21-hydroxylase deficiency

 

Topic mentions per year

Topic mentions per year

1967-2017
0204019672017

Papers overview

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Highly Cited
2006
Highly Cited
2006
OBJECTIVES Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is the most common inherited disorder of adrenal… (More)
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Highly Cited
2002
Highly Cited
2002
Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency results in excessive androgen exposure in the gestational… (More)
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2000
2000
BACKGROUND Glucocorticoids are essential for the normal development and functioning of the adrenal medulla. Whether… (More)
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1997
1997
Premature adrenarche and functional adolescent androgen excess are common disorders which may evolve into polycystic ovary… (More)
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1995
1995
Steroid 21-hydroxylase deficiency is the most frequent cause of congenital adrenal hyperplasia. We have determined the 21… (More)
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Highly Cited
1992
Highly Cited
1992
Genotyping for 10 mutations in the CYP21 gene was performed in 88 families with congenital adrenal hyperplasia due to 21… (More)
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Highly Cited
1988
Highly Cited
1988
The need for a reliable screening test for classical congenital adrenal hyperplasia prompted development of newborn screening… (More)
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1987
1987
Among 80 women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency (40 with the simple virilizing form and 40… (More)
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Highly Cited
1985
Highly Cited
1985
Nonclassical steroid 21-hydroxylase deficiency is an autosomal recessive disorder that is defined by clinical and hormonal… (More)
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1977
1977
Congenital adrenal hyperplasia (C.A.H.) with 21-hydroxylase deficiency is an autosomal recessive disease. HLA genotyping of… (More)
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