Lv4
690 积分 2021-07-20 加入
The role of confirmatory tests in the diagnosis of primary aldosteronism
22小时前
求助中
Liddle Syndrome with a SCNN1A Mutation: A Case Report and Literature Review
4个月前
已完结
Corin and Left Atrial Cardiomyopathy, Hypertension, Arrhythmia, and Fibrosis
6个月前
已完结
Cushing Syndrome
9个月前
已完结
Steroid profile in dried blood spots by liquid chromatography tandem mass spectrometry: Application to newborn screening for congenital adrenal hyperplasia in China
1年前
已完结
Novel human pathological mutations. Gene symbol: CYP17A1. Disease: 17alpha-hydroxylase/17,20-lyase deficiency
1年前
已关闭
Molecular analysis of 12 Chinese patients with 11β‐hydroxylase deficiency and in vitro functional study of 20 CYP11B1 missense variants
1年前
已完结
Clinical, pathophysiologic, genetic and therapeutic progress in Primary Bilateral Macronodular Adrenal Hyperplasia
1年前
已完结
Molecular analysis of 12 Chinese patients with 11β‐hydroxylase deficiency and in vitro functional study of 20 CYP11B1 missense variants
1年前
已完结
Novel human pathological mutations. Gene symbol: CYP17A1. Disease: 17-alpha-hydroxylase/17,20-lyase deficiency
1年前
已关闭
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