ライフサイエンスコーパス: acromegaly

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1 cated gene in samples from 248 patients with acromegaly.

2 ress growth hormone (GH) secretion and treat acromegaly.

3 alogs provide safe and effective therapy for acromegaly.

4 evelop skeletal abnormalities reminiscent of acromegaly.

5 a patient with McCune-Albright syndrome and acromegaly.

6 ing tumors; it is less commonly required for acromegaly.

7 rrent mutation in GPR101 in some adults with acromegaly.

8 de) in patients with inadequately controlled acromegaly.

9 GH-secreting pituitary adenoma and leads to acromegaly - a disorder of disproportionate skeletal, ti

10 For acromegaly and adrenocorticotropin hormone (ACTH)-secret

11 of thyroid dysfunction, hyperparathyroidism, acromegaly and hypercortisolism on bone.

12 reotide was first used for the management of acromegaly and later used for metastatic gastroenteropan

13 like headache was only seen in patients with acromegaly and prolactinoma.

14 Carney complex and, most recently, familial acromegaly and prolactinomas and other tumors caused by

15 ildren treated with GH, and tall stature and acromegaly are associated with an increased incidence of

16 adults; the genetic causes of gigantism and acromegaly are poorly understood.

17 Somatostatin analogues improved acromegaly-associated headache in 64% of cases, although

18 Many patients with acromegaly do not achieve biochemical control despite re

19 lated growth hormone (GH) hypersecretion and acromegaly; however, regulatory mechanisms that promote

20 h hormone leads to gigantism in children and acromegaly in adults; the genetic causes of gigantism an

21 Acromegaly is a human disease of growth hormone (GH) exc

22 Acromegaly is a rare disabling disorder that results in

23 Growth hormone (GH) excess in acromegaly is associated with increased precancerous col

24 be particularly challenging in patients with acromegaly or Cushing's disease.

25 hypertrophy due to valvular aortic stenosis, acromegaly, or growth hormone deficiency, conditions ass

26 This Review discusses acromegaly pathogenesis and management options.

27 nistration of a GH receptor (GHR) blocker in acromegaly patients induced colon p53 and adenomatous po

28 n and cardiac myxomas, Cushing syndrome, and acromegaly were present in 62, 30, 31 and 8 percent of t

29 ituitary-directed treatment in patients with acromegaly who are inadequately controlled using first-g

30 ligible patients aged 18 years or older with acromegaly who were inadequately controlled (5-point, 2

31 utation (p.E308D) in 11 of 248 patients with acromegaly, with the mutation found mostly in tumors.

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