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2017, Advances in Experimental Medicine and Biology, Volume 956, 21
Phaeochromocytomas and paragangliomas are relatively uncommon tumours which may be manifest in many ways, specifically as sustained or paroxysmal hypertension,... 
MEDICINE, RESEARCH & EXPERIMENTAL | LOCALIZATION | METASTATIC PHEOCHROMOCYTOMA | MIBG SCINTIGRAPHY | MANAGEMENT | EFFICACY | Phaeochromocytomas | Review | EXTRAADRENAL PHEOCHROMOCYTOMAS | BIOCHEMICAL-DIAGNOSIS | Treatment | PERIPHERAL VASCULAR DISEASE | Diagnosis | Malignant | Paragangliomas | CLINICAL-PRACTICE | ADRENAL PHEOCHROMOCYTOMAS
Book Chapter
Cancer, ISSN 0008-543X, 06/2012, Volume 118, Issue 11, pp. 2804 - 2812
Journal Article
European Journal of Nuclear Medicine and Molecular Imaging, ISSN 1619-7070, 2012, Volume 39, Issue 12, pp. 1977 - 1995
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 04/2007, Volume 92, Issue 4, pp. 1217 - 1225
Context: Pheochromocytomas are rare tumors of predominantly adrenal origin that often produce and secrete catecholamines. Malignancy occurs in a variable... 
METHYL-P-TYROSINE | METASTATIC PHEOCHROMOCYTOMA | BENIGN PHEOCHROMOCYTOMA | RADIOPHARMACEUTICAL TREATMENT | NEURAL CREST TUMORS | ENDOCRINOLOGY & METABOLISM | I-131 META-IODOBENZYLGUANIDINE | COMBINATION CHEMOTHERAPY | OCTREOTIDE SCINTIGRAPHY | ADVANCED NEUROENDOCRINE TUMORS | FAMILIAL PHEOCHROMOCYTOMA
Journal Article