-
1
-
-
33645116252
-
Genetics of Parkinson disease: Paradigm shifts and future prospects
-
Farrer MJ. Genetics of Parkinson disease: paradigm shifts and future prospects. Nat Rev Genet 2006;7:306-18.
-
(2006)
Nat Rev Genet
, vol.7
, pp. 306-18
-
-
Farrer, M.J.1
-
2
-
-
33746869343
-
Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease
-
Maraganore DM, de Andrade M, Elbaz A, et al. Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease. JAMA 2006;296:661-70.
-
(2006)
JAMA
, vol.296
, pp. 661-70
-
-
Maraganore, D.M.1
De Andrade, M.2
Elbaz, A.3
-
3
-
-
48949092066
-
Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease
-
Ross OA, Wu YR, Lee MC, et al. Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease. Ann Neurol 2008;64:88-92.
-
(2008)
Ann Neurol
, vol.64
, pp. 88-92
-
-
Ross, O.A.1
Wu, Y.R.2
Lee, M.C.3
-
4
-
-
33746079596
-
A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan
-
Di Fonzo A, Wu-Chou YH, Lu CS, et al. A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan. Neurogenetics 2006;7:133-8.
-
(2006)
Neurogenetics
, vol.7
, pp. 133-8
-
-
Di Fonzo, A.1
Wu-Chou, Y.H.2
Lu, C.S.3
-
5
-
-
0036196860
-
A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1
-
Funayama M, Hasegawa K, Kowa H, et al. 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
-
6
-
-
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;44:601-7.
-
(2004)
Neuron
, vol.44
, pp. 601-7
-
-
Zimprich, A.1
Biskup, S.2
Leitner, P.3
-
7
-
-
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
-
8
-
-
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;76:672-80.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 672-80
-
-
Kachergus, J.1
Mata, I.F.2
Hulihan, M.3
-
9
-
-
50049104725
-
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: A case-control study
-
Healy DG, Falchi M, O'Sullivan SS, et al. Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study. Lancet Neurol 2008;7:583-90.
-
(2008)
Lancet Neurol
, vol.7
, pp. 583-90
-
-
Healy, D.G.1
Falchi, M.2
O'Sullivan, S.S.3
-
10
-
-
31344432937
-
LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs
-
Lesage S, Durr A, Tazir M, et al. LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs. N Engl J Med 2006;354:422-3.
-
(2006)
N Engl J Med
, vol.354
, pp. 422-3
-
-
Lesage, S.1
Durr, A.2
Tazir, M.3
-
11
-
-
56149125336
-
Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?
-
Lesage S, Belarbi S, Troiano A, et al. Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease? Neurology 2008;71:1550-2.
-
(2008)
Neurology
, vol.71
, pp. 1550-2
-
-
Lesage, S.1
Belarbi, S.2
Troiano, A.3
-
12
-
-
48849092336
-
LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: A case-control genetic study
-
Hulihan MM, Ishihara-Paul L, Kachergus J, et al. LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study. Lancet Neurol 2008;7:591-4.
-
(2008)
Lancet Neurol
, vol.7
, pp. 591-4
-
-
Hulihan, M.M.1
Ishihara-Paul, L.2
Kachergus, J.3
-
13
-
-
27644455523
-
G2019S LRRK2 mutation in French and North African families with Parkinson's disease
-
Lesage S, Ibanez P, Lohmann E, et al. G2019S LRRK2 mutation in French and North African families with Parkinson's disease. Ann Neurol 2005;58:784-7.
-
(2005)
Ann Neurol
, vol.58
, pp. 784-7
-
-
Lesage, S.1
Ibanez, P.2
Lohmann, E.3
-
15
-
-
0026629509
-
What features improve the accuracy of clinical diagnosis in Parkinson's disease: A clinicopathologic study
-
Hughes AJ, Ben-Shlomo Y, Daniel SE, et al. What features improve the accuracy of clinical diagnosis in Parkinson's disease: a clinicopathologic study. Neurology 1992;42:1142-6.
-
(1992)
Neurology
, vol.42
, pp. 1142-6
-
-
Hughes, A.J.1
Ben-Shlomo, Y.2
Daniel, S.E.3
-
16
-
-
43649108353
-
Long-term outcome of 50 consecutive Parkinson's disease patients treated with subthalamic deep brain stimulation
-
Wider C, Pollo C, Bloch J, et al. Long-term outcome of 50 consecutive Parkinson's disease patients treated with subthalamic deep brain stimulation. Parkinsonism Relat Disord 2008;14:114-9.
-
(2008)
Parkinsonism Relat Disord
, vol.14
, pp. 114-9
-
-
Wider, C.1
Pollo, C.2
Bloch, J.3
-
17
-
-
77649173768
-
Longitudinal data analysis using generalized linear models
-
Liang KY, Zeger SL. Longitudinal data analysis using generalized linear models. Biometrika 1986;73:13-22.
-
(1986)
Biometrika
, vol.73
, pp. 13-22
-
-
Liang, K.Y.1
Zeger, S.L.2
-
18
-
-
33745713892
-
Rate of progression determines the clinical outcome after neural transplantation in Parkinson's disease
-
Linazasoro G. Rate of progression determines the clinical outcome after neural transplantation in Parkinson's disease. Brain 2006;129:E48.
-
(2006)
Brain
, vol.129
-
-
Linazasoro, G.1
-
19
-
-
52949152728
-
Levodopa-induced dyskinesias and their management
-
Del Sorbo F, Albanese A. Levodopa-induced dyskinesias and their management. J Neurol 2008;255(Suppl 4):32-41.
-
(2008)
J Neurol
, vol.255
, Issue.SUPPL. 4
, pp. 32-41
-
-
Del Sorbo, F.1
Albanese, A.2
-
20
-
-
0035068574
-
Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36
-
Valente EM, Bentivoglio AR, Dixon PH, et al. Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36. Am J Hum Genet 2001;68:895-900.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 895-900
-
-
Valente, E.M.1
Bentivoglio, A.R.2
Dixon, P.H.3
-
21
-
-
7044236967
-
PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations
-
Hatano Y, Sato K, Elibol B, et al. PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations. Neurology 2004;63:1482-5.
-
(2004)
Neurology
, vol.63
, pp. 1482-5
-
-
Hatano, Y.1
Sato, K.2
Elibol, B.3
-
22
-
-
22044432781
-
Early-onset parkinsonism associated with PINK1 mutations: Frequency, genotypes, and phenotypes
-
Bonifati V, Rohe CF, Breedveld GJ, et al. Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes. Neurology 2005;65:87-95.
-
(2005)
Neurology
, vol.65
, pp. 87-95
-
-
Bonifati, V.1
Rohe, C.F.2
Breedveld, G.J.3
-
23
-
-
33244482539
-
Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa
-
Ibanez P, Lesage S, Lohmann E, et al. Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa. Brain 2006;129:686-94.
-
(2006)
Brain
, vol.129
, pp. 686-94
-
-
Ibanez, P.1
Lesage, S.2
Lohmann, E.3
|