Article
65 YEARS OF THE DOUBLE HELIX: Genetics informs precision practice in the diagnosis and management of pheochromocytoma.
Endocrine-related cancer - 1 Aug 2018
Neumann Hartmut P, Young William F, Krauss Tobias, Bayley Jean-Pierre, Schiavi Francesca, Opocher Giuseppe, Boedeker Carsten C, Tirosh Amit, Castinetti Frederic, Ruf Juri, Beltsevich Dmitry, Walz Martin, Groeben Harald-Thomas, von Dobschuetz Ernst, Gimm Oliver, Wohllk Nelson, Pfeifer Marija, Lourenço Delmar M, Peczkowska Mariola, Patocs Attila, Ngeow Joanne, Makay Özer, Shah Nalini S, Tischler Arthur, Leijon Helena, Pennelli Gianmaria, Villar Gómez de Las Heras Karina, Links Thera P, Bausch Birke, Eng Charis
Abstract excerpt
Although the authors of the present review have contributed to genetic discoveries in the field of pheochromocytoma research, we can legitimately ask whether these advances have led to improvements in the diagnosis and management of patients with pheochromocytoma. The answer to this question is an emphatic Yes! In the field of molecular genetics, the well-established axiom that familial (genetic) pheochromocytoma...
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