-
1
-
-
3843066722
-
Unraveling the pathogenesis of Parkinson's disease - The contribution of monogenic forms
-
Bonifati V, Oostra BA, Heutink P: Unraveling the pathogenesis of Parkinson's disease - the contribution of monogenic forms. Cell Mol Life Sci 2004; 61: 1729-1750.
-
(2004)
Cell Mol Life Sci
, vol.61
, pp. 1729-1750
-
-
Bonifati, V.1
Oostra, B.A.2
Heutink, P.3
-
2
-
-
0242363670
-
Molecular pathways of neurodegeneration in Parkinson's disease
-
Dawson TM, Dawson VL: Molecular pathways of neurodegeneration in Parkinson's disease. Science 2003; 302: 819-822.
-
(2003)
Science
, vol.302
, pp. 819-822
-
-
Dawson, T.M.1
Dawson, V.L.2
-
3
-
-
0030744876
-
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
-
Polymeropoulos MH, Lavedan C, Leroy E et al: Mutation in the alpha-synuclein gene identified in families 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
-
4
-
-
0242300619
-
alpha-Synuclein locus triplication causes Parkinson's disease
-
Singleton AB, Farrer M, Johnson J et al: Alpha-Synuclein locus triplication causes Parkinson's disease. Science 2003; 302: 841.
-
(2003)
Science
, vol.302
, pp. 841
-
-
Singleton, A.B.1
Farrer, M.2
Johnson, J.3
-
5
-
-
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
-
6
-
-
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
-
7
-
-
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
-
8
-
-
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, Obata F: A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1. Ann Neurol 2002; 51: 296-301.
-
(2002)
Ann Neurol
, vol.51
, pp. 296-301
-
-
Funayama, M.1
Hasegawa, K.2
Kowa, H.3
Saito, M.4
Tsuji, S.5
Obata, F.6
-
9
-
-
8844233579
-
Mutations in LRRK2 Cause autosomal-dominant Parkinsonism with pleomorphic pathology
-
Zimprich A, Biskup S, Leitner P et al: Mutations in LRRK2 Cause autosomal-dominant Parkinsonism with pleomorphic pathology. Neuron 2004; 44: 601-607.
-
(2004)
Neuron
, vol.44
, pp. 601-607
-
-
Zimprich, A.1
Biskup, S.2
Leitner, P.3
-
10
-
-
8844266996
-
Cloning of the gene containing mutations that cause PARK8-Linked Parkinson's disease
-
Paisan-Ruiz C, Jain S, Evans EW et al: Cloning of the gene containing mutations that cause PARK8-Linked Parkinson's disease. Neuron 2004; 44: 595-600.
-
(2004)
Neuron
, vol.44
, pp. 595-600
-
-
Paisan-Ruiz, C.1
Jain, S.2
Evans, E.W.3
-
12
-
-
19944431081
-
A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease
-
Di Fonzo A, Rohe CF, Ferreira J et al: A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease. Lancet 2005; 365: 412-415.
-
(2005)
Lancet
, vol.365
, pp. 412-415
-
-
Di Fonzo, A.1
Rohe, C.F.2
Ferreira, J.3
-
13
-
-
20044394901
-
Clinical and positron emission tomography of Parkinson's disease caused by LRRK2
-
Hernandez DG, Paisan-Ruiz C, McInerney-Leo A et al: Clinical and positron emission tomography of Parkinson's disease caused by LRRK2. Ann Neurol 2005; 57: 453-456.
-
(2005)
Ann Neurol
, vol.57
, pp. 453-456
-
-
Hernandez, D.G.1
Paisan-Ruiz, C.2
McInerney-Leo, A.3
-
14
-
-
20144387207
-
Identification of a novel LRRK2 mutation Linked to autosomal dominant parkinsonism: Evidence of a common founder across european populations
-
Kachergus J, Mata IF, Hulihan M 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 2005; 76: 672-680.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 672-680
-
-
Kachergus, J.1
Mata, I.F.2
Hulihan, M.3
-
15
-
-
20444420103
-
An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family
-
Funayama M, Hasegawa K, Ohta E et al: An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family. Ann Neurol 2005; 57: 918-921.
-
(2005)
Ann Neurol
, vol.57
, pp. 918-921
-
-
Funayama, M.1
Hasegawa, K.2
Ohta, E.3
-
16
-
-
24644497562
-
LRRK2 mutations in Parkinson disease
-
Farrer M, Stone J, Mata IF et al: LRRK2 mutations in Parkinson disease. Neurology 2005; 65: 738-740.
-
(2005)
Neurology
, vol.65
, pp. 738-740
-
-
Farrer, M.1
Stone, J.2
Mata, I.F.3
-
17
-
-
24644486896
-
A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations
-
Zabetian CP, Samii A, Mosley AD et al: A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations. Neurology 2005; 65: 741-744.
-
(2005)
Neurology
, vol.65
, pp. 741-744
-
-
Zabetian, C.P.1
Samii, A.2
Mosley, A.D.3
-
18
-
-
24644431901
-
LRRK2 gene in Parkinson disease: Mutation analysis and case control association study
-
Paisan-Ruiz C, Lang AE, Kawarai T et al: LRRK2 gene in Parkinson disease: Mutation analysis and case control association study. Neurology 2005; 65: 696-700.
-
(2005)
Neurology
, vol.65
, pp. 696-700
-
-
Paisan-Ruiz, C.1
Lang, A.E.2
Kawarai, T.3
-
19
-
-
19944432921
-
A common LRRK2 mutation in idiopathic Parkinson's disease
-
Gilks WP, Abou-Sleiman PM, Gandhi S et al: A common LRRK2 mutation in idiopathic Parkinson's disease. Lancet 2005; 365: 415-416.
-
(2005)
Lancet
, vol.365
, pp. 415-416
-
-
Gilks, W.P.1
Abou-Sleiman, P.M.2
Gandhi, S.3
-
20
-
-
19944432606
-
Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease
-
Nichols WC, Pankratz N, Hernandez D et al: Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease. Lancet 2005; 365: 410-412.
-
(2005)
Lancet
, vol.365
, pp. 410-412
-
-
Nichols, W.C.1
Pankratz, N.2
Hernandez, D.3
-
21
-
-
21144451648
-
LRRK2 R1441G in Spanish patients with Parkinson's disease
-
Mata IF, Taylor JP, Kachergus J et al: LRRK2 R1441G in Spanish patients with Parkinson's disease. Neurosci Lett 2005; 382: 309-311.
-
(2005)
Neurosci Lett
, vol.382
, pp. 309-311
-
-
Mata, I.F.1
Taylor, J.P.2
Kachergus, J.3
-
22
-
-
20644455323
-
The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients
-
Tan EK, Shen H, Tan LC et al: The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients. Neurosci Lett 2005; 384: 327-329.
-
(2005)
Neurosci Lett
, vol.384
, pp. 327-329
-
-
Tan, E.K.1
Shen, H.2
Tan, L.C.3
-
23
-
-
18244394793
-
Clinical features of LRRK2-associated Parkinson's disease in central Norway
-
Aasly JO, Toft M, Fernandez-Mata I et al: Clinical features of LRRK2-associated Parkinson's disease in central Norway. Ann Neurol 2005; 57: 762-765.
-
(2005)
Ann Neurol
, vol.57
, pp. 762-765
-
-
Aasly, J.O.1
Toft, M.2
Fernandez-Mata, I.3
-
24
-
-
20444414834
-
Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation
-
Deng H, Le W, Guo Y, Hunter CB, Xie W, Jankovic J: Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation. Ann Neurol 2005; 57: 933-934.
-
(2005)
Ann Neurol
, vol.57
, pp. 933-934
-
-
Deng, H.1
Le, W.2
Guo, Y.3
Hunter, C.B.4
Xie, W.5
Jankovic, J.6
-
25
-
-
0026514953
-
Accuracy of clinical diagnosis of idiopathic Parkinson's disease: A clinico-pathological study of 100 cases
-
Hughes AJ, Daniel SE, Kilford L, Lees AJ: Accuracy of clinical diagnosis of idiopathic Parkinson's disease: A clinico-pathological study of 100 cases. J Neurol Neurosurg Psychiatry 1992; 55: 181-184.
-
(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
-
27
-
-
33645160640
-
The G6055A (G2019S) mutation in LRRK2 is frequent in both early - And late-onset Parkinson's disease and originates from a common ancestor
-
Goldwurm S, Di Fonzo A, Simons EJ et al: The G6055A (G2019S) mutation in LRRK2 is frequent in both early - and late-onset Parkinson's disease and originates from a common ancestor. J Med Genet 2005; 42: E65.
-
(2005)
J Med Genet
, vol.42
-
-
Goldwurm, S.1
Di Fonzo, A.2
Simons, E.J.3
-
28
-
-
22544465257
-
LRRK2 Haplotype analyses in European and North African families with Parkinson's disease: A common founder for the G2019S mutation dating from the 13th century
-
Lesage S, Leutenegger A-L, Ibanez P et al: LRRK2 Haplotype analyses in European and North African families with Parkinson's disease: A common founder for the G2019S mutation dating from the 13th century. Am J Hum Genet 2005; 77: 330-332.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 330-332
-
-
Lesage, S.1
Leutenegger, A.-L.2
Ibanez, P.3
-
29
-
-
0037032835
-
The protein kinase complement of the human genome
-
Manning G, Whyte DB, Martinez R, Hunter T, Sudarsanam S: The protein kinase complement of the human genome. Science 2002; 298: 1912-1934.
-
(2002)
Science
, vol.298
, pp. 1912-1934
-
-
Manning, G.1
Whyte, D.B.2
Martinez, R.3
Hunter, T.4
Sudarsanam, S.5
-
30
-
-
4444353636
-
Regulation of protein kinases; controlling activity through activation segment conformation
-
Nolen B, Taylor S, Ghosh G: Regulation of protein kinases; controlling activity through activation segment conformation. Mol Cell 2004; 15: 661-675.
-
(2004)
Mol Cell
, vol.15
, pp. 661-675
-
-
Nolen, B.1
Taylor, S.2
Ghosh, G.3
-
31
-
-
18444374405
-
Mutations of the BRAF gene in human cancer
-
Davies H, Bignell GR, Cox C et al: Mutations of the BRAF gene in human cancer. Nature 2002; 417: 949-954.
-
(2002)
Nature
, vol.417
, pp. 949-954
-
-
Davies, H.1
Bignell, G.R.2
Cox, C.3
-
32
-
-
2342605968
-
Autosomal dominant parkinsonism associated with variable synuclein and tau pathology
-
Wszolek ZK, Pfeiffer RF, Tsuboi Y et al: Autosomal dominant parkinsonism associated with variable synuclein and tau pathology. Neurology 2004; 62: 1619-1622.
-
(2004)
Neurology
, vol.62
, pp. 1619-1622
-
-
Wszolek, Z.K.1
Pfeiffer, R.F.2
Tsuboi, Y.3
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