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Year Number of Results
1946 6
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1948 4
1949 3
1950 7
1951 15
1952 20
1953 20
1954 24
1955 25
1956 43
1957 62
1958 49
1959 52
1960 58
1961 50
1962 60
1963 75
1964 60
1965 65
1966 81
1967 103
1968 97
1969 115
1970 101
1971 85
1972 70
1973 75
1974 73
1975 63
1976 86
1977 80
1978 83
1979 107
1980 129
1981 128
1982 106
1983 100
1984 102
1985 140
1986 131
1987 130
1988 131
1989 124
1990 119
1991 110
1992 141
1993 113
1994 106
1995 126
1996 109
1997 144
1998 123
1999 136
2000 156
2001 154
2002 137
2003 140
2004 170
2005 163
2006 201
2007 180
2008 184
2009 216
2010 264
2011 251
2012 265
2013 229
2014 251
2015 241
2016 251
2017 253
2018 247
2019 268
2020 310
2021 296
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2025 57

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9,514 results

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Page 1
Congenital adrenal hyperplasia.
Auer MK, Nordenström A, Lajic S, Reisch N. Auer MK, et al. Lancet. 2023 Jan 21;401(10372):227-244. doi: 10.1016/S0140-6736(22)01330-7. Epub 2022 Dec 8. Lancet. 2023. PMID: 36502822 Review.
Congenital adrenal hyperplasia is a group of autosomal recessive disorders leading to multiple complex hormonal imbalances caused by various enzyme deficiencies in the adrenal steroidogenic pathway. The most common type of congenital adrenal
Congenital adrenal hyperplasia is a group of autosomal recessive disorders leading to multiple complex hormonal imbalan
Congenital Adrenal Hyperplasia.
Witchel SF. Witchel SF. J Pediatr Adolesc Gynecol. 2017 Oct;30(5):520-534. doi: 10.1016/j.jpag.2017.04.001. Epub 2017 Apr 24. J Pediatr Adolesc Gynecol. 2017. PMID: 28450075 Free PMC article. Review.
The congenital adrenal hyperplasias comprise a family of autosomal recessive disorders that disrupt adrenal steroidogenesis. ...For adolescent and adult men, prevention and early treatment of testicular adrenal rest tumors is beneficial. In this articl …
The congenital adrenal hyperplasias comprise a family of autosomal recessive disorders that disrupt adrenal steroidogen …
Congenital Adrenal Hyperplasia.
Fraga NR, Minaeian N, Kim MS. Fraga NR, et al. Pediatr Rev. 2024 Feb 1;45(2):74-84. doi: 10.1542/pir.2022-005617. Pediatr Rev. 2024. PMID: 38296783 Review.
We describe congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency, which is the most common primary adrenal insufficiency in children and adolescents. ...CAH is characterized by androgen excess secondary to impaired steroidogenesis in t …
We describe congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency, which is the most common primary …
Congenital adrenal hyperplasia.
El-Maouche D, Arlt W, Merke DP. El-Maouche D, et al. Lancet. 2017 Nov 11;390(10108):2194-2210. doi: 10.1016/S0140-6736(17)31431-9. Epub 2017 May 30. Lancet. 2017. PMID: 28576284 Review.
Congenital adrenal hyperplasia is a group of autosomal recessive disorders encompassing enzyme deficiencies in the adrenal steroidogenesis pathway that lead to impaired cortisol biosynthesis. ...Challenges in the treatment of congenital adren
Congenital adrenal hyperplasia is a group of autosomal recessive disorders encompassing enzyme deficiencies in the a
Nonclassic Congenital Adrenal Hyperplasia: What Do Endocrinologists Need to Know?
Jha S, Turcu AF. Jha S, et al. Endocrinol Metab Clin North Am. 2021 Mar;50(1):151-165. doi: 10.1016/j.ecl.2020.10.008. Epub 2021 Jan 9. Endocrinol Metab Clin North Am. 2021. PMID: 33518183 Free PMC article. Review.
Congenital adrenal hyperplasia encompasses a group of autosomal recessive defects in cortisol biosynthesis, and 21-hydroxylase deficiency accounts for 95% of such cases. Non-classic 21-hydroxylase deficiency is due to partial enzymatic defects, which present
Congenital adrenal hyperplasia encompasses a group of autosomal recessive defects in cortisol biosynthesis, and 21-hydr
Congenital adrenal hyperplasia: clinical symptoms and diagnostic methods.
Podgórski R, Aebisher D, Stompor M, Podgórska D, Mazur A. Podgórski R, et al. Acta Biochim Pol. 2018;65(1):25-33. doi: 10.18388/abp.2017_2343. Epub 2018 Mar 15. Acta Biochim Pol. 2018. PMID: 29543924 Free article. Review.
The aim of this paper is a straightforward presentation of the steroidogenesis process and the most common type of congenital adrenal hyperplasia (CAH) - 21-hydroxylase deficiency - as well as the analytical diagnostic methods that are used to recognize this …
The aim of this paper is a straightforward presentation of the steroidogenesis process and the most common type of congenital adre
The management of congenital adrenal hyperplasia during preconception, pregnancy, and postpartum.
Maher JY, Gomez-Lobo V, Merke DP. Maher JY, et al. Rev Endocr Metab Disord. 2023 Feb;24(1):71-83. doi: 10.1007/s11154-022-09770-5. Epub 2022 Nov 18. Rev Endocr Metab Disord. 2023. PMID: 36399318 Free PMC article. Review.
Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders of steroidogenesis of the adrenal cortex, most commonly due to 21-hydroxylase deficiency caused by mutations in the CYP21A2 gene. ...Pregnant women with classic CAH need g
Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders of steroidogenesis of the adrenal
Congenital Adrenal Hyperplasia.
Török D. Török D. Exp Suppl. 2019;111:245-260. doi: 10.1007/978-3-030-25905-1_12. Exp Suppl. 2019. PMID: 31588535 Review.
Congenital adrenal hyperplasia (CAH) is a group of seven autosomal recessively inherited disorders of various enzymes participating in adrenal steroid hormone synthesis. ...
Congenital adrenal hyperplasia (CAH) is a group of seven autosomal recessively inherited disorders of various enzymes p
Pregnancy in Congenital Adrenal Hyperplasia.
Reisch N. Reisch N. Endocrinol Metab Clin North Am. 2019 Sep;48(3):619-641. doi: 10.1016/j.ecl.2019.05.011. Endocrinol Metab Clin North Am. 2019. PMID: 31345527 Review.
Fertility rates in classic congenital adrenal hyperplasia caused by 21-hydroxylase deficiency are substantially decreased for various reasons, including hormonal, anatomic, psychosocial, and psychosexual causes. ...Pregnancy reports in rarer forms of conge
Fertility rates in classic congenital adrenal hyperplasia caused by 21-hydroxylase deficiency are substantially decreas …
Congenital Adrenal Hyperplasia.
Kobayashi A, Fujiu K. Kobayashi A, et al. Int Heart J. 2024;65(1):1-3. doi: 10.1536/ihj.23-647. Int Heart J. 2024. PMID: 38296561 Free article. No abstract available.
9,514 results