Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Neurodegenerative Diseases and GBA[original query] |
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Genetic association study of glucocerebrosidase gene L444P mutation in essential tremor and multiple system atrophy in mainland China. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2012 Nov . Sun QY, Guo JF, Han WW, Zuo X, Wang L, Yao LY, Pan Q, Xia K, Yan XX, Tang BS |
Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies. Human molecular genetics 2014 Dec 23 (23): 6139-46. Bras Jose, Guerreiro Rita, Darwent Lee, Parkkinen Laura, Ansorge Olaf, Escott-Price Valentina, Hernandez Dena G, Nalls Michael A, Clark Lorraine N, Honig Lawrence S, Marder Karen, Van Der Flier Wiesje M, Lemstra Afina, Scheltens Philip, Rogaeva Ekaterina, St George-Hyslop Peter, Londos Elisabet, Zetterberg Henrik, Ortega-Cubero Sara, Pastor Pau, Ferman Tanis J, Graff-Radford Neill R, Ross Owen A, Barber Imelda, Braae Anne, Brown Kristelle, Morgan Kevin, Maetzler Walter, Berg Daniela, Troakes Claire, Al-Sarraj Safa, Lashley Tammaryn, Compta Yaroslau, Revesz Tamas, Lees Andrew, Cairns Nigel, Halliday Glenda M, Mann David, Pickering-Brown Stuart, Dickson Dennis W, Singleton Andrew, Hardy Jo |
Heterogeneity among patients with Parkinson's disease: cluster analysis and genetic association. Journal of the neurological sciences 2015 Apr 351 (1-2): 41-5. Ma Ling-Yan, Chan Piu, Gu Zhu-Qin, Li Fang-Fei, Feng T |
Identification of susceptibility loci for cognitive impairment in a cohort of Han Chinese patients with Parkinson's disease. Neuroscience letters 2020 May 135034. Liu Hong-Jun, Li Xiao-Yan, Chen Hui, Yu Hui-Li, Tao Qing-Qing, Wu Zhi-Yi |
Posterior Cortical Atrophy phenotype in a GBA N370S mutation carrier: a case report. BMC neurology 2021 Jan 21 (1): 17. Picillo Marina, Scannapieco Sara, Iavarone Alessandro, Ginevrino Monia, Valente Enza Maria, Barone Pao |
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