In nearly all cases, acromegaly is caused by excess GH from a pituitary adenoma, resulting in elevated circulating levels of GH and, subsequently, IGF-1. Treatment goals are to eliminate morbidity and restore the increased mortality to normal rates. Therapeutic strategies aim to minimize tumor mass and normalize GH and IGF-1 levels. Somatostatin analogues are the medical treatment of choice in acromegaly, as first-line or post-surgical therapy, and have proven efficacy in pituitary tumor volume reduction (TVR)
Somatostatin is a hypothalamic inhibitor of pituitary growth hormone secretion and cell proliferatio...
Somatostatin is an important physiological regulator of neuroendocrine function across multiple biol...
The effects of a 12- to 24-month treatment with depot long-acting octreotide (OCT-LAR) on hormone pr...
In nearly all cases, acromegaly is caused by excess GH from a pituitary adenoma, resulting in elevat...
Acromegaly is a chronic disease with signs and symptoms due to growth hormone (GH) excess. The most ...
The medical approach to patients with secreting or clinically non-functioning pituitary adenoma as m...
Somatostatin analogues (SSA) are well established for the treatment of acromegaly, an acquired diso...
Acromegaly is characterized by increased release of growth hormone and, consequently, insulin-like g...
To cure acromegalic patients, transsphenoidal surgery is considered first, especially for microadeno...
Pegvisomant, a GH receptor antagonist, is a new pharmaceutical approach to acromegaly. It enables IG...
Somatostatin analogs (SA) are widely used in acromegaly, either as first-line or adjuvant treatment ...
Acromegaly is a hormonal disorder which results when pituitary adenoma produces more growth hormone ...
AbstractMono-therapy using long-acting somatostatin analogues and surgery cannot provide optimal bio...
A 46-year-old woman with acromegaly and hyperthyroidism due to a pituitary adenoma. She had high ser...
Optimal biochemical control cannot be attained by long-acting somatostatin analog monotherapy in a l...
Somatostatin is a hypothalamic inhibitor of pituitary growth hormone secretion and cell proliferatio...
Somatostatin is an important physiological regulator of neuroendocrine function across multiple biol...
The effects of a 12- to 24-month treatment with depot long-acting octreotide (OCT-LAR) on hormone pr...
In nearly all cases, acromegaly is caused by excess GH from a pituitary adenoma, resulting in elevat...
Acromegaly is a chronic disease with signs and symptoms due to growth hormone (GH) excess. The most ...
The medical approach to patients with secreting or clinically non-functioning pituitary adenoma as m...
Somatostatin analogues (SSA) are well established for the treatment of acromegaly, an acquired diso...
Acromegaly is characterized by increased release of growth hormone and, consequently, insulin-like g...
To cure acromegalic patients, transsphenoidal surgery is considered first, especially for microadeno...
Pegvisomant, a GH receptor antagonist, is a new pharmaceutical approach to acromegaly. It enables IG...
Somatostatin analogs (SA) are widely used in acromegaly, either as first-line or adjuvant treatment ...
Acromegaly is a hormonal disorder which results when pituitary adenoma produces more growth hormone ...
AbstractMono-therapy using long-acting somatostatin analogues and surgery cannot provide optimal bio...
A 46-year-old woman with acromegaly and hyperthyroidism due to a pituitary adenoma. She had high ser...
Optimal biochemical control cannot be attained by long-acting somatostatin analog monotherapy in a l...
Somatostatin is a hypothalamic inhibitor of pituitary growth hormone secretion and cell proliferatio...
Somatostatin is an important physiological regulator of neuroendocrine function across multiple biol...
The effects of a 12- to 24-month treatment with depot long-acting octreotide (OCT-LAR) on hormone pr...