-
1
-
-
0037428241
-
Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism
-
V. Bonifati, P. Rizzu, M.J. van Baren, O. Schaap, G.J. Breedveld, E. Krieger, M.C. Dekker, F. Squitieri, P. Ibanez, M. Joosse, J.W. van Dongen, N. Vanacore, J.C. van Swieten, A. Brice, G. Meco, C.M. van Duijn, B.A. Oostra, and P. Heutink Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism Science 299 2003 256 259
-
(2003)
Science
, vol.299
, 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
-
2
-
-
0242363670
-
Molecular pathways of neurodegeneration in Parkinson's disease
-
T.M. Dawson, and V.L. Dawson Molecular pathways of neurodegeneration in Parkinson's disease Science 302 2003 819 822
-
(2003)
Science
, vol.302
, pp. 819-822
-
-
Dawson, T.M.1
Dawson, V.L.2
-
3
-
-
0036654314
-
Genetics of parkinsonism
-
K. Gwinn-Hardy Genetics of parkinsonism Mov. Disord. 17 2002 645 656
-
(2002)
Mov. Disord.
, vol.17
, pp. 645-656
-
-
Gwinn-Hardy, K.1
-
4
-
-
18244412384
-
Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in the Parkin gene in affected individuals
-
N. Hattori, T. Kitada, H. Matsumine, S. Asakawa, Y. Yamamura, H. Yoshino, T. Kobayashi, M. Yokochi, M. Wang, A. Yoritaka, T. Kondo, S. Kuzuhara, S. Nakamura, N. Shimizu, and Y. Mizuno Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: evidence for variable homozygous deletions in the Parkin gene in affected individuals Ann. Neurol. 44 1998 935 941
-
(1998)
Ann. Neurol.
, vol.44
, pp. 935-941
-
-
Hattori, N.1
Kitada, T.2
Matsumine, H.3
Asakawa, S.4
Yamamura, Y.5
Yoshino, H.6
Kobayashi, T.7
Yokochi, M.8
Wang, M.9
Yoritaka, A.10
Kondo, T.11
Kuzuhara, S.12
Nakamura, S.13
Shimizu, N.14
Mizuno, Y.15
-
5
-
-
0032433332
-
Genetic linkage analysis of complex genetic traits by using affected sibling pairs
-
E.R. Hauser, and M. Boehnke Genetic linkage analysis of complex genetic traits by using affected sibling pairs Biometrics 54 1998 1238 1246
-
(1998)
Biometrics
, vol.54
, pp. 1238-1246
-
-
Hauser, E.R.1
Boehnke, M.2
-
6
-
-
0036830525
-
A susceptibility gene for late-onset idiopathic Parkinson's disease
-
A.A. Hicks, H. Petursson, T. Jonsson, H. Stefansson, H.S. Johannsdottir, J. Sainz, M.L. Frigge, A. Kong, J.R. Gulcher, K. Stefansson, and S. Sveinbjornsdottir A susceptibility gene for late-onset idiopathic Parkinson's disease Ann. Neurol. 52 2002 549 555
-
(2002)
Ann. Neurol.
, vol.52
, pp. 549-555
-
-
Hicks, A.A.1
Petursson, H.2
Jonsson, T.3
Stefansson, H.4
Johannsdottir, H.S.5
Sainz, J.6
Frigge, M.L.7
Kong, A.8
Gulcher, J.R.9
Stefansson, K.10
Sveinbjornsdottir, S.11
-
7
-
-
0035940582
-
Improved accuracy of clinical diagnosis of Lewy body Parkinson's disease
-
A.J. Hughes, S.E. Daniel, and A.J. Lees Improved accuracy of clinical diagnosis of Lewy body Parkinson's disease Neurology 57 2001 1497 1499
-
(2001)
Neurology
, vol.57
, pp. 1497-1499
-
-
Hughes, A.J.1
Daniel, S.E.2
Lees, A.J.3
-
8
-
-
0032531924
-
Parkinson's disease. Second of two parts
-
A.E. Lang, and A.M. Lozano Parkinson's disease. Second of two parts N. Engl. J. Med. 339 1998 1130 1143
-
(1998)
N. Engl. J. Med.
, vol.339
, pp. 1130-1143
-
-
Lang, A.E.1
Lozano, A.M.2
-
9
-
-
12244264435
-
Genetic Power Calculator: Design of linkage and association genetic mapping studies of complex traits
-
S. Purcell, S.S. Cherny, and P.C. Sham Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits Bioinformatics 19 2003 149 150
-
(2003)
Bioinformatics
, vol.19
, pp. 149-150
-
-
Purcell, S.1
Cherny, S.S.2
Sham, P.C.3
-
10
-
-
10044275502
-
Analysis of the PINK1 gene in a large cohort of cases with Parkinson's disease
-
in press.
-
E. Rogaeva, J. Johnson, A.E. Lang, T. Kawarai, C. Gulick, K. Gwinn-Hardy, T. Kawarai, C. Sato, A. Morgan, J. Werner, R. Nussbaum, A. Petit, M.S. Okun, A. McInerney, R. Mandel, J.L. Groen, H.H. Fernandez, R. Postuma, K.D. Foote, S. Salehi-Rad, Y. Liang, S. Reimsnider, A. Tandon, J. Hardy, P. St George-Hyslop, A.B. Singleton, Analysis of the PINK1 gene in a large cohort of cases with Parkinson's disease, Arch. Neurol., in press.
-
Arch. Neurol.
-
-
Rogaeva, E.1
Johnson, J.2
Lang, A.E.3
Kawarai, T.4
Gulick, C.5
Gwinn-Hardy, K.6
Kawarai, T.7
Sato, C.8
Morgan, A.9
Werner, J.10
Nussbaum, R.11
Petit, A.12
Okun, M.S.13
McInerney, A.14
Mandel, R.15
Groen, J.L.16
Fernandez, H.H.17
Postuma, R.18
Foote, K.D.19
Salehi-Rad, S.20
Liang, Y.21
Reimsnider, S.22
Tandon, A.23
Hardy, J.24
St George-Hyslop, P.25
Singleton, A.B.26
more..
-
11
-
-
2442668926
-
Hereditary early-onset Parkinson's disease caused by mutations in PINK1
-
E.M. Valente, P.M. Abou-Sleiman, V. Caputo, M.M.K. Muqit, K. Harvey, S. Gispert, Z. Ali, D. Del Turco, A.R. Bentivoglio, D.G. Healy, A. Albanese, R. Nussbaum, R. González-Maldonado, T. Deller, S. Salvi, P. Cortelli, W.P. Gilks, D.S. Latchman, R.J. Harvey, B. Dallapiccola, G. Auburger, and N.W. Wood Hereditary early-onset Parkinson's disease caused by mutations in PINK1 Science 304 2004 1158 1160
-
(2004)
Science
, vol.304
, pp. 1158-1160
-
-
Valente, E.M.1
Abou-Sleiman, P.M.2
Caputo, V.3
Muqit, M.M.K.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
González-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..
|