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Mutations of the ret protooncogene in German multiple endocrine neoplasia families: relation between genotype and phenotype. German Medullary Thyroid Carcinoma Study Group.
Frank-Raue K, Höppner W, Frilling A, Kotzerke J, Dralle H, Haase R, Mann K, Seif F, Kirchner R, Rendl J, Deckart HF, Ritter MM, Hampel R, Klempa J, Scholz GH, Raue F. Frank-Raue K, et al. Among authors: dralle h. J Clin Endocrinol Metab. 1996 May;81(5):1780-3. doi: 10.1210/jcem.81.5.8626834. J Clin Endocrinol Metab. 1996. PMID: 8626834
Primary hyperparathyroidism in multiple endocrine neoplasia type 2A.
Raue F, Kraimps JL, Dralle H, Cougard P, Proye C, Frilling A, Limbert E, Llenas LF, Niederle B. Raue F, et al. Among authors: dralle h. J Intern Med. 1995 Oct;238(4):369-73. doi: 10.1111/j.1365-2796.1995.tb01212.x. J Intern Med. 1995. PMID: 7595174
Early malignant progression of hereditary medullary thyroid cancer.
Machens A, Niccoli-Sire P, Hoegel J, Frank-Raue K, van Vroonhoven TJ, Roeher HD, Wahl RA, Lamesch P, Raue F, Conte-Devolx B, Dralle H; European Multiple Endocrine Neoplasia (EUROMEN) Study Group. Machens A, et al. Among authors: dralle h. N Engl J Med. 2003 Oct 16;349(16):1517-25. doi: 10.1056/NEJMoa012915. N Engl J Med. 2003. PMID: 14561794 Free article.
785 results