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[Adrenal hirsutism (3-beta-hydroxysteroid dehydrogenase deficiency). Studies using chromatographic separation of the urinary 17-ketosteroid fraction. 3. On the differential diagnosis of adrenal hirsutism (M. Cushing, congenital adrenogenital syndrome)].

作者信息

Göbel P

出版信息

Endokrinologie. 1968 Feb;52(5):289-314.

PMID:4236371
Abstract
摘要

相似文献

1
[Adrenal hirsutism (3-beta-hydroxysteroid dehydrogenase deficiency). Studies using chromatographic separation of the urinary 17-ketosteroid fraction. 3. On the differential diagnosis of adrenal hirsutism (M. Cushing, congenital adrenogenital syndrome)].[肾上腺性多毛症(3-β-羟类固醇脱氢酶缺乏症)。利用尿17-酮类固醇组分色谱分离的研究。3. 关于肾上腺性多毛症的鉴别诊断(库欣综合征、先天性肾上腺皮质增生症)]
Endokrinologie. 1968 Feb;52(5):289-314.
2
[Adrenal hirsutism (3-beta-hydroxysteroid dehydrogenase deficiency). Chromatographic separation of the urinary 17-ketosteroid fraction. 3. Differential diagnosis of adrenal hirsutism (Cushing congenital adrenogenital syndrome)].
Dtsch Zahn Mund Kieferheilkd Zentralbl Gesamte. 1967;52(5):289-314.
3
[Adrenal hirsutism (3beta-hydroxysteroid dehydrogenase deficiency). Studies using a chromatographic separation of the 17-ketosteroid fraction in the urine. 1. Dehydroepiandrosterone-forming adrenocortical adenoma].
Endokrinologie. 1967;52(1):22-36.
4
[Adrenal hirsutism (3-beta-hydroxysteroid dehydrogenase deficiency). Studies using a chromatographic separation of the urinary 17-ketosteroid fraction. 2. Dehydroepiandrosterone-forming adrenal hyperplasia and constitutional hirsutism].[肾上腺性多毛症(3-β-羟基类固醇脱氢酶缺乏症)。利用尿17-酮类固醇组分色谱分离法的研究。2. 形成脱氢表雄酮的肾上腺增生和体质性多毛症]
Endokrinologie. 1967;52(3):168-201.
5
[Gas chromatography determination of urinary pregnanediol and -triol and its significance for the differentiation of adrenal hirsutism in women].[气相色谱法测定尿孕二醇和孕三醇及其对女性肾上腺性多毛症鉴别诊断的意义]
Endokrinologie. 1969;54(5):374-91.
6
[Pattern of urinary neutral 17-ketosteroids on the basis of thin layer chromatography].基于薄层色谱法的尿中中性17-酮类固醇模式
Z Klin Chem Klin Biochem. 1967 Jul;5(4):153-5.
7
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.
8
Partial 3 -hydroxysteroid dehydrogenase (3 -HSD) deficiency in a family with congenital adrenal hyperplasia: evidence for increasing 3 -HSD activity with age.
Pediatrics. 1971 Nov;48(5):756-65.
9
[On the differential diagnosis of hirsutism].[关于多毛症的鉴别诊断]
Z Haut Geschlechtskr. 1968 Apr 1;43(7):277-80.
10
The determination of urinary pregnanetriol and the neutral 17-ketosteroids by gas-liquid chromatography.通过气液色谱法测定尿孕三醇和中性17-酮类固醇。
Steroids. 1971 Aug;18(2):113-28. doi: 10.1016/0039-128x(71)90019-5.