LRRK2 in Parkinson’s disease: genetic and clinical studies from patients
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Title
LRRK2 in Parkinson’s disease: genetic and clinical studies from patients
Authors
Keywords
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Journal
FEBS Journal
Volume 276, Issue 22, Pages 6455-6463
Publisher
Wiley
Online
2009-10-06
DOI
10.1111/j.1742-4658.2009.07344.x
References
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Related references
Note: Only part of the references are listed.- LRRK2 and neurodegeneration
- (2009) Gabriel Santpere et al. ACTA NEUROPATHOLOGICA
- LRRK2 G2385R modulates age at onset in Parkinson's disease: A multi-center pooled analysis
- (2009) E.K. Tan et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- Ashkenazi Parkinson’s disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries
- (2009) Anat Bar-Shira et al. NEUROGENETICS
- Lrrk2 R1441G-related Parkinson’s disease: evidence of a common founding event in the seventh century in Northern Spain
- (2009) Ignacio F. Mata et al. NEUROGENETICS
- Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease
- (2008) Owen A. Ross et al. ANNALS OF NEUROLOGY
- Lrrk2 R1628P in non-Chinese Asian races
- (2008) Eng-King Tan et al. ANNALS OF NEUROLOGY
- Uniting Chinese across Asia: the LRRK2 Gly2385Arg risk variant
- (2008) E. K. Tan et al. EUROPEAN JOURNAL OF NEUROLOGY
- LRRK2 R1628P increases risk of Parkinson’s disease: replication evidence
- (2008) E. K. Tan et al. HUMAN GENETICS
- Leucine-rich repeat kinase 2 (LRRK2): A key player in the pathogenesis of Parkinson's disease
- (2008) Payal N. Gandhi et al. JOURNAL OF NEUROSCIENCE RESEARCH
- Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
- (2008) Daniel G Healy et al. LANCET NEUROLOGY
- The LRRK2 Arg1628Pro variant is a risk factor for Parkinson’s disease in the Chinese population
- (2008) Chin-Song Lu et al. NEUROGENETICS
- LRRK2 G2019S and R1441G mutations associated with Parkinson’s disease are common in the Basque Country, but relative prevalence is determined by ethnicity
- (2008) A. Gorostidi et al. NEUROGENETICS
- Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease
- (2008) K. Haugarvoll et al. NEUROLOGY
- Hyposmia in G2019S LRRK2-related parkinsonism: Clinical and pathologic data
- (2008) L. Silveira-Moriyama et al. NEUROLOGY
- Progression of dopaminergic dysfunction in a LRRK2 kindred: A multitracer PET study
- (2008) R. Nandhagopal et al. NEUROLOGY
- Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism
- (2008) Owen A. Ross et al. PARKINSONISM & RELATED DISORDERS
- Myocardial123metaiodobenzylguanidine uptake in genetic Parkinson's disease
- (2007) Aldo Quattrone et al. MOVEMENT DISORDERS
- Case control analysis of LRRK2 Gly2385Arg in Alzheimer's disease
- (2007) E.K. Tan et al. NEUROBIOLOGY OF AGING
- A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease
- (2007) L. Warren et al. PARKINSONISM & RELATED DISORDERS
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