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

Year Number of Results
1976 1
1977 1
1980 1
1982 3
1983 1
1984 2
1985 2
1986 2
1987 1
1988 3
1989 2
1990 2
1991 2
1992 3
1993 4
1994 2
1995 6
1996 2
1997 3
1998 5
1999 12
2000 5
2001 8
2002 3
2003 3
2004 5
2005 10
2006 21
2007 22
2008 17
2009 12
2010 20
2011 22
2012 20
2013 36
2014 32
2015 38
2016 44
2017 30
2018 33
2019 34
2020 33
2021 24
2022 18
2023 20
2024 10

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516 results

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Quoted phrase not found in phrase index: "Growth hormone-producing pituitary gland adenoma"
Page 1
Acromegaly: pathogenesis, diagnosis, and management.
Fleseriu M, Langlois F, Lim DST, Varlamov EV, Melmed S. Fleseriu M, et al. Lancet Diabetes Endocrinol. 2022 Nov;10(11):804-826. doi: 10.1016/S2213-8587(22)00244-3. Epub 2022 Oct 6. Lancet Diabetes Endocrinol. 2022. PMID: 36209758 Review.
Growth hormone-secreting pituitary adenomas that cause acromegaly arise as monoclonal expansions of differentiated somatotroph cells and are usually sporadic. They are almost invariably benign, yet they can be locally invasive and show progressive g …
Growth hormone-secreting pituitary adenomas that cause acromegaly arise as monoclonal expansions of differentiat …
Diagnosis and Treatment of Acromegaly: An Update.
Ershadinia N, Tritos NA. Ershadinia N, et al. Mayo Clin Proc. 2022 Feb;97(2):333-346. doi: 10.1016/j.mayocp.2021.11.007. Mayo Clin Proc. 2022. PMID: 35120696 Review.
Acromegaly is typically caused by a growth hormone-secreting pituitary adenoma, driving excess secretion of insulin-like growth factor 1. ...Early diagnosis and adequate treatment are essential to mitigate excess mortality associated with …
Acromegaly is typically caused by a growth hormone-secreting pituitary adenoma, driving excess secretion …
Diagnosis and Treatment of Pituitary Adenomas: A Review.
Molitch ME. Molitch ME. JAMA. 2017 Feb 7;317(5):516-524. doi: 10.1001/jama.2016.19699. JAMA. 2017. PMID: 28170483 Review.
Prolactinomas account for 32% to 66% of adenomas and present with amenorrhea, loss of libido, galactorrhea, and infertility in women and loss of libido, erectile dysfunction, and infertility in men; they are generally treated with the dopamine agonists cabergoline and bromocripti …
Prolactinomas account for 32% to 66% of adenomas and present with amenorrhea, loss of libido, galactorrhea, and infertility in women and los …
Somatostatin Analogs in Clinical Practice: a Review.
Gomes-Porras M, Cárdenas-Salas J, Álvarez-Escolá C. Gomes-Porras M, et al. Int J Mol Sci. 2020 Feb 29;21(5):1682. doi: 10.3390/ijms21051682. Int J Mol Sci. 2020. PMID: 32121432 Free PMC article. Review.
Acromegaly pathogenesis and treatment.
Melmed S. Melmed S. J Clin Invest. 2009 Nov;119(11):3189-202. doi: 10.1172/JCI39375. Epub 2009 Nov 2. J Clin Invest. 2009. PMID: 19884662 Free PMC article. Review.
Dysregulated growth hormone (GH) hypersecretion is usually caused by a GH-secreting pituitary adenoma and leads to acromegaly - a disorder of disproportionate skeletal, tissue, and organ growth. ...Somatostatin receptor (SSTR) ligands inhibit GH …
Dysregulated growth hormone (GH) hypersecretion is usually caused by a GH-secreting pituitary adenoma and leads …
Pituitary-Tumor Endocrinopathies.
Melmed S. Melmed S. N Engl J Med. 2020 Mar 5;382(10):937-950. doi: 10.1056/NEJMra1810772. N Engl J Med. 2020. PMID: 32130815 Review. No abstract available.
Acromegaly.
Chanson P, Salenave S, Kamenicky P. Chanson P, et al. Handb Clin Neurol. 2014;124:197-219. doi: 10.1016/B978-0-444-59602-4.00014-9. Handb Clin Neurol. 2014. PMID: 25248589 Review.
Acromegaly is due to excessive production of growth hormone (GH), generally by a pituitary GH-secreting adenoma. ...The diagnosis is confirmed by elevated serum GH concentrations that cannot be suppressed by an oral glucose load, and by increased level …
Acromegaly is due to excessive production of growth hormone (GH), generally by a pituitary GH-secreting adenoma. …
Pediatric pituitary adenomas.
Walz PC, Drapeau A, Shaikhouni A, Eide J, Rugino AJ, Mohyeldin A, Carrau R, Prevedello D. Walz PC, et al. Childs Nerv Syst. 2019 Nov;35(11):2107-2118. doi: 10.1007/s00381-019-04293-y. Epub 2019 Jul 13. Childs Nerv Syst. 2019. PMID: 31302729 Review.
BACKGROUND: Pediatric pituitary adenomas are a rare medical entity that makes up a small portion of intracranial tumors in children and adolescents. ...We will also discuss our current treatment paradigm using endoscopic, open, and combined approaches to treat these tumors …
BACKGROUND: Pediatric pituitary adenomas are a rare medical entity that makes up a small portion of intracranial tumors in children a …
Acromegaly in the elderly patients.
Ambrosio MR, Gagliardi I, Chiloiro S, Ferreira AG, Bondanelli M, Giampietro A, Bianchi A, Marinis L, Fleseriu M, Zatelli MC. Ambrosio MR, et al. Endocrine. 2020 Apr;68(1):16-31. doi: 10.1007/s12020-020-02206-7. Epub 2020 Feb 14. Endocrine. 2020. PMID: 32060689 Review.
BACKGROUND: Acromegaly is a rare disease characterized by a chronic exposition to growth hormone (GH) and insulin-like growth factor-1 (IGF-1), caused in most cases by a pituitary GH-secreting adenoma. ...Recent epidemiological data report an im …
BACKGROUND: Acromegaly is a rare disease characterized by a chronic exposition to growth hormone (GH) and insulin-like grow …
Acromegaly: Medical and Surgical Considerations.
Giantini-Larsen AM, Uribe-Cardenas R, Juthani RG. Giantini-Larsen AM, et al. Otolaryngol Clin North Am. 2022 Apr;55(2):331-341. doi: 10.1016/j.otc.2021.12.007. Epub 2022 Mar 4. Otolaryngol Clin North Am. 2022. PMID: 35256175 Review.
Acromegaly results from excessive secretion of insulinlike growth factor-1 and growth hormone, which most commonly occurs because of pituitary somatotrophinoma. Diagnostic features of acromegaly include elevated insulinlike growth factor-1 and …
Acromegaly results from excessive secretion of insulinlike growth factor-1 and growth hormone, which most commonly occu …
516 results