Hereditäres Phäochromozytom und Paragangliom
Author:
Publisher
Springer Berlin Heidelberg
Link
https://link.springer.com/content/pdf/10.1007/978-3-662-63317-5_35
Reference40 articles.
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2. Berends A, Buitenwerf E, de Krijger RR, Veeger N, van der Horst-Schrivers A, Links TP, Kerstens MN (2018) Incidence of pheochromocytoma and sympathetic paraganglioma in the Netherlands: a nationwide study and systematic review. Eur J Intern Med 51:68–73. https://doi.org/10.1016/j.ejim.2018.01.015
3. Brink I, Schaefer O, Walz M, Neumann HP (2006) Fluorine-18 DOPA PET imaging of paraganglioma syndrome. Clin Nucl Med 31(1):39–41. https://doi.org/10.1097/01.rlu.0000191577.39458.a0
4. Burnichon N, Rohmer V, Amar L, Herman P, Leboulleux S, Darrouzet V, Niccoli P, Gaillard D, Chabrier G, Chabolle F, Coupier I, Thieblot P, Lecomte P, Bertherat J, Wion-Barbot N, Murat A, Venisse A, Plouin PF, Jeunemaitre X, Gimenez-Roqueplo AP, PGL.NET network et al (2009) The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas. J Clin Endocrinol Metab 94(8):2817–2827. https://doi.org/10.1210/jc.2008-2504
5. Eisenhofer G, Lenders JW, Linehan WM, Walther MM, Goldstein DS, Keiser HR (1999) Plasma normetanephrine and metanephrine for detecting pheochromocytoma in von Hippel-Lindau disease and multiple endocrine neoplasia type 2. N Engl J Med 340(24):1872–1879. https://doi.org/10.1056/NEJM199906173402404
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