首页 文献索引 SCI期刊 AI助手
期刊目录筛选

期刊名:Therapeutic advances in endocrinology and metabolism

缩写:THER ADV ENDOCRINOL

ISSN:2042-0188

e-ISSN:2042-0196

IF/分区:7.8/Q1

文章目录 更多期刊信息

共收录本刊相关文章索引40
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Romina Lomonaco,Janet Chen,Kenneth Cusi Romina Lomonaco
Endocrinologists are encountering patients with obesity-related complications such as metabolic syndrome (MetS) and type 2 diabetes mellitus (T2DM) on a daily basis. Nonalcoholic fatty liver disease (NAFLD) is a liver condition characterize...
Andreas Soejitno,Pande Kadek Aditya Prayudi Andreas Soejitno
A continuous search for a permanent cure for diabetes mellitus is underway with several remarkable discoveries over the past few decades. One of these is the potential of pancreatic stem/progenitor cells to rejuvenate functional β cells. H...
David A Liebner,Manisha H Shah David A Liebner
Therapeutic options for advanced, unresectable radioiodine-resistant thyroid cancers have historically been limited. Recent progress in understanding the pathogenesis of the various subtypes of thyroid cancer has led to increased interest i...
Alaa E El-Sisi,Sahar K Hegazy,Shereen S Metwally et al. Alaa E El-Sisi et al.
Objective: This study investigated the possibility that genetic factors, such as polymorphism of K inward rectifier subunit (Kir6.2), E23K, and Arg(972) polymorphism of insulin receptor sub-strate-1 (IRS-1), may predispos...
Christian M Girgis,Bernard L Champion,Jack R Wall Christian M Girgis
Graves' disease is the most common cause of hyperthyroidism in the developed world. It is caused by an immune defect in genetically susceptible individuals in whom the production of unique antibodies results in thyroid hormone excess and gl...
Robin Lachmann Robin Lachmann
Phenylketonuria (PKU) is an inherited disorder of amino acid metabolism caused by deficiency of the enzyme phenylalanine hydroxylase (PAH). Historically PKU was a common genetic cause of severe learning difficulties and developmental delay,...
Shashithej K Narayana,David R Woods,Christopher J Boos Shashithej K Narayana
Amiodarone is a highly effective and well-established antiarrrhythmic drug. It can be used to treat supraventricular and ventricular tachyarrhythmias and has the added advantage of being well tolerated in patients with impaired left ventric...