Advances in Cystic Fibrosis Research in Qatar: A Commentary-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Advances in Cystic Fibrosis Research in Qatar: A Commentary

Published:2023-02-28 Issue:3 Volume:13 Page:448
ISSN:2075-4426
Container-title:Journal of Personalized Medicine
language:en
Short-container-title:JPM

Author:

Hammoudeh Samer¹,Janahi Ibrahim A.²³^ORCID

Affiliation:

1. Research Affairs, Academic Health System, Hamad Medical Corporation, Doha P.O. Box 3050, Qatar

2. Medical Education, Sidra Medicine, Doha P.O. Box 26999, Qatar

3. Pediatric Pulmonology, Pediatric Medicine, Sidra Medicine, Doha P.O. Box 26999, Qatar

Abstract

Cystic fibrosis is a genetic disorder caused by a Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene defect. Many across the globe suffer the debilitating symptoms. The aim of this commentary is to briefly cover various aspects related to the disease in the Arab world and then in Qatar.

Funder

Qatar National Library

Publisher

MDPI AG

Subject

Medicine (miscellaneous)

Link

https://www.mdpi.com/2075-4426/13/3/448/pdf

Reference30 articles.

1. CFTR gene variants, epidemiology and molecular pathology;Bareil;Arch. Pédiatr.,2020

2. Cystic fibrosis;Shteinberg;Lancet,2021

3. Cystic fibrosis in the year 2020: A disease with a new face;Acta Paediatr.,2020

4. Ramalho, S.S., Silva, I.A.L., Amaral, M.D., and Farinha, C.M. (2021). Rare Trafficking CFTR Mutations Involve Distinct Cellular Retention Machineries and Require Different Rescuing Strategies. Int. J. Mol. Sci., 23.

5. Increasing life expectancy in cystic fibrosis: Advances and challenges;McBennett;Pediatr. Pulmonol.,2022

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