This thesis describes the long-term consequences of growth hormone and insulin-like growth factor I excess in patients cured from acromegaly for a mean duration of 17 years. Regarding the considerable prevalence of diverse morbidity in these patients, during the active phase of the disease but even more so after 17 years of disease cure, we suggest the screening of acromegalic patients on highly frequent comorbidities, such as osteoarthritis, vertebral fractures, colonic polyps, and colonic diverticulae. It is of great concern to recognize the long-term consequences of the disease in order to offer the patients adequate follow-up and multidisciplinary care. The aim should be to control the persisting complex morbidity as much as possible in...
Copyright © 2012 Zdenko Killinger et al. This is an open access article distributed under the Creati...
Acromegaly is a rare chronic, systemic disorder caused by excessive growth hormone (GH) secretion fr...
In the majority of cases, acromegaly is due to GH hypersecretion by a somatotroph pituitary tumor. T...
In this thesis, a number of observations are described in acromegaly patients with cured or biochemi...
This review focuses on the systemic complications of acromegaly. Mortality in this disease is increa...
Introduction: Acromegaly is a rare clinical condition characterized by chronic growth hormone (GH) ...
Objective: Growth hormone (GH) and insulin-like growth factor 1 (IGF-1) excess results in both rever...
[Abstract] Acromegaly and gigantism are due to excess GH production, usually as a result of a pituit...
Item does not contain fulltextOBJECTIVE: Arthropathy is an invalidating complication of acromegaly, ...
This thesis defines mortality in acromegaly in a modern patient cohort, elucidates underlying explan...
Introduction: Acromegaly is a chronic disease resulting from increased secretion of growth hormone. ...
Acromegaly is a rare disorder caused by chronic growth hormone (GH) hypersecretion. While diagnostic...
Current treatment of acromegaly restores a normal life expectancy in most cases. So, the study of pe...
Objective: The aim of the study was to evaluate the impact of the genomic deletion of exon 3 of the ...
Acromegaly is a rare disorder caused by chronic growth hormone (GH) hypersecretion. While diagnostic...
Copyright © 2012 Zdenko Killinger et al. This is an open access article distributed under the Creati...
Acromegaly is a rare chronic, systemic disorder caused by excessive growth hormone (GH) secretion fr...
In the majority of cases, acromegaly is due to GH hypersecretion by a somatotroph pituitary tumor. T...
In this thesis, a number of observations are described in acromegaly patients with cured or biochemi...
This review focuses on the systemic complications of acromegaly. Mortality in this disease is increa...
Introduction: Acromegaly is a rare clinical condition characterized by chronic growth hormone (GH) ...
Objective: Growth hormone (GH) and insulin-like growth factor 1 (IGF-1) excess results in both rever...
[Abstract] Acromegaly and gigantism are due to excess GH production, usually as a result of a pituit...
Item does not contain fulltextOBJECTIVE: Arthropathy is an invalidating complication of acromegaly, ...
This thesis defines mortality in acromegaly in a modern patient cohort, elucidates underlying explan...
Introduction: Acromegaly is a chronic disease resulting from increased secretion of growth hormone. ...
Acromegaly is a rare disorder caused by chronic growth hormone (GH) hypersecretion. While diagnostic...
Current treatment of acromegaly restores a normal life expectancy in most cases. So, the study of pe...
Objective: The aim of the study was to evaluate the impact of the genomic deletion of exon 3 of the ...
Acromegaly is a rare disorder caused by chronic growth hormone (GH) hypersecretion. While diagnostic...
Copyright © 2012 Zdenko Killinger et al. This is an open access article distributed under the Creati...
Acromegaly is a rare chronic, systemic disorder caused by excessive growth hormone (GH) secretion fr...
In the majority of cases, acromegaly is due to GH hypersecretion by a somatotroph pituitary tumor. T...