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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
Sevgi Beyazgül,Shahla Shafaati Laleh Sevgi Beyazgül
Background: Neonatal sleep is critical for brain maturation and autonomic nervous system regulation. Disruptions in sleep patterns and vagal tone may contribute to the risk of sudden infant death syndrome (SIDS). ...
Song Su,Yuexia Bai,Yi Lu et al. Song Su et al.
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder, with plexiform neurofibromas occurring in approximately 20%-50% of patients. A 12-year-old girl underwent surgery due to unbearable pain caused by diffuse neurofibrom...
Sergio Melgarejo,Gabriela Reyes Valenzuela,Matías Juanes et al. Sergio Melgarejo et al.
The HECW2 gene, essential for neurodevelopment, plays a critical role in maintaining cellular homeostasis and regulating key pathways in the nervous system. Deleterious variants in the HECW2 gene have been associated with developmental dela...
Gamze Sarıkaya Uzan,Ali Han Yaramış,Ece Sönmezler et al. Gamze Sarıkaya Uzan et al.
Objective: Pontocerebellar hypoplasia (PCH) encompasses a heterogeneous group of neurodevelopmental disorders, currently comprising 28 subtypes listed in the Online Mendelian Inheritance in Man (OMIM) database (as of May ...
Fen Zhao,Xizan Yue,Guangyu Wang et al. Fen Zhao et al.
Background: Neurofibromatosis type 1 (NF1) is an autosomal dominant neurocutaneous syndrome. NF1-related vasculopathy represents a clinically significant yet underrecognized complication. Moyamoya syndrome, a rare cerebro...
Dilsu Dicle Erkan,Oğuz Lafcı,Ülkühan Öztoprak et al. Dilsu Dicle Erkan et al.
Hereditary spastic paraplegia (HSP) represents a genetically heterogeneous group of neurodegenerative disorders characterized by progressive axonal degeneration of corticospinal upper motor neurons, leading to lower limb-predominant spastic...
Kalliopi Megari,Dimitra V Katsarou,Evangelos Mantsos et al. Kalliopi Megari et al.
Background: Cancer is one of the most lethal chronic diseases, which has been the reason for the majority of losses of lives globally. Adolescents with cancer experience a lower quality of life compared to both their heal...