-
1
-
-
18244394793
-
Clinical features of LRRK2-associated Parkinson's disease in central Norway
-
J.O. Aasly, M. Toft, I. Fernandez-Mata, J. Kachergus, M. Hulihan, L.R. White, and M. Farrer Clinical features of LRRK2-associated Parkinson's disease in central Norway Ann. Neurol. 57 2005 762 765
-
(2005)
Ann. Neurol.
, vol.57
, pp. 762-765
-
-
Aasly, J.O.1
Toft, M.2
Fernandez-Mata, I.3
Kachergus, J.4
Hulihan, M.5
White, L.R.6
Farrer, M.7
-
2
-
-
0030858820
-
The Clock Drawing Test for dementia of the Alzheimer's type: A comparison of three scoring methods in a memory disorders clinic
-
H. Brodaty, and C.M. Moore The Clock Drawing Test for dementia of the Alzheimer's type: a comparison of three scoring methods in a memory disorders clinic Int. J. Geriatr. Psychiatry 12 1997 619 627
-
(1997)
Int. J. Geriatr. Psychiatry
, vol.12
, pp. 619-627
-
-
Brodaty, H.1
Moore, C.M.2
-
3
-
-
0027194791
-
Gene dose of apolipoprotein e type 4 allele and the risk of Alzheimer's disease in late onset families
-
E.H. Corder, A.M. Saunders, W.J. Strittmatter, D.E. Schmechel, P.C. Gaskell, G.W. Small, A.D. Roses, J.L. Haines, and M.A. Pericak-Vance Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families Science 261 1993 921 923
-
(1993)
Science
, vol.261
, pp. 921-923
-
-
Corder, E.H.1
Saunders, A.M.2
Strittmatter, W.J.3
Schmechel, D.E.4
Gaskell, P.C.5
Small, G.W.6
Roses, A.D.7
Haines, J.L.8
Pericak-Vance, M.A.9
-
4
-
-
19944431081
-
A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease
-
Italian Parkinson Genetics Network V.
-
A. Di Fonzo, C.F. Rohe, J. Ferreira, H.F. Chien, L. Vacca, F. Stocchi, L. Guedes, E. Fabrizio, M. Manfredi, N. Vanacore, S. Goldwurm, G. Breedveld, C. Sampaio, G. Meco, E. Barbosa, B.A. Oostra, V. Bonifati Italian Parkinson Genetics Network A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease Lancet 365 2005 412 415
-
(2005)
Lancet
, vol.365
, pp. 412-415
-
-
Di Fonzo, A.1
Rohe, C.F.2
Ferreira, J.3
Chien, H.F.4
Vacca, L.5
Stocchi, F.6
Guedes, L.7
Fabrizio, E.8
Manfredi, M.9
Vanacore, N.10
Goldwurm, S.11
Breedveld, G.12
Sampaio, C.13
Meco, G.14
Barbosa, E.15
Oostra, B.A.16
Bonifati17
-
5
-
-
7044238416
-
Neurodegenerative diseases: A decade of discoveries paves the way for therapeutic breakthroughs
-
M.S. Forman, J.Q. Trojanowski, and V.M. Lee Neurodegenerative diseases: a decade of discoveries paves the way for therapeutic breakthroughs Nat. Med. 10 2005 1055 1063
-
(2005)
Nat. Med.
, vol.10
, pp. 1055-1063
-
-
Forman, M.S.1
Trojanowski, J.Q.2
Lee, V.M.3
-
6
-
-
19944432921
-
A common LRRK2 mutation in idiopathic Parkinson's disease
-
W.P. Gilks, P.M. Abou-Sleiman, S. Gandhi, S. Jain, A. Singleton, A.J. Lees, K. Shaw, K.P. Bhatia, V. Bonifati, N.P. Quinn, J. Lynch, D.G. Healy, J.L. Holton, T. Revesz, and N.W. Wood A common LRRK2 mutation in idiopathic Parkinson's disease Lancet 365 2005 415 416
-
(2005)
Lancet
, vol.365
, pp. 415-416
-
-
Gilks, W.P.1
Abou-Sleiman, P.M.2
Gandhi, S.3
Jain, S.4
Singleton, A.5
Lees, A.J.6
Shaw, K.7
Bhatia, K.P.8
Bonifati, V.9
Quinn, N.P.10
Lynch, J.11
Healy, D.G.12
Holton, J.L.13
Revesz, T.14
Wood, N.W.15
-
7
-
-
0024362650
-
The Informant Questionnaire on Cognitive Decline in the Elderly (IQCODE): Socio-demographic correlates, reliability, validity and some norms
-
A.F. Jorm, and P.A. Jacomb The Informant Questionnaire on Cognitive Decline in the Elderly (IQCODE): socio-demographic correlates, reliability, validity and some norms Psychol. Med. 19 1989 1015 1022
-
(1989)
Psychol. Med.
, vol.19
, pp. 1015-1022
-
-
Jorm, A.F.1
Jacomb, P.A.2
-
8
-
-
20144387207
-
Identification of a novel LRRK2 mutation linked to autosomal dominant Parkinsonism: Evidence of a common founder across European populations
-
J. Kachergus, I.F. Mata, M. Hulihan, J.P. Taylor, S. Lincoln, J. Aasly, J.M. Gibson, O.A. Ross, T. Lynch, J. Wiley, H. Payami, J. Nutt, D.M. Maraganore, K. Czyzewski, M. Styczynska, Z.K. Wszolek, M.J. Farrer, and M. Toft Identification of a novel LRRK2 mutation linked to autosomal dominant Parkinsonism: evidence of a common founder across European populations Am. J. Hum. Genet. 76 2005 672 680
-
(2005)
Am. J. Hum. Genet.
, vol.76
, pp. 672-680
-
-
Kachergus, J.1
Mata, I.F.2
Hulihan, M.3
Taylor, J.P.4
Lincoln, S.5
Aasly, J.6
Gibson, J.M.7
Ross, O.A.8
Lynch, T.9
Wiley, J.10
Payami, H.11
Nutt, J.12
Maraganore, D.M.13
Czyzewski, K.14
Styczynska, M.15
Wszolek, Z.K.16
Farrer, M.J.17
Toft, M.18
-
9
-
-
10344254833
-
Mixed dementia: Emerging concepts and therapeutic implications
-
K.M. Langa, N.L. Foster, and E.B. Larson Mixed dementia: emerging concepts and therapeutic implications JAMA 292 2004 2901 2908
-
(2004)
JAMA
, vol.292
, pp. 2901-2908
-
-
Langa, K.M.1
Foster, N.L.2
Larson, E.B.3
-
10
-
-
0034719092
-
Research evaluation and diagnosis of probable Alzheimer's disease over the last two decades: I
-
O.L. Lopez, J.T. Becker, W. Klunk, J. Saxton, R.L. Hamilton, D.I. Kaufer, R.A. Sweet, C. Cidis Meltzer, S. Wisniewski, M.I. Kamboh, and S.T. DeKosky Research evaluation and diagnosis of probable Alzheimer's disease over the last two decades: I Neurology 55 2000 1854 1862
-
(2000)
Neurology
, vol.55
, pp. 1854-1862
-
-
Lopez, O.L.1
Becker, J.T.2
Klunk, W.3
Saxton, J.4
Hamilton, R.L.5
Kaufer, D.I.6
Sweet, R.A.7
Cidis Meltzer, C.8
Wisniewski, S.9
Kamboh, M.I.10
Dekosky, S.T.11
-
11
-
-
9144224226
-
Dementia with Lewy bodies
-
I. McKeith, J. Mintzer, D. Aarsland, D. Burn, H. Chiu, J. Cohen-Mansfield, D. Dickson, B. Dubois, J.E. Duda, H. Feldman, S. Gauthier, G. Halliday, B. Lawlor, C. Lippa, O.L. Lopez, J. Carlos Machado, J. O'Brien, J. Playfer, and W. Reid Dementia with Lewy bodies Lancet Neurol. 3 2004 19 28
-
(2004)
Lancet Neurol.
, vol.3
, pp. 19-28
-
-
McKeith, I.1
Mintzer, J.2
Aarsland, D.3
Burn, D.4
Chiu, H.5
Cohen-Mansfield, J.6
Dickson, D.7
Dubois, B.8
Duda, J.E.9
Feldman, H.10
Gauthier, S.11
Halliday, G.12
Lawlor, B.13
Lippa, C.14
Lopez, O.L.15
Carlos MacHado, J.16
O'Brien, J.17
Playfer, J.18
Reid, W.19
-
12
-
-
0006164301
-
Consensus guidelines for the clinical and pathologic diagnosis of dementia with Lewy bodies (DLB): Report of the consortium on DLB international workshop
-
I.G. McKeith, D. Galasko, K. Kosaka, E.K. Perry, D.W. Dickson, L.A. Hansen, D.P. Salmon, J. Lowe, S.S. Mirra, E.J. Byrne, G. Lennox, N.P. Quinn, J.A. Edwardson, P.G. Ince, C. Bergeron, A. Burns, B.L. Miller, S. Lovestone, D. Collerton, E.N. Jansen, C. Ballard, R.A. de Vos, G.K. Wilcock, K.A. Jellinger, and R.H. Perry Consensus guidelines for the clinical and pathologic diagnosis of dementia with Lewy bodies (DLB): report of the consortium on DLB international workshop Neurology 47 1996 1113 1124
-
(1996)
Neurology
, vol.47
, pp. 1113-1124
-
-
McKeith, I.G.1
Galasko, D.2
Kosaka, K.3
Perry, E.K.4
Dickson, D.W.5
Hansen, L.A.6
Salmon, D.P.7
Lowe, J.8
Mirra, S.S.9
Byrne, E.J.10
Lennox, G.11
Quinn, N.P.12
Edwardson, J.A.13
Ince, P.G.14
Bergeron, C.15
Burns, A.16
Miller, B.L.17
Lovestone, S.18
Collerton, D.19
Jansen, E.N.20
Ballard, C.21
De Vos, R.A.22
Wilcock, G.K.23
Jellinger, K.A.24
Perry, R.H.25
more..
-
13
-
-
0021271971
-
Clinical diagnosis of Alzheimer's disease: Report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease
-
G. McKhann, D. Drachman, M. Folstein, R. Katzman, D. Price, and E.M. Stadlan Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease Neurology 34 1984 939 944
-
(1984)
Neurology
, vol.34
, pp. 939-944
-
-
McKhann, G.1
Drachman, D.2
Folstein, M.3
Katzman, R.4
Price, D.5
Stadlan, E.M.6
-
14
-
-
0018425438
-
A new depression scale designed to be sensitive to change
-
S.A. Montgomery, and M. Åsberg A new depression scale designed to be sensitive to change Br. J. Psychiatry 134 1979 382 389
-
(1979)
Br. J. Psychiatry
, vol.134
, pp. 382-389
-
-
Montgomery, S.A.1
Åsberg, M.2
-
15
-
-
0034895326
-
The genetics of late-onset Alzheimer's disease
-
A.J. Myers, and A.M. Goate The genetics of late-onset Alzheimer's disease Curr. Opin. Neurol. 14 2001 433 440
-
(2001)
Curr. Opin. Neurol.
, vol.14
, pp. 433-440
-
-
Myers, A.J.1
Goate, A.M.2
-
16
-
-
19944432606
-
Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease
-
W.C. Nichols, N. Pankratz, D. Hernandez, C. Paisan-Ruiz, S. Jain, C.A. Halter, V.E. Michaels, T. Reed, A. Rudolph, C.W. Shults, A. Singleton, and T. Foroud Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease Lancet 365 2005 410 412
-
(2005)
Lancet
, vol.365
, pp. 410-412
-
-
Nichols, W.C.1
Pankratz, N.2
Hernandez, D.3
Paisan-Ruiz, C.4
Jain, S.5
Halter, C.A.6
Michaels, V.E.7
Reed, T.8
Rudolph, A.9
Shults, C.W.10
Singleton, A.11
Foroud, T.12
-
17
-
-
8844266996
-
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
-
C. Paisan-Ruiz, S. Jain, E.W. Evans, W.P. Gilks, J. Simon, M. van der Brug, A.L. de Munain, S. Aparicio, A.M. Gil, N. Khan, J. Johnson, J.R. Martinez, D. Nicholl, I.M. Carrera, A.S. Pena, R. de Silva, A. Lees, J.F. Marti-Masso, J. Perez-Tur, N.W. Wood, and A.B. Singleton Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease Neuron 44 2004 595 600
-
(2004)
Neuron
, vol.44
, pp. 595-600
-
-
Paisan-Ruiz, C.1
Jain, S.2
Evans, E.W.3
Gilks, W.P.4
Simon, J.5
Van Der Brug, M.6
De Munain, A.L.7
Aparicio, S.8
Gil, A.M.9
Khan, N.10
Johnson, J.11
Martinez, J.R.12
Nicholl, D.13
Carrera, I.M.14
Pena, A.S.15
De Silva, R.16
Lees, A.17
Marti-Masso, J.F.18
Perez-Tur, J.19
Wood, N.W.20
Singleton, A.B.21
more..
-
18
-
-
0030770726
-
Complete genomic screen in late-onset familial Alzheimer disease. Evidence for a new locus on chromosome 12
-
M.A. Pericak-Vance, M.P. Bass, L.H. Yamaoka, P.C. Gaskell, W.K. Scott, H.A. Terwedow, M.M. Menold, P.M. Conneally, G.W. Small, J.M. Vance, A.M. Saunders, A.D. Roses, and J.L. Haines Complete genomic screen in late-onset familial Alzheimer disease. Evidence for a new locus on chromosome 12 JAMA 278 1997 1237 1241
-
(1997)
JAMA
, vol.278
, pp. 1237-1241
-
-
Pericak-Vance, M.A.1
Bass, M.P.2
Yamaoka, L.H.3
Gaskell, P.C.4
Scott, W.K.5
Terwedow, H.A.6
Menold, M.M.7
Conneally, P.M.8
Small, G.W.9
Vance, J.M.10
Saunders, A.M.11
Roses, A.D.12
Haines, J.L.13
-
19
-
-
3142514201
-
Protein aggregation and neurodegenerative disease
-
C.A. Ross, and M.A. Poirier Protein aggregation and neurodegenerative disease Nat. Med. 10 Suppl. 2004 10 17
-
(2004)
Nat. Med.
, vol.10
, Issue.SUPPL.
, pp. 10-17
-
-
Ross, C.A.1
Poirier, M.A.2
-
20
-
-
0033913161
-
Fine mapping of the chromosome 12 late-onset Alzheimer disease locus: Potential genetic and phenotypic heterogeneity
-
W.K. Scott, J.M. Grubber, P.M. Conneally, G.W. Small, C.M. Hulette, C.K. Rosenberg, A.M. Saunders, A.D. Roses, J.L. Haines, and M.A. Pericak-Vance Fine mapping of the chromosome 12 late-onset Alzheimer disease locus: potential genetic and phenotypic heterogeneity Am. J. Hum. Genet. 66 2000 922 932
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 922-932
-
-
Scott, W.K.1
Grubber, J.M.2
Conneally, P.M.3
Small, G.W.4
Hulette, C.M.5
Rosenberg, C.K.6
Saunders, A.M.7
Roses, A.D.8
Haines, J.L.9
Pericak-Vance, M.A.10
-
21
-
-
0030882856
-
Alpha-synuclein in Lewy bodies
-
M.G. Spillantini, M.L. Schmidt, V.M. Lee, J.Q. Trojanowski, R. Jakes, and M. Goedert Alpha-synuclein in Lewy bodies Nature 388 1997 839 840
-
(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
-
22
-
-
0028223015
-
Clinical and neuropathological criteria for frontotemporal dementia
-
The Lund and Manchester Groups
-
The Lund and Manchester Groups Clinical and neuropathological criteria for frontotemporal dementia J. Neurol. Neurosurg. Psychiatry 57 1994 416 418
-
(1994)
J. Neurol. Neurosurg. Psychiatry
, vol.57
, pp. 416-418
-
-
-
23
-
-
16344371939
-
LRRK2 mutations and Parkinsonism
-
M. Toft, I.F. Mata, J.M. Kachergus, O.A. Ross, and M.J. Farrer LRRK2 mutations and Parkinsonism Lancet 365 2005 1229 1230
-
(2005)
Lancet
, vol.365
, pp. 1229-1230
-
-
Toft, M.1
Mata, I.F.2
Kachergus, J.M.3
Ross, O.A.4
Farrer, M.J.5
-
24
-
-
0031460466
-
German-Canadian family (family A) with Parkinsonism, amyotrophy, and dementia: Longitudinal observations
-
Z.K. Wszolek, P. Vieregge, R.J. Uitti, T. Gasser, O. Yasuhara, P. McGeer, K. Berry, D.B. Calne, Vingerhoets FJG, C. Klein, and R.F. Pfeiffer German-Canadian family (family A) with Parkinsonism, amyotrophy, and dementia: longitudinal observations Parkinsonism Relat. Disord. 3 1997 125 139
-
(1997)
Parkinsonism Relat. Disord.
, vol.3
, pp. 125-139
-
-
Wszolek, Z.K.1
Vieregge, P.2
Uitti, R.J.3
Gasser, T.4
Yasuhara, O.5
McGeer, P.6
Berry, K.7
Calne, D.B.8
Fjg, V.9
Klein, C.10
Pfeiffer, R.F.11
-
25
-
-
8844233579
-
Mutations in LRRK2 cause autosomal-dominant Parkinsonism with pleomorphic pathology
-
A. Zimprich, S. Biskup, P. Leitner, P. Lichtner, M. Farrer, S. Lincoln, J. Kachergus, M. Hulihan, R.J. Uitti, D.B. Calne, A.J. Stoessl, R.F. Pfeiffer, N. Patenge, I.C. Carbajal, P. Vieregge, F. Asmus, B. Muller-Myhsok, D.W. Dickson, T. Meitinger, T.M. Strom, Z.K. Wszolek, and T. Gasser Mutations in LRRK2 cause autosomal-dominant Parkinsonism with pleomorphic pathology Neuron 44 2004 601 607
-
(2004)
Neuron
, vol.44
, pp. 601-607
-
-
Zimprich, A.1
Biskup, S.2
Leitner, P.3
Lichtner, P.4
Farrer, M.5
Lincoln, S.6
Kachergus, J.7
Hulihan, M.8
Uitti, R.J.9
Calne, D.B.10
Stoessl, A.J.11
Pfeiffer, R.F.12
Patenge, N.13
Carbajal, I.C.14
Vieregge, P.15
Asmus, F.16
Muller-Myhsok, B.17
Dickson, D.W.18
Meitinger, T.19
Strom, T.M.20
Wszolek, Z.K.21
Gasser, T.22
more..
|