-
1
-
-
33846572874
-
Projected number of people with Parkinson disease in the most populous nations, 2005 through 2030
-
Dorsey E.R., Constantinescu R., Thompson J.P., Biglan K.M., Holloway R.G., Kieburtz K., et al. Projected number of people with Parkinson disease in the most populous nations, 2005 through 2030. Neurology 68 5 (2007) 384-386
-
(2007)
Neurology
, vol.68
, Issue.5
, pp. 384-386
-
-
Dorsey, E.R.1
Constantinescu, R.2
Thompson, J.P.3
Biglan, K.M.4
Holloway, R.G.5
Kieburtz, K.6
-
2
-
-
69149089036
-
Molecular pathogenesis of Parkinson disease: insights from genetic studies
-
Gasser T. Molecular pathogenesis of Parkinson disease: insights from genetic studies. Expert Rev Mol Med 11 (2009) e22
-
(2009)
Expert Rev Mol Med
, vol.11
-
-
Gasser, T.1
-
3
-
-
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 3 (2002) 296-301
-
(2002)
Ann Neurol
, vol.51
, Issue.3
, pp. 296-301
-
-
Funayama, M.1
Hasegawa, K.2
Kowa, H.3
Saito, M.4
Tsuji, S.5
Obata, F.6
-
4
-
-
9144261126
-
The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval
-
Zimprich A., Muller-Myhsok B., Farrer M., Leitner P., Sharma M., Hulihan M., et al. The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval. Am J Hum Genet 74 1 (2004) 11-19
-
(2004)
Am J Hum Genet
, vol.74
, Issue.1
, pp. 11-19
-
-
Zimprich, A.1
Muller-Myhsok, B.2
Farrer, M.3
Leitner, P.4
Sharma, M.5
Hulihan, M.6
-
5
-
-
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 4 (2004) 601-607
-
(2004)
Neuron
, vol.44
, Issue.4
, pp. 601-607
-
-
Zimprich, A.1
Biskup, S.2
Leitner, P.3
Lichtner, P.4
Farrer, M.5
Lincoln, S.6
-
6
-
-
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 4 (2004) 595-600
-
(2004)
Neuron
, vol.44
, Issue.4
, 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
-
7
-
-
33746079596
-
A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan
-
Di Fonzo A., Wu-Chou Y.H., Lu C.S., van Doeselaar M., Simons E.J., Rohe C.F., et al. A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan. Neurogenetics 7 3 (2006) 133-138
-
(2006)
Neurogenetics
, vol.7
, Issue.3
, pp. 133-138
-
-
Di Fonzo, A.1
Wu-Chou, Y.H.2
Lu, C.S.3
van Doeselaar, M.4
Simons, E.J.5
Rohe, C.F.6
-
8
-
-
33847267765
-
Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia
-
Farrer M.J., Stone J.T., Lin C.H., Dachsel J.C., Hulihan M.M., Haugarvoll K., et al. Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia. Parkinsonism Relat Disord 13 2 (2007) 89-92
-
(2007)
Parkinsonism Relat Disord
, vol.13
, Issue.2
, pp. 89-92
-
-
Farrer, M.J.1
Stone, J.T.2
Lin, C.H.3
Dachsel, J.C.4
Hulihan, M.M.5
Haugarvoll, K.6
-
9
-
-
53749090842
-
LRRK2 R1628P increases risk of Parkinson's disease: replication evidence
-
Tan E.K., Tan L.C., Lim H.Q., Li R., Tang M., Yih Y., et al. LRRK2 R1628P increases risk of Parkinson's disease: replication evidence. Hum Genet 124 3 (2008) 287-288
-
(2008)
Hum Genet
, vol.124
, Issue.3
, pp. 287-288
-
-
Tan, E.K.1
Tan, L.C.2
Lim, H.Q.3
Li, R.4
Tang, M.5
Yih, Y.6
-
10
-
-
48949092066
-
Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease
-
Ross O.A., Wu Y.R., Lee M.C., Funayama M., Chen M.L., Soto A.I., et al. Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease. Ann Neurol 64 1 (2008) 88-92
-
(2008)
Ann Neurol
, vol.64
, Issue.1
, pp. 88-92
-
-
Ross, O.A.1
Wu, Y.R.2
Lee, M.C.3
Funayama, M.4
Chen, M.L.5
Soto, A.I.6
-
11
-
-
70450202383
-
LRRK2 R1628P variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China
-
Zhang Z., Burgunder J.M., An X., Wu Y., Chen W., Zhang J., et al. LRRK2 R1628P variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China. Mov Disord 24 13 (2009) 1902-1905
-
(2009)
Mov Disord
, vol.24
, Issue.13
, pp. 1902-1905
-
-
Zhang, Z.1
Burgunder, J.M.2
An, X.3
Wu, Y.4
Chen, W.5
Zhang, J.6
-
12
-
-
31344439221
-
LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews
-
Ozelius L.J., Senthil G., Saunders-Pullman R., Ohmann E., Deligtisch A., Tagliati M., et al. LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews. N Engl J Med 354 4 (2006) 424-425
-
(2006)
N Engl J Med
, vol.354
, Issue.4
, pp. 424-425
-
-
Ozelius, L.J.1
Senthil, G.2
Saunders-Pullman, R.3
Ohmann, E.4
Deligtisch, A.5
Tagliati, M.6
-
13
-
-
31344432937
-
LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs
-
Lesage S., Durr A., Tazir M., Lohmann E., Leutenegger A.L., Janin S., et al. LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs. N Engl J Med 354 4 (2006) 422-423
-
(2006)
N Engl J Med
, vol.354
, Issue.4
, pp. 422-423
-
-
Lesage, S.1
Durr, A.2
Tazir, M.3
Lohmann, E.4
Leutenegger, A.L.5
Janin, S.6
-
14
-
-
20144387207
-
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations
-
Kachergus J., Mata I.F., Hulihan M., Taylor J.P., Lincoln S., Aasly J., et al. Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations. Am J Hum Genet 76 4 (2005) 672-680
-
(2005)
Am J Hum Genet
, vol.76
, Issue.4
, pp. 672-680
-
-
Kachergus, J.1
Mata, I.F.2
Hulihan, M.3
Taylor, J.P.4
Lincoln, S.5
Aasly, J.6
-
15
-
-
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 3 Pt 1 (1995) 502-505
-
(1995)
Neurology
, vol.45
, Issue.3 PART 1
, 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
-
16
-
-
42049094200
-
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease
-
Haugarvoll K., Rademakers R., Kachergus J.M., Nuytemans K., Ross O.A., Gibson J.M., et al. Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease. Neurology 70 16 Pt 2 (2008) 1456-1460
-
(2008)
Neurology
, vol.70
, Issue.16 PART 2
, pp. 1456-1460
-
-
Haugarvoll, K.1
Rademakers, R.2
Kachergus, J.M.3
Nuytemans, K.4
Ross, O.A.5
Gibson, J.M.6
-
17
-
-
41049086705
-
Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients
-
Nuytemans K., Rademakers R., Theuns J., Pals P., Engelborghs S., Pickut B., et al. Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients. Eur J Hum Genet 16 4 (2008) 471-479
-
(2008)
Eur J Hum Genet
, vol.16
, Issue.4
, pp. 471-479
-
-
Nuytemans, K.1
Rademakers, R.2
Theuns, J.3
Pals, P.4
Engelborghs, S.5
Pickut, B.6
-
18
-
-
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 9 (2004) 1619-1622
-
(2004)
Neurology
, vol.62
, Issue.9
, 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
-
19
-
-
70450177430
-
Neuropathology of Parkinson's disease with the R1441G mutation in LRRK2
-
Marti-Masso J.F., Ruiz-Martinez J., Bolano M.J., Ruiz I., Gorostidi A., Moreno F., et al. Neuropathology of Parkinson's disease with the R1441G mutation in LRRK2. Mov Disord 24 13 (2009) 1998-2001
-
(2009)
Mov Disord
, vol.24
, Issue.13
, pp. 1998-2001
-
-
Marti-Masso, J.F.1
Ruiz-Martinez, J.2
Bolano, M.J.3
Ruiz, I.4
Gorostidi, A.5
Moreno, F.6
-
20
-
-
21144451648
-
LRRK2 R1441G in Spanish patients with Parkinson's disease
-
Mata I.F., Taylor J.P., Kachergus J., Hulihan M., Huerta C., Lahoz C., et al. LRRK2 R1441G in Spanish patients with Parkinson's disease. Neurosci Lett 382 3 (2005) 309-311
-
(2005)
Neurosci Lett
, vol.382
, Issue.3
, pp. 309-311
-
-
Mata, I.F.1
Taylor, J.P.2
Kachergus, J.3
Hulihan, M.4
Huerta, C.5
Lahoz, C.6
-
21
-
-
77956545219
-
Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the seventh century in Northern Spain
-
Mata I.F., Hutter C.M., Gonzalez-Fernandez M.C., de Pancorbo M.M., Lezcano E., Huerta C., et al. Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the seventh century in Northern Spain. Neurogenetics 10 4 (2009) 347-353
-
(2009)
Neurogenetics
, vol.10
, Issue.4
, pp. 347-353
-
-
Mata, I.F.1
Hutter, C.M.2
Gonzalez-Fernandez, M.C.3
de Pancorbo, M.M.4
Lezcano, E.5
Huerta, C.6
-
22
-
-
33845204840
-
Parkinson's disease due to the R1441G mutation in Dardarin: a founder effect in the Basques
-
Simon-Sanchez J., Marti-Masso J.F., Sanchez-Mut J.V., Paisan-Ruiz C., Martinez-Gil A., Ruiz-Martinez J., et al. Parkinson's disease due to the R1441G mutation in Dardarin: a founder effect in the Basques. Mov Disord 21 11 (2006) 1954-1959
-
(2006)
Mov Disord
, vol.21
, Issue.11
, pp. 1954-1959
-
-
Simon-Sanchez, J.1
Marti-Masso, J.F.2
Sanchez-Mut, J.V.3
Paisan-Ruiz, C.4
Martinez-Gil, A.5
Ruiz-Martinez, J.6
-
23
-
-
67549117509
-
Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism
-
Ross O.A., Spanaki C., Griffith A., Lin C.H., Kachergus J., Haugarvoll K., et al. Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism. Parkinsonism Relat Disord 15 6 (2009) 466-467
-
(2009)
Parkinsonism Relat Disord
, vol.15
, Issue.6
, pp. 466-467
-
-
Ross, O.A.1
Spanaki, C.2
Griffith, A.3
Lin, C.H.4
Kachergus, J.5
Haugarvoll, K.6
-
24
-
-
67650501546
-
Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease
-
Lesage S., Condroyer C., Lannuzel A., Lohmann E., Troiano A., Tison F., et al. Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease. J Med Genet 46 7 (2009) 458-464
-
(2009)
J Med Genet
, vol.46
, Issue.7
, pp. 458-464
-
-
Lesage, S.1
Condroyer, C.2
Lannuzel, A.3
Lohmann, E.4
Troiano, A.5
Tison, F.6
-
25
-
-
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 3 (1997) 125-139
-
(1997)
Parkinsonism Relat Disord
, vol.3
, Issue.3
, pp. 125-139
-
-
Wszolek, Z.K.1
Vieregge, P.2
Uitti, R.J.3
Gasser, T.4
Yasuhara, O.5
McGeer, P.6
-
26
-
-
28544441181
-
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data
-
Khan N.L., Jain S., Lynch J.M., Pavese N., Abou-Sleiman P., Holton J.L., et al. Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data. Brain 128 Pt 12 (2005) 2786-2796
-
(2005)
Brain
, vol.128
, Issue.PART 12
, pp. 2786-2796
-
-
Khan, N.L.1
Jain, S.2
Lynch, J.M.3
Pavese, N.4
Abou-Sleiman, P.5
Holton, J.L.6
-
27
-
-
32244446461
-
LRRK2 G2019S is a common mutation in Spanish patients with late-onset Parkinson's disease
-
Infante J., Rodriguez E., Combarros O., Mateo I., Fontalba A., Pascual J., et al. LRRK2 G2019S is a common mutation in Spanish patients with late-onset Parkinson's disease. Neurosci Lett 395 3 (2006) 224-226
-
(2006)
Neurosci Lett
, vol.395
, Issue.3
, pp. 224-226
-
-
Infante, J.1
Rodriguez, E.2
Combarros, O.3
Mateo, I.4
Fontalba, A.5
Pascual, J.6
-
28
-
-
48849092336
-
LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case- control genetic study
-
Hulihan M.M., Ishihara-Paul L., Kachergus J., Warren L., Amouri R., Elango R., et al. LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case- control genetic study. Lancet Neurol 7 7 (2008) 591-594
-
(2008)
Lancet Neurol
, vol.7
, Issue.7
, pp. 591-594
-
-
Hulihan, M.M.1
Ishihara-Paul, L.2
Kachergus, J.3
Warren, L.4
Amouri, R.5
Elango, R.6
-
29
-
-
50049104725
-
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. Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study. Lancet Neurol 7 7 (2008) 583-590
-
(2008)
Lancet Neurol
, vol.7
, Issue.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
-
31
-
-
33749021352
-
LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago
-
Zabetian C.P., Hutter C.M., Yearout D., Lopez A.N., Factor S.A., Griffith A., et al. LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago. Am J Hum Genet 79 4 (2006) 752-758
-
(2006)
Am J Hum Genet
, vol.79
, Issue.4
, pp. 752-758
-
-
Zabetian, C.P.1
Hutter, C.M.2
Yearout, D.3
Lopez, A.N.4
Factor, S.A.5
Griffith, A.6
-
32
-
-
50249165832
-
LRRK2: bridging the gap between sporadic and hereditary Parkinson's disease
-
Elbaz A. LRRK2: bridging the gap between sporadic and hereditary Parkinson's disease. Lancet Neurol 7 7 (2008) 562-564
-
(2008)
Lancet Neurol
, vol.7
, Issue.7
, pp. 562-564
-
-
Elbaz, A.1
-
33
-
-
33748621731
-
Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations
-
Ishihara L., Warren L., Gibson R., Amouri R., Lesage S., Durr A., et al. Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations. Arch Neurol 63 9 (2006) 1250-1254
-
(2006)
Arch Neurol
, vol.63
, Issue.9
, pp. 1250-1254
-
-
Ishihara, L.1
Warren, L.2
Gibson, R.3
Amouri, R.4
Lesage, S.5
Durr, A.6
-
34
-
-
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 2 (2006) 388-393
-
(2006)
Ann Neurol
, vol.59
, Issue.2
, 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
-
35
-
-
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 2 (2006) 315-322
-
(2006)
Ann Neurol
, vol.59
, Issue.2
, 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
-
36
-
-
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 6 (2007) 626-628
-
(2007)
J Neurol Neurosurg Psychiatry
, vol.78
, Issue.6
, pp. 626-628
-
-
Gaig, C.1
Marti, M.J.2
Ezquerra, M.3
Rey, M.J.4
Cardozo, A.5
Tolosa, E.6
-
37
-
-
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 6 (2005) 918-921
-
(2005)
Ann Neurol
, vol.57
, Issue.6
, pp. 918-921
-
-
Funayama, M.1
Hasegawa, K.2
Ohta, E.3
Kawashima, N.4
Komiyama, M.5
Kowa, H.6
-
38
-
-
64249149785
-
Familial parkinsonism: study of original Sagamihara PARK8 (I2020T) kindred with variable clinicopathologic outcomes
-
Hasegawa K., Stoessl A.J., Yokoyama T., Kowa H., Wszolek Z.K., and Yagishita S. Familial parkinsonism: study of original Sagamihara PARK8 (I2020T) kindred with variable clinicopathologic outcomes. Parkinsonism Relat Disord 15 4 (2009) 300-306
-
(2009)
Parkinsonism Relat Disord
, vol.15
, Issue.4
, pp. 300-306
-
-
Hasegawa, K.1
Stoessl, A.J.2
Yokoyama, T.3
Kowa, H.4
Wszolek, Z.K.5
Yagishita, S.6
-
39
-
-
33846587090
-
A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan
-
Fung H.C., Chen C.M., Hardy J., Singleton A.B., and Wu Y.R. A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan. BMC Neurol 6 (2006) 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
-
40
-
-
50649115505
-
LRRK2 Gly2385Arg mutation and clinical features in a Chinese population with early-onset Parkinson's disease compared to late-onset patients
-
Chan D.K., Ng P.W., Mok V., Yeung J., Fang Z.M., Clarke R., et al. LRRK2 Gly2385Arg mutation and clinical features in a Chinese population with early-onset Parkinson's disease compared to late-onset patients. J Neural Transm 115 9 (2008) 1275-1277
-
(2008)
J Neural Transm
, vol.115
, Issue.9
, pp. 1275-1277
-
-
Chan, D.K.1
Ng, P.W.2
Mok, V.3
Yeung, J.4
Fang, Z.M.5
Clarke, R.6
-
41
-
-
70349267492
-
LRRK2 R1628P contributes to Parkinson's disease susceptibility in Chinese Han populations from mainland China
-
Yu L., Hu F., Zou X., Jiang Y., Liu Y., He X., et al. LRRK2 R1628P contributes to Parkinson's disease susceptibility in Chinese Han populations from mainland China. Brain Res 1296 (2009) 113-116
-
(2009)
Brain Res
, vol.1296
, pp. 113-116
-
-
Yu, L.1
Hu, F.2
Zou, X.3
Jiang, Y.4
Liu, Y.5
He, X.6
-
42
-
-
34250199013
-
Localization of Parkinson's disease-associated LRRK2 in normal and pathological human brain
-
Higashi S., Biskup S., West A.B., Trinkaus D., Dawson V.L., Faull R.L., et al. Localization of Parkinson's disease-associated LRRK2 in normal and pathological human brain. Brain Res 1155 (2007) 208-219
-
(2007)
Brain Res
, vol.1155
, pp. 208-219
-
-
Higashi, S.1
Biskup, S.2
West, A.B.3
Trinkaus, D.4
Dawson, V.L.5
Faull, R.L.6
-
43
-
-
33846562487
-
Parkinson's disease-associated mutations in LRRK2 link enhanced GTP-binding and kinase activities to neuronal toxicity
-
West A.B., Moore D.J., Choi C., Andrabi S.A., Li X., Dikeman D., et al. Parkinson's disease-associated mutations in LRRK2 link enhanced GTP-binding and kinase activities to neuronal toxicity. Hum Mol Genet 16 2 (2007) 223-232
-
(2007)
Hum Mol Genet
, vol.16
, Issue.2
, pp. 223-232
-
-
West, A.B.1
Moore, D.J.2
Choi, C.3
Andrabi, S.A.4
Li, X.5
Dikeman, D.6
-
44
-
-
67649813448
-
Mutant LRRK2(R1441G) BAC transgenic mice recapitulate cardinal features of Parkinson's disease
-
Li Y., Liu W., Oo T.F., Wang L., Tang Y., Jackson-Lewis V., et al. Mutant LRRK2(R1441G) BAC transgenic mice recapitulate cardinal features of Parkinson's disease. Nat Neurosci 12 7 (2009) 826-828
-
(2009)
Nat Neurosci
, vol.12
, Issue.7
, pp. 826-828
-
-
Li, Y.1
Liu, W.2
Oo, T.F.3
Wang, L.4
Tang, Y.5
Jackson-Lewis, V.6
|