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

Year Number of Results
1963 5
1964 6
1966 1
1967 2
1968 9
1969 11
1970 7
1971 16
1972 4
1973 12
1974 5
1975 3
1976 7
1977 3
1978 5
1979 3
1980 6
1981 11
1982 6
1983 3
1984 3
1985 11
1986 6
1987 2
1988 8
1989 5
1990 5
1991 8
1992 5
1993 9
1994 10
1995 21
1996 4
1997 8
1998 6
1999 15
2000 15
2001 16
2002 18
2003 15
2004 10
2005 21
2006 22
2007 14
2008 12
2009 9
2010 14
2011 15
2012 15
2013 16
2014 13
2015 10
2016 14
2017 21
2018 18
2019 10
2020 19
2021 11
2022 15
2023 11
2024 5

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579 results

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Page 1
Adrenal myelolipomas.
Calissendorff J, Juhlin CC, Sundin A, Bancos I, Falhammar H. Calissendorff J, et al. Lancet Diabetes Endocrinol. 2021 Nov;9(11):767-775. doi: 10.1016/S2213-8587(21)00178-9. Epub 2021 Aug 24. Lancet Diabetes Endocrinol. 2021. PMID: 34450092 Free PMC article. Review.
Adrenal myelolipomas are benign, lipomatous tumours with elements of myeloid cells, most of which present as adrenal incidentalomas and comprise 3.3-6.5% of all adrenal masses. ...Patients with congenital adrenal hyperplasia exhibit a higher pre …
Adrenal myelolipomas are benign, lipomatous tumours with elements of myeloid cells, most of which present as adrenal incidenta …
Approach to androgen excess in women: Clinical and biochemical insights.
Cussen L, McDonnell T, Bennett G, Thompson CJ, Sherlock M, O'Reilly MW. Cussen L, et al. Clin Endocrinol (Oxf). 2022 Aug;97(2):174-186. doi: 10.1111/cen.14710. Epub 2022 Mar 29. Clin Endocrinol (Oxf). 2022. PMID: 35349173 Free PMC article. Review.
Identification of women with non-PCOS pathology within large cohorts of patients presenting with androgen excess represents a diagnostic challenge for the endocrinologist, and rare pathology including nonclassic congenital adrenal hyperplasia, severe insulin resista …
Identification of women with non-PCOS pathology within large cohorts of patients presenting with androgen excess represents a diagnostic cha …
Approach to Investigation of Hyperandrogenism in a Postmenopausal Woman.
Hirschberg AL. Hirschberg AL. J Clin Endocrinol Metab. 2023 Apr 13;108(5):1243-1253. doi: 10.1210/clinem/dgac673. J Clin Endocrinol Metab. 2023. PMID: 36409990 Free PMC article. Review.
Postmenopausal hyperandrogenism is a condition caused by relative or absolute androgen excess originating from the ovaries and/or the adrenal glands. Hirsutism, in other words, increased terminal hair growth in androgen-dependent areas of the body, is considered the …
Postmenopausal hyperandrogenism is a condition caused by relative or absolute androgen excess originating from the ovaries and/or the adr …
Management of Incidentalomas.
Reidelberger K, Fingeret A. Reidelberger K, et al. Surg Clin North Am. 2021 Dec;101(6):1081-1096. doi: 10.1016/j.suc.2021.06.006. Surg Clin North Am. 2021. PMID: 34774270 Review.
This review details the epidemiology, considerations, and recommendations for management of common incidental manifestations in surgical patients, including Meckel diverticulum, adrenal incidentaloma, thyroid nodule, solitary pulmonary nodule, small bowel intussusception, …
This review details the epidemiology, considerations, and recommendations for management of common incidental manifestations in surgical pat …
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. ...Classic patients are treated with glucocorticoid substitutio …
Congenital adrenal hyperplasia (CAH) due to 21alpha-hydroxylase deficiency (21OHD) or 11beta-hydroxylase deficiency (11OHD) ar …
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 the a …
We describe congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency, which is the most common primary adrenal …
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. ...Congenital causes of adrenal ins …
Adrenal insufficiency encompasses a group of congenital and acquired disorders that lead to inadequate steroid production by t …
Pheochromocytoma/Paraganglioma: Is This a Genetic Disorder?
Fishbein L. Fishbein L. Curr Cardiol Rep. 2019 Jul 31;21(9):104. doi: 10.1007/s11886-019-1184-y. Curr Cardiol Rep. 2019. PMID: 31367972 Review.
Pheochromocytomas and paragangliomas (PCC/PGL) are neuroendocrine tumors of the adrenal medulla and extra-adrenal ganglia which often over-secrete catecholamines leading to cardiovascular morbidity and even mortality. ...
Pheochromocytomas and paragangliomas (PCC/PGL) are neuroendocrine tumors of the adrenal medulla and extra-adrenal ganglia whic …
Adrenal hyperplasias in childhood: An update.
Pitsava G, Stratakis CA. Pitsava G, et al. Front Endocrinol (Lausanne). 2022 Aug 3;13:937793. doi: 10.3389/fendo.2022.937793. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35992119 Free PMC article. Review.
Most cases are due to defects in the cyclic AMP/protein kinase A (cAMP/PKA) pathway, although a few cases remain without an identified genetic defect. Another cause of adrenal hyperplasia in childhood is congenital adrenal hyperplasia, a group of autosomal re …
Most cases are due to defects in the cyclic AMP/protein kinase A (cAMP/PKA) pathway, although a few cases remain without an identified genet …
579 results