Genotype-phenotype correlations in a chinese population with familial amyotrophic lateral sclerosis

WC Liu, XG Li, Y Sun, XT Yu, Y Wang, N Liu… - Neurological …, 2022 - Taylor & Francis
Objective This study aimed to determine the distribution of the most commonly mutated
genes (SOD1, TARDBP, FUS/TLS, and C9ORF72) associated with familial amyotrophic …

Genetic Analysis of the ZNF512B, SLC41A1, and ALDH2 Polymorphisms in Parkinson's Disease in the Iranian Population

F Madadi, MS Khaniani, EE Shandiz… - Genetic testing and …, 2016 - liebertpub.com
Aims: Parkinson's disease (PD) is one of the most common neurodegenerative disorders; its
etiology includes both genetic and environmental factors and their interactions. The …

[HTML][HTML] The clinical assessment of amyotrophic lateral sclerosis patients' prognosis by ZNF512B gene, neck flexor muscle power score and body mass index (BMI)

CJ Yu, L Wang, SL Mao, Y Zhang, LL Song, LY Cai… - BMC neurology, 2018 - Springer
Background Assessment on the prognosis of amyotrophic lateral sclerosis (ALS) is
becoming a focus of research in recent years since there is no effective treatment. The aim of …

Meta-analysis of the association between ZNF512B polymorphism rs2275294 and risk of amyotrophic lateral sclerosis

P Ning, X Yang, B Yang, Q Zhao, H Huang, R An… - Neurological …, 2018 - Springer
Amyotrophic lateral sclerosis (ALS), the most common motor neuron disease, appears to
result from the combination of genetic and environmental factors. Whether the rs2275294 …

肌萎缩侧索硬化中锌指蛋白512B 基因, 颈屈肌肌力, 体重指数的意义

宋玲玲, 俞春江 - 中国临床神经科学, 2016 - cqvip.com
肌萎缩侧索硬化是一种同时累及上, 下运动神经元的进行性神经系统变性疾病.
肌萎缩侧索硬化患者生存时间短, 病死率高, 其病因及发病机制不明确, 目前尚无有效治疗方法 …

Comment on: Factors associated with increased pain in primary dysmenorrhea: analysis through a multivariate ordered logistic regression model

S Khazaei, SM Hanis, K Mansori - Journal of Pediatric and …, 2017 - jpagonline.org
We read the article written by Marıa I. Tomás-Rodrıguez and colleagues published in the
Journal of Pediatric and Adolescent Gynecology. Their purpose was to determine possible …

Difficulty in determining the association of a single nucleotide polymorphism in the ZNF512B gene with the risk and prognosis of amyotrophic lateral sclerosis

S Tetsuka - 臨床神経学, 2017 - jstage.jst.go.jp
The advent of next-generation sequencing technology is expected to accelerate the
identification of novel genes, and this technology will likely supersede Sanger sequencing …

Lack of association between the P413L variant of chromogranin B and ALS risk or age at onset: a meta-analysis

X Yang, S Li, D Xing, P Li, C Li, L Qi, Y Xu… - … Lateral Sclerosis and …, 2018 - Taylor & Francis
Background: Amyotrophic lateral sclerosis (ALS), the most common motor neuron disease,
is thought to result from interaction of genetic and environmental risk factors. Whether the …