Adrenal phaechromocytomas and extra-adrenal sympathetic paragangliomas (PPGLs) are
rare neuroendocrine tumours, characterised by production of the catecholamines …

Objective: The aim was to formulate clinical practice guidelines for pheochromocytoma and
paraganglioma (PPGL). Participants: The Task Force included a chair selected by the …

The treatment of hormone hypersecretory syndromes caused by neuroendocrine tumors
(NETs) can be a major challenge. NETs originating from the small intestine often secrete …

PHEOs/PGLs are the most inherited tumors among (neuro) endocrine tumors. Future
approaches in genetics, including whole-genome sequencing, will allow the discovery of …

Neuroendocrine (carcinoid) tumors (NETs) are endocrine neoplasms occurring most
frequently in gastrointestinal and bronchopulmonary (BP) systems. The majority of patients …

Abstract Pheochromocytomas (PCCs) and paragangliomas (PGLs) are rare, heterogeneous
neuroendocrine neoplasms of the autonomous nervous system of chromaffin cell origin that …

Dopamine is a catecholamine that acts both as a neurotransmitter and as a hormone,
exerting its functions via dopamine (DA) receptors that are present in a broad variety of …

Warburg's metabolic hypothesis is based on the assumption that a cancer cell's respiration
must be under attack, leading to its damage, in order to obtain increased glycolysis …

Pheochromocytoma (PCC) and paraganglioma are rare neuroendocrine tumors of the
adrenal medulla and sympathetic and parasympathetic paraganglia, for which mutations in …

Introduction. Pheochromocytomas (PHEO) and paragangliomas (PGL) are rare
neuroendocrine tumors with an estimated occurrence of 2 to 5 patients per million per year …