Multiple endocrine neoplasia type 2
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Oncology
Link
http://link.springer.com/content/pdf/10.1007/s11864-004-0022-6.pdf
Reference43 articles.
1. Brandi ML, Gagel RF, Angeli A, et al.: Guidelines for diagnosis and therapy of MEN type 1 and type 2? J Clin Endocrinol Metab 2001, 86:5658–5671.
2. Eng C, Clayton D, Schuffenecker I, et al.: The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis? JAMA 1996, 276:1575–1579. This paper provides useful data of genotype-phenotype correlations in a large MEN-2 study cohort.
3. Nunziata V, Giannattasio R, Di Giovanni G, et al.: Hereditary localized pruritus in affected members of a kindred with multiple endocrine neoplasia type 2A (Sipple’s syndrome)? Clin Endocrinol (Oxf) 1989, 30:57–63.
4. Verdy M, Weber AM, Roy CC, et al.: Hirschsprung’s disease in a family with multiple endocrine neoplasia type 2? J Pediatr Gastroenterol Nutr 1982, 1:603–607.
5. Gagel RF, Tashjian AH Jr, Cummings T, et al.: The clinical outcome of prospective screening for multiple endo-crine neoplasia type 2a: an 18-year experience? N Engl J Med 1988, 318:478–484.
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