Cargando…

Analysis of genetic polymorphisms associated with leukoaraiosis in the southern Chinese population: A case–control study

Leukoaraiosis (LA) is a frequent neuroimaging finding commonly observed on brain MRIs of elderly people with prevalence ranging from 50% to 100%. Multiple susceptibility genes or genetic risk factors for LA have been identified in subjects of European descent. Here, we report the first replication s...

Descripción completa

Detalles Bibliográficos
Autores principales:	Huang, Wen-Qing, Ye, Hui-Ming, Li, Fang-Fang, Yi, Ke-Hui, Zhang, Ya, Cai, Liang-Liang, Lin, Hui-Nuan, Lin, Qing, Tzeng, Chi-Meng
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer Health 2016
Materias:	5300
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008527/ https://www.ncbi.nlm.nih.gov/pubmed/27583843 http://dx.doi.org/10.1097/MD.0000000000003857

Ejemplares similares

DNA Methylation Profiling Reveals the Change of Inflammation-Associated ZC3H12D in Leukoaraiosis
por: Huang, Wen-Qing, et al.
Publicado: (2018)

Incidence and risk factors of leukoaraiosis from 4683 hospitalized patients: A cross-sectional study
por: Lin, Qing, et al.
Publicado: (2017)

Effects of citicoline therapy on the network connectivity of the corpus callosum in patients with leukoaraiosis
por: Feng, Liang, et al.
Publicado: (2017)

The Associations of PMF1, ICAM1, AGT, TRIM65, FBF1, and ACOX1 Variants With Leukoaraiosis in Chinese Population
por: Huang, Wen-Qing, et al.
Publicado: (2019)

Correlation between prefrontal-striatal pathway impairment and cognitive impairment in patients with leukoaraiosis
por: Wang, Shuangkun, et al.
Publicado: (2017)

The association of uric acid with leukoaraiosis
por: Li, Jun-Jing, et al.
Publicado: (2016)

Perimesencephalic nonaneurysmal subarachnoid hemorrhage caused by transverse sinus thrombosis: A case report and review of literature
por: Fu, Fang-Wang, et al.
Publicado: (2017)

Correlation between Calpain-10 single-nucleotide polymorphisms and obstructive sleep apnea/hypopnoea syndrome with ischemic stroke in a Chinese population: A population-based study
por: Zhang, Wei, et al.
Publicado: (2017)

Gray Matter Loss and Related Functional Connectivity Alterations in A Chinese Family With Benign Adult Familial Myoclonic Epilepsy
por: Zeng, Ling-Li, et al.
Publicado: (2015)

Systolic Blood Pressure Variability is a Novel Risk Factor for Rebleeding in Acute Subarachnoid Hemorrhage: A Case–Control Study
por: Lin, Qing-Song, et al.
Publicado: (2016)

APOE Polymorphism Affects Brain Default Mode Network in Healthy Young Adults: A STROBE Article
por: Su, Yun Yan, et al.
Publicado: (2015)

Relationship between annualized case volume and in-hospital motality in subarachnoid hemorrhage: A systematic review and meta-analysis
por: Huang, Jian-Yi, et al.
Publicado: (2021)

Genetic mutation analysis of hereditary spastic paraplegia: A retrospective study
por: Cui, Fang, et al.
Publicado: (2020)

Correlation study of CYP2C19 gene polymorphism and clopidogrel resistance in Han Chinese patients with cerebral infarction in Guizhou region
por: Shi, Guo-Xian, et al.
Publicado: (2021)

BDNF Val66Met Polymorphism on Functional MRI During n-Back Working Memory Tasks
por: Chen, Chih-Chung, et al.
Publicado: (2015)

Examining the Association Between Quadriceps Strength and Cognitive Performance in the Elderly
por: Chen, Wei-Liang, et al.
Publicado: (2015)

Pathogenic variants of PROC gene caused type II activity deficiency in a Chinese family: A case report
por: Zhu, Hui, et al.
Publicado: (2021)

The effectiveness and safety of dual antiplatelet therapy in ischemic cerebrovascular disease with intracranial and extracranial arteriostenosis in Chinese patients: A randomized and controlled trail
por: Zuo, Feng-Tong, et al.
Publicado: (2017)

Interhemispheric Connectivity in Drug-Naive Benign Childhood Epilepsy With Centrotemporal Spikes: Combining Function and Diffusion MRI
por: Wu, Yun, et al.
Publicado: (2015)

TNFAIP3 gene rs7749323 polymorphism is associated with late onset myasthenia gravis
por: Yang, Hong-Wei, et al.
Publicado: (2017)

PI3K polymorphism in patients with sporadic Parkinson’s disease
por: Su, Jiali, et al.
Publicado: (2022)

Tonifying spleen and replenishing kidney method of traditional Chinese medicine for myasthenia gravis: A protocol for systematic review and meta-analysis
por: Lu, Bibo, et al.
Publicado: (2021)

Pathogenesis and research progress in leukoaraiosis
por: Sun, Lingqi, et al.
Publicado: (2022)

Early Statin Use and the Progression of Alzheimer Disease: A Total Population-Based Case-Control Study
por: Lin, Feng-Cheng, et al.
Publicado: (2015)

Extranodal natural killer/T-cell lymphoma nasal type with central nervous system involvement mimicked tuberculous meningitis: A case report
por: Yang, Yina, et al.
Publicado: (2019)

Sympathetic skin response and heart rate variability in predicting autonomic disorders in patients with Parkinson disease
por: Ke, Jiang-Qiong, et al.
Publicado: (2017)

Study on optimization and evaluation system of traditional Chinese medicine rehabilitation program for swallowing disorder after stroke
por: Tang, Qiang, et al.
Publicado: (2021)

A case of cerebral hyperperfusion following spontaneous recanalization of occluded middle cerebral artery: Reperfusion injury or true cerebral hyperperfusion syndrome?
por: Xu, Ziqi, et al.
Publicado: (2017)

Pathophysiology of Small-Fiber Sensory System in Parkinson's Disease: Skin Innervation and Contact Heat Evoked Potential
por: Lin, Chin-Hsien, et al.
Publicado: (2016)

Efficacy and Safety of Topiramate for Essential Tremor: A Meta-Analysis of Randomized Controlled Trials
por: Chang, Kuo-Hsuan, et al.
Publicado: (2015)

Susceptibility Weighted Imaging (SWI) Recommended as a Regular Magnetic Resonance Diagnosis for Vascular Dementia to Identify Independent Idiopathic Normal Pressure Hydrocephalus Before Ventriculo-Peritoneal (V-P) Shunt Treatment: A Case Study
por: Huang, Wen-Qing, et al.
Publicado: (2019)

Electromyographic study assessing swallowing function in subacute stroke patients with respiratory muscle weakness
por: Liaw, Mei-Yun, et al.
Publicado: (2021)

Single nucleotide polymorphisms in the non-coding region of STIM1 gene are associated with Parkinson disease risk in Chinese Han population
por: Lou, Danning, et al.
Publicado: (2020)

Contactin-associated protein-2 and anti-aquaporin-4 antibody positive autoimmune encephalitis secondary to herpes simplex encephalitis: A case report
por: Zhang, Lin-Ming, et al.
Publicado: (2023)

STK39, But Not BST1, HLA-DQB1, and SPPL2B Polymorphism, Is Associated With Han-Chinese Parkinson's Disease in Taiwan
por: Chang, Kuo-Hsuan, et al.
Publicado: (2015)

Early enteral nutrition supplemented with probiotics improved the clinical outcomes in severe head injury: Some promising findings from Chinese patients
por: Yi, Li-Juan, et al.
Publicado: (2019)

Calcified extra-axial cavernous malformation arising from lower cranial nerves: A case report and literature review
por: Ke, Daibo, et al.
Publicado: (2021)

Inter-practitioner comparisons of nerve conduction studies with standardized techniques in normal subjects: Reap as you sow
por: Zhao, Bing, et al.
Publicado: (2020)

The effects of paroxetine therapy on depressive symptom and motor function in the treatment of depression with Parkinson’s disease: A meta-analysis
por: Jiang, Li-Lin, et al.
Publicado: (2023)

The Association Between Genetic Polymorphism rs703842 in CYP27B1 and Multiple Sclerosis: A Meta-Analysis
por: Jiang, Tao, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_46fn864joucmkf7c7c89unkig3