Congenital Leptin Deficiency Due to Homozygosity for the Δ133G Mutation: Report of Another Case and Evaluation of Response to Four Years of Leptin Therapy-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Congenital Leptin Deficiency Due to Homozygosity for the Δ133G Mutation: Report of Another Case and Evaluation of Response to Four Years of Leptin Therapy

Published:2004-10 Issue:10 Volume:89 Page:4821-4826
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

Gibson William T.,Farooqi I. Sadaf,Moreau Mary,DePaoli Alex M.,Lawrence Elizabeth,O’Rahilly Stephen,Trussell Rebecca A.

Publisher

The Endocrine Society

Subject

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

Cited by 233 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. Novel compound heterozygous mutations in LEP responsible for obesity in a Chinese family;Molecular Genetics and Metabolism Reports;2024-09

2. Differentiating monogenic and syndromic obesities from polygenic obesity: Assessment, diagnosis, and management;Obesity Pillars;2024-09

3. Medical semiology of patients with monogenic obesity: A systematic review;Obesity Reviews;2024-07-02

4. Changes in hippocampal volume, synaptic plasticity and amylin sensitivity in an animal model of type 2 diabetes are associated with increased vulnerability to amyloid-beta in advancing age;Frontiers in Aging Neuroscience;2024-06-21

5. Unexpected identification of obesity-associated mutations in LEP and MC4R genes in patients with anorexia nervosa;Scientific Reports;2024-03-25

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