Retraction Note: Impact of flexible assertive community treatment model (FACT) on community rehabilitation of schizophrenia in Southern China [0.03%]
撤回 notice: 关于灵活的肯定社区治疗模式(FACT)对中国南部精神分裂症患者社区康复的影响
Yinglin Zhao,Shaoxiong Zheng,Handi Zhang et al.
Yinglin Zhao et al.
Genetic and expressional insights into the association of TRAPPC10 variants with neurodevelopmental disorders [0.03%]
TRAPPC10变异与神经发育障碍的遗传和表达研究见解
Peng-Yu Wang,Wen-Hui Liu,Yu-Jie Gu et al.
Peng-Yu Wang et al.
Correction to: Gene-gene interaction network analysis indicates CNTN2 is a candidate gene for idiopathic generalized epilepsy [0.03%]
基因-基因互作网络分析表明CNTN2是特发性全面性癫痫的候选基因
Zhi-Jian Lin,Jun-Wei He,Sheng-Yin Zhu et al.
Zhi-Jian Lin et al.
Published Erratum
Neurogenetics. 2025 Jan 28;26(1):24. DOI:10.1007/s10048-025-00802-1 2025
Phenotypic variability in progressive encephalopathy with brain atrophy and thin corpus callosum: insights from two families [0.03%]
脑萎缩和穹隆纤细进行性脑病的表型变异：来自两个家系的启示
Busra Aynekin,Sinan Akbaş,Ayten Gulec et al.
Busra Aynekin et al.
The cytoskeleton, composed of microtubules, intermediate filaments and actin filaments is vital for various cellular functions, particularly within the nervous system, where microtubules play a key role in intracellular transport, cell morp...
Case Reports
Neurogenetics. 2025 Jan 24;26(1):23. DOI:10.1007/s10048-025-00799-7 2025
The molecular mechanism of nitric oxide in memory consolidation and its role in the pathogenesis of memory-related disorders [0.03%]
一氧化氮在记忆巩固中的分子机制及其在记忆相关障碍疾病发病机制中的作用
Zainab I Bahdar,Ejlal Abu-El-Rub,Rawan Almazari et al.
Zainab I Bahdar et al.
Memory is a dynamic process of encoding, storing, and retrieving information. It includes sensory, short-term, and long-term memory, each with unique characteristics. Nitric oxide (NO) is a biological messenger synthesized on demand by neur...
Neuroinflammation and neurodegeneration in Huntington's disease: genetic hallmarks, role of metals and organophosphates [0.03%]
亨廷顿舞蹈病的神经炎症和神经退行性病变：遗传标志、金属元素及有机磷化合物的作用
Omkar Kumar Kunwar,Shamsher Singh
Omkar Kumar Kunwar
Huntington's disease (HDs) is a fatal, autosomal dominant, and hereditary neurodegenerative disorder characterized by progressive motor dysfunction, cognitive decline, and psychiatric disturbances. HD is well linked to mutation in the HTT g...
Neuronal ceroid lipofuscinosis 11 (CLN11) presenting with early-onset cone-rod dystrophy and learning difficulties [0.03%]
以早发性视锥视杆营养不良和学习困难为表现的神经元 ceroid 溶酶体贮积症 11 型 (CLN11)
Gustavo Maximiano-Alves,Renata do Amaral Moreto Caravelas,Trajano Aguiar Pires Gonçalves et al.
Gustavo Maximiano-Alves et al.
Neuronal Ceroid Lipofuscinosis 11 (CLN11) is an ultra-rare subtype of adult-onset Neuronal Ceroid Lipofuscinosis. Its phenotype is variable and not fully known. A 21-year-old man was evaluated in our neurogenetic outpatient clinic for early...
Case Reports
Neurogenetics. 2025 Jan 15;26(1):20. DOI:10.1007/s10048-025-00800-3 2025
ATXN2 polyglutamine intermediate repeats length expansions in Malaysian patients with amyotrophic lateral sclerosis (ALS) [0.03%]
马来亚Lou Gehrig病患者中ATXN2多聚谷氨酰胺中间重复序列长度的扩大变异
Suzanna Edgar,Nurul Angelyn Zulhairy-Liong,Melina Ellis et al.
Suzanna Edgar et al.
Intermediate CAG repeats from 29 to 33 in the ATXN2 gene contributes to the risk of amyotrophic lateral sclerosis (ALS) in European and Asian populations. In this study, 148 ALS patients of multiethnic descent: Chinese (56.1%), Malay (24.3%...
Novel compound heterozygous mutations in the LARS2 gene in a Chinese family with hearing loss [0.03%]
LARS2基因新杂合突变导致的一家系听力损失表型分析
Mengyi Lu,Kai Zhou,Xiuyun Yang et al.
Mengyi Lu et al.
Background: Mutations in the LARS2 gene are correlated with Perrault syndrome, a rare autosomal recessive genetic disorder, that is typically characterized by sensorineural hearing loss and ovarian insufficiency. ...
Case Reports
Neurogenetics. 2025 Jan 7;26(1):17. DOI:10.1007/s10048-024-00797-1 2025
Computational modeling design of novel NMDAR agonist for the treatment of Schizophrenia [0.03%]
新型NMDAR激活剂的计算机模拟设计用于治疗精神分裂症
Amena Khatun Manica,Mariam Omowunmi Daud,Michael Olanrewaju Faloyo et al.
Amena Khatun Manica et al.
Schizophrenia (SZ) is a complex, chronic mental disorder characterized by positive symptoms (such as delusions and hallucinations), negative symptoms (including anhedonia, alogia, avolition, and social withdrawal), and cognitive deficits (a...