-
1
-
-
0030744876
-
Mutation in the alpha-synuclein gene identified in familles with Parkinson's disease
-
Polymeropoulos MH, Lavedan C, Leroy E, et al. Mutation in the alpha-synuclein gene identified in familles with Parkinson's disease. Science 1997;276:2045-2047.
-
(1997)
Science
, vol.276
, pp. 2045-2047
-
-
Polymeropoulos, M.H.1
Lavedan, C.2
Leroy, E.3
-
2
-
-
0030882856
-
Alpha-synuclein in Lewy bodies
-
Spillantini MG, Schmidt ML, Lee VM, Trojanowski JQ, Jakes R, Goedert M. Alpha-synuclein in Lewy bodies. Nature 1997;388:839-480.
-
(1997)
Nature
, vol.388
, pp. 839-480
-
-
Spillantini, M.G.1
Schmidt, M.L.2
Lee, V.M.3
Trojanowski, J.Q.4
Jakes, R.5
Goedert, M.6
-
3
-
-
0032499264
-
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
-
Kitada T, Asakawa S, Hattori N, et al. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 1998;392:605-608.
-
(1998)
Nature
, vol.392
, pp. 605-608
-
-
Kitada, T.1
Asakawa, S.2
Hattori, N.3
-
4
-
-
0037428241
-
Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism
-
Bonifati V, Rizzu P, Van Baren MJ, et al. Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism. Science 2003;299:256-259.
-
(2003)
Science
, vol.299
, pp. 256-259
-
-
Bonifati, V.1
Rizzu, P.2
Van Baren, M.J.3
-
5
-
-
2442668926
-
Hereditary early-onset Parkinson's disease caused by mutations in PINK1
-
Valente EM, Abou-Sleiman PM, Caputo V, et al. Hereditary early-onset Parkinson's disease caused by mutations in PINK1. Science 2004;304:1158-1160.
-
(2004)
Science
, vol.304
, pp. 1158-1160
-
-
Valente, E.M.1
Abou-Sleiman, P.M.2
Caputo, V.3
-
6
-
-
5644254800
-
PINK1 (PARK6) associated Parkinson disease in Ireland
-
Healy DG, Abou-Sleiman PM, Ross OA, et al. PINK1 (PARK6) associated Parkinson disease in Ireland. Neurology 2004;63:1486-1488.
-
(2004)
Neurology
, vol.63
, pp. 1486-1488
-
-
Healy, D.G.1
Abou-Sleiman, P.M.2
Ross, O.A.3
-
7
-
-
7044236967
-
PARK6-linked autoaomal recessive early-onset parkinsonism in Asian populations
-
Hatano Y, Sato K, Elibol B, et al. PARK6-linked autoaomal recessive early-onset parkinsonism in Asian populations. Neurology 2004;63:1482-1485.
-
(2004)
Neurology
, vol.63
, pp. 1482-1485
-
-
Hatano, Y.1
Sato, K.2
Elibol, B.3
-
8
-
-
0035526282
-
Phenotypic characterisation of autosomal recessive PARK6-linked parkinsonism in three unrelated Italian families
-
Bentivoglio AR, Cortelli P, Valente EM, et al. Phenotypic characterisation of autosomal recessive PARK6-linked parkinsonism in three unrelated Italian families. Mov Disord 2001;16:999-1006.
-
(2001)
Mov Disord
, vol.16
, pp. 999-1006
-
-
Bentivoglio, A.R.1
Cortelli, P.2
Valente, E.M.3
-
9
-
-
0036895554
-
Clinical and subclinical dopaminergic dysfunction in PARK6-linked parkinsonism: An 18F-dopa PET study
-
Khan NL, Valente EM, Bentivoglio AR, et al. Clinical and subclinical dopaminergic dysfunction in PARK6-linked parkinsonism: an 18F-dopa PET study. Ann Neurol 2002;52:849-853.
-
(2002)
Ann Neurol
, vol.52
, pp. 849-853
-
-
Khan, N.L.1
Valente, E.M.2
Bentivoglio, A.R.3
-
10
-
-
0036136951
-
PARK6-linked parkinsonism occurs in several European families
-
Valente EM, Brancati F, Ferraris A, et al. PARK6-linked parkinsonism occurs in several European families. Ann Neurol 2002;51:14-18.
-
(2002)
Ann Neurol
, vol.51
, pp. 14-18
-
-
Valente, E.M.1
Brancati, F.2
Ferraris, A.3
|