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期刊名:International journal of developmental neuroscience

缩写:INT J DEV NEUROSCI

ISSN:0736-5748

e-ISSN:1873-474X

IF/分区:1.4/Q4

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共收录本刊相关文章索引1585条
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Qi Zhang,Ying Ren,Song Su et al. Qi Zhang et al.
Background: The cohesin complex is a multifunctional unit that plays a crucial role in DNA repair, replication, chromosome segregation, and gene expression. Dysfunctions in this complex can lead to a spectrum of developme...
Rahul Bharat,Uzaina Uzaina,Kakoli Das et al. Rahul Bharat et al.
Parents of children with autism spectrum disorder (ASD) often encounter significant challenges in accessing timely diagnosis and appropriate support services. This study explores the experiences of parents navigating autism-related services...
Jiali Luo,Junjiao Ping,Jing Wan et al. Jiali Luo et al.
Background: Accumulating evidence suggests that dysregulated inflammatory signalling pathway plays a crucial role in the development and pathogenesis of clinical features in schizophrenia. SOCS3, a key regulator of inflam...
Zeynep Soy,Mevhibe Saricaoglu,Ozden Erkan Ogul et al. Zeynep Soy et al.
This study aims to examine the impact of anodal transcranial direct stimulation (tDCS) targeting the cerebellum (CER) and the supplementary motor area (SMA) on both balance function and resting-state beta activity. A cohort of 28 healthy yo...
Jianxi Liu,Nannan Xia,Kang Hu et al. Jianxi Liu et al.
Background and purpose: An understanding of the modular structure of brain functional networks and their changes with age is beneficial in uncovering the neural mechanisms that underlie cognitive decline during the ageing...
Sema Öznur Çeltik,Arif Önder,Berhan Akdağ et al. Sema Öznur Çeltik et al.
This study aimed to evaluate serum levels of matrix metalloproteinase-9 (MMP-9), telomerase, sirtuin-1 (SIRT1) and nitric oxide (NO) in children diagnosed with cognitive disengagement syndrome (CDS). The sample included 22 children with 'pu...
Turgay Cokyaman,Zeynep Alara Saltik,Nihan Ecmel Turan Turgay Cokyaman
Pathogenic variants of sacsin (SACS) gene cause autosomal recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS). It is a hereditary neurological disorder manifested with gait ataxia, intentional tremor, lower limb pyramidal signs and pes...
Risa Kagaya,Hiroyuki Maki,Hiroshi Matsuda et al. Risa Kagaya et al.
Background: This study aimed to assess cerebrocerebellar connectivity in patients with hemimegalencephaly (HME) using 18F-fluorodeoxyglucose positron emission tomography (FDG-PET) and diffusion tensor imaging (DTI), as un...
Miguel López-Zamora,Nadia Porcar-Gozalbo,Isabel López-Chicheri et al. Miguel López-Zamora et al.
Prematurity has been linked to an increased risk of neurodevelopmental disorders, including dyslexia, due to neonatal complications that can impact brain maturation, such as intraventricular haemorrhage, periventricular leukomalacia and res...
Pinar Ozkan Kart,Cihad Özdemir,Temel Kayikcioglu et al. Pinar Ozkan Kart et al.
Objective: The aim of this study was to examine the possible effect of HFOs detected in children with SeLECTS, who have rolandic spikes with or without ADHD, in predicting cognitive comorbidities with the fully automatic ...