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1963
2025

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

Year Number of Results
1963 3
1964 2
1968 7
1969 5
1970 5
1971 3
1972 4
1973 4
1974 7
1975 3
1976 8
1977 1
1978 3
1979 6
1980 1
1981 4
1982 6
1983 5
1984 2
1985 3
1986 2
1987 5
1988 2
1989 4
1990 4
1991 2
1992 7
1993 6
1994 1
1995 5
1996 3
1997 6
1998 5
1999 10
2000 5
2001 7
2002 5
2003 8
2004 9
2005 10
2006 5
2007 16
2008 9
2009 12
2010 15
2011 14
2012 9
2013 5
2014 15
2015 7
2016 12
2017 10
2018 11
2019 7
2020 11
2021 22
2022 14
2023 10
2024 8
2025 0

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369 results

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Page 1
Cushing's syndrome.
Lacroix A, Feelders RA, Stratakis CA, Nieman LK. Lacroix A, et al. Lancet. 2015 Aug 29;386(9996):913-27. doi: 10.1016/S0140-6736(14)61375-1. Epub 2015 May 21. Lancet. 2015. PMID: 26004339 Review.
Congenital Hypothyroidism in Preterm Newborns - The Challenges of Diagnostics and Treatment: A Review.
Klosinska M, Kaczynska A, Ben-Skowronek I. Klosinska M, et al. Front Endocrinol (Lausanne). 2022 Mar 18;13:860862. doi: 10.3389/fendo.2022.860862. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35370986 Free PMC article. Review.
The decreased level of thyroxine regardless of cause may lead to delayed mental development. Congenital hypothyroidism (CH) is a disorder highly prevalent in premature neonates and it originates from maternal factors, perinatal and labor complications, genetic abnormali
The decreased level of thyroxine regardless of cause may lead to delayed mental development. Congenital hypothyroidism (CH) is a diso …
Hypothalamic syndrome.
Müller HL, Tauber M, Lawson EA, Özyurt J, Bison B, Martinez-Barbera JP, Puget S, Merchant TE, van Santen HM. Müller HL, et al. Nat Rev Dis Primers. 2022 Apr 21;8(1):24. doi: 10.1038/s41572-022-00351-z. Nat Rev Dis Primers. 2022. PMID: 35449162 Review.
Hypothalamic syndrome (HS) is a rare disorder caused by disease-related and/or treatment-related injury to the hypothalamus, most commonly associated with rare, non-cancerous parasellar masses, such as craniopharyngiomas, germ cell tumours, gliomas, cysts of Rathke's pouch …
Hypothalamic syndrome (HS) is a rare disorder caused by disease-related and/or treatment-related injury to the hypothalamus, most com …
Male and Female Hypogonadism.
Richard-Eaglin A. Richard-Eaglin A. Nurs Clin North Am. 2018 Sep;53(3):395-405. doi: 10.1016/j.cnur.2018.04.006. Nurs Clin North Am. 2018. PMID: 30100005 Review.
Secondary hypogonadism is the result of a dysfunction within the hypothalamus and/or pituitary. Diagnosis of hypogonadism requires a comprehensive health history, evaluation of the signs and symptoms, complete physical examination, as well as laboratory and diagnostic test …
Secondary hypogonadism is the result of a dysfunction within the hypothalamus and/or pituitary. Diagnosis of hypogonadism requires a …
Development of the Pituitary Gland.
Alatzoglou KS, Gregory LC, Dattani MT. Alatzoglou KS, et al. Compr Physiol. 2020 Mar 12;10(2):389-413. doi: 10.1002/cphy.c150043. Compr Physiol. 2020. PMID: 32163208 Review.
Endocrine cells of the pituitary gland are organized into structural and functional networks that contribute to the coordinated response of endocrine cells to stimuli; these cellular networks are formed during embryonic development and are maintained or may be modified in adultho …
Endocrine cells of the pituitary gland are organized into structural and functional networks that contribute to the coordinated response of …
Hypoglycaemia in adrenal insufficiency.
Lee SC, Baranowski ES, Sakremath R, Saraff V, Mohamed Z. Lee SC, et al. Front Endocrinol (Lausanne). 2023 Nov 20;14:1198519. doi: 10.3389/fendo.2023.1198519. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 38053731 Free PMC article. Review.
Adrenal insufficiency encompasses a group of congenital and acquired disorders that lead to inadequate steroid production by the adrenal glands, mainly glucocorticoids, mineralocorticoids and androgens. ...Adrenal insufficiency may be primary, affecting the adrenal gland's …
Adrenal insufficiency encompasses a group of congenital and acquired disorders that lead to inadequate steroid production by the adre …
Clinical review: Klinefelter syndrome--a clinical update.
Groth KA, Skakkebæk A, Høst C, Gravholt CH, Bojesen A. Groth KA, et al. J Clin Endocrinol Metab. 2013 Jan;98(1):20-30. doi: 10.1210/jc.2012-2382. Epub 2012 Nov 1. J Clin Endocrinol Metab. 2013. PMID: 23118429 Review.
The role of steroid hormones in the sexual differentiation of the human brain.
Bakker J. Bakker J. J Neuroendocrinol. 2022 Feb;34(2):e13050. doi: 10.1111/jne.13050. Epub 2021 Oct 27. J Neuroendocrinol. 2022. PMID: 34708466 Free article. Review.
Both clinical and neuroimaging data obtained in patients with altered androgen levels/actions (i.e., congenital adrenal hyperplasia or complete androgen insensitivity syndrome [CAIS]), point to an important role of (prenatal) androgens in inducing typical male neural and p …
Both clinical and neuroimaging data obtained in patients with altered androgen levels/actions (i.e., congenital adrenal hyperplasia o …
Clinical advances in the pharmacotherapy of congenital adrenal hyperplasia.
Prete A, Auchus RJ, Ross RJ. Prete A, et al. Eur J Endocrinol. 2021 Nov 30;186(1):R1-R14. doi: 10.1530/EJE-21-0794. Eur J Endocrinol. 2021. PMID: 34735372 Free PMC article. Review.
BACKGROUND: Patients with 21-hydroxylase deficiency congenital adrenal hyperplasia (21OHD-CAH) have poor health outcomes with increased mortality, short stature, impaired fertility, and increased cardiovascular risk factors such as obesity. ...METHODS: Narrative review of …
BACKGROUND: Patients with 21-hydroxylase deficiency congenital adrenal hyperplasia (21OHD-CAH) have poor health outcomes with increas …
369 results