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Bausch, Birke; Schiavi, Francesca; Ni, Ying; Welander, Jenny; Patocs, Attila; Ngeow, Joanne; Wellner, Ulrich; Malinoc, Angelica; Taschin, Elisa; Barbon, Giovanni; Lanza, Virginia; Söderkvist, Peter; Stenman, Adam; Larsson, Catharina; Svahn, Fredrika; Chen, Jin-Lian; Marquard, Jessica; Fraenkel, Merav; Walter, Martin Alexander; Peczkowska, Mariola; ... (2017). Clinical Characterization of the Pheochromocytoma and Paraganglioma Susceptibility Genes SDHA, TMEM127, MAX, and SDHAF2 for Gene-Informed Prevention. JAMA oncology, 3(9), pp. 1204-1212. American Medical Association 10.1001/jamaoncol.2017.0223
Klingler, Jan-Helge; Krüger, Marie T; Lemke, Johannes R; Jilg, Cordula; Van Velthoven, Vera; Zentner, Josef; Neumann, Hartmut P H; Gläsker, Sven (2013). Sequence variations in the von Hippel-Lindau tumor suppressor gene in patients with intracranial aneurysms. Journal of stroke and cerebrovascular diseases, 22(4), pp. 437-43. New York, N.Y.: W.B. Saunders 10.1016/j.jstrokecerebrovasdis.2013.01.016
Hentschel, Michael; Rottenburger, Christof; Boedeker, Carsten C; Neumann, Hartmut P H; Brink, Ingo (2012). Is there an optimal scan time for 6-[F-18]fluoro-L-DOPA PET in pheochromocytomas and paragangliomas? Clinical nuclear medicine, 37(2), e24-9. Philadelphia, Pa.: Lippincott Williams & Wilkins 10.1097/RLU.0b013e318238f550
Frank-Raue, Karin; Rybicki, Lisa A; Erlic, Zoran; Schweizer, Heiko; Winter, Aurelia; Milos, Ioana; Toledo, Sergio P A; Toledo, Rodrigo A; Tavares, Marcos R; Alevizaki, Maria; Mian, Caterina; Siggelkow, Heide; Hüfner, Michael; Wohllk, Nelson; Opocher, Giuseppe; Dvo?áková, Sárka; Bendlova, Bela; Czetwertynska, Ma?gorzata; Skasko, El?bieta; Barontini, Marta; ... (2011). Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10. Human mutation, 32(1), pp. 51-8. Hoboken, N.J.: Wiley-Blackwell 10.1002/humu.21385
