-
1
-
-
50049104725
-
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: A case-control study
-
International LRRK2 Consortium
-
Healy DG, Falchi M, O'Sullivan SS, et al; International LRRK2 Consortium. Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study. Lancet Neurol 2008;7:583-590.
-
(2008)
Lancet Neurol
, vol.7
, pp. 583-590
-
-
Healy, D.G.1
Falchi, M.2
O'Sullivan, S.S.3
-
2
-
-
80051505298
-
Phenotype in parkinsonian and nonparkinsonian LRRK2 G2019S mutation carriers
-
Marras C, Schüle B, Munhoz RP, et al. Phenotype in parkinsonian and nonparkinsonian LRRK2 G2019S mutation carriers. Neurology 2011;77:325-333.
-
(2011)
Neurology
, vol.77
, pp. 325-333
-
-
Marras, C.1
Schüle, B.2
Munhoz, R.P.3
-
3
-
-
81955164797
-
Clinical and brain imaging characteristics in leucine-rich repeat kinase 2-associated PD and asymptomatic mutation carriers
-
Brockmann K, Gröger A, Di Santo A, et al. Clinical and brain imaging characteristics in leucine-rich repeat kinase 2-associated PD and asymptomatic mutation carriers. Mov Disord 2011;26:2335-2342.
-
(2011)
Mov Disord
, vol.26
, pp. 2335-2342
-
-
Brockmann, K.1
Gröger, A.2
Di Santo, A.3
-
4
-
-
34147125812
-
Evaluation of LRRK2 G2019S penetrance: Relevance for genetic counseling in Parkinson disease
-
Goldwurm S, Zini M, Mariani L, et al. Evaluation of LRRK2 G2019S penetrance: relevance for genetic counseling in Parkinson disease. Neurology 2007;68:1141-1143.
-
(2007)
Neurology
, vol.68
, pp. 1141-1143
-
-
Goldwurm, S.1
Zini, M.2
Mariani, L.3
-
5
-
-
81955167499
-
High frequency and reduced penetrance of LRRK2 G2019S mutation among Parkinson's disease patients in Cantabria (Spain)
-
Sierra M, González-Aramburu I, Sánchez-Juan P, et al. High frequency and reduced penetrance of LRRK2 G2019S mutation among Parkinson's disease patients in Cantabria (Spain). Mov Disord 2011;26:2343-2346.
-
(2011)
Mov Disord
, vol.26
, pp. 2343-2346
-
-
Sierra, M.1
González-Aramburu, I.2
Sánchez-Juan, P.3
-
6
-
-
0038147327
-
Movement disorders Society Scientific Issues Committee report: Sic Task Force appraisal of clinical diagnostic criteria for parkinsonian disorders
-
Movement Disorders Society Scientific Issues Committee
-
Litvan I, Bhatia KP, Burn DJ, et al; Movement Disorders Society Scientific Issues Committee. Movement disorders Society Scientific Issues Committee report: SIC Task Force appraisal of clinical diagnostic criteria for parkinsonian disorders. Mov Disord 2003;18:467-486.
-
(2003)
Mov Disord
, vol.18
, pp. 467-486
-
-
Litvan, I.1
Bhatia, K.P.2
Burn, D.J.3
-
7
-
-
0042591659
-
The Unified Parkinson's Disease Rating Scale (UPDRS): Status and recommendations
-
Movement Disorder Society Task Force on Rating Scales for Parkinson's Disease
-
Movement Disorder Society Task Force on Rating Scales for Parkinson's Disease. The Unified Parkinson's Disease Rating Scale (UPDRS): status and recommendations. Mov Disord 2003;18:738-750.
-
(2003)
Mov Disord
, vol.18
, pp. 738-750
-
-
-
9
-
-
79955081027
-
Substantia nigra hyperechogenicity with LRRK2 G2019S mutations
-
Brüggemann N, Hagenah J, Stanley K, et al. Substantia nigra hyperechogenicity with LRRK2 G2019S mutations. Mov Disord 2011;26:885-888.
-
(2011)
Mov Disord
, vol.26
, pp. 885-888
-
-
Brüggemann, N.1
Hagenah, J.2
Stanley, K.3
-
10
-
-
34548150884
-
Cross-sectional study discloses a positive family history for Parkinson's disease and male gender as epidemiological risk factors for substantia nigra hyperechogenicity
-
Schweitzer KJ, Behnke S, Liepelt I, et al. Cross-sectional study discloses a positive family history for Parkinson's disease and male gender as epidemiological risk factors for substantia nigra hyperechogenicity. J Neural Transm 2007;114:1167-1171.
-
(2007)
J Neural Transm
, vol.114
, pp. 1167-1171
-
-
Schweitzer, K.J.1
Behnke, S.2
Liepelt, I.3
-
11
-
-
76949094278
-
Transcranial sonography for diagnosis of Parkinson's disease
-
Mehnert S, Reuter I, Schepp K, Maaser P, Stolz E, Kaps M. Transcranial sonography for diagnosis of Parkinson's disease. BMC Neurol 2010;10:9.
-
(2010)
BMC Neurol
, vol.10
, pp. 9
-
-
Mehnert, S.1
Reuter, I.2
Schepp, K.3
Maaser, P.4
Stolz, E.5
Kaps, M.6
-
12
-
-
72849145914
-
Transcranial ultrasound as a risk marker for Parkinson's disease
-
Berg D. Transcranial ultrasound as a risk marker for Parkinson's disease. Mov Disord 2009;24:S677-S683.
-
(2009)
Mov Disord
, vol.24
-
-
Berg, D.1
-
13
-
-
18144397394
-
Five-year follow-up study of hyperechogenicity of the substantia nigra in Parkinson's disease
-
Berg D, Merz B, Reiners K, Naumann M, Becker G. Five-year follow-up study of hyperechogenicity of the substantia nigra in Parkinson's disease. Mov Disord 2005;20:383-385.
-
(2005)
Mov Disord
, vol.20
, pp. 383-385
-
-
Berg, D.1
Merz, B.2
Reiners, K.3
Naumann, M.4
Becker, G.5
-
15
-
-
0038408929
-
Olfaction in neurodegenerative disorder
-
Hawkes C. Olfaction in neurodegenerative disorder. Mov Disord 2003;18:364-372.
-
(2003)
Mov Disord
, vol.18
, pp. 364-372
-
-
Hawkes, C.1
-
16
-
-
84859834711
-
Lewy pathology and neurodegeneration in premotor Parkinson's disease
-
Del Tredici K, Braak H. Lewy pathology and neurodegeneration in premotor Parkinson's disease. Mov Disord 2012;27:597-607.
-
(2012)
Mov Disord
, vol.27
, pp. 597-607
-
-
Del Tredici, K.1
Braak, H.2
-
17
-
-
77952998970
-
Olfactory dysfunction, Central cholinergic integrity and cognitive impairment in Parkinson's disease
-
Bohnen NI, Müller ML, Kotagal V, et al. Olfactory dysfunction, central cholinergic integrity and cognitive impairment in Parkinson's disease. Brain 2010;133:1747-1754.
-
(2010)
Brain
, vol.133
, pp. 1747-1754
-
-
Bohnen, N.I.1
Müller, M.L.2
Kotagal, V.3
-
18
-
-
80051513364
-
Olfactory dysfunction in LRRK2 G2019S mutation carriers
-
Saunders-Pullman R, Stanley K, Wang C, et al. Olfactory dysfunction in LRRK2 G2019S mutation carriers. Neurology 2011;77:319-324.
-
(2011)
Neurology
, vol.77
, pp. 319-324
-
-
Saunders-Pullman, R.1
Stanley, K.2
Wang, C.3
-
19
-
-
80052962219
-
Olfactory deficits and cardiac 123I-MIBG in Parkinson's disease related to the LRRK2 R1441G and G2019S mutations
-
Ruiz-Martínez J, Gorostidi A, Goyenechea E, et al. Olfactory deficits and cardiac 123I-MIBG in Parkinson's disease related to the LRRK2 R1441G and G2019S mutations. Mov Disord 2011;26:2026-2031.
-
(2011)
Mov Disord
, vol.26
, pp. 2026-2031
-
-
Ruiz-Martínez, J.1
Gorostidi, A.2
Goyenechea, E.3
-
21
-
-
64549084210
-
A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations
-
French Parkinson's Disease Genetics Study Group
-
Lohmann E, Leclere L, De Anna F, et al; French Parkinson's Disease Genetics Study Group. A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations. Parkinsonism Relat Disord 2009;15:273-276.
-
(2009)
Parkinsonism Relat Disord
, vol.15
, pp. 273-276
-
-
Lohmann, E.1
Leclere, L.2
De Anna, F.3
-
22
-
-
79959814706
-
123I-MIBG cardiac uptake and smell identification in parkinsonian patients with LRRK2 mutations
-
Valldeoriola F, Gaig C, Muxí A, et al. 123I-MIBG cardiac uptake and smell identification in parkinsonian patients with LRRK2 mutations. J Neurol 2011;258:1126-1132.
-
(2011)
J Neurol
, vol.258
, pp. 1126-1132
-
-
Valldeoriola, F.1
Gaig, C.2
Muxí, A.3
-
23
-
-
0037333666
-
Staging of brain pathology related to sporadic Parkinson's disease
-
Braak H, Del Tredici K, Rüb U, de Vos RA, Jansen Steur EN, Braak E. Staging of brain pathology related to sporadic Parkinson's disease. Neurobiol Aging 2003;24:197-211.
-
(2003)
Neurobiol Aging
, vol.24
, pp. 197-211
-
-
Braak, H.1
Del Tredici, K.2
Rüb, U.3
De Vos, R.A.4
Jansen Steur, E.N.5
Braak, E.6
-
24
-
-
84859846991
-
Defining at-risk populations for Parkinson's disease: Lessons from ongoing studies
-
Berg D, Marek K, Ross GW, Poewe W. Defining at-risk populations for Parkinson's disease: lessons from ongoing studies. Mov Disord 2012;27:656-665.
-
(2012)
Mov Disord
, vol.27
, pp. 656-665
-
-
Berg, D.1
Marek, K.2
Ross, G.W.3
Poewe, W.4
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