2026-10-02 · 12 篇
乌干达CMV流行人群中先天性巨细胞病毒感染的患病率
Prevalence of Congenital Cytomegalovirus Infection in a CMV-Endemic Ugandan Population.
NF2相关神经鞘瘤病（NF2-SWN）中前庭神经鞘瘤对氯沙坦的反应：病例系列研究
Response of Vestibular Schwannomas in NF2-Related Schwannomatosis (NF2-SWN) to Losartan: A Case Series.
成人人工耳蜗植入：长期听觉剥夺后的结局
Cochlear implants in adults: outcomes in prolonged auditory deprivation.
大剂量核黄素对Brown-Vialetto-Van Laere综合征的显著疗效：一例病例报告
Excellent response to high-dose Riboflavin in Brown-Vialetto-Van Laere syndrome: A case report.
双侧剑伤样硬斑病伴双侧眼部受累及听力损失：一例罕见病例报告并文献复习。
Bilateral en coup de sabre with bilateral ophthalmic involvement and hearing loss: A rare case report with review of literature.
天气变量与睡眠结构之间的关联：一项使用消费者睡眠数据的大规模分析
Associations between weather variables and sleep architecture: A large-scale analysis using consumer sleep data.
病例报告：与亚急性甲状腺炎相关的颅内高压
Case Report: Intracranial hypertension occurring in association with subacute thyroiditis.
AI辅助、以缺陷为导向的运动干预后肥胖儿童身体成分和姿势控制的改善
Improvements in body composition and postural control in children with obesity following an AI-assisted, deficit-oriented exercise intervention.
病例报告：由新型复合杂合FBXO7变异引起的新生儿起病帕金森-锥体综合征
Case Report: Neonatal-onset parkinsonian-pyramidal syndrome caused by novel compound heterozygous FBXO7 variants.
瑞美吉泮治疗眩晕相关前庭和耳蜗症状：一项真实世界回顾性研究
Rimegepant for vestibular and cochlear symptoms associated with vertigo in a real-world retrospective study.
17α-羟化酶/17,20-裂解酶缺陷症扩展的基因型-表型谱：九例系列报道，包括一种新发突变、疑似TART样病变及多系统受累
Extended genotype-phenotype spectrum of 17α-hydroxylase/17,20-lyase deficiency: a nine-case series featuring a novel mutation, suspected TART-like lesions, and multisystem involvement.
一例成人起病原发性侧索硬化样综合征患者中的ATP1A3 p.Arg995His新发变异
A De Novo ATP1A3 p.Arg995His Variant in a Patient With an Adult-Onset Primary Lateral Sclerosis-Like Syndrome.