期刊文献+
共找到2篇文章
< 1 >
每页显示 20 50 100
Gangliosides in nervous system development,regeneration,and pathologies 被引量:1
1
作者 Juliana F.Vasques Renata Guedes de Jesus Gonçalves +3 位作者 Almir Jordão da Silva-Junior Robertta Silva Martins Fernanda Gubert Rosalia Mendez-Otero 《Neural Regeneration Research》 SCIE CAS CSCD 2023年第1期81-86,共6页
Gangliosides,sialic acid-containing sphingolipids,are major constituents of neuronal membranes.According to the number of sialic acids and the structure of the oligosaccharide chain,gangliosides can be classified as s... Gangliosides,sialic acid-containing sphingolipids,are major constituents of neuronal membranes.According to the number of sialic acids and the structure of the oligosaccharide chain,gangliosides can be classified as simple or complex and grouped in different ganglio-series.Hundreds of gangliosides have been identified in vertebrate cells,with different expression patterns during development and related to several physiological processes,especially in the nervous system.While GD3 and its O-acetylated form,9acGD3,are highly expressed in early developmental stages,GM1,GD1a,GD1b,and GT1b are the most abundant ganglioside species in the mature nervous system.Mutations in enzymes involved in ganglioside metabolism can lead to the accumulation of specific species,a condition termed gangliosidosis and usually marked by severe neurological impairment.Changes in ganglioside levels have also been described in several neurodegenerative diseases,such as Alzheimer’s and Parkinson’s.In this review,we summarized recent information about the roles of GD3,9acGD3,GM1,GD1a,GD1b,GT1b,and other ganglioside species in nervous system development and regeneration,as well as clinical trials evaluating possible therapeutic applications of these molecules. 展开更多
关键词 9acGD3 GANGLIOSIDES GD1a gd1b GD3 GLYCOLIPIDS GM1 GM2 GM3 GM4 GT1b
下载PDF
男性幼儿双下肢无力1周伴眼睑下垂3d 被引量:1
2
作者 郎长会 田茂强 束晓梅 《中国当代儿科杂志》 CAS CSCD 北大核心 2022年第8期923-927,共5页
患儿1岁7个月,以双下肢无力、眼睑下垂起病,呈进行性加重并出现呼吸不规则。神经系统体格检查:嗜睡状,双眼睑下垂,双上肢肌力4级,双下肢肌力3级,腱反射消失。实验室检查提示脑脊液蛋白细胞分离,H反射消失,血清抗GD1b抗体IgG阳性。最终... 患儿1岁7个月,以双下肢无力、眼睑下垂起病,呈进行性加重并出现呼吸不规则。神经系统体格检查:嗜睡状,双眼睑下垂,双上肢肌力4级,双下肢肌力3级,腱反射消失。实验室检查提示脑脊液蛋白细胞分离,H反射消失,血清抗GD1b抗体IgG阳性。最终该患儿诊断为吉兰-巴雷综合征(Guillain-Barrésyndrome,GBS)、Miller-Fisher综合征与Bickerstaff脑干脑炎重叠综合征,治疗上予免疫球蛋白、血浆置换、呼吸支持等治疗后患儿恢复出院。儿童GBS、Miller-Fisher综合征与Bickerstaff脑干脑炎重叠综合征可同时出现周围神经及脑干损害,临床异质性强,其中抗GD1b抗体相关的GBS、Miller-Fisher综合征与Bickerstaff脑干脑炎重叠综合征有特殊临床表现及复杂神经电生理变化,诊断较困难。因此对有双下肢乏力、眼睑下垂患儿尽早完善神经传导速度检查,重点关注H反射。 展开更多
关键词 MILLER-FISHER综合征 吉兰-巴雷综合征 BICKERSTAFF脑干脑炎 gd1b抗体 上睑下垂 幼儿
下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部