International Journal of Developmental Neuroscience This is an RSS file. You can use it to subscribe to this data in your favourite RSS reader or to display this data on your own website or blog.

Experience of treatment in critical Guillain-Barre Syndrome case after COVID-19 vaccination
CONCLUSIONS: For patients with previous radiculitis, COVID-19 vaccination may increase the susceptibility to GBS. Thus, it is recommended to extend the vaccination interval for these patients and ensure that any potential increased risk is continually assessed.PMID:38590219 | DOI:10.1002/jdn.10325 (Source: International Journal of Developmental Neuroscience)
Source: International Journal of Developmental Neuroscience - April 9, 2024 Category: Neuroscience Authors: Chunying Zhu Huan Wang Yingfu Zhang Wentao Wang Jia Wang Wei Li Source Type: research

Gut-brain barrier dysfunction bridge autistic-like behavior in mouse model of maternal separation stress: A behavioral, histopathological, and molecular study
Int J Dev Neurosci. 2024 Apr 7. doi: 10.1002/jdn.10329. Online ahead of print.ABSTRACTAutism spectrum disorder (ASD) is a fast-growing neurodevelopmental disorder throughout the world. Experiencing early life stresses (ELS) like maternal separation (MS) is associated with autistic-like behaviors. It has been proposed that disturbance in the gut-brain axis-mediated psychiatric disorders following MS. The role of disruption in the integrity of gut-brain barrier in ASD remains unclear. Addressing this knowledge gap, in this study we aimed to investigate role of the gut-brain barrier integrity in mediating autistic-like behavi...
Source: International Journal of Developmental Neuroscience - April 7, 2024 Category: Neuroscience Authors: Negin Rowshan Maryam Anjomshoa Anahita Farahzad Elham Bijad Hossein Amini-Khoei Source Type: research

Compound heterozygous mutations in three Chinese patients of Segawa syndrome and their treatment outcomes
Int J Dev Neurosci. 2024 Apr 2. doi: 10.1002/jdn.10328. Online ahead of print.ABSTRACTSegawa syndrome is a rare autosomal recessive form of dopa-responsive dystonia resulting from TH gene dysfunction. Patients typically exhibit symptoms such as generalized dystonia, rigidity, tremors, infantile Parkinsonism, and pseudo-spastic paraplegia. Levodopa is often an effective treatment. Due to its rarity, high heterogeneity, and poorly understood pathological mutation and phenotype spectrums, as well as genotype-phenotype and genotype-treatment outcome correlations, Segawa syndrome poses diagnostic and therapeutic challenges. In ...
Source: International Journal of Developmental Neuroscience - April 3, 2024 Category: Neuroscience Authors: Jie Zhang Yaxin Huang Yulei Hu Bing Bai Source Type: research

Single nucleotide polymorphisms of ANKK1, DDR4, and GRIN2B genes predict behavior in a prospective cohort of Mexican children and adolescents
This study explores the links between SNPs in candidate genes involved in central nervous system (CNS) physiology and their implications for the behavioral and emotional aspects in children and teenagers. A total of 590 participants, aged 7-15 years, from the Early Life Exposures In Mexico To Environmental Toxicants (ELEMENT) cohort study in Mexico City, underwent genotyping for at least one of 15 CNS gene-related SNPs at different timepoints. We employed multiple linear regression models to assess the potential impact of genetic variations on behavioral and cognitive traits, as measured by the Behavioral Assessment System...
Source: International Journal of Developmental Neuroscience - March 26, 2024 Category: Neuroscience Authors: Barbara Moctezuma Ángel Santiago Ana Burguete-Garc ía Jesus Mart ínez-Barnetche Claudia Morales-G ómez Carmen Hernandez-Chavez Gabriela Gil Karen E Peterson Martha M Tellez-Rojo Hector Lamadrid-Figueroa Source Type: research