Pregnane-3α,17α,20α-Triol and Pregnane-3α,17α,20α-Triol-11-One Excretion by Patients with Adrenocortical Dysfunction1-Reference-Cited by-同舟云学术

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Pregnane-3α,17α,20α-Triol and Pregnane-3α,17α,20α-Triol-11-One Excretion by Patients with Adrenocortical Dysfunction1

Published:1957-12-01 Issue:12 Volume:36 Page:1726-1735
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Cox R. I.,Finkelstein M.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Cited by 59 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. Non-Classic Disorder of Adrenal Steroidogenesis and Clinical Dilemmas in 21-Hydroxylase Deficiency Combined with Backdoor Androgen Pathway. Mini-Review and Case Report;International Journal of Molecular Sciences;2020-06-29

2. Successful Pregnancy in a Case of Congenital Adrenogenital Syndrome;The Journal of The Asian federation of Obstetrics and Gynaecology;2010-05-24

3. Urinary pregnanetriol-3-glucuronide excretion in neonates and the use of urinary pregnanetriol-3-glucuronide/creatinine ratio in differentiating 21-hydroxylase deficiency;Screening;1996-05

4. Changes of Several Adrenal Δ⁴-Steroids Measured by HPLC-UV Spectrometry in Neonatal Patients with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency;Hormone Research;1990

5. Identification of 5β-pregnane and 5β-androstane derivatives in adrenal venous and peripheral blood plasma of the female possum (Trichosurus vulpecula);Journal of Steroid Biochemistry;1989-04

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