Rare forms of autosomal recessive neurodegenerative ataxia
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Pediatrics, Perinatology and Child Health
Reference77 articles.
1. Neuromyopathy and vitamin E deficiency in man;Burck;Neuropediatrics,1981
2. Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping;Ben Hamida;Nat Genet,1993
3. Friedreich’s ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families;Ben Hamida;Neurology,1993
4. Ataxia with isolated vitamin E deficiency;Cavalier;Am J Hum Genet,1998
5. Friedreich-like ataxia with retinitis pigmentosa caused by the His101Gln mutation of the alpha-tocopherol transfer protein gene;Yokota;Ann Neurol,1997
Cited by 41 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. First case of Autosomal recessive spastic ataxia of Charlevoix-Saguenay in the Middle east;2024-09-02
2. Autosomal and X-Linked Degenerative Ataxias: From Genetics to Promising Therapeutics;Contemporary Clinical Neuroscience;2023
3. Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies;Orphanet Journal of Rare Diseases;2022-05-12
4. Clinical features and molecular genetics of autosomal recessive ataxia in the Turkish population;Journal of Pediatric Neurosciences;2020
5. The Hepatic Fate of Vitamin E;Vitamin E in Health and Disease;2018-10-24
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