Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Hui-Qin Lim"'
Publikováno v:
In Basal Ganglia June 2014 4(2):71-73
Publikováno v:
Parkinsonism & Related Disorders. 14:569-571
Co-existence of Parkinson's disease (PD) and essential tremor (ET) suggests a possible overlapping pathophysiology between these two conditions. PD patients with leucine-rich repeat kinase-2 ( LRRK2 ) mutations have been reported to present initially
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a2c273851124d7abc513c0e9fa4dd47
https://doi.org/10.1016/j.parkreldis.2007.12.003
https://doi.org/10.1016/j.parkreldis.2007.12.003
Autor:
Hui-Qin Lim, Yih Yuen, Jianjun Liu, Louis C.S. Tan, Stephanie Fook-Chong, R. Pavanni, Meng-Cheong Wong, Y. Zhao, Eng-King Tan, Jasinda H. Lee
Publikováno v:
Movement Disorders. 22:1816-1818
A common LRRK2 missense variant, Gly2385Arg, has been found to be a genetic risk factor for Parkinson's disease (PD) in ethnic Chinese and Japanese. However, the presence of the variant in other non-Chinese Asian patients has not been fully clarified
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c4faa8b96e612c91b8b27915fea3abf
https://doi.org/10.1002/mds.21658
https://doi.org/10.1002/mds.21658
Autor:
R. Pavanni, Meng-Ling Chen, R. Li, Yih Yuen, Hui-Qin Lim, Kumar M. Prakash, Ruey-Meei Wu, Chin-Hslen Lin, Yi Zhao, Louis C. Tan, Chun-Hwei Tai, Eng-King Tan
Publikováno v:
Human genetics. 126(3)
Mutations in the GIGYF2 gene at the PARK11 locus have recently been reported in Parkinson’s disease (PD). However, the pathogenicity of some of these mutations has been debated. We conducted a comprehensive genetic analysis of the entire GIGYF2 gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4de462ef7feb25e6e5b22dd014c9aaaf
https://pubmed.ncbi.nlm.nih.gov/19449032
https://pubmed.ncbi.nlm.nih.gov/19449032
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 23(5)
A heterozygous 2264C-->T variant (P755L) in LRRK2 gene has been reported to be a likely pathogenic variant among ethnic Chinese patients with Parkinson's disease (PD). In a case control study, we performed genetic analysis of the P755L variant in an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::790a33ee8d97ac4020f8d57a84503be6
https://pubmed.ncbi.nlm.nih.gov/18265005
https://pubmed.ncbi.nlm.nih.gov/18265005
Autor:
Yi Zhao, R. Pavanni, R. Li, Hui-Qin Lim, Kumar M. Prakash, Louis C. Tan, Michelle Tang, Eng-King Tan, Stephanie Fook-Chong, Yuen Yih
Publikováno v:
Human Genetics. 124:287-288
We showed that the frequency of a LRRK2 variant (c.4883G > C, R1628P) was higher in Parkinson’s disease (PD) compared to controls (8.4 vs. 3.4%, P = 0.046, OR 2.5, 95% CI 1.1–5.6). In the multivariate logistic regression (with adjustments made fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8abae91fb6d25035819e3302ea281a9
https://doi.org/10.1007/s00439-008-0544-2
https://doi.org/10.1007/s00439-008-0544-2
Autor:
Eng-King Tan, Chin-Hslen Lin, Chun-Hwei Tai, Tan, Louis C., Meng-Ling Chen, Li, R., Hui-Qin Lim, Pavanni, Ratnagopal, Yih Yuen, Prakash, K. M., Yi Zhao, Ruey-Meei Wu
Publikováno v:
Human Genetics; Sep2009, Vol. 126 Issue 3, p425-430, 6p, 3 Charts, 1 Graph