-
1
-
-
33644822969
-
Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease
-
D Berg K Schweitzer P Leitner 2005 Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease Brain 128 3000 3011
-
(2005)
Brain
, vol.128
, pp. 3000-3011
-
-
Berg, D.1
Schweitzer, K.2
Leitner, P.3
-
2
-
-
38549097049
-
The prevalence of LRRK2 Gly2385Arg variant in Chinese Han population with Parkinson's disease
-
L Cao T Zhang Q Xiao 2007 The prevalence of LRRK2 Gly2385Arg variant in Chinese Han population with Parkinson's disease Mov Disord 22 2439 2442
-
(2007)
Mov Disord
, vol.22
, pp. 2439-2442
-
-
Cao, L.1
Zhang, T.2
Xiao, Q.3
-
3
-
-
0942300688
-
Comparison of environmental and genetic factors for Parkinson's disease between Chinese and Caucasians
-
DKY Chan D Cordato Bui Triet G Mellick 2004 Comparison of environmental and genetic factors for Parkinson's disease between Chinese and Caucasians Neuroepidemiology 23 13 22
-
(2004)
Neuroepidemiology
, vol.23
, pp. 13-22
-
-
Chan, D.K.Y.1
Cordato, D.2
Bui, T.3
Mellick, G.4
-
4
-
-
44749090091
-
PARK2 mutations and clinical features in a Chinese population with early onset Parkinson's disease
-
doi 10.1007/s00702-007-0011-6
-
Chan DKY, Mok V, Ng PW et al (2008) PARK2 mutations and clinical features in a Chinese population with early onset Parkinson's disease. J Neural Transm doi 10.1007/s00702-007-0011-6
-
(2008)
J Neural Transm
-
-
Chan, D.K.Y.1
Mok, V.2
Ng, P.W.3
-
5
-
-
33746079596
-
A common missense variant in the LRRK2 gene, Gly2385Arg, associated with parkinson's diseae risk in Taiwan
-
A Di Fonzo YH Wu-Chou CS Lu 2006 A common missense variant in the LRRK2 gene, Gly2385Arg, associated with parkinson's diseae risk in Taiwan Neurogenetics 7 133 138
-
(2006)
Neurogenetics
, vol.7
, pp. 133-138
-
-
Di Fonzo, A.1
Wu-Chou, Y.H.2
Lu, C.S.3
-
6
-
-
33847226901
-
Leucine-rich repeat kinase 2 G2385R variant is a risk factor for Parkinson disease in Asian population
-
M Funayama Y Li H Tomiyama 2007 Leucine-rich repeat kinase 2 G2385R variant is a risk factor for Parkinson disease in Asian population NeuroReport 18 273 275
-
(2007)
NeuroReport
, vol.18
, pp. 273-275
-
-
Funayama, M.1
Li, Y.2
Tomiyama, H.3
-
7
-
-
33846587090
-
A common genetic factor for Parkinson's disease in ethnic Chinese population in Taiwan
-
HC Fung CM Chen J Hardy AB Singleton YR Wu 2006 A common genetic factor for Parkinson's disease in ethnic Chinese population in Taiwan BMC Neurol 6 47
-
(2006)
BMC Neurol
, vol.6
, pp. 47
-
-
Fung, H.C.1
Chen, C.M.2
Hardy, J.3
Singleton, A.B.4
Wu, Y.R.5
-
8
-
-
19944432921
-
A common LRRK2 mutation in idiopathic Parkinson's disease
-
9457
-
WP Gilks PM Abou-Sleiman S Gandhi 2005 A common LRRK2 mutation in idiopathic Parkinson's disease Lancet 365 9457 415 416
-
(2005)
Lancet
, vol.365
, pp. 415-416
-
-
Gilks, W.P.1
Abou-Sleiman, P.M.2
Gandhi, S.3
-
9
-
-
27744446035
-
The I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease
-
NM_004562.1
-
Lu C, Simons E, Wu-Chou Y et al (2005) The I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease. Parkinsonism and related disorders 11(8):521-522. NM_004562.1 http://www.ncbi.nlm.nih.gov/entrez/viewer.fcgi?val=83722281&from=121&to= 7704&view=gbwithparts
-
(2005)
Parkinsonism and Related Disorders
, vol.11
, Issue.8
, pp. 521-522
-
-
Lu, C.1
Simons, E.2
Wu-Chou, Y.3
-
10
-
-
8844266996
-
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
-
4
-
C Paisan-Ruiz S Jain EW Evans 2004 Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease Neuron 44 4 595 600
-
(2004)
Neuron
, vol.44
, pp. 595-600
-
-
Paisan-Ruiz, C.1
Jain, S.2
Evans, E.W.3
-
11
-
-
33846358949
-
The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: Genetic and functional evidence
-
EK Tan Y Zhao L Skipper 2007 The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence Hum Genet 120 857 863
-
(2007)
Hum Genet
, vol.120
, pp. 857-863
-
-
Tan, E.K.1
Zhao, Y.2
Skipper, L.3
-
12
-
-
32044458576
-
LRRK2: A common pathway for parkinsonism, pathogenesis and prevention?
-
JP Taylor IF Mata MJ Farrer 2006 LRRK2: a common pathway for parkinsonism, pathogenesis and prevention? Trends Mol Med 12 76 82
-
(2006)
Trends Mol Med
, vol.12
, pp. 76-82
-
-
Taylor, J.P.1
Mata, I.F.2
Farrer, M.J.3
-
13
-
-
8844233579
-
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
-
4
-
A Zimprich S Biskup P Leitner 2004 Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology Neuron 44 4 601 607
-
(2004)
Neuron
, vol.44
, pp. 601-607
-
-
Zimprich, A.1
Biskup, S.2
Leitner, P.3
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