Genetic Profiles and Three-year Follow-up Study of Chinese Males With Congenital Hypogonadotropic Hypogonadism-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Genetic Profiles and Three-year Follow-up Study of Chinese Males With Congenital Hypogonadotropic Hypogonadism

Published:2021-09 Issue:9 Volume:18 Page:1500-1510
ISSN:1743-6095
Container-title:The Journal of Sexual Medicine
language:en
Short-container-title:The Journal of Sexual Medicine

Author:

Zhang Luyao,Gao Yuting,Du Qin,Liu Liyi,Li Yanbing,Dey Subrata Kumar,Banerjee Santasree,Liao Zhihong

Funder

Guangzhou Municipal Science and Technology Project

Guangzhou Science Technology and Innovation Commission

Publisher

Elsevier BV

Subject

Urology,Reproductive Medicine,Endocrinology,Endocrinology, Diabetes and Metabolism,Psychiatry and Mental health

Reference41 articles.

1. Clinical management of congenital hypogonadotropic hypogonadism;Young;Endocr Rev,2019

2. Chinese society of endocrinology: chinese consensus statement on idiopathic hypogonadotropic hypogonadism;Chin J Internal Med,2015

3. Genetics of congenital hypogonadotropic hypogonadism: peculiarities and phenotype of an oligogenic disease;Cangiano;Hum Genet,2021

4. New genetic findings in a large cohort of congenital hypogonadotropic hypogonadism;Amato;Eur J Endocrinol,2019

5. Identification of gene variants in a cohort of hypogonadotropic hypogonadism: diagnostic utility of custom NGS panel and WES in unravelling genetic complexity of the disease;Gach;Mol Cell Endocrinol,2020

Cited by 6 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. The impact of impaired intrauterine growth on male fertility: A systematic review and meta‐analysis;Andrology;2024-07-09

2. Digenic CHD7 and SMCHD1 inheritance Unveils phenotypic variability in a family mainly presenting with hypogonadotropic hypogonadism;Heliyon;2024-01

3. Gonadotropins for pubertal induction in males with hypogonadotropic hypogonadism: systematic review and meta-analysis;European Journal of Endocrinology;2023-12-21

4. Phenotypic and genotypic landscape of PROKR2 in neuroendocrine disorders;Frontiers in Endocrinology;2023-02-08

5. Genetic spectrum of Kallmann syndrome: Single‐center experience and systematic review;Clinical Endocrinology;2022-09-30

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