Rapid progressive course of later-onset Pompe disease in Chinese patients-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Rapid progressive course of later-onset Pompe disease in Chinese patients

Published:2011-11 Issue:3 Volume:104 Page:284-288
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Yang Chih-Chao,Chien Yin-Hsiu,Lee Ni-Chung,Chiang Shu-Chuan,Lin Shuan-Pei,Kuo Yung-Ting,Chen Shun-Sheng,Jong Yuh-Jyh,Hwu Wuh-Liang

Funder

Taiwanese National Science Council

Genzyme Corporation

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference30 articles.

1. Glycogen storage disease type II: acid alpha-glucosidase (acid maltase) deficiency;Hirschhorn,2001

2. A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease;Kishnani;J. Pediatr.,2006

3. Clinical manifestation and natural course of late-onset Pompe's disease in 54 Dutch patients;Hagemans;Brain,2005

4. The natural course of non-classic Pompe's disease; a review of 225 published cases;Winkel;J. Neurol.,2005

5. Late onset Pompe disease: clinical and neurophysiological spectrum of 38 patients including long-term follow-up in 18 patients;Muller-Felber;Neuromuscul. Disord.,2007

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. High‐risk screening for late‐onset Pompe disease in China: An expanded multicenter study;Journal of Inherited Metabolic Disease;2024-09-03

2. Newborn Screening for 6 Lysosomal Storage Disorders in China;JAMA Network Open;2024-05-13

3. Diagnostic delay in late‐onset Pompe disease among Chinese patients: A retrospective study;JIMD Reports;2023-12-20

4. GAA variants associated with reduced enzymatic activity but lack of Pompe-related symptoms, incidentally identified by exome sequencing;Molecular Genetics and Metabolism Reports;2023-09

5. Motor Responses in Pediatric Pompe Disease in the ADVANCE Participant Cohort;Journal of Neuromuscular Diseases;2022-11-08

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