Autosomal-recessive syndrome with alopecia, hypogonadism, progressive extra-pyramidal disorder, white matter disease, sensory neural deafness, diabetes mellitus, and low IGF1
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference27 articles.
1. Diagnostic reliability of a single IGF-I measurement in 237 adults with total anterior hypopituitarism and severe GH deficiency
2. Primary hypogonadism and partial alopecia in three sibs with Müllerian hypoplasia in the affected females
3. Muscle Force and Endurance in Untreated and Human Growth Hormone or Insulin-Like Growth Factor-l-Treated Patients with Growth Hormone Deficiency or Laron Syndrome
4. Is IGF binding protein-3 assessment helpful for the diagnosis of GH deficiency?
5. A familial syndrome of deafness, alopecia, and hypogonadism
Cited by 45 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. Woodhouse-Sakati syndrome: A review;Revue Neurologique;2024-02
2. Nine Hereditary Movement Disorders First Described in Asia: Their History and Evolution;Journal of Movement Disorders;2023-09-30
3. Three Siblings With Woodhouse-Sakati Syndrome: A Case Report of A New Saudi Family;Cureus;2022-12-05
4. Woodhouse-Sakati Syndrome Presenting With Psychotic Features After Starting Trihexyphenidyl: A Case Report;Cureus;2022-08-01
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