-
1
-
-
33646763903
-
Biochemical staging of synucleinopathy and amyloid deposition in dementia with Lewy bodies
-
Deramecourt V, Bombois S, Maurage CA et al: Biochemical staging of synucleinopathy and amyloid deposition in dementia with Lewy bodies. J Neuropathol Exp Neurol 2006; 65: 278-288.
-
(2006)
J Neuropathol Exp Neurol
, vol.65
, pp. 278-288
-
-
Deramecourt, V.1
Bombois, S.2
Maurage, C.A.3
-
2
-
-
0032543684
-
Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17
-
Hutton M, Lendon CL, Rizzu P et al: Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17. Nature 1998; 393: 702-705.
-
(1998)
Nature
, vol.393
, pp. 702-705
-
-
Hutton, M.1
Lendon, C.L.2
Rizzu, P.3
-
3
-
-
0033951680
-
Significant association between the tau gene A0/A0 genotype and Parkinson's disease
-
Pastor P, Ezquerra M, Munoz E et al: Significant association between the tau gene A0/A0 genotype and Parkinson's disease. Ann Neurol 2000; 47: 242-245.
-
(2000)
Ann Neurol
, vol.47
, pp. 242-245
-
-
Pastor, P.1
Ezquerra, M.2
Munoz, E.3
-
4
-
-
70549088602
-
Genome-wide association study reveals genetic risk underlying Parkinson's disease
-
Simon-Sanchez J, Schulte C, Bras JM et al: Genome-wide association study reveals genetic risk underlying Parkinson's disease. Nat Genet 2009; 41: 1308-1312.
-
(2009)
Nat Genet
, vol.41
, pp. 1308-1312
-
-
Simon-Sanchez, J.1
Schulte, C.2
Bras, J.M.3
-
5
-
-
0037335814
-
Prevalence and characteristics of dementia in Parkinson disease: An 8-year prospective study
-
Aarsland D, Andersen K, Larsen JP, Lolk A, Kragh-Sorensen P: Prevalence and characteristics of dementia in Parkinson disease: an 8-year prospective study. Arch Neurol 2003; 60: 387-392.
-
(2003)
Arch Neurol
, vol.60
, pp. 387-392
-
-
Aarsland, D.1
Andersen, K.2
Larsen, J.P.3
Lolk, A.4
Kragh-Sorensen, P.5
-
6
-
-
40149099986
-
Cognitive impairment in 873 patients with idiopathic Parkinson's disease,Results from the German Study on Epidemiology of Parkinson's Disease with Dementia (GEPAD)
-
Riedel O, Klotsche J, Spottke A et al: Cognitive impairment in 873 patients with idiopathic Parkinson's disease. Results from the German Study on Epidemiology of Parkinson's Disease with Dementia (GEPAD). J Neurol 2008; 255: 255-264.
-
(2008)
J Neurol
, vol.255
, pp. 255-264
-
-
Riedel, O.1
Klotsche, J.2
Spottke, A.3
-
7
-
-
77953011321
-
Relationships between age and late progression of Parkinson's disease: A clinico-pathological study
-
Kempster PA, O'Sullivan SS, Holton JL, Revesz T, Lees AJ.: Relationships between age and late progression of Parkinson's disease: a clinico-pathological study. Brain 2010; 133: 1755-1762.
-
(2010)
Brain
, vol.133
, pp. 1755-1762
-
-
Kempster, P.A.1
O'Sullivan, S.S.2
Holton, J.L.3
Revesz, T.4
Lees, A.J.5
-
8
-
-
0026088977
-
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
-
Goate A, Chartier-Harlin MC, Mullan M et al: Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease. Nature 1991; 349: 704-706.
-
(1991)
Nature
, vol.349
, pp. 704-706
-
-
Goate, A.1
Chartier-Harlin, M.C.2
Mullan, M.3
-
9
-
-
0029087026
-
Candidate gene for the chromosome 1 familial Alzheimer's disease locus
-
Levy-Lahad E, Wasco W, Poorkaj P et al: Candidate gene for the chromosome 1 familial Alzheimer's disease locus. Science 1995; 269: 973-977.
-
(1995)
Science
, vol.269
, pp. 973-977
-
-
Levy-Lahad, E.1
Wasco, W.2
Poorkaj, P.3
-
10
-
-
0029101491
-
Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene
-
Rogaev EI, Sherrington R, Rogaeva EA et al: Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene. Nature 1995; 376: 775-778.
-
(1995)
Nature
, vol.376
, pp. 775-778
-
-
Rogaev, E.I.1
Sherrington, R.2
Rogaeva, E.A.3
-
11
-
-
0029004341
-
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
-
Sherrington R, Rogaev EI, Liang Y et al: Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease. Nature 1995; 375: 754-760.
-
(1995)
Nature
, vol.375
, pp. 754-760
-
-
Sherrington, R.1
Rogaev, E.I.2
Liang, Y.3
-
12
-
-
33746910649
-
Null mutations in progranulin cause ubiquitinpositive frontotemporal dementia linked to chromosome 17q21
-
Cruts M, Gijselinck I, van der Zee J et al: Null mutations in progranulin cause ubiquitinpositive frontotemporal dementia linked to chromosome 17q21. Nature 2006; 442: 920-924.
-
(2006)
Nature
, vol.442
, pp. 920-924
-
-
Cruts, M.1
Gijselinck, I.2
Van Der Zee, J.3
-
13
-
-
70350673956
-
A new subtype of frontotemporal lobar degeneration with FUS pathology
-
Neumann M, Rademakers R, Roeber S, Baker M, Kretzschmar HA, Mackenzie IR.: A new subtype of frontotemporal lobar degeneration with FUS pathology. Brain 2009; 132: 2922-2931.
-
(2009)
Brain
, vol.132
, pp. 2922-2931
-
-
Neumann, M.1
Rademakers, R.2
Roeber, S.3
Baker, M.4
Kretzschmar, H.A.5
Mackenzie, I.R.6
-
14
-
-
33749632259
-
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
Neumann M, Sampathu DM, Kwong LK et al: Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 2006; 314: 130-133.
-
(2006)
Science
, vol.314
, pp. 130-133
-
-
Neumann, M.1
Sampathu, D.M.2
Kwong, L.K.3
-
15
-
-
35348939603
-
Clinical diagnostic criteria for dementia associated with Parkinson's disease
-
quiz 1837
-
Emre M, Aarsland D, Brown R et al: Clinical diagnostic criteria for dementia associated with Parkinson's disease. Mov Disord 2007; 22: 1689-1707, quiz 1837.
-
(2007)
Mov Disord
, vol.22
, pp. 1689-1707
-
-
Emre, M.1
Aarsland, D.2
Brown, R.3
-
16
-
-
79960819049
-
Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1
-
Winkelmann J, Czamara D, Schormair B et al: Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. PLoS Genet 2011; 7: e1002171.
-
(2011)
PLoS Genet
, vol.7
, pp. e1002171
-
-
Winkelmann, J.1
Czamara, D.2
Schormair, B.3
-
17
-
-
84944145877
-
-
(ESP) NGESP. Exome Variant Server,Accessed on December 1, 2012
-
(ESP) NGESP. Exome Variant Server. Available at http://evs.gs.washington.edu/EVS/Accessed on December 1, 2012.
-
-
-
-
18
-
-
84856708923
-
Tau deficiency induces parkinsonism with dementia by impairing APP-mediated iron export
-
Lei P, Ayton S, Finkelstein DI et al: Tau deficiency induces parkinsonism with dementia by impairing APP-mediated iron export. Nat Med 2012; 18: 291-295.
-
(2012)
Nat Med
, vol.18
, pp. 291-295
-
-
Lei, P.1
Ayton, S.2
Finkelstein, D.I.3
-
19
-
-
80052967403
-
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: A case-control study
-
Ross OA, Soto-Ortolaza AI, Heckman MG et al: Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study. Lancet Neurol 2011; 10: 898-908.
-
(2011)
Lancet Neurol
, vol.10
, pp. 898-908
-
-
Ross, O.A.1
Soto-Ortolaza, A.I.2
Heckman, M.G.3
-
20
-
-
32444432146
-
Abeta and tau form soluble complexes that may promote self aggregation of both into the insoluble forms observed in Alzheimer's disease
-
Guo JP, Arai T, Miklossy J, McGeer PL: Abeta and tau form soluble complexes that may promote self aggregation of both into the insoluble forms observed in Alzheimer's disease. Proc Natl Acad Sci USA 2006;103:1953-1958.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 1953-1958
-
-
Guo, J.P.1
Arai, T.2
Miklossy, J.3
McGeer, P.L.4
-
21
-
-
84876797754
-
Substrate determinants in the C99 juxtamembrane domains differentially affect gamma-secretase cleavage specificity and modulator pharmacology
-
Ousson S, Saric A, Baguet A et al: Substrate determinants in the C99 juxtamembrane domains differentially affect gamma-secretase cleavage specificity and modulator pharmacology. J Neurochem 2013; 125: 610-619.
-
(2013)
J Neurochem
, vol.125
, pp. 610-619
-
-
Ousson, S.1
Saric, A.2
Baguet, A.3
-
23
-
-
84873058848
-
Amine oxidase activity of beta-amyloid precursor protein modulates systemic and local catecholamine levels
-
Duce JA, Ayton S, Miller AA et al: Amine oxidase activity of beta-amyloid precursor protein modulates systemic and local catecholamine levels. Mol Psychiatry 2013; 18: 245-254.
-
(2013)
Mol Psychiatry
, vol.18
, pp. 245-254
-
-
Duce, J.A.1
Ayton, S.2
Miller, A.A.3
-
24
-
-
77956647381
-
Iron-export ferroxidase activity of beta-amyloid precursor protein is inhibited by zinc in Alzheimer's disease
-
Duce JA, Tsatsanis A, Cater MA et al: Iron-export ferroxidase activity of beta-amyloid precursor protein is inhibited by zinc in Alzheimer's disease. Cell 2010; 142: 857-867.
-
(2010)
Cell
, vol.142
, pp. 857-867
-
-
Duce, J.A.1
Tsatsanis, A.2
Cater, M.A.3
-
25
-
-
0023638828
-
Increased nigral iron content in postmortem parkinsonian brain
-
Dexter DT, Wells FR, Agid F et al: Increased nigral iron content in postmortem parkinsonian brain. Lancet 1987; 2: 1219-1220.
-
(1987)
Lancet
, vol.2
, pp. 1219-1220
-
-
Dexter, D.T.1
Wells, F.R.2
Agid, F.3
|