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Journal Abstract Search

212 related items for PubMed ID: 9736899

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  • 4. Rudolf-Virchow-Preis 1995. The role of RET proto-oncogene mutation analysis in the diagnosis of multiple endocrine neoplasia type 2 (MEN 2) gene carriers and in the discrimination of sporadic and familial medullary thyroid carcinomas and pheochromocytomas.
    Komminoth P.
    Verh Dtsch Ges Pathol; 1995; 79():L-LV. PubMed ID: 8600671
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  • 7. Familial isolated hyperparathyroidism caused by single adenoma: a distinct entity different from multiple endocrine neoplasia.
    Watanabe T, Tsukamoto F, Shimizu T, Sugimoto T, Taguchi T, Nishisho I, Nakazawa H, Shiba E, Shishiba Y, Takai S.
    Endocr J; 1998 Oct; 45(5):637-46. PubMed ID: 10395244
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  • 8. Obvious mRNA and protein expression but absence of mutations of the RET proto-oncogene in parathyroid tumors.
    Kimura T, Yoshimoto K, Tanaka C, Ohkura T, Iwahana H, Miyauchi A, Sano T, Itakura M.
    Eur J Endocrinol; 1996 Mar; 134(3):314-9. PubMed ID: 8616528
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  • 10. Distinction between sporadic and hereditary medullary thyroid carcinoma (MTC) by mutation analysis of the RET proto-oncogene. "Study Group Multiple Endocrine Neoplasia Austria (SMENA)".
    Fink M, Weinhüsel A, Niederle B, Haas OA.
    Int J Cancer; 1996 Aug 22; 69(4):312-6. PubMed ID: 8797874
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  • 11. Analysis of the RET proto-oncogene in sporadic parathyroid adenomas.
    Williams GH, Rooney S, Carss A, Cummins G, Thomas GA, Williams ED.
    J Pathol; 1996 Oct 22; 180(2):138-41. PubMed ID: 8976870
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  • 15. Sporadic multiple endocrine neoplasia type 2A.
    Yamashita S.
    Intern Med; 1999 Feb 22; 38(2):80. PubMed ID: 10225659
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  • 18. Mutation analysis of glial cell line-derived neurotrophic factor, a ligand for an RET/coreceptor complex, in multiple endocrine neoplasia type 2 and sporadic neuroendocrine tumors.
    Marsh DJ, Zheng Z, Arnold A, Andrew SD, Learoyd D, Frilling A, Komminoth P, Neumann HP, Ponder BA, Rollins BJ, Shapiro GI, Robinson BG, Mulligan LM, Eng C.
    J Clin Endocrinol Metab; 1997 Sep 22; 82(9):3025-8. PubMed ID: 9284737
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  • 20. The RET protooncogene in sporadic pheochromocytomas: frequent MEN 2-like mutations and new molecular defects.
    Beldjord C, Desclaux-Arramond F, Raffin-Sanson M, Corvol JC, De Keyzer Y, Luton JP, Plouin PF, Bertagna X.
    J Clin Endocrinol Metab; 1995 Jul 22; 80(7):2063-8. PubMed ID: 7608256
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