-
Baker, H.1
Joh, T.2
Reis, D.3
-
77
-
-
0028278417
-
Sparing of the dopaminergic neurons containing calbindin-D28k and of the dopaminergic mesocortical projections in weaver mutant mouse
-
Caspar P, Ben Jelloun N, Febvret A. Sparing of the dopaminergic neurons containing calbindin-D28k and of the dopaminergic mesocortical projections in weaver mutant mouse. Neuroscience 1994;61:293-305.
-
(1994)
Neuroscience
, vol.61
, pp. 293-305
-
-
Caspar, P.1
Ben Jelloun, N.2
Febvret, A.3
-
78
-
-
0023100259
-
Selective loss of monoaminergic neurons in weaver mutant mice - An immunocytochemical study
-
Gupta M, Feiten D, Ghetti B. Selective loss of monoaminergic neurons in weaver mutant mice - an immunocytochemical study. Brain Res 1987;402:379-382.
-
(1987)
Brain Res
, vol.402
, pp. 379-382
-
-
Gupta, M.1
Feiten, D.2
Ghetti, B.3
-
79
-
-
0020046462
-
Dopamine deficiency in the weaver mutant mouse
-
Schmidt M, Sawyer B, Perry K, Fuller R, Foreman M, Ghetti B. Dopamine deficiency in the weaver mutant mouse. J Neurosci 1982;2:376-380.
-
(1982)
J Neurosci
, vol.2
, pp. 376-380
-
-
Schmidt, M.1
Sawyer, B.2
Perry, K.3
Fuller, R.4
Foreman, M.5
Ghetti, B.6
-
80
-
-
0028864538
-
Early postnatal changes of the dopaminergic mesencephalic neurons in the weaver mouse
-
Verney C, Febvret-Muzerelie A, Caspar P. Early postnatal changes of the dopaminergic mesencephalic neurons in the weaver mouse. Brain Res Dev Brain Res 1995;89:115-119.
-
(1995)
Brain Res Dev Brain Res
, vol.89
, pp. 115-119
-
-
Verney, C.1
Febvret-Muzerelie, A.2
Caspar, P.3
-
81
-
-
0029115971
-
A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation
-
Paul N, Cox D, Bhat D, Faham M, Myers R, Peterson A. A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation. Nat Genet 1995;11:126-129.
-
(1995)
Nat Genet
, vol.11
, pp. 126-129
-
-
Paul, N.1
Cox, D.2
Bhat, D.3
Faham, M.4
Myers, R.5
Peterson, A.6
-
82
-
-
0029864810
-
The human homologue of the weaver mouse gene in familial and sporadic Parkinson's disease
-
Bandmann O, Davis M, Marsden CD, Wood NW. The human homologue of the weaver mouse gene in familial and sporadic Parkinson's disease. Neuroscience 1996;72:877-879.
-
(1996)
Neuroscience
, vol.72
, pp. 877-879
-
-
Bandmann, O.1
Davis, M.2
Marsden, C.D.3
Wood, N.W.4
-
83
-
-
0029942337
-
Histochemical detection of apoptosis in Parkinson's disease
-
Mochizuki H, Goto K, Mori H, Mizuno Y. Histochemical detection of apoptosis in Parkinson's disease. J Neurol Sci 1996;137:120-123.
-
(1996)
J Neurol Sci
, vol.137
, pp. 120-123
-
-
Mochizuki, H.1
Goto, K.2
Mori, H.3
Mizuno, Y.4
-
84
-
-
84889219801
-
Neurons from bcl-2-deficient mice are more susceptible to dopamine-induced oxidative stress
-
Hochman A, Offen D, Sternin H, Korsmeyer S, Ziv I, Melamed E. Neurons from bcl-2-deficient mice are more susceptible to dopamine-induced oxidative stress. Mov Disord 1996;11:592-593.
-
(1996)
Mov Disord
, vol.11
, pp. 592-593
-
-
Hochman, A.1
Offen, D.2
Sternin, H.3
Korsmeyer, S.4
Ziv, I.5
Melamed, E.6
-
85
-
-
0030249597
-
Dopamine neurons from transgenic mice with a knockout of the p53 gene resist MPTP neurotoxicity
-
Trimmer P, Smith T, Jung A, Bennett J. Dopamine neurons from transgenic mice with a knockout of the p53 gene resist MPTP neurotoxicity. Neurodegeneration 1996;5:233-239.
-
(1996)
Neurodegeneration
, vol.5
, pp. 233-239
-
-
Trimmer, P.1
Smith, T.2
Jung, A.3
Bennett, J.4
-
86
-
-
0027750939
-
Electron transfer complexes I and IV of platelets are abnormal in Parkinson's disease but normal in Parkinson-plus syndromes
-
Bennecke R, Struemper P, Weiss H. Electron transfer complexes I and IV of platelets are abnormal in Parkinson's disease but normal in Parkinson-plus syndromes. Brain 1993;116:1451-1463.
-
(1993)
Brain
, vol.116
, pp. 1451-1463
-
-
Bennecke, R.1
Struemper, P.2
Weiss, H.3
-
87
-
-
0029050583
-
Low platelet mitochondrial complex I and complex II/III activity in early untreated Parkinson's disease
-
Haas R, Nasirian F, Nakano K, et al. Low platelet mitochondrial complex I and complex II/III activity in early untreated Parkinson's disease. Ann Neurol 1995;37:714-722.
-
(1995)
Ann Neurol
, vol.37
, pp. 714-722
-
-
Haas, R.1
Nasirian, F.2
Nakano, K.3
-
88
-
-
0024390719
-
Mitochondrial complex I deficiency in Parkinson's disease
-
Schapira A, Cooper J, Dexter D, Jenner P, Clark J, Marsden CD. Mitochondrial complex I deficiency in Parkinson's disease [Letter]. Lancet 1989;I:1269.
-
(1989)
Lancet
, vol.1
, pp. 1269
-
-
Schapira, A.1
Cooper, J.2
Dexter, D.3
Jenner, P.4
Clark, J.5
Marsden, C.D.6
-
89
-
-
0029908226
-
Origin and functional consequences of the complex I defect in Parkinson's disease
-
Swerdlow R, Parks J, Miller S, et al. Origin and functional consequences of the complex I defect in Parkinson's disease. Ann Neurol 1996;40:663-671.
-
(1996)
Ann Neurol
, vol.40
, pp. 663-671
-
-
Swerdlow, R.1
Parks, J.2
Miller, S.3
-
90
-
-
0025047351
-
Normal mitochondrial genome in brain from patients with Parkinson's disease and complex I defects
-
Lestienne P, Nelson I, Riederer P, Jellinger K, Reichmann H. Normal mitochondrial genome in brain from patients with Parkinson's disease and complex I defects. J Neurochem 1990;55:1810-1812.
-
(1990)
J Neurochem
, vol.55
, pp. 1810-1812
-
-
Lestienne, P.1
Nelson, I.2
Riederer, P.3
Jellinger, K.4
Reichmann, H.5
-
91
-
-
0026548217
-
Quantitation of a mitochondrial DNA deletion in Parkinson's disease
-
Mann VM, Cooper JM, Schapira AHV. Quantitation of a mitochondrial DNA deletion in Parkinson's disease. FEBS Lett 1992;299:218-222.
-
(1992)
FEBS Lett
, vol.299
, pp. 218-222
-
-
Mann, V.M.1
Cooper, J.M.2
Schapira, A.H.V.3
-
92
-
-
0027397842
-
PCR analysis of platelet mtDNA: Lack of specific changes in Parkinson's disease
-
Sandy MS, Langston JM, Smith MT, Di Monte DA. PCR analysis of platelet mtDNA: lack of specific changes in Parkinson's disease. Mov Disord 1993;8:74-82.
-
(1993)
Mov Disord
, vol.8
, pp. 74-82
-
-
Sandy, M.S.1
Langston, J.M.2
Smith, M.T.3
Di Monte, D.A.4
-
93
-
-
0029880474
-
Mitochondrial NADH dehydrogenase and CYP2D6 genotypes in Lewy-body parkinsonism
-
Kösel S, Lücking CB, Egensberger R, Mehraein P, Graeber MB. Mitochondrial NADH dehydrogenase and CYP2D6 genotypes in Lewy-body parkinsonism. J Neurosci Res 1996;44:174-183.
-
(1996)
J Neurosci Res
, vol.44
, pp. 174-183
-
-
Kösel, S.1
Lücking, C.B.2
Egensberger, R.3
Mehraein, P.4
Graeber, M.B.5
-
94
-
-
0027200741
-
Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients
-
Shoffner J, Brown M, Torroni A, et al. Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients. Genomics 1993;17:171-184.
-
(1993)
Genomics
, vol.17
, pp. 171-184
-
-
Shoffner, J.1
Brown, M.2
Torroni, A.3
-
95
-
-
0025010120
-
Mitochondrial DNA analysis in Parkinson's disease
-
Schapira A, Holt I, Sweeney M, Harding AE, Jenner P, Marsden CD. Mitochondrial DNA analysis in Parkinson's disease. Mov Disord 1990;5:294-297.
-
(1990)
Mov Disord
, vol.5
, pp. 294-297
-
-
Schapira, A.1
Holt, I.2
Sweeney, M.3
Harding, A.E.4
Jenner, P.5
Marsden, C.D.6
-
96
-
-
0030915207
-
Mitochondrial DNA polymorphisms in pathologically proven Parkinson's disease
-
Bandmann O, Sweeney M, Daniel S, Marsden CD, Wood NW. Mitochondrial DNA polymorphisms in pathologically proven Parkinson's disease. J Neurol 1997;244:262-265.
-
(1997)
J Neurol
, vol.244
, pp. 262-265
-
-
Bandmann, O.1
Sweeney, M.2
Daniel, S.3
Marsden, C.D.4
Wood, N.W.5
-
97
-
-
0025834561
-
A clinical and genetic study of familial Parkinson's disease
-
Maraganore D, Harding AE, Marsden CD. A clinical and genetic study of familial Parkinson's disease. Mov Disord 1991;6:205-211.
-
(1991)
Mov Disord
, vol.6
, pp. 205-211
-
-
Maraganore, D.1
Harding, A.E.2
Marsden, C.D.3
-
99
-
-
1842335744
-
Maternal inheritance of Parkinson's disease
-
Wooten G, Currie L, Bennett J, Harrison M, Trugman J, Parker W. Maternal inheritance of Parkinson's disease. Ann Neurol 1997;41:265-268.
-
(1997)
Ann Neurol
, vol.41
, pp. 265-268
-
-
Wooten, G.1
Currie, L.2
Bennett, J.3
Harrison, M.4
Trugman, J.5
Parker, W.6
-
100
-
-
0030744876
-
Mutation in the α-synuclein gene identified in families with Parkinson's disease
-
Polymeropoulos MH, Lavedan C, Leroy E, et al. Mutation in the α-synuclein gene identified in families with Parkinson's disease. Science 1997;276:2045-2047.
-
(1997)
Science
, vol.276
, pp. 2045-2047
-
-
Polymeropoulos, M.H.1
Lavedan, C.2
Leroy, E.3
|