Microfilter paper method for 17 alpha-hydroxyprogesterone radioimmunoassay: its application for rapid screening for congenital adrenal hyperplasia.

Suppr

超能文献

作者信息

Pang S, Hotchkiss J, Drash A L, Levine L S, New M I

出版信息

J Clin Endocrinol Metab. 1977 Nov;45(5):1003-8. doi: 10.1210/jcem-45-5-1003.

DOI:10.1210/jcem-45-5-1003

PMID:925125

Abstract

摘要

相似文献

Microfilter paper method for 17 alpha-hydroxyprogesterone radioimmunoassay: its application for rapid screening for congenital adrenal hyperplasia.

J Clin Endocrinol Metab. 1977 Nov;45(5):1003-8. doi: 10.1210/jcem-45-5-1003.

Diagnosis of congenital adrenal hyperplasia based on plasma 21-deoxycortisol level determined with a specific radioimmunoassay.基于用特定放射免疫测定法测定的血浆21-脱氧皮质醇水平诊断先天性肾上腺皮质增生症。

Mater Med Pol. 1984 Apr-Dec;16(2-4):95-8.

[Micro-filter paper method for 17 alpha-hydroxyprogesterone radioimmunoassay. Application for diagnosis of 21-hydroxylase deficiency (author's transl)].

Horumon To Rinsho. 1979 Sep;27(9):1048-53.

Neonatal screening for 21-hydroxylase deficiency: a microfilter paper method for 17-alpha-hydroxyprogesterone assay.

J Endocrinol Invest. 1982 Mar-Apr;5(2):87-90. doi: 10.1007/BF03350496.

Estimation of 17 alpha-hydroxyprogesterone in dried blood spots for mass screening of newborn infants with congenital adrenal hyperplasia.干血斑中17α-羟孕酮的测定用于先天性肾上腺皮质增生症新生儿的大规模筛查。

Acta Med Iugosl. 1983;37(2):95-100.

[Serum 17 alpha-hydroxyprogesterone, 21-deoxycortisol and cortisol levels in congenital adrenal gland hyperplasia].

Horumon To Rinsho. 1977 Sep;25(9):981-8.

Early diagnosis of congenital adrenal hyperplasia by measurement of 17-hydroxyprogesterone.

Clin Endocrinol (Oxf). 1975 Jul;4(4):451-54. doi: 10.1111/j.1365-2265.1975.tb01553.x.

[Neonatal mass-screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency. I. Microfilter paper methods for radioimmunoassay of 17 alpha-hydroxyprogesterone].[新生儿21-羟化酶缺乏所致先天性肾上腺皮质增生症的群体筛查。I. 17α-羟孕酮放射免疫测定的微量滤纸法]

Nihon Naibunpi Gakkai Zasshi. 1983 Dec 20;59(12):1845-9. doi: 10.1507/endocrine1927.59.12_1845.

Rapid assay of plasma 21-deoxycortisol and 11-deoxycortisol in congenital adrenal hyperplasia.

Clin Endocrinol (Oxf). 1979 Apr;10(4):367-75. doi: 10.1111/j.1365-2265.1979.tb02091.x.

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.

引用本文的文献

Editorial: Special Issue "Genetic Newborn Screening".社论：“新生儿基因筛查”特刊

Genes (Basel). 2025 Aug 26;16(9):1006. doi: 10.3390/genes16091006.

Maria Iandolo New (1928-2024): Pioneering pediatric endocrinologist.玛丽亚·扬多洛·纽（1928 - 2024）：杰出的儿科内分泌学家。

Proc Natl Acad Sci U S A. 2025 Feb 4;122(5):e2424275122. doi: 10.1073/pnas.2424275122. Epub 2025 Jan 29.

Genetics and Pathophysiology of Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.21-羟化酶缺乏所致经典型先天性肾上腺皮质增生症的遗传学与病理生理学

J Clin Endocrinol Metab. 2025 Jan 21;110(Supplement_1):S1-S12. doi: 10.1210/clinem/dgae535.

Barriers to the Management of Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.21-羟化酶缺乏所致经典型先天性肾上腺皮质增生症管理中的障碍

J Clin Endocrinol Metab. 2025 Jan 21;110(Supplement_1):S67-S73. doi: 10.1210/clinem/dgae710.

History of Adrenal Research: From Ancient Anatomy to Contemporary Molecular Biology.肾上腺研究史：从古代解剖学到当代分子生物学。

Endocr Rev. 2023 Jan 12;44(1):70-116. doi: 10.1210/endrev/bnac019.

Moderate congenital adrenal hyperplasia in two girls diagnosed by newborn screening.两名经新生儿筛查诊断为中度先天性肾上腺增生症的女童。

Pediatr Endocrinol Diabetes Metab. 2021;27(4):291-297. doi: 10.5114/pedm.2021.109123.

Two girls with a neonatal screening-negative 21-hydroxylase deficiency requiring treatment with hydrocortisone for virilization in late childhood.两名女孩患有新生儿筛查阴性的21-羟化酶缺乏症，在儿童晚期因男性化需用氢化可的松治疗。

Clin Pediatr Endocrinol. 2021;30(3):143-148. doi: 10.1297/cpe.30.143. Epub 2021 Jul 10.

[Newborn screening for congenital hypothyroidism and congenital adrenal hyperplasia: Benefits and costs of a successful public health program].[先天性甲状腺功能减退症和先天性肾上腺皮质增生症的新生儿筛查：一项成功的公共卫生项目的益处与成本]

Med Sci (Paris). 2021 May;37(5):528-534. doi: 10.1051/medsci/2021053. Epub 2021 May 18.

Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.先天性肾上腺皮质增生症-病理生理学、诊断和治疗的最新见解。

Endocr Rev. 2022 Jan 12;43(1):91-159. doi: 10.1210/endrev/bnab016.

Newborn Screening for CAH-Challenges and Opportunities.先天性肾上腺皮质增生症的新生儿筛查——挑战与机遇

Int J Neonatal Screen. 2021 Feb 13;7(1):11. doi: 10.3390/ijns7010011.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验