Pheochromocytoma in MEN 2A Syndrome. Study of 54 Patients
Author:
Publisher
Springer Science and Business Media LLC
Subject
Surgery
Link
http://link.springer.com/content/pdf/10.1007/s00268-008-9734-2.pdf
Reference34 articles.
1. Casanova S, Rosenberg-Bourgin M, Farkas D, Calmettes C, Feingold N, Heshmati HM et al (1993) Pheochromocytoma in multiple endocrine neoplasia type 2A: survey of 100 cases. Clin Endocrinol 38:531–537
2. Modigliani E, Vasen HM, Rue K, Dralle H, Frilling A et al (1995) Pheochromocytoma in multiple endocrine neoplasia type 2A: European study. The Euromen Study Group. J Intern Med 238:363–367
3. Toledo SPA, Cortina MA, Toledo RA (2006) Impact of RET protooncogen analysis on the management of multiple endocrine neoplasia type 2. Clinics 61:59–70
4. Brandi ML, Gagel RF, Angeli A, Bilerkian SP, Beck-Peccoz P et al (2001) Guidelines for diagnosis and therapy of MEN type 1 and 2. J Clin Endocrinol Metab 86:5658–5671
5. Gimm O, Koch CA, Januszewicz A, Opocher G, Neumann HP (2004) The genetic basis of pheochromocytoma. Front Horm Res 31:45–60
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