Development of a patient-reported outcome measure for upper limb function in Duchenne muscular dystrophy: DMD Upper Limb PROM-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Development of a patient-reported outcome measure for upper limb function in Duchenne muscular dystrophy: DMD Upper Limb PROM

Published:2016-09-26 Issue:2 Volume:59 Page:224-231
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:Dev Med Child Neurol

Author:

Klingels K¹²,Mayhew A G³,Mazzone E S⁴,Duong T⁵,Decostre V⁶,Werlauff U⁷,Vroom E⁸,Mercuri E⁴,Goemans N M⁹,

Affiliation:

1. Department of Rehabilitation Sciences; KU Leuven; Leuven Belgium

2. Rehabilitation Research Center (REVAL); Biomed; Hasselt University; Diepenbeek Belgium

3. John Walton Muscular Dystrophy Research Centre; Institute of Genetic Medicine; Newcastle upon Tyne UK

4. Department of Paediatric Neurology; Catholic University; Rome Italy

5. Department of Neurology; Stanford University School of Medicine; Stanford CA USA

6. Institut de Myologie; GH Pitié Salpêtrière; Paris France

7. Danish National Rehabilitation Center for Neuromuscular Diseases; Aarhus Denmark

8. Duchenne Parent Project; Veenendaal the Netherlands

9. Department of Child Neurology; University Hospitals Leuven; Leuven Belgium

Funder

Duchenne Parent Project, the Netherlands

Publisher

Wiley

Subject

Clinical Neurology,Developmental Neuroscience,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/dmcn.13277/fullpdf

Reference21 articles.

1. North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophy;Mazzone;Neuromuscul Disord,2010

2. Moving towards meaningful measurement: Rasch analysis of the North Star Ambulatory Assessment in Duchenne muscular dystrophy;Mayhew;Dev Med Child Neurol,2011

3. The 6-minute walk test in Duchenne/Becker muscular dystrophy: longitudinal observations;McDonald;Muscle Nerve,2010

4. Upper limb strength and function changes during a one-year follow-up in non-ambulant patients with Duchenne muscular dystrophy: an observational multicenter trial;Seferian;PLoS ONE,2015

5. Patterns of decline in upper limb function of boys and men with DMD: an international survey;Janssen;J Neurol,2014

Cited by 40 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. Evaluation of fatigue and fatigability in people with Duchenne muscular dystrophy using a dynamic arm support – a pilot study;Disability and Rehabilitation: Assistive Technology;2024-09-12

2. Effect of Aquatic Exercise on Functional Activity in Duchenne Muscular Dystrophy: Case Report;Journal of The Korean Society of Physical Medicine;2024-08-31

3. Lower urinary tract symptoms in children with Duchenne muscular dystrophy: An evaluation in terms of functional level, posture, and muscle strength;Neurourology and Urodynamics;2024-08-16

4. Relationship Between Hand Strength and Function in Duchenne Muscular Dystrophy and Spinal Muscular Atrophy: Implications for Clinical Trials;Journal of Neuromuscular Diseases;2024-07-02

5. Patient-Reported Outcome Measures in Neuromuscular Diseases: A Scoping Review;Journal of Neuromuscular Diseases;2024-04-30

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

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