-
1
-
-
0001835824
-
Paralysis agitans: Clinical and genetic study
-
Mjönes H. Paralysis agitans: clinical and genetic study. Acta Psychiatr Scand Suppl 1949; 54: 1-195.
-
(1949)
Acta Psychiatr Scand Suppl
, vol.54
, pp. 1-195
-
-
Mjönes, H.1
-
2
-
-
0033608187
-
Parkinson disease in twins: An aetiologic study
-
Tanner CM, Ottman R, Goldman SM, Ellenberg J, Chan P, Mayeux R et al. Parkinson disease in twins: an aetiologic study. JAMA 1999; 281: 341-6.
-
(1999)
JAMA
, vol.281
, pp. 341-346
-
-
Tanner, C.M.1
Ottman, R.2
Goldman, S.M.3
Ellenberg, J.4
Chan, P.5
Mayeux, R.6
-
3
-
-
0032913951
-
The role of inheritance in sporadic Parkinson's disease: Evidence from a longitudinal study of dopaminergic function in twins
-
Piccini P, Burn DJ, Ceravolo R, Maragonore D, Brooks DJ. The role of inheritance in sporadic Parkinson's disease: evidence from a longitudinal study of dopaminergic function in twins. Ann Neurol 1999; 45: 577-82.
-
(1999)
Ann Neurol
, vol.45
, pp. 577-582
-
-
Piccini, P.1
Burn, D.J.2
Ceravolo, R.3
Maragonore, D.4
Brooks, D.J.5
-
4
-
-
0034649710
-
Familial aggregation of Parkinson's disease on Iceland
-
Sveinbjornsdottir S, Hicks AA, Jonsson T, Petursson H, Gugmundsson G, Frigge ML et al. Familial aggregation of Parkinson's disease on Iceland. N Engl J Med 2000; 343: 1765-70.
-
(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
-
5
-
-
0032543684
-
Association of missense and 5′-splice site mutations in tau with the inherited dementia FTDP-17
-
Hutton M, Lendon CL, Rizzu P, Baker M, Froelich S, Houlden H et al. Association of missense and 5′-splice site mutations in tau with the inherited dementia FTDP-17. Nature 1998; 393: 702-5.
-
(1998)
Nature
, vol.393
, pp. 702-705
-
-
Hutton, M.1
Lendon, C.L.2
Rizzu, P.3
Baker, M.4
Froelich, S.5
Houlden, H.6
-
6
-
-
0034718577
-
Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese
-
Gwinn-Hardy K, Chen JY, Liu HC, Liu TY, Boss M, Seltzer W et al. Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese. Neurology 2000; 55: 800-5.
-
(2000)
Neurology
, vol.55
, pp. 800-805
-
-
Gwinn-Hardy, K.1
Chen, J.Y.2
Liu, H.C.3
Liu, T.Y.4
Boss, M.5
Seltzer, W.6
-
7
-
-
0036765066
-
Ethnic differences in the expression of neurodegenerative disease: Machado-Joseph disease in Africans and Caucasians
-
Subramony SH, Hernandez D, Adam A, Smith-Jefferson S, Hussey J, Gwinn-Hardy K et al. Ethnic differences in the expression of neurodegenerative disease: Machado-Joseph disease in Africans and Caucasians. Move Disord 2002; 17: 1068-71.
-
(2002)
Move Disord
, vol.17
, pp. 1068-1071
-
-
Subramony, S.H.1
Hernandez, D.2
Adam, A.3
Smith-Jefferson, S.4
Hussey, J.5
Gwinn-Hardy, K.6
-
8
-
-
0030744876
-
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
-
Polymeropoulous MH, Lavedan C, Leroy E, Ide SE, Dehejia A, Dutra A et al. Mutation in the alpha-synuclein gene identified in families with Parkinson's disease. Science 1997; 276: 2045-7.
-
(1997)
Science
, vol.276
, pp. 2045-2047
-
-
Polymeropoulous, M.H.1
Lavedan, C.2
Leroy, E.3
Ide, S.E.4
Dehejia, A.5
Dutra, A.6
-
9
-
-
0031990490
-
Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease
-
Kruger R, Kuhn W, Muller T, Woitalla D, Graeber M, Kosel S et al. Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease. Nat Genet 1998; 18: 106-8.
-
(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
-
10
-
-
0030882856
-
Alpha-synuclein in Lewy-bodies
-
Spillantini MG, Schmidt ML, Lee VM, Trojanowski JQ, Jakes R, Goedert M. Alpha-synuclein in Lewy-bodies. Nature 1997; 388: 839-40.
-
(1997)
Nature
, vol.388
, pp. 839-840
-
-
Spillantini, M.G.1
Schmidt, M.L.2
Lee, V.M.3
Trojanowski, J.Q.4
Jakes, R.5
Goedert, M.6
-
11
-
-
0242300619
-
α-Synuclein locus triplication causes Parkinson's disease
-
Singleton AB, Farrer M, Johnson J, Singleton A, Hague S, Kachergus J et al. α-Synuclein locus triplication causes Parkinson's disease. Science 2003; 302: 841.
-
(2003)
Science
, vol.302
, pp. 841
-
-
Singleton, A.B.1
Farrer, M.2
Johnson, J.3
Singleton, A.4
Hague, S.5
Kachergus, J.6
-
12
-
-
0031787871
-
Accelerated in vitro fibril formation by a mutant alpha-synuclein linked to early-onset Parkinson disease
-
Conway KA, Harper JD, Lansbury PT. Accelerated in vitro fibril formation by a mutant alpha-synuclein linked to early-onset Parkinson disease. Nat Med 1998; 4: 131820.
-
(1998)
Nat Med
, vol.4
, pp. 131820
-
-
Conway, K.A.1
Harper, J.D.2
Lansbury, P.T.3
-
13
-
-
15144345616
-
Hereditary form of parkinsonism-dementia
-
Muenter MD, Forno LS, Hornykiewicz O, Kish SJ, Maraganore DM, Caselli RJ et al. Hereditary form of parkinsonism-dementia. Ann Neurol 1998; 43: 768-81.
-
(1998)
Ann Neurol
, vol.43
, pp. 768-781
-
-
Muenter, M.D.1
Forno, L.S.2
Hornykiewicz, O.3
Kish, S.J.4
Maraganore, D.M.5
Caselli, R.J.6
-
14
-
-
0032499264
-
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
-
Kitada T, Asakawa S, Hattori N, Matsumine H, Yamamura Y, Ivlinoshima S et al. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 1998; 392: 605-8.
-
(1998)
Nature
, vol.392
, pp. 605-608
-
-
Kitada, T.1
Asakawa, S.2
Hattori, N.3
Matsumine, H.4
Yamamura, Y.5
Ivlinoshima, S.6
-
15
-
-
0342368772
-
Association between early-onset Parkinson's disease and mutations in the parkin gene
-
French Parkinson's Disease Genetics Study Group
-
Lucking CB, Durr A, Bonifati V, Vaughan J, De Michele G, Gasser T et al. Association between early-onset Parkinson's disease and mutations in the parkin gene. French Parkinson's Disease Genetics Study Group. N Engl J Med 2000; 342: 1560-7.
-
(2000)
N Engl J Med
, vol.342
, pp. 1560-1567
-
-
Lucking, C.B.1
Durr, A.2
Bonifati, V.3
Vaughan, J.4
De Michele, G.5
Gasser, T.6
-
16
-
-
0030015934
-
Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile parkinsonism
-
Ishikawa A, Tsuji S. Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile parkinsonism. Neurology 1996; 47: 160-6.
-
(1996)
Neurology
, vol.47
, pp. 160-166
-
-
Ishikawa, A.1
Tsuji, S.2
-
17
-
-
0028198309
-
Familial juvenile parkinsonism: Clinical and pathological study in a family
-
Takahashi H, Omaha E, Suzuki S, Horikawa Y, Ishikawa A, Morita T et al. Familial juvenile parkinsonism: clinical and pathological study in a family. Neurology 1994; 44: 437-41.
-
(1994)
Neurology
, vol.44
, pp. 437-441
-
-
Takahashi, H.1
Omaha, E.2
Suzuki, S.3
Horikawa, Y.4
Ishikawa, A.5
Morita, T.6
-
18
-
-
0032190090
-
The ubiquitin pathway in Parkinson's disease
-
Leroy E, Boyer R, Auburger G, Leube B, Ulm G, Mezey E et al. The ubiquitin pathway in Parkinson's disease. Nature 1998; 395: 451-2.
-
(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
-
19
-
-
0037428241
-
Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism
-
Bonifati V, Rizzu P, van Baten MJ, Schaap O, Breedveld GJ, Krieger E et al. Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism. Science 2003; 299: 256-9.
-
(2003)
Science
, vol.299
, pp. 256-259
-
-
Bonifati, V.1
Rizzu, P.2
Van Baten, M.J.3
Schaap, O.4
Breedveld, G.J.5
Krieger, E.6
-
20
-
-
0042232353
-
The role of pathogenic DJ-1 mutations in Parkinson's disease
-
Abou-Sleiman PM, Healy DG, Quinn N, Lees AJ, Wood NW. The role of pathogenic DJ-1 mutations in Parkinson's disease. Ann Neurol 2003; 54: 283-6.
-
(2003)
Ann Neurol
, vol.54
, pp. 283-286
-
-
Abou-Sleiman, P.M.1
Healy, D.G.2
Quinn, N.3
Lees, A.J.4
Wood, N.W.5
-
21
-
-
0031951197
-
A susceptibility locus for Parkinson's disease maps to chromosome 2p13
-
Gasser T, Muller-Myhsok B, Wszolek ZK, Oehlmann R, Calne DB, Bonifati V et al. A susceptibility locus for Parkinson's disease maps to chromosome 2p13. Nat Genet 1998; 18: 262-5.
-
(1998)
Nat Genet
, vol.18
, pp. 262-265
-
-
Gasser, T.1
Muller-Myhsok, B.2
Wszolek, Z.K.3
Oehlmann, R.4
Calne, D.B.5
Bonifati, V.6
-
22
-
-
0035068574
-
Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-36
-
Valente EM, Bentivoglio AR, Dixon PH, Ferraris A, lalongo T, Frontali M et al. Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-36. Am J Hum Genet 2001; 68: 895-900.
-
(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
Lalongo, T.5
Frontali, M.6
-
23
-
-
0036196860
-
A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1
-
Funayama M, Hasegawa K, Kowa H, Saito M, Tsuji S, Obata F. A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1. Ann Neurol 2002; 51: 296-301.
-
(2002)
Ann Neurol
, vol.51
, pp. 296-301
-
-
Funayama, M.1
Hasegawa, K.2
Kowa, H.3
Saito, M.4
Tsuji, S.5
Obata, F.6
-
24
-
-
0036830525
-
A susceptibility gene for late-onset idiopathic Parkinson's disease
-
Hicks AA, Petursson H, Jonsson T, Stefansson H, Johannsdottir HS, Sainz J et al. A susceptibility gene for late-onset idiopathic Parkinson's disease. Ann Neurol 2002; 52: 549-55.
-
(2002)
Ann Neurol
, vol.52
, pp. 549-555
-
-
Hicks, A.A.1
Petursson, H.2
Jonsson, T.3
Stefansson, H.4
Johannsdottir, H.S.5
Sainz, J.6
-
25
-
-
18444364221
-
Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations
-
Pankratz N, Nichols WC, Uniacke SK, Halter C, Rudolph A, Shults C et al. Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations. Am J Hum Genet 2002; 71: 124-35.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 124-135
-
-
Pankratz, N.1
Nichols, W.C.2
Uniacke, S.K.3
Halter, C.4
Rudolph, A.5
Shults, C.6
-
26
-
-
0027407565
-
Apolipoprotein E: High-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease
-
Strittmatter WJ, Saunders AM, Schmechel D, Pericak-Vance M, Enghild J, Salvesen GS et al. Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease. Proc Natl Acad Sci USA 1993; 90: 1977-81.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 1977-1981
-
-
Strittmatter, W.J.1
Saunders, A.M.2
Schmechel, D.3
Pericak-Vance, M.4
Enghild, J.5
Salvesen, G.S.6
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