Two Australian families with inclusion-body myopathy, Paget’s disease of bone and frontotemporal dementia: Novel clinical and genetic findings-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Two Australian families with inclusion-body myopathy, Paget’s disease of bone and frontotemporal dementia: Novel clinical and genetic findings

Published:2010-05 Issue:5 Volume:20 Page:330-334
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Kumar Kishore R.,Needham Merrilee,Mina Kym,Davis Mark,Brewer Janice,Staples Christopher,Ng Karl,Sue Carolyn M.,Mastaglia Frank L.

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference18 articles.

1. Valosin-containing protein disease: inclusion body myopathy with Paget’s disease of the bone and fronto-temporal dementia;Weihl;Neuromuscul Disord,2009

2. Valosin-containing protein gene mutations: clinical and neuropathologic features;Guyant-Maréchal;Neurology,2006

3. Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene;Haubenberger;Neurology,2005

4. Pathological consequences of VCP mutations on human striated muscle;Hübbers;Brain,2007

5. Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia;Watts;Clin Genet,2007

Cited by 51 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. MRI based semi-quantitative scoring system analysis of thigh muscles in patients with VCP disease;2023-10-17

2. Case report: Frontotemporal dementia and amyotrophic lateral sclerosis caused by a missense variant (p.Arg89Trp) in the valosin-containing protein gene;Frontiers in Genetics;2023-05-26

3. Multisystem Proteinopathy Due to VCP Mutations: A Review of Clinical Heterogeneity and Genetic Diagnosis;Genes;2022-05-27

4. Valosin Containing Protein (VCP): A Multistep Regulator of Autophagy;International Journal of Molecular Sciences;2022-02-09

5. Pain in neurodegenerative diseases with atypical parkinsonis a systematic review on prevalence, clinical presentation, and findings from experimental studies;Journal of Integrative Neuroscience;2021-12-30

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