Clinical and molecular profiles of patients with Xia-Gibbs syndrome: a cohort in Japan [0.03%]
Xia- Gibbs综合征患者的临床和分子特征：日本队列研究
Hironao Shirai,Yoshiki Oitani,Eriko Nishi et al.
Hironao Shirai et al.
Background: Xia-Gibbs syndrome (XGS) is a rare neurodevelopmental disorder caused by pathogenic variants in the AT-hook DNA binding motif containing 1 (AHDC1) gene. More than 100 patients with XGS have been reported. In t...
A scoping review of functional near-infrared spectroscopy studies of reading development in children aged 6-12 [0.03%]
儿童阅读发展近红外光谱研究的范围回顾（年龄6-12岁）
Devon A Bode,Saisha S Rankaduwa,Laura M Elliott et al.
Devon A Bode et al.
Significance: Functional near-infrared spectroscopy (fNIRS) offers several advantages for neuroimaging in children, yet its use in research on cognitive development, particularly reading, remains limited. ...
Toward etiology-specific and radiomics-based approaches in cytotoxic lesions of the corpus callosum [0.03%]
向以病因特异性和影像组学为基础的脑室周围白质软化灶研究方法发展
Hasan Tekgül,Yavuz Ataş,Seda Kanmaz et al.
Hasan Tekgül et al.
Pediatric neuromyelitis optica spectrum disorders in Dakar: Insights from a preliminary multicentric case series in Senegal [0.03%]
达喀尔儿童视神经脊髓炎谱系病的初步多中心病例系列研究——来自塞内加尔的见解
Ndiaga Matar Gaye,Rokhaya Diagne,Khalifa Ababacar Mbaye et al.
Ndiaga Matar Gaye et al.
Aim: To describe the epidemiological, diagnostic, therapeutic, and outcome aspects of pediatric neuromyelitis optica spectrum disorders (NMOSD) in Dakar, Senegal. ...
A lipidation inhibitor rescues impaired neurite outgrowth caused by the CDC42 mutation associated with Takenouchi-Kosaki syndrome in Neuro2A cells [0.03%]
CDC42突变引起的Takenouchi-Kosaki综合征的神经元突起生长缺陷可以被脂基化抑制剂在Neuro2A细胞中挽救
Etsuko Daimon,Yukinao Shibukawa,Natsuko Yamazaki et al.
Etsuko Daimon et al.
Background: Takenouchi-Kosaki syndrome (TKS), caused by the CDC42 c.191A>G (p.Tyr64Cys; Y64C) variant, characterized by a range of clinical manifestations, including developmental delay with intellectual disability (ID). ...
Electroencephalogram abnormalities in children presenting with language development delay [0.03%]
语言发育迟缓儿童的脑电图异常
Merve Yavuz,Feyza Gülağız,Aycan Ünalp et al.
Merve Yavuz et al.
Background: EEG abnormalities are frequently reported in children with developmental language disorders, particularly in language-associated regions, though existing data remain inconsistent. ...
Neurocognitive profiles of attentional networks in children with Tic disorders [0.03%]
注意网络的神经认知特征在抽动障碍儿童中的表现
Xinyu Yang,Xiaofei Ye,Dandan Zheng et al.
Xinyu Yang et al.
Objective: Tic disorders (TD) are childhood-onset neurodevelopmental conditions marked by sudden, rapid, recurrent motor and/or vocal tics. This study aimed to investigate attentional network functioning in children with ...
The global research hotspots and future trends of infantile epileptic spasms syndrome: A bibliometric analysis of trends and themes [0.03%]
婴幼儿痉挛症研究热点及未来趋势的文献计量分析
Zhenzhen Wang,Danqing Hu,Xin Dong et al.
Zhenzhen Wang et al.
Objective: This study aims to investigate research trends, key contributors, and emerging topics in the field of infantile epileptic spasms syndrome (IESS). ...
Evaluation of perinatal arterial ischemic stroke patients: Underlying etiologic factors and long-term prognosis [0.03%]
围产期动脉缺血性卒中患者的病因及长期预后分析
Çisem Duman Kayar,Rıdvan Avcı,Fulya Kürekçi et al.
Çisem Duman Kayar et al.
Background: Perinatal arterial ischemic stroke (PAIS) is a major cause of long-term neurological impairments. Understanding its etiologic and prognostic factors is essential for improving outcomes. ...
Quantitative interpretation using ADC values for subjective MRI classification of neonatal hypoxic-ischemic encephalopathy [0.03%]
基于ADC值的新生儿缺氧缺血性脑病MRI主观分级的定量分析
Katsumi Hayakawa,Koichi Tanda,Masakazu Nishimoto et al.
Katsumi Hayakawa et al.
Background: MRI-based classification of hypoxic-ischemic encephalopathy (HIE), particularly using diffusion-weighted imaging (DWI), remains susceptible to subjective bias in determining the presence or absence of diffusio...