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2013 2
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Parkinson's disease GWAS-linked Park16 carriers show greater motor progression.
Deng X, Xiao B, Allen JC, Ng E, Foo JN, Lo YL, Tan LCS, Tan EK. Deng X, et al. J Med Genet. 2019 Nov;56(11):765-768. doi: 10.1136/jmedgenet-2018-105661. Epub 2019 Feb 27. J Med Genet. 2019. PMID: 30814270 Free PMC article.
Using longitudinal linear mixed model analysis, there was a greater rate of deterioration in the motor function as measured by the UPDRS scores compared with non-carriers after 5 years from the date of diagnosis (p=0.009). In addition, we demonstrated that PARK16 variant c …
Using longitudinal linear mixed model analysis, there was a greater rate of deterioration in the motor function as measured by the UPDRS …
Association analysis of PARK16-18 variants and Parkinson's disease in a Chinese population.
Zhou LL, Zhang X, Bao QQ, Liu RP, Gong MY, Mao GY, Zou M, Zhu JH. Zhou LL, et al. J Clin Neurosci. 2014 Jun;21(6):1029-32. doi: 10.1016/j.jocn.2013.09.015. Epub 2013 Nov 14. J Clin Neurosci. 2014. PMID: 24373818
However, rs11248051 or rs3129882 displayed no association with PD phenotypes or clinical scores. Our results suggest that rs11248051 and rs3129882 are risk factors for sporadic PD in a Chinese population, and their genetic interplay contributes to an elevated risk for PD p …
However, rs11248051 or rs3129882 displayed no association with PD phenotypes or clinical scores. Our results suggest that rs11248051 …
Distinct patterns of imprecise consonant articulation among Parkinson's disease, progressive supranuclear palsy and multiple system atrophy.
Tykalova T, Rusz J, Klempir J, Cmejla R, Ruzicka E. Tykalova T, et al. Brain Lang. 2017 Feb;165:1-9. doi: 10.1016/j.bandl.2016.11.005. Epub 2016 Nov 25. Brain Lang. 2017. PMID: 27894006
Here, the patterns and degree of consonant articulation deficits across voiced and voiceless stop plosives in 16 PD, 16 PSP, 16 MSA and 16 healthy control speakers were evaluated using acoustic and perceptual methods. Imprecise consonant articulation was observed across al …
Here, the patterns and degree of consonant articulation deficits across voiced and voiceless stop plosives in 16 PD, 16 PSP, 16 MSA and 16 h …
The effect of the PARK16 rs11240572 variant on brain structure in Parkinson's disease.
Gu LY, Dai SB, Zhou C, Gao T, Wu JJ, Fang Y, Guan XJ, Guo T, Zheng R, Jin C, Xu XJ, Song Z, Tian J, Yin X, Zhang MM, Zhang BR, Yan Y, Pu J. Gu LY, et al. Brain Struct Funct. 2021 Nov;226(8):2665-2673. doi: 10.1007/s00429-021-02359-9. Epub 2021 Aug 9. Brain Struct Funct. 2021. PMID: 34373950
In non-carriers, left basal ganglia GMV was positively correlated with UPDRS III (r = 0.365, p = 0.034) and bradykinesia (r = 0.352, p = 0.042), but negatively correlated with MMSE (r = - 0.344, p = 0.047), while in carriers negative correlation between basal ganglia GMV and MMSE …
In non-carriers, left basal ganglia GMV was positively correlated with UPDRS III (r = 0.365, p = 0.034) and bradykinesia (r = 0.352, p = 0.0 …
RAB7L1 interacts with LRRK2 to modify intraneuronal protein sorting and Parkinson's disease risk.
MacLeod DA, Rhinn H, Kuwahara T, Zolin A, Di Paolo G, McCabe BD, Marder KS, Honig LS, Clark LN, Small SA, Abeliovich A. MacLeod DA, et al. Neuron. 2013 Feb 6;77(3):425-39. doi: 10.1016/j.neuron.2012.11.033. Neuron. 2013. PMID: 23395371 Free PMC article.
Deficiency of the PARK16 locus gene RAB7L1 in primary rodent neurons, or of a RAB7L1 ortholog in Drosophila dopamine neurons, recapitulated degeneration observed with expression of a familial PD mutant form of LRRK2, whereas RAB7L1 overexpression rescued the LRRK2 mutant p …
Deficiency of the PARK16 locus gene RAB7L1 in primary rodent neurons, or of a RAB7L1 ortholog in Drosophila dopamine neurons, recapitulated …
Objective Measures of Swallowing Function Applied to the Dysphagia Population: A One Year Experience.
Kendall KA, Ellerston J, Heller A, Houtz DR, Zhang C, Presson AP. Kendall KA, et al. Dysphagia. 2016 Aug;31(4):538-46. doi: 10.1007/s00455-016-9711-0. Epub 2016 Apr 22. Dysphagia. 2016. PMID: 27106909
Reflux-related dysphagia (36 %), nonspecific pharyngeal dysphagia (24 %), Parkinson disease (16 %), esophageal abnormality (13 %), and brain insult (10 %) were the most common diagnoses. ...This preliminary study indicates that reflux disease is common in pat …
Reflux-related dysphagia (36 %), nonspecific pharyngeal dysphagia (24 %), Parkinson disease (16 %), esophageal abnormal …