The Barth Syndrome Registry: Distinguishing disease characteristics and growth data from a longitudinal study-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

The Barth Syndrome Registry: Distinguishing disease characteristics and growth data from a longitudinal study

Published:2012-10-08 Issue:11 Volume:158A Page:2726-2732
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Roberts Amy E.,Nixon Connie,Steward Colin G.,Gauvreau Kimberly,Maisenbacher Melissa,Fletcher Matthew,Geva Judith,Byrne Barry J.,Spencer Carolyn T.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.35609/fullpdf

Reference34 articles.

1. Heart transplantation for Barth syndrome;Adwani;Pediatr Cardiol,1997

2. An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes;Barth;J Neurol Sci,1983

3. X-linked cardioskeletal myopathy and neutropenia (Barth syndrome)-MIM 302060;Barth;J Pediatr,1999

4. X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): An update;Barth;Am J Med Genet Part A,2004

5. Arrhythmogenic right ventricular cardiomyopathy: Clinical registry and database, evaluation of therapies, pathology registry, DNA banking;Basso;Eur Heart J,2004

Cited by 106 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. ECG findings are poor predictors for adverse events and cardiac death in Barth syndrome;Progress in Pediatric Cardiology;2024-12

2. Barth syndrome in an adult patient: an overview of the problem and case report. A review;Terapevticheskii arkhiv;2024-09-14

3. A Barth Syndrome Patient-Derived D75H Point Mutation in TAFAZZIN Drives Progressive Cardiomyopathy in Mice;International Journal of Molecular Sciences;2024-07-27

4. Tafazzin deficiency causes substantial remodeling in the lipidome of a mouse model of Barth Syndrome cardiomyopathy;Frontiers in Molecular Medicine;2024-04-29

5. Stem cell models of TAFAZZIN deficiency reveal novel tissue-specific pathologies in Barth Syndrome;2024-04-29

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