Recent Advances in Genetics, Diagnosis, Localization, and Treatment of Pheochromocytoma

By Karel Pacak, W. Marston Linehan, Graeme Eisenhofer, M. Walther, D. Goldstein. Annals of Internal Medicine, 2001

607 citations recorded by the source corpus.

Subfields: Cancer Research, Endocrinology, Diabetes and Metabolism, Surgery

View Paper: https://www.semanticscholar.org/paper/f48e0313ce3f28d2e62b6509109fa2af290ba9ff

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Citations in the corpus

• The clinically inapparent adrenal mass: update in diagnosis and management. (2004, background): “These autosomally inherited disorders are associated with mutations of the RET protooncogene, which encodes a tyrosine kinase receptor involved in the regulation of cell growth and differentiation (94).”
• Biochemical diagnosis of pheochromocytoma: which test is best? (2002, neutral): “Age, mean (SD) [range], y 33 (14) [8-63] 47 (15) [17-78] 38 (14) [11-76] 47 (14) [8-77] DIAGNOSIS OF PHEOCHROMOCYTOMA”