-
1
-
-
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., and Obata F. A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1. Ann Neurol 51 (2002) 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
-
2
-
-
0034952990
-
Analysis of alpha-synuclein, parkin, tau, and UCH-L1 in a Japanese family with autosomal dominant parkinsonism
-
Hasegawa K., Funayama M., Matsuura N., Furusawa H., Sakai F., Kowa H., et al. Analysis of alpha-synuclein, parkin, tau, and UCH-L1 in a Japanese family with autosomal dominant parkinsonism. Eur Neurol 46 (2001) 20-24
-
(2001)
Eur Neurol
, vol.46
, pp. 20-24
-
-
Hasegawa, K.1
Funayama, M.2
Matsuura, N.3
Furusawa, H.4
Sakai, F.5
Kowa, H.6
-
3
-
-
8844266996
-
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
-
Paisan-Ruiz C., Jain S., Evans E.W., Gilks W.P., Simon J., van der Brug M., et al. 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
-
4
-
-
8844233579
-
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
-
Zimprich A., Biskup S., Leitner P., Lichtner P., Farrer M., Lincoln S., et al. 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
-
5
-
-
50049104725
-
International LRRK2 Consortium. Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
-
Healy D.G., Falchi M., O'Sullivan S.S., Bonifati V., Durr A., Bressman S., et al. International LRRK2 Consortium. Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study. Lancet Neurol 7 (2008) 583-590
-
(2008)
Lancet Neurol
, vol.7
, pp. 583-590
-
-
Healy, D.G.1
Falchi, M.2
O'Sullivan, S.S.3
Bonifati, V.4
Durr, A.5
Bressman, S.6
-
6
-
-
20444420103
-
An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family
-
Funayama M., Hasegawa K., Ohta E., Kawashima N., Komiyama M., Kowa H., et al. An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family. Ann Neurol 57 (2005) 918-921
-
(2005)
Ann Neurol
, vol.57
, pp. 918-921
-
-
Funayama, M.1
Hasegawa, K.2
Ohta, E.3
Kawashima, N.4
Komiyama, M.5
Kowa, H.6
-
7
-
-
0018027296
-
A big family of paralysis agitans
-
[Translated by the authors] [Japanese]
-
Nukada H., Kowa H., Saitoh T., Tazaki Y., and Miura S. A big family of paralysis agitans. Rinsho Shinkeigaku 18 (1978) 627-634 [Translated by the authors] [Japanese]
-
(1978)
Rinsho Shinkeigaku
, vol.18
, pp. 627-634
-
-
Nukada, H.1
Kowa, H.2
Saitoh, T.3
Tazaki, Y.4
Miura, S.5
-
8
-
-
28544434193
-
PET in LRRK2 mutations: comparison to sporadic Parkinson's disease and evidence for presymptomatic compensation
-
Adams J.R., van Netten H., Schulzer M., Mak E., Mckenzie J., Strongosky A., et al. PET in LRRK2 mutations: comparison to sporadic Parkinson's disease and evidence for presymptomatic compensation. Brain 128 (2005) 2777-2785
-
(2005)
Brain
, vol.128
, pp. 2777-2785
-
-
Adams, J.R.1
van Netten, H.2
Schulzer, M.3
Mak, E.4
Mckenzie, J.5
Strongosky, A.6
-
10
-
-
0000244524
-
Disorders of movement and system degenerations
-
Graham D.I., and Lantos P.L. (Eds), Arnold, New York
-
Lowe J.S., and Leigh N. Disorders of movement and system degenerations. In: Graham D.I., and Lantos P.L. (Eds). Greenfield's neuropathology. 7th ed. vol. 2 (2002), Arnold, New York 325-372
-
(2002)
Greenfield's neuropathology. 7th ed.
, vol.2
, pp. 325-372
-
-
Lowe, J.S.1
Leigh, N.2
-
11
-
-
0030915893
-
The distribution and dynamic density of oligodendroglial cytoplasmic inclusions (GCIs) in multiple system atrophy: a correlation between the density of GCIs and the degree of involvement of striatonigral and olivopontocerebellar systems
-
Inoue M., Yagishita S., Ryo M., Hasegawa K., Amano N., and Matsushita M. The distribution and dynamic density of oligodendroglial cytoplasmic inclusions (GCIs) in multiple system atrophy: a correlation between the density of GCIs and the degree of involvement of striatonigral and olivopontocerebellar systems. Acta Neuropathol (Berl) 93 (1997) 585-591
-
(1997)
Acta Neuropathol (Berl)
, vol.93
, pp. 585-591
-
-
Inoue, M.1
Yagishita, S.2
Ryo, M.3
Hasegawa, K.4
Amano, N.5
Matsushita, M.6
-
12
-
-
0037383761
-
Colocalization of tau and alpha-synuclein epitopes in Lewy bodies
-
Ishizawa T., Mattila P., Davies P., Wang D., and Dickson D.W. Colocalization of tau and alpha-synuclein epitopes in Lewy bodies. J Neuropathol Exp Neurol 62 (2003) 389-397
-
(2003)
J Neuropathol Exp Neurol
, vol.62
, pp. 389-397
-
-
Ishizawa, T.1
Mattila, P.2
Davies, P.3
Wang, D.4
Dickson, D.W.5
-
13
-
-
3042830032
-
Lewy body-related α-synucleinopathy in aging
-
Saito Y., Ruberu N.N., Sawabe M., Arai T., Kazama H., Hosoi T., et al. Lewy body-related α-synucleinopathy in aging. J Neuropathol Exp Neurol 63 (2004) 742-749
-
(2004)
J Neuropathol Exp Neurol
, vol.63
, pp. 742-749
-
-
Saito, Y.1
Ruberu, N.N.2
Sawabe, M.3
Arai, T.4
Kazama, H.5
Hosoi, T.6
-
14
-
-
35848934109
-
Neurocirculatory and nigrostriatal abnormalities in Parkinson disease from LRRK2 mutation
-
Goldstein D.S., Imrich R., Peckham E., Holmes C., Lopez G., Crews C., et al. Neurocirculatory and nigrostriatal abnormalities in Parkinson disease from LRRK2 mutation. Neurology 69 (2007) 1580-1584
-
(2007)
Neurology
, vol.69
, pp. 1580-1584
-
-
Goldstein, D.S.1
Imrich, R.2
Peckham, E.3
Holmes, C.4
Lopez, G.5
Crews, C.6
-
15
-
-
0031460466
-
German-Canadian family (family A) with parkinsonism, amyotrophy, and dementia: longitudinal observations
-
Wszolek Z.K., Vieregge P., Uitti R.J., Gasser T., Yasuhara O., McGeer P., et al. 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
-
16
-
-
0029049738
-
Western Nebraska family (family D) with autosomal dominant parkinsonism
-
Wszolek Z.K., Pfeiffer B., Fulgham J.R., Parisi J.E., Thompson B.M., Uitti R.J., et al. Western Nebraska family (family D) with autosomal dominant parkinsonism. Neurology 45 (1995) 502-505
-
(1995)
Neurology
, vol.45
, pp. 502-505
-
-
Wszolek, Z.K.1
Pfeiffer, B.2
Fulgham, J.R.3
Parisi, J.E.4
Thompson, B.M.5
Uitti, R.J.6
-
17
-
-
2342605968
-
Autosomal dominant parkinsonism associated with variable synuclein and tau pathology
-
Wszolek Z.K., Pfeiffer R.F., Tsuboi Y., Uitti R.J., McComb R.D., Stoessl A.J., et al. Autosomal dominant parkinsonism associated with variable synuclein and tau pathology. Neurology 62 (2004) 1619-1622
-
(2004)
Neurology
, vol.62
, pp. 1619-1622
-
-
Wszolek, Z.K.1
Pfeiffer, R.F.2
Tsuboi, Y.3
Uitti, R.J.4
McComb, R.D.5
Stoessl, A.J.6
-
18
-
-
32044466285
-
LRRK2 and Lewy body disease
-
Ross O.A., Toft M., Whittle A.J., Johnson J.L., Papapetropoulos S., Mash D.C., et al. LRRK2 and Lewy body disease. Ann Neurol 59 (2006) 388-393
-
(2006)
Ann Neurol
, vol.59
, pp. 388-393
-
-
Ross, O.A.1
Toft, M.2
Whittle, A.J.3
Johnson, J.L.4
Papapetropoulos, S.5
Mash, D.C.6
-
19
-
-
33750308194
-
Parkinsonism, LRRK2 G2019S, and tau neuropathology
-
Rajput A., Dickson D.W., Robinson C.A., Ross O.A., Dachsel J.C., Lincoln S.J., et al. Parkinsonism, LRRK2 G2019S, and tau neuropathology. Neurology 67 (2006) 1506-1508
-
(2006)
Neurology
, vol.67
, pp. 1506-1508
-
-
Rajput, A.1
Dickson, D.W.2
Robinson, C.A.3
Ross, O.A.4
Dachsel, J.C.5
Lincoln, S.J.6
-
20
-
-
32044432395
-
Biochemical and pathological characterization of LRRK2
-
Giasson B.I., Covy J.P., Bonini N.M., Hurtig H.I., Farrer M.J., Trojanowski J.Q., et al. Biochemical and pathological characterization of LRRK2. Ann Neurol 59 (2006) 315-322
-
(2006)
Ann Neurol
, vol.59
, pp. 315-322
-
-
Giasson, B.I.1
Covy, J.P.2
Bonini, N.M.3
Hurtig, H.I.4
Farrer, M.J.5
Trojanowski, J.Q.6
-
21
-
-
34249714900
-
G2019S LRRK2 mutation causing Parkinson's disease without Lewy bodies
-
Gaig C., Marti M.J., Ezquerra M., Rey M.J., Cardozo A., and Tolosa E. G2019S LRRK2 mutation causing Parkinson's disease without Lewy bodies. J Neurol Neurosurg Psychiatry 78 (2007) 626-628
-
(2007)
J Neurol Neurosurg Psychiatry
, vol.78
, pp. 626-628
-
-
Gaig, C.1
Marti, M.J.2
Ezquerra, M.3
Rey, M.J.4
Cardozo, A.5
Tolosa, E.6
-
22
-
-
34247617699
-
LRRK2 G2019S substitution in frontotemporal lobar degeneration with ubiquitin-immunoreactive neuronal inclusions
-
Dachsel J.C., Ross O.A., Mata I.F., Kachergus J., Toft M., Cannon A., et al. LRRK2 G2019S substitution in frontotemporal lobar degeneration with ubiquitin-immunoreactive neuronal inclusions. Acta Neuropathol (Berl) 113 (2007) 601-606
-
(2007)
Acta Neuropathol (Berl)
, vol.113
, pp. 601-606
-
-
Dachsel, J.C.1
Ross, O.A.2
Mata, I.F.3
Kachergus, J.4
Toft, M.5
Cannon, A.6
-
23
-
-
33847750732
-
Neuropathology of Parkinson's disease associated with the LRRK2 Ile1371Val mutation
-
Giordana M.T., D'Agostino C., Albani G., Mauro A., Di Fonzo A., Antonini A., et al. Neuropathology of Parkinson's disease associated with the LRRK2 Ile1371Val mutation. Mov Disord 22 (2007) 275-278
-
(2007)
Mov Disord
, vol.22
, pp. 275-278
-
-
Giordana, M.T.1
D'Agostino, C.2
Albani, G.3
Mauro, A.4
Di Fonzo, A.5
Antonini, A.6
|