Results 81 to 90 of about 20,619 (221)

[Pregnancy in active acromegaly]

open access: yes, 2008
A 29-year-old woman with a long-lasting history of oligoamenorrhea, fell pregnant shortly after being diagnosed with acromegaly. LABORATORY TESTS AND IMAGING: A high IGF-1 concentration and an oral glucose tolerance test confirmed the diagnosis.
Christ, E, Sahli, R
core   +1 more source

Very Long‐Term Follow‐Up of Multidimensional Health‐Related Quality of Life After Endoscopic Endonasal Surgery for Pituitary Adenomas: A Prospective Cohort Study

open access: yesHead &Neck, Volume 48, Issue 4, Page 1088-1096, April 2026.
ABSTRACT Background To evaluate postoperative health‐related quality of life (HRQoL) for pituitary adenoma patients, multidimensional assessment is important. Available data is limited on long‐term follow‐up. Methods Prospectively, 52 nonfunctioning (NFA) and functioning (FA) pituitary adenoma patients were included.
Gonneke E. Joustra   +7 more
wiley   +1 more source

Feline Acromegaly [PDF]

open access: yesTopics in Companion Animal Medicine, 2012
Acromegaly, or hypersomatotropism, results from chronic, excessive secretion of growth hormone in the adult animal. The anabolic effects of growth hormone are exerted through the intermediary hormone, insulin-like growth factor 1, which is produced in the liver under the influence of growth hormone.
openaire   +2 more sources

Diagnostic challenges and management of a patient with acromegaly due to ectopic growth hormone-releasing hormone secretion from a bronchial carcinoid tumour

open access: yesEndocrinology, Diabetes & Metabolism Case Reports, 2017
A male patient presented at the age of 30 with classic clinical features of acromegaly and was found to have elevated growth hormone levels, not suppressing during an oral glucose tolerance test.
Nikolaos Kyriakakis   +6 more
doaj   +1 more source

Somatostatin receptor ligands in acromegaly: clinical response and factors predicting resistance

open access: yes, 2017
Introduction: Somatostatin (SST) receptor ligands (SRL), in particular those of first generation (Octreotide and Lanreotide), are widely used in medical treatment of acromegaly, but they assure biochemical control of disease (and the possibility of an ...
Paragliola, Rosa Maria   +1 more
core   +1 more source

Knowledge, Attitude, and Practice of Diabetes Mellitus Management in the Age Group Above 40 Years' Patients Attending the Medical Outpatient Department of the Tertiary Care Center, Nepal: A Cross‐Sectional Study

open access: yesHealth Science Reports, Volume 9, Issue 4, April 2026.
ABSTRACT Background and Aims Diabetes Mellitus (DM) is a chronic metabolic disease and a major global health issue that has reached alarming levels. Developing countries including Nepal face particular challenges due to financial constraints in disease management.
Dinesh Kumar Lamsal   +7 more
wiley   +1 more source

Hip Structure Analyses in Acromegaly: Decrease of Cortical Bone Thickness After Treatment: A Longitudinal Cohort Study

open access: yesJBMR Plus, 2019
Long‐standing growth hormone (GH) excess causes the skeletal clinical signs of acromegaly with typical changes in bone geometry, including increased cortical bone thickness (CBT).
Kristin Godang   +8 more
doaj   +1 more source

Current treatment of Acromegaly

open access: yes, 2019
Acromegaly is a rare endocrine disordered, cause by excessive production of Growth Hormone usually by pituitary adenoma. The most common finding is the enlargement of the extremities hence the name “acromegaly”.
Kounnas, Ioannis
core  

Prevalence of thyroid diseases in patients with acromegaly: results of an Italian multi-center study

open access: yes, 2002
Acromegaly is frequently associated with the presence of thyroid disorders, however the exact prevalence is still controversial. An Italian multicenter study was performed on 258 patients with active acromegaly (high levels of IGF-I and lack of ...
E. Martino   +14 more
core   +1 more source

Adaptive Servo‐Ventilation for Glottic Closure in a Patient With Adult‐Onset Congenital Central Hypoventilation Syndrome: A Case Report

open access: yesRespirology Case Reports, Volume 14, Issue 4, April 2026.
We report a genetically confirmed case of adult‐onset congenital central hypoventilation syndrome (CCHS) in a 69‐year‐old man whose condition became clinically manifest following transsphenoidal surgery for a pituitary microadenoma, complicated by high‐grade atrioventricular block and recurrent postoperative type 2 respiratory failure.
Sushil Agwan   +2 more
wiley   +1 more source

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