Abstract This Consensus Statement from an international, multidisciplinary workshop
sponsored by the Pituitary Society offers evidence-based graded consensus …

Neuroendocrine neoplasms (NENs) can develop in almost any organ and span a spectrum
from well-differentiated and indolent neuroendocrine tumours (NETs) to poorly differentiated …

Recent data suggest an increase in the overall incidence of parathyroid disorders, with
primary hyperparathyroidism (PHPT) being the most prevalent parathyroid disorder. PHPT is …

Corticotroph tumours are primarily sporadic monoclonal neoplasms and only rarely found in
genetic syndromes. Recurrent mutations in the ubiquitin specific protease 8 (USP8) gene …

Abetted by widespread usage of acid-suppressing proton pump inhibitors (PPIs), the
mitogenic actions of the peptide hormone gastrin are being revisited as a recurring theme in …

Multiple endocrine neoplasia type 1 (MEN1) is a rare inherited syndrome caused by
inactivating heterozygote mutations of the MEN1 gene affecting parathyroid glands …

Abstract Context Germline CDKN1B pathogenic variants result in multiple endocrine
neoplasia type 4 (MEN4), an autosomal dominant hereditary tumor syndrome variably …

Purpose Multiple endocrine neoplasia type 4 (MEN4) is a rare multiglandular endocrine
neoplasia syndrome, associated with a wide tumor spectrum but hallmarked by primary …

Hereditary Primary Hyperparathyroidism - Endocrinology and Metabolism Clinics Skip to
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Gastric neuroendocrine tumors (G-NET) are rare tumors arising from enterochromaffin-like
cells of the gastric mucosa. They belong to a larger group called gastroenteropancreatic …