Progressive dystonia symptomatic of juvenile GM2 gangliosidosis
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Reference29 articles.
1. The gangliosidoses. In: eds. The metabolic basis of inherited diseases. 6th edition. New York: McGraw-Hill, 1989: 1807-1842.
2. The clinical spectrum of hexosaminidase deficiency diseases
3. Juvenile spinal muscular atrophy: A new hexosaminidase deficiency phenotype
4. Hexosaminidase-A Deficiency Presenting as Atypical Juvenile-onset Spinal Muscular Atrophy
5. Chronic GM2 gangliosidosis masquerading as atypical Friedreich ataxia: Clinical, morphologic, and biochemical studies of nine cases
Cited by 34 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Role of Botulinum Toxin in Treatment of Secondary Dystonia: A Case Series and Overview of Literature;Toxins;2024-06-24
2. Abnormally accumulated GM2 ganglioside contributes to skeletal deformity in Tay-Sachs disease mice;2024-02-16
3. Clinical and genetic features of a case with juvenile onset sandhoff disease;BMC Neurology;2023-06-21
4. Neurodegeneration with progressive dystonia: Juvenile-onset Tay–Sachs disease;Annals of Indian Academy of Neurology;2022
5. Metabolic Disorders With Associated Movement Abnormalities;Movement Disorders in Childhood;2022
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3