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Evaluation of deficiency of 21-hydroxylation in patients with congenital adrenal hyperplasia.

作者信息

Galal O M, Rudd B T, Drayer N M

出版信息

Arch Dis Child. 1968 Aug;43(230):410-4. doi: 10.1136/adc.43.230.410.

DOI:10.1136/adc.43.230.410
PMID:4298539
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2019993/
Abstract
摘要

相似文献

1
Evaluation of deficiency of 21-hydroxylation in patients with congenital adrenal hyperplasia.先天性肾上腺皮质增生症患者21-羟化酶缺乏症的评估。
Arch Dis Child. 1968 Aug;43(230):410-4. doi: 10.1136/adc.43.230.410.
2
[Plasma 17-OH progesterone. Determination in normal children and in congenital adrenal hyperplasia due to the 21-hydroxylation deficiency].[血浆17-羟孕酮。正常儿童及21-羟化酶缺乏所致先天性肾上腺皮质增生症患儿的测定]
Nouv Presse Med. 1974 Dec 21;3(44):2621-4.
3
Unusual type of congenital adrenal hyperplasia probably due to deficiency of 3-beta-hydroxysteroid dehydrogenase. Case report of a surviving girl and steroid studies.一种不寻常类型的先天性肾上腺增生,可能是由于3-β-羟基类固醇脱氢酶缺乏所致。一名存活女童的病例报告及类固醇研究。
J Clin Endocrinol Metab. 1970 Jun;30(6):719-26. doi: 10.1210/jcem-30-6-719.
4
The simultaneous assay of cortisol and 17alpha-hydroxyprogesterone in the plasma of patients with congenital adrenal hyperplasia.先天性肾上腺皮质增生症患者血浆中皮质醇和17α-羟孕酮的同步检测
Acta Endocrinol (Copenh). 1973 Oct;74(2):316-30. doi: 10.1530/acta.0.0740316.
5
Congenital adrenal hyperplasia: simultaneous determination of plasma aldosterone and 17-hydroxyprogesterone.先天性肾上腺皮质增生症:血浆醛固酮和17-羟孕酮的同步测定
Acta Endocrinol (Copenh). 1978 Jan;87(1):148-57. doi: 10.1530/acta.0.0870148.
6
Single dose dexamethasone in treatment of congenital adrenocortical hyperplasia.单剂量地塞米松治疗先天性肾上腺皮质增生症。
Metabolism. 1971 Sep;20(9):897-901. doi: 10.1016/0026-0495(71)90052-7.
7
Identical male twins with congenital adrenal hyperplasia. Comparison of growth, serum and urinary steroids.患有先天性肾上腺皮质增生症的同卵男性双胞胎。生长情况、血清及尿类固醇的比较。
West J Med. 1976 Apr;124(4):335-8.
8
Experience with long-term therapy in congenital adrenal hyperplasia.
J Pediatr. 1974 Jul;85(1):12-9. doi: 10.1016/s0022-3476(74)80277-5.
9
Congenital adrenal hyperplasia due to deficiency of 11 -hydroxylation of 17 -hydroxylated steroids.由于17-羟化类固醇11-羟化作用缺乏所致的先天性肾上腺皮质增生症。
J Clin Endocrinol Metab. 1971 Sep;33(3):501-8. doi: 10.1210/jcem-33-3-501.
10
Exchangeable sodium and aldosterone secretion in children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Pediatr Res. 1970 Mar;4(2):145-56. doi: 10.1203/00006450-197003000-00005.

引用本文的文献

1
Congenital adrenal hyperplasia in a 66-year-old female.一名66岁女性的先天性肾上腺增生症。
Postgrad Med J. 1981 May;57(667):317-20. doi: 10.1136/pgmj.57.667.317.
2
Androgens levels in plasma and urine of patients with virilizing congenital adrenal hyperplasia.先天性肾上腺皮质增生症男性化患者血浆和尿液中的雄激素水平。
Proc R Soc Med. 1970 Oct;63(10):1039-40. doi: 10.1177/003591577006301032.
3
Adrenal insufficiency in two male infants.两名男婴肾上腺功能不全。
Proc R Soc Med. 1970 May;63(5):488-9. doi: 10.1177/003591577006300532.
4
Should we screen for congenital adrenal hyperplasia? A review of 117 cases.我们应该筛查先天性肾上腺增生症吗?117例病例回顾。
Arch Dis Child. 1987 Jul;62(7):659-62. doi: 10.1136/adc.62.7.659.

本文引用的文献

1
ALDOSTERONE SECRETION RATE IN CONGENITAL ADRENAL HYPERPLASIA. A DISCUSSION OF THE THEORIES ON THE PATHOGENESIS OF THE SALT-LOSING FORM OF THE SYNDROME.先天性肾上腺皮质增生症中的醛固酮分泌率。关于该综合征失盐型发病机制理论的讨论。
J Clin Invest. 1965 Sep;44(9):1505-13. doi: 10.1172/JCI105257.
2
AN ALDOSTERONE BIOSYNTHETIC DEFECT IN A SALT-LOSING DISORDER.一种失盐性疾病中的醛固酮生物合成缺陷。
J Clin Endocrinol Metab. 1964 Jul;24:669-72. doi: 10.1210/jcem-24-7-669.
3
The adrenogenital syndrome.肾上腺性征异常综合征
N Engl J Med. 1963 Jun 13;268:1342-51 contd. doi: 10.1056/NEJM196306132682406.
4
17alpha-Hydroxyprogesterone--a salt-losing steroid: relation to congenital adrenal hyperplasia.
J Clin Endocrinol Metab. 1961 Aug;21:909-22. doi: 10.1210/jcem-21-8-909.
5
Adrenogenital syndrome: uncomplicated and hypertensive forms.
Pediatrics. 1958 Apr;21(4):661-7.
6
The determination of 17,21-dihydroxy-20-ketosteroids in urine and plasma.尿液和血浆中17,21 - 二羟基 - 20 - 酮类固醇的测定
J Biol Chem. 1954 Oct;210(2):923-32.