메뉴 건너뛰기




Volumn 65, Issue 2, 2001, Pages 111-126

Genetics of parkinsonism: A review

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA SYNUCLEIN; CELL PROTEIN; HYDROLASE; PARKIN; UBIQUITIN; UNCLASSIFIED DRUG;

EID: 0035020181     PISSN: 00034800     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0003480001008557     Document Type: Article
Times cited : (49)

References (120)
  • 4
    • 0026589459 scopus 로고
    • Mutant debrisoquine hydroxylation genes in Parkinsons-disease
    • Armstrong, M., Daly, A. K., Cholerton, S., Bateman, D. N. & Idle, J. R. (1992). Mutant Debrisoquine Hydroxylation Genes In Parkinsons-Disease. Lancet 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
  • 6
    • 0029010415 scopus 로고
    • Sequence of the superoxide-dismutase 1 (Sod 1) gene in familial Parkinsons-disease
    • Bandmann, O., Davis, M. B., Marsden, C. D. & Harding, A. K. (1995). Sequence Of the Superoxide-Dismutase 1 (Sod 1) Gene In Familial Parkinsons-Disease. J. Neurol. Neurosurg. Psych. 59, 90-91.
    • (1995) J. Neurol. Neurosurg. Psych. , vol.59 , pp. 90-91
    • Bandmann, O.1    Davis, M.B.2    Marsden, C.D.3    Harding, A.E.4
  • 7
    • 0029864810 scopus 로고    scopus 로고
    • The human homolog of the weaver mouse gene in familial and sporadic Parkinsons-discase
    • Bandmann, O., Davis, M. B., Marsden, C. D. & Wood, N. W. (1990). The Human Homolog Of the Weaver Mouse Gene In Familial and Sporadic Parkinsons-Discase. Neuroscience. 72, 877-879.
    • (1996) Neuroscience , vol.72 , pp. 877-879
    • Bandmann, O.1    Davis, M.B.2    Marsden, C.D.3    Wood, N.W.4
  • 8
  • 9
    • 0030692086 scopus 로고    scopus 로고
    • Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease
    • Bandmann, O., Vaughan, J., Holmans, P., Marsden, C. D. & Wood, N. W. (1997b). Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease. Lancet 350, 1136-1139.
    • (1997) Lancet , vol.350 , pp. 1136-1139
    • Bandmann, O.1    Vaughan, J.2    Holmans, P.3    Marsden, C.D.4    Wood, N.W.5
  • 11
    • 0030054522 scopus 로고    scopus 로고
    • Multiple loci for multiple sclerosis [news; comment]
    • Bell, J. I. & Lathrop, G. M. (1996). Multiple loci for multiple sclerosis [news; comment]. Nat. Genet. 13, 377-378.
    • (1996) Nat. Genet. , vol.13 , pp. 377-378
    • Bell, J.I.1    Lathrop, G.M.2
  • 12
    • 0033532119 scopus 로고    scopus 로고
    • Neurogenetic correlates of Parkinson's disease: Apolipoprotein-E and cytochrome P450 2D6 genetic polymorphism
    • Bon, M. A., Jansen Steur, E. N., De Vos. H. A. & Vermes, I. (1999). Neurogenetic correlates of Parkinson's disease: apolipoprotein-E and cytochrome P450 2D6 genetic polymorphism. Neurosci. Lett. 266, 149-151.
    • (1999) Neurosci. Lett. , vol.266 , pp. 149-151
    • Bon, M.A.1    Jansen Steur, E.N.2    De Vos, R.A.3    Vermes, I.4
  • 13
    • 0028106191 scopus 로고
    • Genetic-polymorphism of cytochrome-P450 2d6 in idiopathic disease and diffuse Lewy Body disease
    • Bordet, R., Broly, F., Destee, A. & Libersa, C. (1994). Genetic-Polymorphism Of Cytochrome-P450 2d6 In Idiopathic Disease and Diffuse Lewy Body Disease. Clin. Neuropharn. 17, 484-488.
    • (1994) Clin. Neuropharn. , vol.17 , pp. 484-488
    • Bordet, R.1    Broly, F.2    Destee, A.3    Libersa, C.4
  • 15
    • 0029006495 scopus 로고
    • Towards a new understanding of dopamine-receptors
    • Carlsson, A. (1995). Towards a New Understanding Of Dopamine-Receptors. Clin. Neuropharm. 18, S 6-S 13.
    • (1995) Clin. Neuropharm. , vol.18 , pp. S6-S13
    • Carlsson, A.1
  • 16
    • 85006913319 scopus 로고    scopus 로고
    • Identification of a novel Parkin gene mutation associated with autosomal dominant familial parkinsonism with Lewy bodies
    • Chen, R., Gosavi, N. S., Tan, L., Forno, L. S., Tanner, C. M., Langston, J. W. & Chan, P. (2000). Identification of a novel Parkin gene mutation associated with autosomal dominant familial Parkinsonism with Lewy bodies. Neurology 54 (suppl 3), A427.
    • (2000) Neurology , vol.54 , pp. A427
    • Chen, R.1    Gosavi, N.S.2    Tan, L.3    Forno, L.S.4    Tanner, C.M.5    Langston, J.W.6    Chan, P.7
  • 18
    • 0031787871 scopus 로고    scopus 로고
    • Accelerated in vitro fibril formation by a mutant alpha-synuclein linked to early-onset Parkinson disease
    • Conway, K. A., Harper, J. D. & Lansbury, P. T. (1998). Accelerated in vitro fibril formation by a mutant alpha-synuclein linked to early-onset Parkinson disease. Nat. Med. 4, 1318-1320.
    • (1998) Nat. Med. , vol.4 , pp. 1318-1320
    • Conway, K.A.1    Harper, J.D.2    Lansbury, P.T.3
  • 20
    • 0031013848 scopus 로고    scopus 로고
    • Prevalence of parkinsonism and Parkinson's disease in Europe: The EUROPARKINSON collaborative study. European community concerted action on the epidemiology of Parkinson's disease
    • De Rijk, M., Tzourio, C. & Breteler, M. (1997). 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. Psych. 62, 10-15.
    • (1997) J. Neurol. Neurosurg. Psych. , vol.62 , pp. 10-15
    • De Rijk, M.1    Tzourio, C.2    Breteler, M.3
  • 22
    • 0029835547 scopus 로고    scopus 로고
    • Genetic-variability of the Cyp 2d6 gene is not a risk factor for sporadic Parkinsons-disease
    • Diederich, N., Hilger. G., Goetz, C. G., Keipes, M., Hentges, F., Vieregge, P. & Metz, H. (1996). Genetic-Variability Of the Cyp 2d6 Gene Is Not a Risk Factor For Sporadic Parkinsons-Disease. Ann. Neurol. 40, 463-465.
    • (1996) Ann. Neurol. , vol.40 , pp. 463-465
    • Diederich, N.1    Hilger, G.2    Goetz, C.G.3    Keipes, M.4    Hentges, F.5    Vieregge, P.6    Metz, H.7
  • 23
    • 0032573597 scopus 로고    scopus 로고
    • Aggregates from mutant and wild-type alpha-synuclein proteins and NAC peptide induce apoptotic cell death in human neuroblastoma cells by formation of beta-sheet and amyloid-like filaments
    • El-Agnaf, O. M., Jakes, R., Curran, M. D., Middleton, D., Ingenito, R., Bianchi, E., Pessi, A., Neill, D. & Wallace, A. (1998). Aggregates from mutant and wild-type alpha-synuclein proteins and NAC peptide induce apoptotic cell death in human neuroblastoma cells by formation of beta-sheet and amyloid-like filaments. FEBS Lett. 440, 71-75.
    • (1998) FEBS Lett. , vol.440 , pp. 71-75
    • El-Agnaf, O.M.1    Jakes, R.2    Curran, M.D.3    Middleton, D.4    Ingenito, R.5    Bianchi, E.6    Pessi, A.7    Neill, D.8    Wallace, A.9
  • 26
    • 0024347981 scopus 로고
    • Assessment of genetic risk for Alzheimer's disease among first degree relatives
    • Farrer, L. A., O'Sullivan, D. M., Cupples, L. A., Growden, J. H. & Myers, R. H. (1989). Assessment of genetic risk for Alzheimer's disease among first degree relatives. Ann. Neurol. 25, 485-493.
    • (1989) Ann. Neurol. , vol.25 , pp. 485-493
    • Farrer, L.A.1    O'Sullivan, D.M.2    Cupples, L.A.3    Growden, J.H.4    Myers, R.H.5
  • 27
    • 0032862949 scopus 로고    scopus 로고
    • The genetics of disorders with synuclein pathology and parkinsonism
    • Farrer, M., Gwinn-Hardy, K., Mutton, M., Hardy, J. (1999). The genetics of disorders with synuclein pathology and parkinsonism. Hum. Mol. Genet. 8, 1901-1905.
    • (1999) Hum. Mol. Genet. , vol.8 , pp. 1901-1905
    • Farrer, M.1    Gwinn-Hardy, K.2    Mutton, M.3    Hardy, J.4
  • 29
    • 0034704752 scopus 로고    scopus 로고
    • A drosophila model of Parkinson's disease
    • Feany, M. B., Bender, W. W. (2000). A Drosophila model of Parkinson's disease. Nature 404, 394-398.
    • (2000) Nature , vol.404 , pp. 394-398
    • Feany, M.B.1    Bender, W.W.2
  • 34
    • 0033583215 scopus 로고    scopus 로고
    • Mutant and wild type human alpha-synucleins assemble into elongated filaments with distinct morphologies in vitro
    • Giasson, B. I., Uryu, K., Trojanowski, J. Q. & Lee, V. M. (1999). Mutant and wild type human alpha-synucleins assemble into elongated filaments with distinct morphologies in vitro. J. Biol. Chem. 274, 7619-7622.
    • (1999) J. Biol. Chem. , vol.274 , pp. 7619-7622
    • Giasson, B.I.1    Uryu, K.2    Trojanowski, J.Q.3    Lee, V.M.4
  • 35
    • 0032214501 scopus 로고    scopus 로고
    • Tau mutations cause frontotemporal dementias
    • Goedert, M., Crowther, R. A., Spillantini, M. G. (1998). Tau mutations cause frontotemporal dementias. Neuron 21, 955-958.
    • (1998) Neuron , vol.21 , pp. 955-958
    • Goedert, M.1    Crowther, R.A.2    Spillantini, M.G.3
  • 41
    • 0028963983 scopus 로고
    • An allelic association study of monoamine oxidase-B in Parkinson's disease
    • Ho, S., Kapadi, A., Ramsden, D. & Williams, A. (1995). An allelic association study of monoamine oxidase-B in Parkinson's disease. Ann. Neurol. 37, 403-405.
    • (1995) Ann. Neurol. , vol.37 , pp. 403-405
    • Ho, S.1    Kapadi, A.2    Ramsden, D.3    Williams, A.4
  • 42
    • 0033007372 scopus 로고    scopus 로고
    • Cytochrome P4502D6 (debrisoquine 4-hydroxylase) and Parkinson's disease in Chinese and Caucasians
    • Ho, S. L., Kung, M. H. W., Li, L. S. W., Lauder, I. J. & Ramsden, D. B. (1999). Cytochrome P4502D6 (debrisoquine 4-hydroxylase) and Parkinson's disease in Chinese and Caucasians, Eur. J. Neurol. 6, 323-329.
    • (1999) Eur. J. Neurol. , vol.6 , pp. 323-329
    • Ho, S.L.1    Kung, M.H.W.2    Li, L.S.W.3    Lauder, I.J.4    Ramsden, D.B.5
  • 44
    • 0026514953 scopus 로고
    • Accuracy of clinical diagnosis of idiopathic Parkinson's disease: A clinico-pathological study of 100 cases
    • Hughes, A., Daniel, S., Kilford, L. & Lees, A. (1992). Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. J. Neurol. Neurosurg. Psych. 55, 181-184.
    • (1992) J. Neurol. Neurosurg. Psych. , vol.55 , pp. 181-184
    • Hughes, A.1    Daniel, S.2    Kilford, L.3    Lees, A.4
  • 46
    • 0023149678 scopus 로고
    • 4-Phenylpyridine (4PP) and MPTP: The relationship between striatal MPP+ concentrations and neurotoxicity
    • Irwin, I., Langston, J. W. & DeLanney, L. R. (1987). 4-Phenylpyridine (4PP) and MPTP: the relationship between striatal MPP+ concentrations and neurotoxicity. Life Sciences 40, 731-740.
    • (1987) Life Sciences , vol.40 , pp. 731-740
    • Irwin, I.1    Langston, J.W.2    DeLanney, L.R.3
  • 47
    • 0029785290 scopus 로고    scopus 로고
    • Fluorodopa positron emission tomography with an inhibitor of catechol-O-methyl-transferase - Effect of the plasma 3-O-methyldopa fraction on data-analysis
    • Ishikawa, T., Dhawan, V., Chaly, T., Robeson, W., Belakhlef, A., Mandel, F., Dahl, R., Marouleff, C. & Eidelberg, D. (1996). Fluorodopa Positron Emission Tomography With an Inhibitor Of Catechol-O-Methyl-transferase - Effect Of the Plasma 3-O-Methyldopa Fraction On Data-Analysis. J. Cereb. Blood Flou Metab. 16, 854-863.
    • (1996) J. Cereb. Blood Flou Metab. , vol.16 , pp. 854-863
    • Ishikawa, T.1    Dhawan, V.2    Chaly, T.3    Robeson, W.4    Belakhlef, A.5    Mandel, F.6    Dahl, R.7    Marouleff, C.8    Eidelberg, D.9
  • 48
    • 0032500599 scopus 로고    scopus 로고
    • Binding of alpha-synuclein to brain vesicles is abolished by familial Parkinson's disease mutation
    • Jensen, P. H., Nielsen, M. S., Jakes, R., Dotti, G. & Goedert, M. (1998). Binding of alpha-synuclein to brain vesicles is abolished by familial Parkinson's disease mutation, J. Biol. Chem. 273, 26292-20294.
    • (1998) J. Biol. Chem. , vol.273 , pp. 26292-120294
    • Jensen, P.H.1    Nielsen, M.S.2    Jakes, R.3    Dotti, G.4    Goedert, M.5
  • 52
  • 53
    • 0020680904 scopus 로고
    • Chronic parkinsonism in humans due to a product of meperidine-analog synthesis
    • Langston, J., Ballard, P., Tetrud, J. & Irwin, I. (1983). Chronic parkinsonism in humans due to a product of meperidine-analog synthesis. Science 219, 979-980.
    • (1983) Science , vol.219 , pp. 979-980
    • Langston, J.1    Ballard, P.2    Tetrud, J.3    Irwin, I.4
  • 56
    • 0033525009 scopus 로고    scopus 로고
    • Low frequency of pathogenic mutations in the ubiquitin carboxy-terminal hydrolase gene in familial Parkinson's disease
    • Lincoln, S., Vaughan, J., Wood, N., Baker, M., Adamson, J., Gwinn-Hardy, K., Lynch, T., Hardy, J. & Farrer, M. (1999). Low frequency of pathogenic mutations in the ubiquitin carboxy-terminal hydrolase gene in familial Parkinson's disease. Neuroreport 10, 427-429.
    • (1999) Neuroreport , vol.10 , pp. 427-429
    • Lincoln, S.1    Vaughan, J.2    Wood, N.3    Baker, M.4    Adamson, J.5    Gwinn-Hardy, K.6    Lynch, T.7    Hardy, J.8    Farrer, M.9
  • 57
    • 0342368772 scopus 로고    scopus 로고
    • Association between early-onset Parkinson's disease and mutations in the parkin gene
    • Luecking, C. B., Durr, A., Bonifati, V. & Vaughan, J. (2000). Association between early-onset Parkinson's disease and mutations in the parkin gene. N. Engl. J. Med. 342, 1545-1620.
    • (2000) N. Engl. J. Med. , vol.342 , pp. 1545-1620
    • Luecking, C.B.1    Durr, A.2    Bonifati, V.3    Vaughan, J.4
  • 58
    • 0033941972 scopus 로고    scopus 로고
    • Case-control study of debrisoquine 4-hydroxylase, N-acetyltransferase2 and apolipoprotein E gene polymorphisms in Parkinson's disease
    • Maraganore, D. M. (2000). Case-Control Study of Debrisoquine 4-Hydroxylase, N-Acetyltransferase2 and Apolipoprotein E Gene Polymorphisms in Parkinson's Disease. Mov. Disord. 15, 714-719.
    • (2000) Mov. Disord. , vol.15 , pp. 714-719
    • Maraganore, D.M.1
  • 59
    • 0033544368 scopus 로고    scopus 로고
    • Case-control study of the ubiquitin carboxy-terminal hydrolase L1 gene in Parkinson's disease
    • Maraganore, D. M., Farrer, M. J., Hardy, J. A., Lincoln, S. J., McDonnell, S. K. & Rocca, W. A. (1999). Case-control study of the ubiquitin carboxy-terminal hydrolase L1 gene in Parkinson's disease. Neurology 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
  • 61
    • 0023280977 scopus 로고
    • Parkinson's disease in twins
    • Marsden, C. D. (1987). Parkinson's disease in twins [letter]. J. Neurol. Neurosurg. Psych. 50, 105-106.
    • (1987) J. Neurol. Neurosurg. Psych. , vol.50 , pp. 105-106
    • Marsden, C.D.1
  • 62
    • 0034681471 scopus 로고    scopus 로고
    • Dopaminergic loss and inclusion body formation in alpha-synuclein mice: Implications for neurodegenerative disorders
    • Masliah, E., Rockenstein, E., Veinbergs, I., Mallory, M., Hashimoto, M., Takeda, A., Sagara, Y., Sisk, A. & Mucke, L. (2000). Dopaminergic loss and inclusion body formation in alpha-synuclein mice: Implications for neurodegenerative disorders. Science 287, 1265-1269.
    • (2000) Science , vol.287 , pp. 1265-1269
    • Masliah, E.1    Rockenstein, E.2    Veinbergs, I.3    Mallory, M.4    Hashimoto, M.5    Takeda, A.6    Sagara, Y.7    Sisk, A.8    Mucke, L.9
  • 65
    • 0034722106 scopus 로고    scopus 로고
    • The ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism does not confer protection against idiopathic Parkinson's disease
    • Mellick, G. D. & Silburn, P. A. (2000). The ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism does not confer protection against idiopathic Parkinson's disease. Neurosci. Lett. 293, 127-130.
    • (2000) Neurosci. Lett. , vol.293 , pp. 127-130
    • Mellick, G.D.1    Silburn, P.A.2
  • 66
    • 0027953659 scopus 로고
    • Smoking associated protection from Alzheimer's and Parkinson's disease
    • Morens, D. M., Grandinetti, A., Reed, D. & White, L. R. (1994). Smoking associated protection from Alzheimer's and Parkinson's disease. Lancet 343, 356-357.
    • (1994) Lancet , vol.343 , pp. 356-357
    • Morens, D.M.1    Grandinetti, A.2    Reed, D.3    White, L.R.4
  • 67
    • 0031721141 scopus 로고    scopus 로고
    • Pathologic and biochemical studies of juvenile parkinsonism linked to chromosome 6q
    • Mori, H., Kondo, T. & Yokochi, M. (1998). Pathologic and biochemical studies of juvenile parkinsonism linked to chromosome 6q. Neuroloyy 51, 890-892.
    • (1998) Neurology , vol.51 , pp. 890-892
    • Mori, H.1    Kondo, T.2    Yokochi, M.3
  • 69
    • 0033515471 scopus 로고    scopus 로고
    • Narhi, L., Wood, S. J., Steavenson, S., Jiang, Y., Wu, G. M., Anafi. D., Kaufman, S. A., Martin, F., Sitney, K., Denis, P., Louis, J. C., Wypyeh, J., Biere, A. L. & Citron, M. (1999). Both familial Parkinson's disease mutations accelerate alpha-synuclein aggregation [published erratum appears in J. Biol. Chem. 274. 13728]. J. Biol. Chen. 274. 9843-9846.
    • J. Biol. Chen. , vol.274 , pp. 9843-9846
  • 71
    • 0025964041 scopus 로고
    • The absolute number of nerve cells in substantia nigra in normal subjects and in patients with Parkinson's disease estimated with an unbiased stereological method
    • Pakkenberg, B., Moller, A., Gundersen, H. J., Mouritzen Dam, A., Pakkenberg, H. (1991). The absolute number of nerve cells in substantia nigra in normal subjects and in patients with Parkinson's disease estimated with an unbiased stereological method. J. Neurol. Neurosurg. Psych. 54, 30-33.
    • (1991) J. Neurol. Neurosurg. Psych. , vol.54 , pp. 30-33
    • Pakkenberg, B.1    Moller, A.2    Gundersen, H.J.3    Mouritzen Dam, A.4    Pakkenberg, H.5
  • 72
    • 0024843373 scopus 로고
    • Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (Striatonigral degeneration. Olivopontocerebellar atrophy and shy-drager syndrome)
    • Papp, M. I. Kahn, J. E., Lantos, P. L. (1989). Glial Cytoplasmic Inclusions In the CNS Of Patients With Multiple System Atrophy (Striatonigral Degeneration. Olivopontocerebellar Atrophy and Shy-Drager Syndrome). J. Neurol. Sci. 94, 79-100.
    • (1989) J. Neurol. Sci. , vol.94 , pp. 79-100
    • Papp, M.I.1    Kahn, J.E.2    Lantos, P.L.3
  • 74
    • 0024848034 scopus 로고
    • Abnormalities of the electron transport chain in idiopathic Parkinson's disease
    • Parker, W. D., Boyson, S. J. & Parks, J. K. (1989). Abnormalities of the electron transport chain in idiopathic Parkinson's disease. Ann. Neurol. 26, 719-723.
    • (1989) Ann. Neurol. , vol.26 , pp. 719-723
    • Parker, W.D.1    Boyson, S.J.2    Parks, J.K.3
  • 76
    • 0033951680 scopus 로고    scopus 로고
    • Significant association between the tau gene A0/A0 genotype and Parkinson's disease
    • Pastor, P., Ezquerra, M., Munoz, E., Marti, M. J., Blesa, R., Tolosa, E. & Oliva, R. (2000). Significant association between the tau gene A0/A0 genotype and Parkinson's disease. Ann. Neurol. 47, 242-245.
    • (2000) Ann. Neurol. , vol.47 , pp. 242-245
    • Pastor, P.1    Ezquerra, M.2    Munoz, E.3    Marti, M.J.4    Blesa, R.5    Tolosa, E.6    Oliva, R.7
  • 77
    • 0029115971 scopus 로고
    • A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation
    • Patil, N., Cox, D. R., Bhat, D., Faham, M., Myers, R. M. & Peterson, A. S. (1995). A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation [see comments]. Nat.Genet. 11, 126-129.
    • (1995) Nat.Genet. , vol.11 , pp. 126-129
    • Patil, N.1    Cox, D.R.2    Bhat, D.3    Faham, M.4    Myers, R.M.5    Peterson, A.S.6
  • 78
    • 0028060492 scopus 로고
    • Increased risk of Parkinsons-disease in parents and siblings of patients
    • Payami, H., Larsen, K., Bernard, S. & Nutt, J. (1994). Increased Risk Of Parkinsons-Disease In Parents and Siblings Of Patients. Ann. Neurol. 36, 659-661.
    • (1994) Ann. Neurol. , vol.36 , pp. 659-661
    • Payami, H.1    Larsen, K.2    Bernard, S.3    Nutt, J.4
  • 79
    • 0032913951 scopus 로고    scopus 로고
    • The role of inheritance in sporadic Parkinson's disease: Evidence from a longitudinal study of dopaminergic function in twins
    • Piccini, P., Burn, D. J., Ceravolo, R., Maraganore, D. & Brooks, D. J. (1999). The role of inheritance in sporadic Parkinson's disease: evidence from a longitudinal study of dopaminergic function in twins. Ann. Neurol. 45, 577-582.
    • (1999) Ann. Neurol. , vol.45 , pp. 577-582
    • Piccini, P.1    Burn, D.J.2    Ceravolo, R.3    Maraganore, D.4    Brooks, D.J.5
  • 82
    • 2542507783 scopus 로고    scopus 로고
    • 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
    • Plante-Bordeneuve, V., Taussig, D., Thomas, F., Said, G., Wood, N. W., Marsden, C. D. & Harding, A. E. (1997). 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 48, 1589-1593.
    • (1997) Neurology , vol.48 , pp. 1589-1593
    • Plante-Bordeneuve, V.1    Taussig, D.2    Thomas, F.3    Said, G.4    Wood, N.W.5    Marsden, C.D.6    Harding, A.E.7
  • 85
    • 0024474837 scopus 로고
    • Multiple system atrophy - The nature of the beast
    • Quinn, N. P. (1989). Multiple System Atrophy - the Nature Of the Beast. J. Neurol. Neurosurg. Psych. S 78-89.
    • (1989) J. Neurol. Neurosurg. Psych. , pp. S78-89
    • Quinn, N.P.1
  • 86
    • 0031907725 scopus 로고    scopus 로고
    • P450 enzymes and Parkinson's disease: The story so far
    • Riedl, A. G., Watts, P. M., Jenner, P. &Marsden, C. D. (1998). P450 enzymes and Parkinson's disease: the story so far. Mov. Disord. 13, 212-220.
    • (1998) Mov. Disord. , vol.13 , pp. 212-220
    • Riedl, A.G.1    Watts, P.M.2    Jenner, P.3    Marsden, C.D.4
  • 87
    • 0029914688 scopus 로고    scopus 로고
    • Apolipoprotein E and Alzheimer's disease
    • Roses, A. D. & Strittmatter, W. J. (1996). Apolipoprotein E and Alzheimer's Disease. Ann. Rev. Neurosci. 19, 53-77.
    • (1996) Ann. Rev. Neurosci. , vol.19 , pp. 53-77
    • Roses, A.D.1    Strittmatter, W.J.2
  • 88
    • 0032794767 scopus 로고    scopus 로고
    • A family history of Parkinson's disease and its effect on other PD risk factors
    • Rybicki, B. A., Johnson, C. C., Peterson, E. L., Kortsha, G. X. & Gorell, J. M. (1999). A family history of Parkinson's disease and its effect on other PD risk factors. Neuroepiden. 18, 270-278.
    • (1999) Neuroepiden. , vol.18 , pp. 270-278
    • Rybicki, B.A.1    Johnson, C.C.2    Peterson, E.L.3    Kortsha, G.X.4    Gorell, J.M.5
  • 91
    • 0033589692 scopus 로고    scopus 로고
    • Prevalence of progressive supranuclear palsy and multiple system atrophy: A cross-sectional study
    • Schrag, A., Ben-Shlomo, Y., Quinn, N. P. (1999). Prevalence of progressive supranuclear palsy and multiple system atrophy: a cross-sectional study. Lancet 354, 1771-1775.
    • (1999) Lancet , vol.354 , pp. 1771-1775
    • Schrag, A.1    Ben-Shlomo, Y.2    Quinn, N.P.3
  • 92
    • 0033009603 scopus 로고    scopus 로고
    • Neurofibrillary degeneration in progressive supranuclear palsy and corticobasal degeneration: Tau pathologies with exclusively 'exon 10' isoforms
    • Sergeant, N., Wattez, A. & Delacourte, A. (1999). Neurofibrillary degeneration in progressive supranuclear palsy and corticobasal degeneration: Tau pathologies with exclusively 'exon 10' isoforms. J. Neurochem. 72, 1243-1249.
    • (1999) J. Neurochem. , vol.72 , pp. 1243-1249
    • Sergeant, N.1    Wattez, A.2    Delacourte, A.3
  • 95
    • 0000355051 scopus 로고
    • Report of familial cases of parkinsonism: Evidence of a dominant trait in a patient's family
    • Spellman, G. (1962). Report of familial cases of parkinsonism: evidence of a dominant trait in a patient's family. JAMA 179, 372-374.
    • (1962) JAMA , vol.179 , pp. 372-374
    • Spellman, G.1
  • 96
    • 0031912715 scopus 로고    scopus 로고
    • A sibship test for linkage in the presence of association: The sib transmission/disequilibrium test
    • Spielman, R. S. & Ewens, W. J. (1998). A sibship test for linkage in the presence of association: the sib transmission/disequilibrium test [see comments]. Am. J. Hum. Genet. 62, 450-458.
    • (1998) Am. J. Hum. Genet. , vol.62 , pp. 450-458
    • Spielman, R.S.1    Ewens, W.J.2
  • 97
    • 0031949084 scopus 로고    scopus 로고
    • Frontotemporal dementia and parkinsonism linked to chromosome 17: A new group of tauopathies
    • Spillantini, M. G., Bird, T. D. & Ghetti, B. (1998). Frontotemporal dementia and Parkinsonism linked to chromosome 17: a new group of tauopathies. Brain Pathol. 8, 387-402.
    • (1998) Brain Pathol. , vol.8 , pp. 387-402
    • Spillantini, M.G.1    Bird, T.D.2    Ghetti, B.3
  • 99
    • 0041721143 scopus 로고    scopus 로고
    • Determination of the GSTMt gene deletion frequency in Parkinson's disease by allele specific PCR
    • Stroombergen, M. C. M. J., Waring, R. H., Bennett, P. & Williams, A. C. (1996). Determination of the GSTMt gene deletion frequency in Parkinson's disease by allele specific PCR. Parkinsonism & Related Disord. 2, 151-154.
    • (1996) Parkinsonism & Related Disord. , vol.2 , pp. 151-154
    • Stroombergen, M.C.M.J.1    Waring, R.H.2    Bennett, P.3    Williams, A.C.4
  • 100
    • 0032476121 scopus 로고    scopus 로고
    • Differential expression of the parkin gene in the human brain and peripheral leukocytes
    • Sunada, Y., Saito, F. & Matsunnira, K. (1998). Differential expression of the parkin gene in the human brain and peripheral leukocytes. Neurosci. Lett. 254, 180-182.
    • (1998) Neurosci. Lett. , vol.254 , pp. 180-182
    • Sunada, Y.1    Saito, F.2    Matsunnira, K.3
  • 101
    • 0343025316 scopus 로고
    • Genetic linkage studies in autosomal dominant parkinsonisin: Evaluation of candidate genes
    • Supala, A., Wszolek, Z. K. & Trofatter, J. (1994). Genetic linkage studies in autosomal dominant parkinsonisin: evaluation of candidate genes. Mov. Disord. 9, 32.
    • (1994) Mov. Disord. , vol.9 , pp. 32
    • Supala, A.1    Wszolek, Z.K.2    Trofatter, J.3
  • 104
    • 0033837202 scopus 로고    scopus 로고
    • Variability and validity of polymorphism association studies in Parkinson's disease
    • Tan, E. K., Khajavi, M., Thornby, J. I., Nagamitsu, S., Jankovic, J., Ashizawa, T. (2000). Variability and validity of polymorphism association studies in Parkinson's disease. Neurology. 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
  • 105
    • 0026608742 scopus 로고
    • Epidemiology of Parkinson's disease
    • Tanner, C. M. (1992). Epidemiology of Parkinson's disease. Neurologic Clinics 10, 317-329.
    • (1992) Neurologic Clinics , vol.10 , pp. 317-329
    • Tanner, C.M.1
  • 107
    • 0027200680 scopus 로고
    • A novel cytochrome P-450IID6 mutant gene associated with Parkinson's disease
    • Tsuneoka, Y., Matsuo, Y., Iwahashi, K., Takeuchi, H. & Ichikawa, Y. (1993). A novel cytochrome P-450IID6 mutant gene associated with Parkinson's disease. J. Biochem. 114, 263-266.
    • (1993) J. Biochem. , vol.114 , pp. 263-266
    • Tsuneoka, Y.1    Matsuo, Y.2    Iwahashi, K.3    Takeuchi, H.4    Ichikawa, Y.5
  • 111
    • 85006849310 scopus 로고    scopus 로고
    • Further evidence for a chromosome 4p haplotype segregating with Parkinson's disease in an independent Italian kindred
    • Vaughan, J. R., Farrer, M., De Michele, G., Volpe, G., Hardy, J. & Wood, N. W. (1999). Further evidence for a chromosome 4p haplotype segregating with Parkinson's disease in an independent Italian Kindred. Am.J. Hum. Genet. 65, A496.
    • (1999) Am.J. Hum. Genet. , vol.65 , pp. A496
    • Vaughan, J.R.1    Farrer, M.2    De Michele, G.3    Volpe, G.4    Hardy, J.5    Wood, N.W.6
  • 115
    • 0020623657 scopus 로고
    • 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. (1983). Parkinson's disease in 65 pairs of twins and in a set of quadruplets. Neurology 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
  • 116
    • 0030986997 scopus 로고    scopus 로고
    • Multiple system atrophy: A review of 203 pathologically proven cases
    • Wenning, G. K., Tison, F., BenShlomo, Y., Daniel, S. E., Quinn, N. P. (1997). Multiple system atrophy: A review of 203 pathologically proven cases. Mov. Disord. 12, 133-147.
    • (1997) Mov. Disord. , vol.12 , pp. 133-147
    • Wenning, G.K.1    Tison, F.2    BenShlomo, Y.3    Daniel, S.E.4    Quinn, N.P.5
  • 118
    • 0031471890 scopus 로고    scopus 로고
    • Genetic aspects of parkinsonism
    • Wood, N. (1997). Genetic aspects of parkinsonism. Baillieres Clin. Neurol. 6, 37-53.
    • (1997) Baillieres Clin. Neurol. , vol.6 , pp. 37-53
    • Wood, N.1
  • 120
    • 0027358350 scopus 로고
    • Worldwide occurrence of Parkinson's disease: An updated review
    • Zhang, Z. X. & Roman, G. C. (1993). Worldwide occurrence of Parkinson's disease: an updated review. Neuroepidem. 12, 195-208.
    • (1993) Neuroepidem. , vol.12 , pp. 195-208
    • Zhang, Z.X.1    Roman, G.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.