Elucidating the Underlying Molecular Pathogenesis ofNR3C2Mutants Causing Autosomal Dominant Pseudohypoaldosteronism Type 1-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Elucidating the Underlying Molecular Pathogenesis ofNR3C2Mutants Causing Autosomal Dominant Pseudohypoaldosteronism Type 1

Published:2006-11 Issue:11 Volume:91 Page:4552-4561
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

Riepe Felix G.,Finkeldei Johannes,de Sanctis Luisa,Einaudi Silvia,Testa Alberto,Karges Beate,Peter Michael,Viemann Matthias,Grötzinger Joachim,Sippell Wolfgang G.,Fejes-Toth Geza,Krone Nils

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/91/11/4552/9063884/jcem4552.pdf

Cited by 55 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. NR3C2 microdeletions—an underrecognized cause of pseudohypoaldosteronism type 1A: a case report and literature review;Laboratory Medicine;2024-03-16

2. Hypoaldosteronism, pseudohypoaldosteronism and salt loss;Steroids in the Laboratory and Clinical Practice;2023

3. Mineralocorticoid Resistance;Endocrinology;2023

4. Mineralocorticoid Resistance;Endocrinology;2023

5. Depression and Autoimmune Hypothyroidism—Their Relationship and the Effects of Treating Psychiatric and Thyroid Disorders on Changes in Clinical and Biochemical Parameters Including BDNF and Other Cytokines—A Systematic Review;Pharmaceuticals;2022-03-24

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