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pregnanetriolone
Papers overview
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2012
2012
BACKGROUND
The clinical differential diagnosis of classic 21-hydroxylase deficiency (C21OHD) and cytochrome P450 oxidoreductase… Expand
Highly Cited
2006
Highly Cited
2006
CONTEXT
Although the "backdoor" pathway to dihydrotestosterone has been postulated in the fetal-to-early-infantile period of… Expand
2004
2004
Elevated blood 17alpha-hydroxyprogesterone (17OHP) level, although widely used for the screening of classical 21-hydroxylase… Expand
1982
1982
Three patients with male pseudohermaphroditism due to 17,20-desmolase deficiency were studied at a pubertal age. Patients 1 and 2… Expand
1978
1978
Three otherwise healthy relatives of patients with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency and salt… Expand
Highly Cited
1972
Highly Cited
1972
In a child with male pseudohermaphroditism (ambiguous external genitalia, XY sex chromosomal constitution and normal… Expand
1971
1971
Abstract A gas chromatographic method for the determination of urinary steroids on glass capillary columns is described. The… Expand
Highly Cited
1970
Highly Cited
1970
ABSTRACT The case of a girl, aged 6 1/2 yr, with probable 3β-hydroxysteroid dehydrogenase deficiency is described. To our… Expand
1966
1966
A gas chromatographic method for the determination of urinary regnanetriol (5β-pregnane-3α,17α,20α-triol), pregnanetriolone (3… Expand
1965
1965
Abstract A method using gas-liquid chromatography (GLC) has been devised for the routine determination of urinary pregnanediol… Expand