Reply: Wheelchair use in genetically confirmed FSHD1 from a large cohort study in Chinese population-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Reply: Wheelchair use in genetically confirmed FSHD1 from a large cohort study in Chinese population

Published:2022-03-18 Issue:6 Volume:145 Page:e55-e56
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:

Author:

Katz Natalie K¹,Hogan John²,Delbango Ryan²,Cernik Colin³,Tawil Rabi⁴,Statland Jeffrey M⁵

Affiliation:

1. Department of Neurology, Children’s Mercy Hospital , Kansas City, MO 64118 , USA

2. Department of Artificial Intelligence, AIbytes, LLC , Hurley, NY 12443 , USA

3. Department of Biostatistics, University of Kansas Medical Center , Kansas City, KS 66160 , USA

4. Department of Neurology, University of Rochester Medical Center , Rochester, NY 14642 , USA

5. Department of Neurology, University of Kansas Medical Center , Kansas City, KS 66160 , USA

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

https://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awac098/43780767/awac098.pdf

Reference3 articles.

1. Wheelchair use in genetically-confirmed FSHD1 from a large cohort study in Chinese population;Qiu;Brain.,2022

2. Risk of functional impairment in Facioscapulohumeral muscular dystrophy;Statland;Muscle Nerve,2014

3. Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype;Ricci;Ann Neurol,1999

同舟云学术

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