-
1
-
-
0032497504
-
Parkinson's disease. First of two parts
-
Lang AE, Lozano AM. Parkinson's disease. First of two parts. N Engl J Med 1998;339:1044-1053.
-
(1998)
N Engl J Med
, vol.339
, pp. 1044-1053
-
-
Lang, A.E.1
Lozano, A.M.2
-
2
-
-
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
-
3
-
-
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
-
4
-
-
39749165843
-
Role of heterozygous mutations in Parkinson's disease genes
-
Hedrich K, Klein C, Rogaeva E, et al. Role of heterozygous mutations in Parkinson's disease genes. Lancet Neurol 2007;69:140-147.
-
(2007)
Lancet Neurol
, vol.69
, pp. 140-147
-
-
Hedrich, K.1
Klein, C.2
Rogaeva, E.3
-
5
-
-
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;354:422-423.
-
(2006)
N Engl J Med
, vol.354
, pp. 422-423
-
-
Lesage, S.1
Durr, A.2
Tazir, M.3
-
6
-
-
31344439221
-
LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews
-
Ozelius LJ, Senthil G, Saunders-Pullman R, et al. LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews. N Engl J Med 2006;354:424-425.
-
(2006)
N Engl J Med
, vol.354
, pp. 424-425
-
-
Ozelius, L.J.1
Senthil, G.2
Saunders-Pullman, R.3
-
7
-
-
0035940582
-
Improved accuracy of clinical diagnosis of Lewy body Parkinson's disease
-
Hughes AJ, Daniel SE, Lees AJ. Improved accuracy of clinical diagnosis of Lewy body Parkinson's disease. Neurology 2001;57:1497-1499.
-
(2001)
Neurology
, vol.57
, pp. 1497-1499
-
-
Hughes, A.J.1
Daniel, S.E.2
Lees, A.J.3
-
8
-
-
24644431901
-
LRRK2 gene in Parkinson's Disease: Mutation analysis and case control association study
-
Paisan-Ruiz C, Lang AE, Kawarai T, et al. LRRK2 gene in Parkinson's 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
-
9
-
-
0036895446
-
Language lateralization in monozygotic twin pairs concordant and discordant for handedness
-
Sommer IE, Ramsey NF, Mandl RC, Kahn RS. Language lateralization in monozygotic twin pairs concordant and discordant for handedness. Brain 2002;125:2710-2718.
-
(2002)
Brain
, vol.125
, pp. 2710-2718
-
-
Sommer, I.E.1
Ramsey, N.F.2
Mandl, R.C.3
Kahn, R.S.4
-
10
-
-
28544446980
-
G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort
-
Bras JM, Guerreiro RJ, Ribeiro MH, et al. G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort. Mov Disord 2005;20:1653-1655.
-
(2005)
Mov Disord
, vol.20
, pp. 1653-1655
-
-
Bras, J.M.1
Guerreiro, R.J.2
Ribeiro, M.H.3
-
11
-
-
33646271123
-
Parkinson's disease and LRRK2: Frequency of a common mutation in U.S. movement disorder clinics
-
Kay DM, Zabetian CP, Factor SA, et al. Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics. Mov Disord 2006;21:519-523.
-
(2006)
Mov Disord
, vol.21
, pp. 519-523
-
-
Kay, D.M.1
Zabetian, C.P.2
Factor, S.A.3
-
12
-
-
33750305328
-
Recurrent LRRK2 (Park8) mutations in early-onset Parkinson's disease
-
Hedrich K, Winkler S, Hagenah J, et al. Recurrent LRRK2 (Park8) mutations in early-onset Parkinson's disease. Mov Disord 2006;21:1506-1510.
-
(2006)
Mov Disord
, vol.21
, pp. 1506-1510
-
-
Hedrich, K.1
Winkler, S.2
Hagenah, J.3
-
13
-
-
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
-
14
-
-
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;58:784-787.
-
(2005)
Ann Neurol
, vol.58
, pp. 784-787
-
-
Lesage, S.1
Ibanez, P.2
Lohmann, E.3
-
15
-
-
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
-
16
-
-
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
-
17
-
-
0037422553
-
Color and genomic ancestry in Brazilians
-
Parra FC, Amado RC, Lambertucci JR, Rocha J, Antunes CM, Pena SD. Color and genomic ancestry in Brazilians. Proc Natl Acad Sci USA 2003;100:177-182.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 177-182
-
-
Parra, F.C.1
Amado, R.C.2
Lambertucci, J.R.3
Rocha, J.4
Antunes, C.M.5
Pena, S.D.6
-
18
-
-
28544441181
-
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: Clinical, pathological, olfactory and functional imaging and genetic data
-
Khan NL, Jain S, Lynch JM, et al. Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data. Brain 2005;128:2786-2796.
-
(2005)
Brain
, vol.128
, pp. 2786-2796
-
-
Khan, N.L.1
Jain, S.2
Lynch, J.M.3
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