-
1
-
-
84858693790
-
Role of Mendelian genes in "sporadic" Parkinson's disease
-
Lesage S, Brice A. Role of Mendelian genes in "sporadic" Parkinson's disease. Parkinsonism Relat Disord 2012; 18: S66-S70.
-
(2012)
Parkinsonism Relat Disord
, vol.18
-
-
Lesage, S.1
Brice, A.2
-
3
-
-
80051534540
-
A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease
-
Zimprich A, Benet-Pages A, Struhal W, et al. A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease. Am J Hum Genet 2011; 89: 168-175.
-
(2011)
Am J Hum Genet
, vol.89
, pp. 168-175
-
-
Zimprich, A.1
Benet-Pages, A.2
Struhal, W.3
-
4
-
-
84856956020
-
Screening for VPS35 mutations in Parkinson's disease
-
Sheerin UM, Charlesworth G, Bras J, et al. Screening for VPS35 mutations in Parkinson's disease. Neurobiol Aging 2012; 33: 838.e1-838.e5.
-
(2012)
Neurobiol Aging
, vol.33
-
-
Sheerin, U.M.1
Charlesworth, G.2
Bras, J.3
-
5
-
-
84861697525
-
The Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's disease
-
Guella I, Soldà G, Cilia R, et al. The Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's disease. Mov Disord 2012; 27: 800-801.
-
(2012)
Mov Disord
, vol.27
, pp. 800-801
-
-
Guella, I.1
Soldà, G.2
Cilia, R.3
-
6
-
-
84861848453
-
Contribution of VPS35 genetic variability to LBD in the Flanders-Belgian population
-
Verstraeten A, Wauters E, Crosiers D, et al. Contribution of VPS35 genetic variability to LBD in the Flanders-Belgian population. Neurobiol Aging 2012; 33: 1844.e11-e13.
-
(2012)
Neurobiol Aging
, vol.33
-
-
Verstraeten, A.1
Wauters, E.2
Crosiers, D.3
-
7
-
-
84862776825
-
Vacuolar protein sorting 35 Asp620Asn mutation is rare in the ethnic Chinese population with Parkinson's disease
-
Zhang Y, Chen S, Xiao Q, et al. Vacuolar protein sorting 35 Asp620Asn mutation is rare in the ethnic Chinese population with Parkinson's disease. Parkinsonism Relat Disord 2012; 18: 638-640.
-
(2012)
Parkinsonism Relat Disord
, vol.18
, pp. 638-640
-
-
Zhang, Y.1
Chen, S.2
Xiao, Q.3
-
8
-
-
33846613222
-
The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease
-
Rogaeva E, Meng Y, Lee JH, et al. The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease. Nat Genet 2007; 39: 168-177.
-
(2007)
Nat Genet
, vol.39
, pp. 168-177
-
-
Rogaeva, E.1
Meng, Y.2
Lee, J.H.3
-
9
-
-
83055181478
-
Frameshift mutations of vacuolar protein sorting genes in gastric and colorectal cancers with microsatellite instability
-
An CH, Kim YR, Kim HS, Kim SS, Yoo NJ, Lee SH. Frameshift mutations of vacuolar protein sorting genes in gastric and colorectal cancers with microsatellite instability. Hum Pathol 2012; 43: 40-47.
-
(2012)
Hum Pathol
, vol.43
, pp. 40-47
-
-
An, C.H.1
Kim, Y.R.2
Kim, H.S.3
Kim, S.S.4
Yoo, N.J.5
Lee, S.H.6
-
10
-
-
84859929853
-
The LRRK2 G2019S mutation is associated with Parkinson disease and concomitant non-skin cancers
-
Inzelberg R, Cohen OS, Aharon-Peretz J, et al. The LRRK2 G2019S mutation is associated with Parkinson disease and concomitant non-skin cancers. Neurology 2012; 78: 781-786.
-
(2012)
Neurology
, vol.78
, pp. 781-786
-
-
Inzelberg, R.1
Cohen, O.S.2
Aharon-Peretz, J.3
-
11
-
-
84862907635
-
VPS35 haploinsufficiency increases Alzheimer's disease neuropathology
-
Wen L, Tang FL, Hong Y, et al. VPS35 haploinsufficiency increases Alzheimer's disease neuropathology. J Cell Biol 2011; 195: 765-779.
-
(2011)
J Cell Biol
, vol.195
, pp. 765-779
-
-
Wen, L.1
Tang, F.L.2
Hong, Y.3
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