pregnanetriolone

 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1961-2016
02419612016

Papers overview

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2016
2016
One major issue of newborn screening programs for 21-hydroxylase deficiency (21OHD) is the high rate of false-positive results… (More)
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2012
2012
BACKGROUND The clinical differential diagnosis of classic 21-hydroxylase deficiency (C21OHD) and cytochrome P450 oxidoreductase… (More)
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2006
2006
CONTEXT Although the "backdoor" pathway to dihydrotestosterone has been postulated in the fetal-to-early-infantile period of… (More)
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2004
2004
Elevated blood 17alpha-hydroxyprogesterone (17OHP) level, although widely used for the screening of classical 21-hydroxylase… (More)
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2000
2000
A 55-year-old woman presented with androgenetic alopecia which had started at age 40. Her clinical history revealed that, unlike… (More)
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1982
1982
Three patients with male pseudohermaphroditism due to 17,20-desmolase deficiency were studied at a pubertal age. Patients 1 and 2… (More)
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1980
1980
The author describes two methods of simultaneous estimation of pregnanetriolone, pregnanetetrol and delta 5-pregnenetriol. These… (More)
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1976
1976
Synthesis of 3H-pregnanetriolone permitted the estimation of pregnanetriolone in urine with a sensitivity in excess of most… (More)
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1975
1975
In healthy persons no or very little pregnanetriolone /PT'one; 3α,17α, 20α -trihydroxy-5β -pregnanll-one/ is excreted in the… (More)
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1966
1966
Polycystic ovaries were found in a 16-year-old female with congenital absence of vagina, male-like external genitalia, and… (More)
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