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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1946 6
1947 4
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 158
2001 154
2002 137
2003 140
2004 170
2005 163
2006 201
2007 180
2008 184
2009 216
2010 264
2011 251
2012 266
2013 229
2014 251
2015 241
2016 251
2017 253
2018 247
2019 268
2020 309
2021 296
2022 311
2023 289
2024 320
2025 326
2026 283

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10,012 results

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Page 1
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.
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 …
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.
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.
Congenital Adrenal Hyperplasia.
Anisowicz SK, Vogt KS. Anisowicz SK, et al. Pediatr Ann. 2025 Feb;54(2):e74-e77. doi: 10.3928/19382359-20241203-02. Epub 2025 Feb 1. Pediatr Ann. 2025. PMID: 39928428 Review.
Congenital adrenal hyperplasia (CAH) is a rare disorder that typically presents in childhood. Affected female infants are most often discovered at birth due to virilized external genitalia, while male infants are diagnosed after newborn screening or, when non …
Congenital adrenal hyperplasia (CAH) is a rare disorder that typically presents in childhood. Affected female infants a …
Challenges in treatment of patients with non-classic congenital adrenal hyperplasia.
Adriaansen BPH, Schröder MAM, Span PN, Sweep FCGJ, van Herwaarden AE, Claahsen-van der Grinten HL. Adriaansen BPH, et al. Front Endocrinol (Lausanne). 2022 Dec 12;13:1064024. doi: 10.3389/fendo.2022.1064024. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36578966 Free PMC article. Review.
Congenital adrenal hyperplasia (CAH) due to 21alpha-hydroxylase deficiency (21OHD) or 11beta-hydroxylase deficiency (11OHD) are congenital conditions with affected adrenal steroidogenesis. ...Elevated precursor steroids are shunted into the unaf …
Congenital adrenal hyperplasia (CAH) due to 21alpha-hydroxylase deficiency (21OHD) or 11beta-hydroxylase deficiency (11 …
Pregnancy in Congenital Adrenal Hyperplasia.
Reisch N, Auchus RJ. Reisch N, et al. Endocrinol Metab Clin North Am. 2024 Sep;53(3):391-407. doi: 10.1016/j.ecl.2024.05.005. Epub 2024 Jun 25. Endocrinol Metab Clin North Am. 2024. PMID: 39084815 Review.
Over the last several decades, children with all forms of classic congenital adrenal hyperplasia (CAH) are identified early and treated appropriately throughout childhood. ...
Over the last several decades, children with all forms of classic congenital adrenal hyperplasia (CAH) are identified e …
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 …
Future Directions in the Management of Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.
Sarafoglou K, Auchus RJ. Sarafoglou K, et al. J Clin Endocrinol Metab. 2025 Jan 21;110(Supplement_1):S74-S87. doi: 10.1210/clinem/dgae759. J Clin Endocrinol Metab. 2025. PMID: 39836617 Free PMC article. Review.
CONTEXT: The traditional management of classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (21OHD) is difficult and often suboptimal. ...
CONTEXT: The traditional management of classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (21OHD) …
Novel treatments for congenital adrenal hyperplasia.
Schröder MAM, Claahsen-van der Grinten HL. Schröder MAM, et al. Rev Endocr Metab Disord. 2022 Jun;23(3):631-645. doi: 10.1007/s11154-022-09717-w. Epub 2022 Feb 23. Rev Endocr Metab Disord. 2022. PMID: 35199280 Free PMC article. Review.
Patients with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (21OHD) need life-long medical treatment to replace the lacking glucocorticoids and potentially lacking mineralocorticoids and to lower elevated adrenal androgens. .. …
Patients with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (21OHD) need life-long medical tr …
10,012 results
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