-
1
-
-
0141741347
-
Parkinson's disease: Mechanisms and models
-
10.1016/S0896-6273(03)00568-3 12971891
-
Dauer W Przedborski S Parkinson's disease: Mechanisms and models Neuron 2003, 39(6):889-909 10.1016/S0896-6273(03)00568-3 12971891
-
(2003)
Neuron
, vol.39
, Issue.6
, pp. 889-909
-
-
Dauer, W.1
Przedborski, S.2
-
2
-
-
0026514953
-
Accuracy of the clinical diagnosis of idiopathic Parkinson's disease: A clinicapathological study of 100 cases
-
1564476
-
Hughes AJ Daniel SE Kilford L Lees AJ Accuracy of the clinical diagnosis of idiopathic Parkinson's disease: A clinicapathological study of 100 cases J Neurol Neurosurg Psychiatry 1992, 55:181-184 1564476
-
(1992)
J Neurol Neurosurg Psychiatry
, vol.55
, pp. 181-184
-
-
Hughes, A.J.1
Daniel, S.E.2
Kilford, L.3
Lees, A.J.4
-
3
-
-
0036654314
-
Genetics of parkinsonism
-
10.1002/mds.10173 12210852
-
Gwinn-Hardy K Genetics of parkinsonism Mov Disord 2002, 17(4):645-656 10.1002/mds.10173 12210852
-
(2002)
Mov Disord
, vol.17
, Issue.4
, pp. 645-656
-
-
Gwinn-Hardy, K.1
-
4
-
-
2442668926
-
Hereditary early-onset Parkinson's disease caused by mutations in PINK1
-
10.1126/science.1096284 15087508
-
Valente EM Abou-Sleiman PM Caputo V Muqit MM Harvey K Gispert S Ali Z Del Turco D Bentivoglio AR Healy DG Albanese A Nussbaum R Gonzalez-Maldonado R Deller T Salvi S Cortelli P Gilks WP Latchman DS Harvey RJ Dallapiccola B Auburger G Wood NW Hereditary early-onset Parkinson's disease caused by mutations in PINK1 Science 2004, 304(5674):1158-1160 10.1126/science.1096284 15087508
-
(2004)
Science
, vol.304
, Issue.5674
, pp. 1158-1160
-
-
Valente, E.M.1
Abou-Sleiman, P.M.2
Caputo, V.3
Muqit, M.M.4
Harvey, K.5
Gispert, S.6
Ali, Z.7
Del Turco, D.8
Bentivoglio, A.R.9
Healy, D.G.10
Albanese, A.11
Nussbaum, R.12
Gonzalez-Maldonado, R.13
Deller, T.14
Salvi, S.15
Cortelli, P.16
Gilks, W.P.17
Latchman, D.S.18
Harvey, R.J.19
Dallapiccola, B.20
Auburger, G.21
Wood, N.W.22
more..
-
5
-
-
0036151884
-
Localization of autosomal recessive early-onset parkinsonism to chromosome 1p36 (PARK7) in an independent dataset
-
10.1002/ana.10106 11835383
-
Bonifati V Breedveld GJ Squitieri F Vanacore N Brustenghi P Harhangi BS Montagna P Cannella M Fabbrini G Rizzu P van Duijn CM Oostra BA Meco G Heutink P Localization of autosomal recessive early-onset parkinsonism to chromosome 1p36 (PARK7) in an independent dataset Ann Neurol 2002, 51(2):253-256 10.1002/ana.10106 11835383
-
(2002)
Ann Neurol
, vol.51
, Issue.2
, pp. 253-256
-
-
Bonifati, V.1
Breedveld, G.J.2
Squitieri, F.3
Vanacore, N.4
Brustenghi, P.5
Harhangi, B.S.6
Montagna, P.7
Cannella, M.8
Fabbrini, G.9
Rizzu, P.10
van Duijn, C.M.11
Oostra, B.A.12
Meco, G.13
Heutink, P.14
-
6
-
-
0030744876
-
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
-
10.1126/science.276.5321.2045 9197268
-
Polymeropoulos MH Lavedan C Leroy E Ide SE Dehejia A Dutra A Pike B Root H Rubenstein J Boyer R Stenroos ES Chandrasekharappa S Athanassiadou A Papapetropoulos T Johnson WG Lazzarini AM Duvoisin RC Di Iorio G Golbe LI Nussbaum RL Mutation in the alpha-synuclein gene identified in families with Parkinson's disease Science 1997, 276(5321):2045-2047 10.1126/science.276.5321.2045 9197268
-
(1997)
Science
, vol.276
, Issue.5321
, pp. 2045-2047
-
-
Polymeropoulos, M.H.1
Lavedan, C.2
Leroy, E.3
Ide, S.E.4
Dehejia, A.5
Dutra, A.6
Pike, B.7
Root, H.8
Rubenstein, J.9
Boyer, R.10
Stenroos, E.S.11
Chandrasekharappa, S.12
Athanassiadou, A.13
Papapetropoulos, T.14
Johnson, W.G.15
Lazzarini, A.M.16
Duvoisin, R.C.17
Di Iorio, G.18
Golbe, L.I.19
Nussbaum, R.L.20
more..
-
7
-
-
0032499264
-
Mutations in the parkin gene cause autossomal recessive juvenile parkinsonism
-
10.1038/33416 9560156
-
Kitada T Asakawa S Hattori N Matsumine H Yamamura Y Minoshima S Yokochi M Mizuno Y Shimizu N Mutations in the parkin gene cause autossomal recessive juvenile parkinsonism Nature 1998, 392:605-608 10.1038/33416 9560156
-
(1998)
Nature
, vol.392
, pp. 605-608
-
-
Kitada, T.1
Asakawa, S.2
Hattori, N.3
Matsumine, H.4
Yamamura, Y.5
Minoshima, S.6
Yokochi, M.7
Mizuno, Y.8
Shimizu, N.9
-
8
-
-
8844266996
-
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
-
10.1016/j.neuron.2004.10.023 15541308
-
Paisan-Ruiz C Jain S Evans EW Gilks WP Simon J van der Brug M Lopez de Munain A Aparicio S Gil AM Khan N Johnson J Martinez JR Nicholl D Carrera IM Pena AS de Silva R Lees A Marti-Masso JF Perez-Tur J Wood NW Singleton AB Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease Neuron 2004, 44(4):595-600 10.1016/ j.neuron.2004.10.023 15541308
-
(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
Lopez de Munain, A.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..
-
9
-
-
8844233579
-
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
-
10.1016/j.neuron.2004.11.005 15541309
-
Zimprich A Biskup S Leitner P Lichtner P Farrer M Lincoln S Kachergus J Hulihan M Uitti RJ Calne DB Stoessl AJ Pfeiffer RF Patenge N Carbajal IC Vieregge P Asmus F Muller-Myhsok B Dickson DW Meitinger T Strom TM Wszolek ZK Gasser T Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology Neuron 2004, 44(4):601-607 10.1016/j.neuron.2004.11.005 15541309
-
(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
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..
-
10
-
-
0242300619
-
alpha-Synuclein locus triplication causes Parkinson's disease
-
10.1126/science.1090278 14593171
-
Singleton AB Farrer M Johnson J Singleton A Hague S Kachergus J Hulihan M Peuralinna T Dutra A Nussbaum R Lincoln S Crawley A Hanson M Maraganore D Adler C Cookson MR Muenter M Baptista M Miller D Blancato J Hardy J Gwinn-Hardy K alpha-Synuclein locus triplication causes Parkinson's disease Science 2003, 302(5646):841 10.1126/science.1090278 14593171
-
(2003)
Science
, vol.302
, Issue.5646
, pp. 841
-
-
Singleton, A.B.1
Farrer, M.2
Johnson, J.3
Singleton, A.4
Hague, S.5
Kachergus, J.6
Hulihan, M.7
Peuralinna, T.8
Dutra, A.9
Nussbaum, R.10
Lincoln, S.11
Crawley, A.12
Hanson, M.13
Maraganore, D.14
Adler, C.15
Cookson, M.R.16
Muenter, M.17
Baptista, M.18
Miller, D.19
Blancato, J.20
Hardy, J.21
Gwinn-Hardy, K.22
more..
-
11
-
-
10744226640
-
DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease
-
Hedrich K Djarmati A Schafer N Hering R Wellenbrock C Weiss PH Hilker R Vieregge P Ozelius LJ Heutink P Bonifati V Schwinger E Lang AE Noth J Bressman SB Pramstaller PP Riess O Klein C DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease Neurology 2004, 62:389-394
-
(2004)
Neurology
, vol.62
, pp. 389-394
-
-
Hedrich, K.1
Djarmati, A.2
Schafer, N.3
Hering, R.4
Wellenbrock, C.5
Weiss, P.H.6
Hilker, R.7
Vieregge, P.8
Ozelius, L.J.9
Heutink, P.10
Bonifati, V.11
Schwinger, E.12
Lang, A.E.13
Noth, J.14
Bressman, S.B.15
Pramstaller, P.P.16
Riess, O.17
Klein, C.18
-
12
-
-
0042232353
-
The role of pathogenic DJ-1 mutations in Parkinson's disease
-
10.1002/ana.10675 12953260
-
Abou-Sleiman PM Healy DG Quinn N Lees AJ Wood NW The role of pathogenic DJ-1 mutations in Parkinson's disease Ann Neurol 2003, 54(3):283-286 10.1002/ana.10675 12953260
-
(2003)
Ann Neurol
, vol.54
, Issue.3
, pp. 283-286
-
-
Abou-Sleiman, P.M.1
Healy, D.G.2
Quinn, N.3
Lees, A.J.4
Wood, N.W.5
-
13
-
-
0037428241
-
Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism
-
10.1126/science.1077209 12446870
-
Bonifati V Rizzu P van Baren MJ Schaap O Breedveld GJ Krieger E Dekker MC Squitieri F Ibanez P Joosse M van Dongen JW Vanacore N van Swieten JC Brice A Meco G van Duijn CM Oostra BA Heutink P Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism Science 2003, 299(5604):256-259 10.1126/science.1077209 12446870
-
(2003)
Science
, vol.299
, Issue.5604
, pp. 256-259
-
-
Bonifati, V.1
Rizzu, P.2
van Baren, M.J.3
Schaap, O.4
Breedveld, G.J.5
Krieger, E.6
Dekker, M.C.7
Squitieri, F.8
Ibanez, P.9
Joosse, M.10
van Dongen, J.W.11
Vanacore, N.12
van Swieten, J.C.13
Brice, A.14
Meco, G.15
van Duijn, C.M.16
Oostra, B.A.17
Heutink, P.18
-
14
-
-
5044235807
-
Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7)
-
10.1002/humu.20089 15365989
-
Hering R Strauss KM Tao X Bauer A Woitalla D Mietz EM Petrovic S Bauer P Schaible W Muller T Schols L Klein C Berg D Meyer PT Schulz JB Wollnik B Tong L Kruger R Riess O Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7) Hum Mutat 2004, 24(4):321-329 10.1002/ humu.20089 15365989
-
(2004)
Hum Mutat
, vol.24
, Issue.4
, pp. 321-329
-
-
Hering, R.1
Strauss, K.M.2
Tao, X.3
Bauer, A.4
Woitalla, D.5
Mietz, E.M.6
Petrovic, S.7
Bauer, P.8
Schaible, W.9
Muller, T.10
Schols, L.11
Klein, C.12
Berg, D.13
Meyer, P.T.14
Schulz, J.B.15
Wollnik, B.16
Tong, L.17
Kruger, R.18
Riess, O.19
-
15
-
-
28544446980
-
G2019S Dardarin Substitution is a Common Cause of Parkinson's Disease in a Portuguese Cohort
-
10.1002/mds.20682 16149095
-
Bras JM Guerreiro RJ Ribeiro MH Januário C Morgadinho AS Oliveira C Cunha L Hardy J Singleton A G2019S Dardarin Substitution is a Common Cause of Parkinson's Disease in a Portuguese Cohort Mov Disord 2005, 20(12):1653-1655 10.1002/mds.20682 16149095
-
(2005)
Mov Disord
, vol.20
, Issue.12
, pp. 1653-1655
-
-
Bras, J.M.1
Guerreiro, R.J.2
Ribeiro, M.H.3
Januário, C.4
Morgadinho, A.S.5
Oliveira, C.6
Cunha, L.7
Hardy, J.8
Singleton, A.9
-
16
-
-
28544441389
-
Genetics of Parkinson's disease: LRRK2 on the rise
-
10.1093/brain/awh676 16311269
-
Brice A Genetics of Parkinson's disease: LRRK2 on the rise Brain 2005, 128(Pt 12):2760-2762 10.1093/brain/awh676 16311269
-
(2005)
Brain
, vol.128
, Issue.PART 12
, pp. 2760-2762
-
-
Brice, A.1
-
17
-
-
31344432937
-
LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs
-
10.1056/NEJMc055540 16436781
-
Lesage S Durr A Tazir M Lohmann E Leutenegger AL Janin S Pollak P Brice A LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs N Engl J Med 2006, 354(4):422-423 10.1056/NEJMc055540 16436781
-
(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
Pollak, P.7
Brice, A.8
-
18
-
-
31344439221
-
LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews
-
10.1056/NEJMc055509 16436782
-
Ozelius LJ Senthil G Saunders-Pullman R Ohmann E Deligtisch A Tagliati M Hunt AL Klein C Henick B Hailpern SM Lipton RB Soto-Valencia J Risch N Bressman SB LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews N Engl J Med 2006, 354(4):424-425 10.1056/NEJMc055509 16436782
-
(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
Hunt, A.L.7
Klein, C.8
Henick, B.9
Hailpern, S.M.10
Lipton, R.B.11
Soto-Valencia, J.12
Risch, N.13
Bressman, S.B.14
-
19
-
-
0032937059
-
Diagnostic criteria for Parkinson disease
-
10.1001/archneur.56.1.33 9923759
-
Gelb DJ Oliver E Gilman S Diagnostic criteria for Parkinson disease Arch Neurol 1999, 56:33-39 10.1001/archneur.56.1.33 9923759
-
(1999)
Arch Neurol
, vol.56
, pp. 33-39
-
-
Gelb, D.J.1
Oliver, E.2
Gilman, S.3
-
20
-
-
27744553995
-
Alpha-synuclein and Parkinson's disease: Implications from the screening of more than 1,900 patients
-
10.1002/mds.20504 15895422
-
Berg D Niwar M Maass S Zimprich A Moller JC Wuellner U Schmitz-Hubsch T Klein C Tan EK Schols L Marsh L Dawson TM Janetzky B Muller T Woitalla D Kostic V Pramstaller PP Oertel WH Bauer P Krueger R Gasser T Riess O Alpha-synuclein and Parkinson's disease: Implications from the screening of more than 1,900 patients Mov Disord 2005, 20(9):1191-1194 10.1002/ mds.20504 15895422
-
(2005)
Mov Disord
, vol.20
, Issue.9
, pp. 1191-1194
-
-
Berg, D.1
Niwar, M.2
Maass, S.3
Zimprich, A.4
Moller, J.C.5
Wuellner, U.6
Schmitz-Hubsch, T.7
Klein, C.8
Tan, E.K.9
Schols, L.10
Marsh, L.11
Dawson, T.M.12
Janetzky, B.13
Muller, T.14
Woitalla, D.15
Kostic, V.16
Pramstaller, P.P.17
Oertel, W.H.18
Bauer, P.19
Krueger, R.20
Gasser, T.21
Riess, O.22
more..
-
21
-
-
4444237208
-
Novel PINK1 mutations in early-onset parkinsonism
-
10.1002/ana.20251 15349870
-
Hatano Y Li Y Sato K Asakawa S Yamamura Y Tomiyama H Yoshino H Asahina M Kobayashi S Hassin-Baer S Lu CS Ng AR Rosales RL Shimizu N Toda T Mizuno Y Hattori N Novel PINK1 mutations in early-onset parkinsonism Ann Neurol 2004, 56(3):424-427 10.1002/ana.20251 15349870
-
(2004)
Ann Neurol
, vol.56
, Issue.3
, pp. 424-427
-
-
Hatano, Y.1
Li, Y.2
Sato, K.3
Asakawa, S.4
Yamamura, Y.5
Tomiyama, H.6
Yoshino, H.7
Asahina, M.8
Kobayashi, S.9
Hassin-Baer, S.10
Lu, C.S.11
Ng, A.R.12
Rosales, R.L.13
Shimizu, N.14
Toda, T.15
Mizuno, Y.16
Hattori, N.17
-
22
-
-
33750725402
-
Digenic parkinsonism: Investigation of the synergistic effects of PRKN and LRRK2
-
10.1016/j.neulet.2006.06.068 17095157
-
Dachsel JC Mata IF Ross OA Taylor JP Lincoln SJ Hinkle KM Huerta C Ribacoba R Blazquez M Alvarez V Farrer MJ Digenic parkinsonism: investigation of the synergistic effects of PRKN and LRRK2 Neurosci Lett 2006, 410(2):80-84 10.1016/j.neulet.2006.06.068 17095157
-
(2006)
Neurosci Lett
, vol.410
, Issue.2
, pp. 80-84
-
-
Dachsel, J.C.1
Mata, I.F.2
Ross, O.A.3
Taylor, J.P.4
Lincoln, S.J.5
Hinkle, K.M.6
Huerta, C.7
Ribacoba, R.8
Blazquez, M.9
Alvarez, V.10
Farrer, M.J.11
-
23
-
-
33750370804
-
Understanding the molecular causes of Parkinson's disease
-
10.1016/j.molmed.2006.09.007 17027339
-
Wood-Kaczmar A Gandhi S Wood NW Understanding the molecular causes of Parkinson's disease Trends Mol Med 2006, 12(11):521-528 10.1016/ j.molmed.2006.09.007 17027339
-
(2006)
Trends Mol Med
, vol.12
, Issue.11
, pp. 521-528
-
-
Wood-Kaczmar, A.1
Gandhi, S.2
Wood, N.W.3
|