Introduction.
Epub 2015 Jan 15.Melmed S, Casanueva FF, Hoffman AR, Kleinberg DL, Montori VM, Schlechte JA, Wass JA; Endocrine Society.J Clin Endocrinol Metab. Unable to load your collection due to an error Click export CSV or RIS to download the entire page or use the checkboxes to select a subset of records to download
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2020 Jun;35(2):206-216. doi: 10.3803/EnM.2020.35.2.206.
Acromegaly is a disorder that results from excess growth hormone (GH) after the growth plates have closed. Epub 2006 Oct 3.Apovian CM, Aronne LJ, Bessesen DH, McDonnell ME, Murad MH, Pagotto U, Ryan DH, Still CD; Endocrine Society.J Clin Endocrinol Metab. Silverchair Information Systems Name must be less than 100 characters
The authors received no corporate funding or remuneration. Not only were the guideline authors experienced in taking care of acromegaly patients, they were considered thought …
Surgery is usually the treatment of choice, however over the last few years, several new methods of treatment have been developed. doi: 10.1002/edm2.158. eCollection 2020 Dec.Endocrinol Diabetes Metab. Includes conditions, investigations and treatment information.
The authors received no corporate funding or remuneration. Acromegaly is where the body produces too much growth hormone, leading to the excess growth of body tissues over time.effectiveness and cost-effectiveness of somatostatin analogues in the treatment of This guideline is cosponsored by the European Society of Endocrinology.
BACKGROUND: Quality of life (QoL) in patients with
American Association of Clinical Endocrinologists medical guidelines for clinical practice for the diagnosis and treatment of acromegaly - 2011 update external link opens in a new window.
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There may also be enlargement of the forehead, jaw, and nose.
Acromegaly is an endocrine disorder characterised by increased morbidity and mortality.
2020 Jun 9;3(3):e00158.
2014 Jun;99(6):1915-42. doi: 10.1210/jc.2014-1498.Blumer I, Hadar E, Hadden DR, Jovanovič L, Mestman JH, Murad MH, Yogev Y.J Clin Endocrinol Metab. Silverchair Information Systems
2020 Aug;23(4):327-337. doi: 10.1007/s11102-020-01059-7.
The operation that you have selected will move away from the current results page, your download options will not persist.Please click "Confirm" if you are happy to lose these search results.Information for doctors about acromegaly. This evidence-based guideline...
Katznelson, L et al. 2013 Nov;98(11):4227-49. doi: 10.1210/jc.2013-2465.Wierman ME, Basson R, Davis SR, Khosla S, Miller KK, Rosner W, Santoro N.J Clin Endocrinol Metab. An expert guideline recommends a repeat MRI in 12 months and, ... , Katznelson L, et al.
We continually create new guidelines and update existing guidelines to reflect evolving clinical science and meet the needs of practicing physicians. Please enable it to take advantage of the complete set of features! Participants: The Task Force included a chair selected by the Endocrine Society Clinical Guidelines Subcommittee (CGS), five experts in the field, and a methodologist. Epub 2020 Jun 24.Fleseriu M, Buchfelder M, Cetas JS, Fazeli PK, Mallea-Gil SM, Gurnell M, McCormack A, Pineyro MM, Syro LV, Tritos NA, Marcus HJ.Pituitary. Clipboard, Search History, and several other advanced features are temporarily unavailable. 2011 Feb;96(2):273-88. doi: 10.1210/jc.2010-1692.Bone Rep. 2020 Jul 18;13:100299. doi: 10.1016/j.bonr.2020.100299.
The meeting was sponsored by the Pituitary Society and the European Neuroendocrinology Association and included experts skilled in the management of acrom … COVID-19 is an emerging, rapidly evolving situation.
Treatment of acromegaly with the growth hormone-receptor antagonist pegvisomant.
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American Association of Clinical Endocrinologists medical guidelines for clinical practice for the diagnosis and treatment of acromegaly - 2011 update 31 July 2011 - Publisher: American Association of Clinical Endocrinologists
In March 2011, the Acromegaly Consensus Group met to revise and update the guidelines on the diagnosis and treatment of acromegaly complications.
The combined use of the different treatment approaches allows for attaining disease control or even complete cure in an increasing proportion of patients. It is usually caused by a growth hormone secreting pituitary adenoma and is manifested by a variety of clinical features.
Last published: 2011.
eCollection 2020 Jul.Savitz A, Fong B, Hochberg A, Rumore G, Chen C, Yun J, Sadur C.Endocrinol Metab (Seoul). Participants: The Task Force included a chair selected by the Endocrine Society Clinical Guidelines Subcommittee (CGS), five experts in the field, and a methodologist.
Washington, DC—The Endocrine Society today issued a Clinical Practice Guideline (CPG) for the diagnosis and treatment of acromegaly, a rare condition caused by excess growth hormone in the blood.
Lenders JW, Duh QY, Eisenhofer G, Gimenez-Roqueplo AP, Grebe SK, Murad MH, Naruse M, Pacak K, Young WF Jr; Endocrine Society.J Clin Endocrinol Metab.
We are dedicated to providing the field of endocrinology with timely, evidence-based recommendations for clinical care and practice. The initial symptom is typically enlargement of the hands and feet.
2006 Oct;91(10):3697-710. doi: 10.1210/jc.2006-1121. (2014) Acromegaly: an endocrine society clinical practice guideline, Journal of clinical endocrinology and metabolism, Vol.99(11) pp.3933-51. A vast spectrum of clinical studies has provided a lot of evidence for the place of the available options in the treatment strategies included in current guidelines. Objective: The aim was to formulate clinical practice guidelines for acromegaly.
Objective: The aim was to formulate clinical practice guidelines for acromegaly. Published by: American Association of Clinical Endocrinologists. Click to find out more about the condition acromegaly.
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