Pheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors
originating from chromaffin cells in the adrenal medulla (PCCs) or extra-adrenal sympathetic …

Abstract Purpose of Review Pheochromocytomas and paragangliomas (PPGLs) are
uncommon catecholamine-producing neuroendocrine neoplasms that usually present with …

Background No randomised controlled trial has ever been done in patients with metastatic
phaeochromocytomas and paragangliomas. Preclinical and first clinical evidence suggested …

Metastatic pheochromocytomas and paragangliomas are rare, highly vascular tumors that
spread primarily to the lymph nodes, skeletal tissue, lungs, and liver. Tumor morbidity is …

While the establishment of human phaeochromocytoma and paraganglioma (PPGL) cell
lines has proven to be particularly difficult over several decades of research, there are other …

Pheochromocytomas and paragangliomas (PPGL) are rare neuroendocrine tumors
characterized by a high frequency of hereditary forms. Based on transcriptome classification …

Osteosarcoma is a rare type of cancer that commonly occurs as a primary bone tumour in
children and adolescents and is associated with a poor clinical outcome. Despite complex …

Research on rare tumors heavily relies on suitable models for basic and translational
research. Paragangliomas (PPGL) are rare neuroendocrine tumors (NET), developing from …

Paragangliomas and pheochromocytomas are rare neuroendocrine tumors characterized by
a large spectrum of hereditary predisposition. Based on gene expression profiling …

Tendons are relatively hypovascular but become hypervascular during both injury and
degeneration. This is due to the angiogenic response, or the formation of new blood vessels …