SCOPUS 정보 검색 플랫폼

1
- 0034049691
- Familial aggregation of Parkinson's disease in a Finnish population
- (2000) J Neurol Neurosurg Psychiatry , vol.69 , pp. 107-109
- Autere, J.M.¹ Moilanen, J.S.² Myllyla, V.V.³ Majamaa, K.⁴

2
- 0035854630
- No pathogenic mutations in the synphilin-1 gene in Parkinson's disease
- (2001) Neurosci Lett , vol.307 , pp. 125-127
- Bandopadhyay, R.¹ De Silva, R.² Khan, N.³ Graham, E.⁴ Vaughan, J.⁵ Engelender, S.⁶ Ross, C.⁷ Morris, H.⁸ Morris, C.⁹ Wood, N.W.¹⁰ Daniel, S.¹¹ Lees, A.¹²

3
- 0035526288
- Clinical features of parkinsonian patients with the alpha-synuclein (G209A) mutation
- (2001) Mov Disord , vol.16 , pp. 1007-1013
- Bostantjopoulou, S.¹ Katsarou, Z.² Papadimitriou, A.³ Veletza, V.⁴ Hatzigeorgiou, G.⁵ Lees, A.⁶

4
- 0026793873
- Parkinson's disease in twins studied with 18F-dopa and positron emission tomography
- (1992) Neurology , vol.42 , pp. 1894-1900
- Burn, D.J.¹ Mark, M.H.² Playford, E.D.³ Maraganore, D.M.⁴ Zimmerman, T.R.⁵ Duvoisin, R.C.⁶ Harding, A.E.⁷ Marsden, C.D.⁸ Brooks, D.J.⁹

5
- 0031900214
- Absence of mutations in the coding region of the alpha-synuclein gene in pathologically proven Parkinson's disease
- (1998) Neurology , vol.50 , pp. 1136-1137
- Chan, P.¹ Jiang, X.² Forno, L.S.³ Di Monte, D.A.⁴ Tanner, C.M.⁵ Langston, J.W.⁶

6
- 0034776095
- Parkin ubiquitinates the alpha-synuclein-interacting protein, synphilin-1: Implications for Lewy-body formation in Parkinson disease
- (2001) Nat Med , vol.7 , pp. 1144-1150
- Chung, K.K.¹ Zhang, Y.² Lim, K.L.³ Tanaka, Y.⁴ Huang, H.⁵ Gao, J.⁶ Ross, C.A.⁷ Dawson, V.L.⁸ Dawson, T.M.⁹

7
- 0015431015
- A genetic study of Wilson's disease: Evidence for heterogeneity
- (1972) Am J Hum Genet , vol.24 , pp. 646-666
- Cox, D.W.¹ Fraser, F.C.² Sass-Kortsak, A.³

8
- 0028971334
- A genetic study of Parkinson's disease
- (1995) J Neural Transm Suppl , vol.45 , pp. 21-25
- De Michele, G.¹ Filla, A.² Marconi, R.³ Volpe, G.⁴ D'Alessio, A.⁵ Scala, R.⁶ Ambrosio, G.⁷ Campanella, G.⁸

9
- 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
- (1997) J Neurol Neurosurg Psychiatry , vol.62 , pp. 10-15
- De Rijk, M.C.¹ Tzourio, C.² Breteler, M.M.³ Dartigues, J.F.⁴ Amaducci, L.⁵ Lopez-Pousa, S.⁶ Manubens-Bertran, J.M.⁷ Alperovitch, A.⁸ Rocca, W.A.⁹

10
- 0035949797
- Genome-wide scan for Parkinson's disease: The GenePD Study
- (2001) Neurology , vol.57 , pp. 1124-1126
- DeStefano, A.L.¹ Golbe, L.I.² Mark, M.H.³ Lazzarini, A.M.⁴ Maher, N.E.⁵ Saint-Hilaire, M.⁶ Feldman, R.G.⁷

11
- 0035836752
- Pathology of PD in monozygotic twins with a 20-year discordance interval
- (2001) Neurology , vol.56 , pp. 981-982
- Dickson, D.¹ Farrer, M.² Lincoln, S.³ Mason, R.P.⁴ Zimmerman, T.R.⁵ Golbe, L.I.⁶ Hardy, J.⁷

12
- 0033016210
- Familial aggregation of Parkinson's disease: A population-based case-control study in Europe: EUROPARKINSON Study Group
- (1999) Neurology , vol.52 , pp. 1876-1882
- Elbaz, A.¹ Grigoletto, F.² Baldereschi, M.³ Breteler, M.M.⁴ Manubens-Bertran, J.M.⁵ Lopez-Pousa, S.⁶ Dartigues, J.F.⁷ Alperovitch, A.⁸ Tzourio, C.⁹ Rocca, W.A.¹⁰

13
- 0035029340
- Genetic analysis of synphilin-1 in familial Parkinson's disease
- (2001) Neurobiol Dis , vol.8 , pp. 317-323
- Farrer, M.¹ Destee, A.² Levecque, C.³ Singleton, A.⁴ Engelender, S.⁵ Becquet, E.⁶ Mouroux, V.⁷ Richard, F.⁸ Defebvre, L.⁹ Crook, R.¹⁰ Hernandez, D.¹¹ Ross, C.A.¹² Hardy, J.¹³ Amouyel, P.¹⁴ Chartier-Harlin, M.C.¹⁵

14
- 0032911910
- A chromosome 4p haplotype segregating with Parkinson's disease and postural tremor
- (1999) Hum Mol Genet , vol.8 , pp. 81-85
- Farrer, M.J.¹ Gwinn-Hardy, K.² Muenter, M.³ DeVrieze, F.W.⁴ Crook, R.⁵ Perez-Tur, J.⁶ Lincoln, S.⁷ Maraganore, D.⁸ Adler, C.⁹ Newman, S.¹⁰ MacElwee, K.¹¹ McCarthy, P.¹² Miller, C.¹³ Waters, C.¹⁴ Hardy, J.¹⁵

15
- 0035880458
- Alpha-synuclein gene haplotypes are associated with Parkinson's disease
- (2001) Hum Mol Genet , vol.10 , pp. 1847-1851
- Farrer, M.¹ Maraganore, D.M.² Lockhart, P.³ Singleton, A.⁴ Lesnick, T.G.⁵ De Andrade, M.⁶ West, A.⁷ De Silva, R.⁸ Hardy, J.⁹ Hernandez, D.¹⁰

16
- 2642607011
- Low frequency of alpha-synuclein mutations in familial Parkinson's disease
- (1998) Ann Neurol , vol.43 , pp. 394-397
- Farrer, M.¹ Wavrant-De Vrieze, F.² Crook, R.³ Boles, L.⁴ Perez-Tur, J.⁵ Hardy, J.⁶ Johnson, W.G.⁷ Steele, J.⁸ Maraganore, D.⁹ Gwinn, K.¹⁰ Lynch, T.¹¹

17
- 0025954066
- Ageing and Parkinson's disease: Substantia nigra regional selectivity
- (1991) Brain , vol.114 , pp. 2283-2301
- Fearnley, J.M.¹ Lees, A.J.²

18
- 0032549088
- The alpha-Synuclein gene and Parkinson's disease
- (1998) Science , vol.279 , pp. 1116-1117

19
- 0034798193
- Genetics of Parkinson's disease
- (2001) J Neurol , vol.248 , pp. 833-840
- Gasser, T.¹

20
- 0031951197
- A susceptibility locus for Parkinson's disease maps to chromosome 2p13
- (1998) Nat Genet , vol.18 , pp. 262-265
- Gasser, T.¹ Müller-Myhsok, B.² Wszolek, Z.K.³ Oehlmann, R.⁴ Calne, D.B.⁵ Bonifati, V.⁶ Bereznai, B.⁷ Fabrizio, E.⁸ Vieregge, P.⁹ Horstmann, R.D.¹⁰

21
- 0024512326
- The significance of the Lewy body in the diagnosis of idiopathic Parkinson's disease
- (1989) Neuropathol Appl Neurobiol , vol.15 , pp. 27-44
- Gibb, W.R.¹ Lees, A.J.²

22
- 0030927756
- Relationship estimation in affected sib pair analysis of late-onset diseases
- (1997) Eur J Hum Genet , vol.5 , pp. 69-77
- Goring, H.H.¹ Ott, J.²

23
- 0001420150
- A susceptibility gene for late-onset idiopathic Parkinson's disease successfully mapped
- (2001) Am J Hum Genet Suppl , vol.69 , pp. 200
- Hicks, A.¹ Petursson, H.² Jónsson, T.³ Stefánsson, H.⁴ Jóhannsdóttir, H.⁵ Sainz, J.⁶ Frigge, M.L.⁷ Kong, A.⁸ Gulcher, J.R.⁹ Stefánsson, K.¹⁰ Sveinbjörnsdóttir, S.¹¹

24
- 0027529253
- Asymptotic properties of affected-sib-pair linkage analysis
- (1993) Am J Hum Genet , vol.52 , pp. 362-374
- Holmans, P.¹

25
- 0026629509
- What features improve the accuracy of clinical diagnosis in Parkinson's disease: A clinicopathologic study
- (1992) Neurology , vol.42 , pp. 1142-1146
- Hughes, A.J.¹ Ben-Schlomo, Y.² Daniel, S.E.³ Lees, A.J.⁴

26
- 0026514953
- Accuracy of the clinical diagnosis of Parkinson's disease: A clinicopathological study of 100 cases
- (1992) J Neurol Neurosurg Psychiatry , vol.55 , pp. 181-184
- Hughes, A.J.¹ Daniel, S.E.² Kilford, L.³ Lees, A.J.⁴

27
- 0030015934
- Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile Parkinsonism
- (1996) Neurology , vol.47 , pp. 160-166
- Ishikawa, A.¹ Tsuji, S.²

28
- 0035838284
- Multiple ligand interaction of α-synuclein produced various forms of protein aggregates in the presence of Aβ25-35, copper, and eosin
- (2001) Brain Res , vol.908 , pp. 93-98
- Kim, Y.S.¹ Lee, D.² Lee, E.K.³ Sung, J.Y.⁴ Chung, K.C.⁵ Kim, J.⁶ Paik, S.R.⁷

29
- 0032499264
- Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
- (1998) Nature , vol.392 , pp. 605-608
- Kitada, T.¹ Asakawa, S.² Hattori, N.³ Matsumine, H.⁴ Yamamura, Y.⁵ Minoshima, S.⁶ Yokochi, M.⁷ Mizuno, Y.⁸ Shimizu, N.⁹

30
- 0002206567
- Classification of parkinsonism
- Koller WC (ed). Marcel Dekker, New York
- (1992) Handbook of Parkinson's disease , pp. 59-103
- Koller, W.C.¹ Hubble, J.P.²

31
- 0031990490
- Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease
- (1998) Nat Genet , vol.18 , pp. 106-108
- Kruger, R.¹ Kuhn, W.² Muller, T.³ Woitalla, D.⁴ Graeber, M.⁵ Kosel, S.⁶ Przuntek, H.⁷ Epplen, J.T.⁸ Schols, L.⁹ Riess, O.¹⁰

32
- 0342950666
- Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotype
- (1999) Ann Neurol , vol.45 , pp. 611-617
- Kruger, R.¹ Vieira-Saecker, A.M.² Kuhn, W.³ Berg, D.⁴ Muller, T.⁵ Kuhnl, N.⁶ Fuchs, G.A.⁷ Storch, A.⁸ Hungs, M.⁹ Woitalla, D.¹⁰ Przuntek, H.¹¹ Epplen, J.T.¹² Schols, L.¹³ Riess, O.¹⁴

33
- 0029046177
- Complete multipoint sib-pair analysis of qualitative and quantitative traits
- (1995) Am J Hum Genet , vol.57 , pp. 439-454
- Kruglyak, L.¹ Lander, E.S.²

34
- 0035049892
- Familial occurrence of Parkinson's disease in a community-based case-control study
- (2001) Parkinsonism Relat Disord , vol.7 , pp. 297-303
- Kuopio, A.¹ Marttila, R.J.² Helenius, H.³ Rinne, U.K.⁴

35
- 0002643609
- Assessment of Parkinson's disease
- Munsat TL (ed). Butterworth, Boston
- (1989) Quantification of neurologic deficit , pp. 285-309
- Lang, A.E.¹ Fahn, S.²

36
- 0035666595
- Sex linked recessive dystonia parkinsonism of Panay, Philippines (XDP)
- (2001) Mol Pathol , vol.54 , pp. 362-368
- Lee, L.V.¹ Munoz, E.L.² Tan, K.T.³ Reyes, M.T.⁴

37
- 0032190090
- The ubiquitin pathway in Parkinson's disease
- (1998) Nature , vol.395 , pp. 451-452
- Leroy, E.¹ Boyer, R.² Auburger, G.³ Leube, B.⁴ Ulm, G.⁵ Mezey, E.⁶ Harta, G.⁷ Brownstein, M.J.⁸ Jonnalagada, S.⁹ Chernova, T.¹⁰ Dehejia, A.¹¹ Lavedan, C.¹² Gasser, T.¹³ Steinbach, P.J.¹⁴ Wilkinson, K.D.¹⁵ Polymeropoulos, M.H.¹⁶

38
- 0342368772
- Association between early-onset Parkinson's disease and mutations in the Parkin gene: French Parkinson's Disease Genetics Study Group
- (2000) N Engl J Med , vol.342 , pp. 1560-1567
- Lücking, C.B.¹ Durr, A.² Bonifati, V.³ Vaughan, J.⁴ De Michele, G.⁵ Gasser, T.⁶ Harhangi, B.S.⁷ Meco, G.⁸ Denefle, P.⁹ Wood, N.W.¹⁰ Agid, Y.¹¹ Brice, A.¹²

39
- 0023258542
- DNA banking: The effects of storage of blood and isolated DNA on the integrity of DNA
- (1987) Am J Med Genet , vol.27 , pp. 379-390
- Madisen, L.¹ Hoar, D.I.² Holroyd, C.D.³ Crisp, M.⁴ Hodes, M.E.⁵

40
- 0042487762
- Refined linkage disequilibrium and physical mapping of the gene locus for X-linked dystonia-parkinsonism (DYT3)
- (1999) Genomics , vol.60 , pp. 320-329
- Nemeth, A.H.¹ Nolte, D.² Dunne, E.³ Niemann, S.⁴ Kostrzewa, M.⁵ Peters, U.⁶ Fraser, E.⁷ Bochukova, E.⁸ Butler, R.⁹ Brown, J.¹⁰ Cox, R.D.¹¹ Levy, E.R.¹² Ropers, H.H.¹³ Monaco, A.P.¹⁴ Muller, U.¹⁵

41
- 85007241941
- Linkage stratification and mutation analysis at the parkin locus identifies mutation positive, Parkinson disease families
- in press
- Hum Genet
- Nichols, W.C.¹ Pankratz, N.² Uniacke, S.K.³ Pauciulo, M.W.⁴ Halter, C.⁵ Rudolph, A.⁶ Conneally, P.M.⁷ Foroud, T.⁸

42
- 0032231941
- PedCheck: A program for identification of genotype incompatibilities in linkage analysis
- (1998) Am J Hum Genet , vol.63 , pp. 259-266
- O'Connell, J.R.¹ Weeks, D.E.²

43
- 0034660568
- Metal-catalyzed oxidation of alpha-synuclein in the presence of copper(II) and hydrogen peroxide
- (2000) Arch Biochem Biophys , vol.378 , pp. 269-277
- Paik, S.R.¹ Shin, H.J.² Lee, J.H.³

44
- 0023237555
- Raised cerebrospinal-fluid copper concentration in Parkinson's disease
- (1987) Lancet , vol.2 , pp. 238-241
- Pall, H.S.¹ Williams, A.C.² Blake, D.R.³ Lunec, J.⁴ Gutteridge, J.M.⁵ Hall, M.⁶ Taylor, A.⁷

45
- 0035526251
- Analysis of the coding and the 5′ flanking regions of the alpha-synuclein gene in patients with Parkinson's disease
- (2001) Mov Disord , vol.16 , pp. 1115-1119
- Pastor, P.¹ Munoz, E.² Ezquerra, M.³ Obach, V.⁴ Marti, M.J.⁵ Valldeoriola, F.⁶ Tolosa, E.⁷ Oliva, R.⁸

46
- 0028060492
- Increased risk of Parkinson's disease in parents and siblings of patients
- (1994) Ann Neurol , vol.36 , pp. 659-661
- Payami, H.¹ Larsen, K.² Bernard, S.³ Nutt, J.⁴

47
- 0031049889
- Dopaminergic function in familial Parkinson's disease: A clinical and 18F-dopa positron emission tomography study
- (1997) Ann Neurol , vol.41 , pp. 222-229
- Piccini, P.¹ Morrish, P.K.² Turjanski, N.³ Sawle, G.V.⁴ Burn, D.J.⁵ Weeks, R.A.⁶ Mark, M.H.⁷ Maraganore, D.M.⁸ Lees, A.J.⁹ Brooks, D.J.¹⁰

48
- 0030744876
- Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
- (1997) Science , vol.276 , pp. 2045-2047
- Polymeropoulos, M.H.¹ Lavedan, C.² Leroy, E.³ Ide, S.E.⁴ Dehejia, A.⁵ Dutra, A.⁶ Pike, B.⁷ Root, H.⁸ Rubenstein, J.⁹ Boyer, R.¹⁰ Stenroos, E.S.¹¹ Chandrasekharappa, S.¹² Athanassiadou, A.¹³ Papapetropoulos, T.¹⁴ Johnson, W.G.¹⁵ Lazzarini, A.M.¹⁶ Duvoisin, R.C.¹⁷ Di Iorio, G.¹⁸ Golbe, L.I.¹⁹ Nussbaum, R.L.²⁰ more..

49
- 0033768752
- Parkinson's disease and environmental factors: Matched case-control study in the Limousin region, France
- (2000) Neuroepidemiology , vol.19 , pp. 333-337
- Preux, P.M.¹ Condet, A.² Anglade, C.³ Druet-Cabanac, M.⁴ Debrock, C.⁵ Macharia, W.⁶ Couratier, P.⁷ Boutros-Toni, F.⁸ Dumas, M.⁹

50
- 0035139204
- The Wilson's disease gene and phenotypic diversity
- (2001) J Hepatol , vol.34 , pp. 165-171
- Riordan, S.M.¹ Williams, R.²

51
- 0035860983
- Complete genomic screen in Parkinson disease: Evidence for multiple genes
- (2001) JAMA , vol.286 , pp. 2239-2244
- Scott, W.K.¹ Nance, M.A.² Watts, R.L.³ Hubble, J.P.⁴ Koller, W.C.⁵ Lyons, K.⁶ Pahwa, R.⁷

52
- 0001291620
- Clinical diagnostic criteria for idiopathic Parkinson's disease
- (1998) Mov Disord , vol.13 , pp. 862
- Siemers, E.R.¹ Hubble, J.² Tuite, P.³ Comella, C.⁴ Kompoliti, K.⁵ Oakes, D.⁶ Wojcieszek, J.⁷ Foroud, T.⁸ Conneally, P.M.⁹

53
- 0034649710
- Familial aggregation of Parkinson's disease in Iceland
- (2000) N Engl J Med , vol.343 , pp. 1765-1770
- Sveinbjornsdottir, S.¹ Hicks, A.A.² Jonsson, T.³ Petursson, H.⁴ Gugmundsson, G.⁵ Frigge, M.L.⁶ Kong, A.⁷ Gulcher, J.R.⁸ Stefansson, K.⁹

54
- 0033608187
- Parkinson's disease in twins: An etiologic study
- (1999) JAMA , vol.281 , pp. 341-346
- Tanner, C.M.¹ Ottmann, R.² Goldman, S.M.³ Ellenberg, J.⁴ Chan, P.⁵ Mayeux, R.⁶ Langston, J.W.⁷

55
- 0000904361
- Parkinson's disease incidence in Olmstead County, MN: 1935-1988
- (1992) Neurology , vol.42 , pp. 194
- Tanner, C.M.¹ Thelen, J.A.² Oxford, K.P.³ Rademacher, D.⁴ Goetz, C.G.⁵ Kurland, L.T.⁶

56
- 0030985136
- Familial Parkinson's disease: A case-control study of families
- (1997) Can J Neurol Sci , vol.24 , pp. 127-132
- Uitti, R.J.¹ Shinotoh, H.² Hayward, M.³ Schulzer, M.⁴ Mak, E.⁵ Calne, D.B.⁶

57
- 0035941201
- Metal-triggered structural transformations, aggregation, and fibrillation of human alpha-synuclein: A possible molecular NK between Parkinson's disease and heavy metal exposure
- (2001) J Biol Chem , vol.276 , pp. 44284-44296
- Uversky, V.N.¹ Li, J.² Fink, A.L.³

58
- 0035068574
- Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on chromosome 1p35-p36
- (2001) Am J Hum Genet , vol.68 , pp. 895-900
- Valente, E.M.¹ Bentivoglio, A.R.² Dixon, P.H.³ Ferraris, A.⁴ Ialongo, T.⁵ Frontali, M.⁶ Albanese, A.⁷ Wood, N.W.⁸

59
- 0034892917
- PARK7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36
- (2001) Am J Hum Genet , vol.69 , pp. 629-634
- Van Duijn, C.M.¹ Dekker, M.C.J.² Bonifati, V.³ Galjaard, R.J.⁴ Houwing-Duistermaat, J.J.⁵ Snijders, P.J.L.M.⁶ Testers, L.⁷ Breedveld, G.J.⁸ Horstink, M.⁹ Sandkuijl, L.A.¹⁰ Van Swieten, J.C.¹¹ Oostra, B.A.¹² Heutink, P.¹³

60
- 6844236385
- Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations: The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD)
- (1998) Hum Mol Genet , vol.7 , pp. 751-753
- Vaughan, J.R.¹ Farter, M.J.² Wszolek, Z.K.³ Gasser, T.⁴ Durr, A.⁵ Agid, Y.⁶ Bonifati, V.⁷ DeMichele, G.⁸ Volpe, G.⁹ Lincoln, S.¹⁰ Breteler, M.¹¹ Meco, G.¹² Brice, A.¹³ Marsden, C.D.¹⁴ Hardy, J.¹⁵ Wood, N.W.¹⁶

61
- 0028360383
- Multifactorial etiology of idiopathic Parkinson disease: A case-control study
- in German
- (1994) Nervenarzt , vol.65 , pp. 390-395
- Vieregge, P.¹ Friedrich, H.J.² Rohl, A.³ Ulm, G.⁴ Heberlein, I.⁵

62
- 0015590978
- Paralysis agitans of early-onset with marked diurnal fluctuation of symptoms
- (1973) Neurology , vol.23 , pp. 239-244
- Yamamura, Y.¹ Sobue, I.² Ando, K.³ Iida, M.⁴ Yanagi, T.⁵ Kondo, C.⁶