Pegvisomant, a GH receptor antagonist, is a new pharmaceutical approach to acromegaly. It enables IGF-I levels to return in the age- and sex-reference range in approximately 90% of patients. This new approach is particularly beneficial in those patients who do not experience control of hormone hypersecretion after surgery and/or medical treatment with somatostatin analogs. In our preliminary experience, out of 16 patients unsuccessfully operated on by transsphenoidal surgery and resistant to 40-mg octreotide-LAR or 120-mg lanreotide for at least 6 months, 13 normalized their IGF-I levels within 6 months from treatment beginning. Normalization of IGF-I levels was accompanied by a significant decrease of ring size. We did not observe any incr...
Acromegaly is characterized by chronic, excess secretion of growth hormone (GH) from a pituitary ade...
Acromegaly management is a significant challenge for endocrinologists. The Acromegaly Consensus Grou...
Acromegaly is characterized by chronic, excess secretion of growth hormone (GH) from a pituitary ade...
Pegvisomant, a GH receptor antagonist, is a new pharmaceutical approach to acromegaly. It enables IG...
Acromegaly, a multisystemic disease resulting from excessive growth hormone (GH) and insulin-like gr...
Currently available medical treatment of acromegaly includes dopamine agonists, slow release formula...
OBJECTIVE: We aimed to investigate the efficacy of pegvisomant in patients with acromegaly resistant...
Somatostatin analogs (SA) are widely used in acromegaly, either as first-line or adjuvant treatment ...
Acromegaly is a chronic disorder invariably caused by a growth hormone (GH)-secreting pituitary tumo...
AbstractMono-therapy using long-acting somatostatin analogues and surgery cannot provide optimal bio...
In nearly all cases, acromegaly is caused by excess GH from a pituitary adenoma, resulting in elevat...
textabstractTreatment of acromegaly with monotherapy long-acting somatostatin analogues (LA-SSA) as ...
Acromegaly is a chronic disease with signs and symptoms due to growth hormone (GH) excess. The most ...
Acromegaly is a rare and severe disease caused by an increased and autonomous secretion of growth ho...
Optimal biochemical control cannot be attained by long-acting somatostatin analog monotherapy in a l...
Acromegaly is characterized by chronic, excess secretion of growth hormone (GH) from a pituitary ade...
Acromegaly management is a significant challenge for endocrinologists. The Acromegaly Consensus Grou...
Acromegaly is characterized by chronic, excess secretion of growth hormone (GH) from a pituitary ade...
Pegvisomant, a GH receptor antagonist, is a new pharmaceutical approach to acromegaly. It enables IG...
Acromegaly, a multisystemic disease resulting from excessive growth hormone (GH) and insulin-like gr...
Currently available medical treatment of acromegaly includes dopamine agonists, slow release formula...
OBJECTIVE: We aimed to investigate the efficacy of pegvisomant in patients with acromegaly resistant...
Somatostatin analogs (SA) are widely used in acromegaly, either as first-line or adjuvant treatment ...
Acromegaly is a chronic disorder invariably caused by a growth hormone (GH)-secreting pituitary tumo...
AbstractMono-therapy using long-acting somatostatin analogues and surgery cannot provide optimal bio...
In nearly all cases, acromegaly is caused by excess GH from a pituitary adenoma, resulting in elevat...
textabstractTreatment of acromegaly with monotherapy long-acting somatostatin analogues (LA-SSA) as ...
Acromegaly is a chronic disease with signs and symptoms due to growth hormone (GH) excess. The most ...
Acromegaly is a rare and severe disease caused by an increased and autonomous secretion of growth ho...
Optimal biochemical control cannot be attained by long-acting somatostatin analog monotherapy in a l...
Acromegaly is characterized by chronic, excess secretion of growth hormone (GH) from a pituitary ade...
Acromegaly management is a significant challenge for endocrinologists. The Acromegaly Consensus Grou...
Acromegaly is characterized by chronic, excess secretion of growth hormone (GH) from a pituitary ade...