Výsledky vyhledávání

Predicting cognitive impairment in outpatients with epilepsy using machine learning techniques

Autor: Han Lin, Han Jiarui, Ji-lan Lin, Shenggen Chen, Wanhui Lin, Feng Lin, Xianyang Chen, Chaofeng Zhu, Huapin Huang, Xue Teng

Publikováno v: Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Scientific Reports

Many studies report predictions for cognitive function but there are few predictions in epileptic patients; therefore, we established a workflow to efficiently predict outcomes of both the Mini-Mental State Examination (MMSE) and Montreal Cognitive A

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b27ae93ae40afe10a81209fb4be0b1c4
https://doaj.org/article/d06ade1ce43f4535aa529274a46757e4

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Sequencing of neurofilament genes identified NEFH Ser787Arg as a novel risk variant of sporadic amyotrophic lateral sclerosis in Chinese subjects

Autor: Ji-lan Lin, Chaodong Wang, Wanhui Lin, Junge Zhu, Zhanjun Wang, Feng Lin, Xu-Ying Li, Huapin Huang, Chaofeng Zhu

Publikováno v: BMC Medical Genomics, Vol 14, Iss 1, Pp 1-8 (2021)
BMC Medical Genomics

Background Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease with neuronal cell inclusions composed of neurofilaments and other abnormal aggregative proteins as pathological hallmarks. Approximately 90% of patients have s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e79ebbdb8e8572b979fa58f00dbe9b2
https://doaj.org/article/cd0b5198e3b1446ca8569dc63bcc28d2

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Novel Variants in the FIG4 Gene Associated With Chinese Sporadic Amyotrophic Lateral Sclerosis With Slow Progression

Autor: Chang-Yun Liu, Ji-Lan Lin, Shu-Yan Feng, Chun-Hui Che, Hua-Pin Huang, Zhang-Yu Zou

Publikováno v: Journal of Clinical Neurology (Seoul, Korea)

Background and Purpose Mutations in the FIG4 gene have been linked to amyotrophic lateral sclerosis (ALS) type 11 in Caucasian populations. The purpose of this study was to identify FIG4 variants in a cohort of 15 familial ALS (FALS) indexes and 275

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5718db20fba1c642aede4de7d9183995
https://doi.org/10.3988/jcn.2022.18.1.41

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Seizure-induced 5-HT release and chronic impairment of serotonergic function in rats

Autor: Huapin Huang, Ji-lan Lin, Chun-Hui Che, Wanhui Lin, Xiaochai Lv, Shenggen Chen, Ming-xing Lin

Publikováno v: Neuroscience Letters. 534:1-6

We analyzed the dynamic concentration change of serotonin (5-HT) and its main metabolite 5-hydroxyindoleacetic acid (5-HIAA) within the epileptic hippocampus in rats. Seizure was induced by systemic injection of pilocarpine (320mg/kg, i.p.). Using el

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8efd2a4236278d80969199ce8f5b3677
https://doi.org/10.1016/j.neulet.2012.12.007

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[Analysis of CLCN1 gene mutations in 2 patients with myotonia congenita]

Autor: Zhi-ting, Chen, Jin, He, Wan-jin, Chen, Sheng-gen, Chen, Ji-lan, Lin, Qin-yong, Ye, Hua-pin, Huang

Publikováno v: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 29(6)

To investigate chloride channel 1 (CLCN1) gene mutation and clinical features of 2 Chinese patients with myotonia congenita.Clinical data of a patient from a family affected with myotonia congenita in addition with a sporadic patient from Fujian prov

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::11ae901859120611189e617337bf90cd
https://pubmed.ncbi.nlm.nih.gov/23225051

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