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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
Rong Li,Sudhanshu Sahu Rong Li
Reelin, an extracellular matrix glycoprotein, plays important roles in neural development. Mutation-induced loss of its functions in mammals leads to severe disorders associated with impaired motor coordination, tremors and ataxia. Little i...
Savas Baris,Cuneyd Yavas Savas Baris
Spastic paraplegia-67, caused by a defect in glycosylphosphatidylinositol (GPI) biosynthesis, is an autosomal recessive neurodevelopmental disorder. It is characterized by dysmorphic features, spasticity, brain abnormalities, hypotonia, imp...
Ayşe Çiğel,Oya Sayın,Seren Gülşen Gürgen et al. Ayşe Çiğel et al.
Introduction: Traumatic brain injury (TBI) is a major public health problem and an essential cause of morbidity and mortality during childhood. The aim of this study was to evaluate the apoptotic effects of MK-801, a nonc...
Zahra Shaddel,Morteza Zendehdel,Hamed Zarei et al. Zahra Shaddel et al.
Relaxin-3 is a member of a structurally related peptide superfamily that includes relaxin and insulin-like peptide hormones, which play a role in regulating stress, memory, nutrition, pregnancy and childbirth, mental illnesses, including an...
Morgan Botdorf,Zehua Cui,Tracy Riggins Morgan Botdorf
Abuse and maltreatment have been associated with negative effects on the developing brain through the hypothalamic-pituitary-adrenal (HPA) axis, the body's central stress response system. Theoretically, similar pathophysiology occurs when c...
Hilal Aydin,Zeynep Esener,Hilmi Bolat et al. Hilal Aydin et al.
Glucose transporter type 1 deficiency syndrome (GLUT1DS) affects all age groups, from infants to adolescents, and involves age-specific symptoms. Nonclassic GLUT1 DS is observed in 10% of cases, in which seizures are not observed, and the c...
Ourida Loumi,Christian R Andres Ourida Loumi
Autism spectrum disorder (ASD) affects more than 80,000 children under the age of 18 in Algeria, making it a major public health problem. It is characterized by communication abnormalities, restricted and stereotyped behaviours and resistan...
Jianhui Zhao,Luzhuang Li,Dianrong Sun et al. Jianhui Zhao et al.
Sotos syndrome is an autosomal dominant disorder resulting from pathogenic variants of the NSD1 gene. In this study, we present five Chinese paediatric cases, including two previously unreported NSD1 variants: a nonsense mutation (c.1486A >...
Concetto Puzzo,Maurizio Oggiano,Micaela Capobianco et al. Concetto Puzzo et al.
In developmental-age kids with specific-learning-disabilities (SLD), functional illiteracy entails poor logical reasoning; in those with attention-deficit/hyperactivity disorder (ADHD), a deficit in prospective memory results in difficulty ...