期刊： NEUROPEDIATRICS, 2020; 51 (1)
Muscular dystrophy-dystroglycanopathies (MDDG) are a group of genetically heterogeneous autosomal recessive disorders characterized by hypoglycosylati......
期刊： NEUROPEDIATRICS, 2020; 51 (1)
Microtubule dynamics plays a crucial role in neuronal development and function. Variants in the tubulin cofactor D ( TBCD ) gene, which encodes one of......
期刊： NEUROPEDIATRICS, 2020; 51 (3)
Familial hemiplegic migraine type 2 (FHM2) is an autosomal dominant inheritance disorder caused by ATP1A2 mutation, and the clinical spectrum is heter......
期刊： NEUROPEDIATRICS, 2020; 51 (5)
The congenital myasthenia syndromes (CMS) are a group of autosomal recessive or autosomal dominant diseases that affect neuromuscular junctions. CMS c......
期刊： NEUROPEDIATRICS, 2019; 50 (2)
Anti-N-methyl-D-aspartate receptor encephalitis (anti-NMDARe) was originally described as a paraneoplastic disease with more than 50% cases involving ......
期刊： NEUROPEDIATRICS, 2018; 49 (3)
Cerebral cavernous malformations (CMs) are vascular malformations affecting any part of the central nervous system. Clinical data and surgical outcome......
期刊： NEUROPEDIATRICS, 2018; 49 (5)
Objective Shunt dependency syndrome after cyst-peritoneal (CP) shunt is a rare but serious complication which leads to increased intracranial pressure......
期刊： NEUROPEDIATRICS, 2017; 48 (6)
Background The unfolded protein response (UPR) includes three cascade pathways, which are responsible for the elimination of overload protein that is ......
期刊： NEUROPEDIATRICS, 2022; 53 (3)
Objective We aimed to analyze the angioarchitecture characters and changes after combined bypass surgery (CBS) in pediatric moyamoya disease (MMD). Me......
期刊： NEUROPEDIATRICS, 2022; 53 (2)
Background Autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy is an inflammatory central nervous system (CNS) disorder that usually pres......
期刊： NEUROPEDIATRICS, 2022; 53 (1)
Background Streptococcus pneumoniae is an important cause of pediatric meningitis. Objective The aim of this study was to analyze the clinical feature......
期刊： NEUROPEDIATRICS, 2022; 53 (6)
Introduction Focal cortical dysplasia (FCD) is a most common cause of intractable focal epilepsy in children. Surgery is considered as a radical optio......
