Oncogenetic testing for persons with hereditary endocrine cancer syndromes [PDF]
Bex, Marie +10 more
core +1 more source
A rare case of a composite phaeochromocytoma-ganglioneuroma in Australia. [PDF]
Pham P +4 more
europepmc +1 more source
PERSPECTIVE: Challenging preoperative α-blockade in phaeochromocytoma surgery: beyond tradition, towards 'safer surgery'. [PDF]
Holscher I +6 more
europepmc +1 more source
Recommendations for bone-directed therapy in patients with neuroendocrine tumour skeletal metastases at the New Zealand National Neuroendocrine Tumour Multidisciplinary Meeting. [PDF]
Radley G +3 more
europepmc +1 more source
Impact of centre volume on adrenalectomy outcomes: European multicentre study based on EUROCRINE® registry. [PDF]
Türk Y +6 more
europepmc +1 more source
Silent adrenal pheochromocytoma coexistent with corticomedullary hyperplasia: a case incidentally discovered [PDF]
Antonio, Ciardi +7 more
core
To screen or not to screen: complexity of <i>SDHA</i> mutation management. [PDF]
Mohamed E +3 more
europepmc +1 more source
Approach to the Management of Gastrointestinal Manifestations in Patients With Phaeochromocytoma and Paraganglioma. [PDF]
Majumder M +5 more
europepmc +1 more source
Genomic testing for RET in the clinic: UK and global perspective. [PDF]
Izatt L.
europepmc +1 more source

