DUOX2 Mutations Are Frequently Associated With Congenital Hypothyroidism in the Korean Population-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

DUOX2 Mutations Are Frequently Associated With Congenital Hypothyroidism in the Korean Population

Published:2016-03-01 Issue:2 Volume:36 Page:145-153
ISSN:2234-3806
Container-title:Annals of Laboratory Medicine
language:en
Short-container-title:Ann Lab Med

Author:

Park Kyoung-Jin¹,Park Hyun-Kyung²,Kim Young-Jin²,Lee Kyoung-Ryul²,Park Jong-Ho¹,Park June-Hee³,Park Hyung-Doo⁴,Lee Soo-Youn⁴,Kim Jong-Won¹⁴

Affiliation:

1. Department of Health Sciences and Technology, Samsung Advanced Institute for Health Sciences and Technology, Sungkyunkwan University, Seoul, Korea

2. Department of Laboratory Medicine, Seoul Clinical Laboratories, Seoul Medical Science Institute, Seoul, Korea

3. Samsung Biomedical Research Institute, Samsung Medical Center, Seoul, Korea

4. Department of Laboratory Medicine & Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea

Funder

Ministry of Health and Welfare

Publisher

Annals of Laboratory Medicine

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

Link

http://synapse.koreamed.org/pdf/10.3343/alm.2016.36.2.145

Reference27 articles.

1. Prevention of intellectual disability through screening for congenital hypothyroidism: how much and at what level?

2. Birth prevalence of disorders detectable through newborn screening by race/ethnicity

3. Increase in congenital hypothyroidism in New York State and in the United States

4. Congenital hypothyroidism in Western Australia 1981-1998

5. A 7-year experience with low blood TSH cutoff levels for neonatal screening reveals an unsuspected frequency of congenital hypothyroidism (CH)

Cited by 62 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. Patients with Thyroid Dyshormonogenesis and DUOX2 Variants: Molecular and Clinical Description and Genotype–Phenotype Correlation;International Journal of Molecular Sciences;2024-08-03

2. Clinical efficacy of multigene panels in the management of congenital hypothyroidism with gland in situ;Medicine;2024-07-19

3. Molecular and Clinical Features of Congenital Hypothyroidism Due to Multiple DUOX2 Variants;Thyroid®;2024-07-01

4. Genetic etiology in patients diagnosed with congenital hypothyroidism with new-generation sequencing: A single-center experience;Archives de Pédiatrie;2024-07

5. Ultrasonographic Development and Progression of a Thyroid Nodule in a Girl with TPO-Mutated Dyshormonogenesis during Levothyroxine Supplementation;International Journal of Thyroidology;2023-05-30

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