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2. [Medullary thyroid gland carcinoma. Sporadic/familial. Screening when and why?]. Frilling A; Liedke MO Internist (Berl); 1998 Jun; 39(6):588-91. PubMed ID: 9677514 [No Abstract] [Full Text] [Related]
3. Genetic basis of endocrine disease: multiple endocrine neoplasia type 2. Mulligan LM; Ponder BA J Clin Endocrinol Metab; 1995 Jul; 80(7):1989-95. PubMed ID: 7608246 [No Abstract] [Full Text] [Related]
4. Mutation analysis of the RET proto-oncogene in Dutch families with MEN 2A, MEN 2B and FMTC: two novel mutations and one de novo mutation for MEN 2A. Landsvater RM; Jansen RP; Hofstra RM; Buys CH; Lips CJ; Ploos van Amstel HK Hum Genet; 1996 Jan; 97(1):11-4. PubMed ID: 8557249 [TBL] [Abstract][Full Text] [Related]
5. [Prophylactic total thyroidectomy in children and adolescents with genetic mutations in the RET-protooncogene]. Spinelli C; Puccini M; Bertocchini A; Lima M; Pacini F; Miccoli P Pediatr Med Chir; 2002; 24(1):53-7. PubMed ID: 11938683 [TBL] [Abstract][Full Text] [Related]
6. 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 [TBL] [Abstract][Full Text] [Related]
7. [From gene to disease; from the RET gene to multiple endocrine neoplasia types 2A and 2B, sporadic and familial medullary thyroid carcinoma, Hirschsprung disease and papillary thyroid carcinoma]. Hofstra RM; van der Luijt RB; Lips CJ Ned Tijdschr Geneeskd; 2001 Nov; 145(46):2217-21. PubMed ID: 11757244 [TBL] [Abstract][Full Text] [Related]
8. [One gene--four diseases: on the importance of mutations in the ret gene in MEN 2A, MEN 2B, Hirschsprung disease and medullary thyroid carcinoma]. Fehmann HC; Göke B Z Gastroenterol; 1994 Jul; 32(7):416-7. PubMed ID: 7975780 [No Abstract] [Full Text] [Related]
9. Very early detection of RET proto-oncogene mutation is crucial for preventive thyroidectomy in multiple endocrine neoplasia type 2 children: presence of C-cell malignant disease in asymptomatic carriers. Sanso GE; Domene HM; Garcia R; Pusiol E; de M; Roque M; Ring A; Perinetti H; Elsner B; Iorcansky S; Barontini M Cancer; 2002 Jan; 94(2):323-30. PubMed ID: 11900218 [TBL] [Abstract][Full Text] [Related]
11. 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; 69(4):312-6. PubMed ID: 8797874 [TBL] [Abstract][Full Text] [Related]
12. Predictive DNA testing for multiple endocrine neoplasia 2: a therapeutic challenge of prophylactic thyroidectomy in very young children. van Heurn LW; Schaap C; Sie G; Haagen AA; Gerver WJ; Freling G; van Amstel HK; Heineman E J Pediatr Surg; 1999 Apr; 34(4):568-71. PubMed ID: 10235324 [TBL] [Abstract][Full Text] [Related]
13. RET proto-oncogene mutations in inherited and sporadic medullary thyroid cancer. Blaugrund JE; Johns MM; Eby YJ; Ball DW; Baylin SB; Hruban RH; Sidransky D Hum Mol Genet; 1994 Oct; 3(10):1895-7. PubMed ID: 7849720 [No Abstract] [Full Text] [Related]
14. Diagnosis of multiple endocrine neoplasia [MEN] 2A, 2B and familial medullary thyroid cancer [FMTC] by multiplex PCR and heteroduplex analyses of RET proto-oncogene mutations. Kambouris M; Jackson CE; Feldman GL Hum Mutat; 1996; 8(1):64-70. PubMed ID: 8807338 [TBL] [Abstract][Full Text] [Related]
15. Analysis of RET proto-oncogene abnormalities in patients with MEN 2A, MEN 2B, familial or sporadic medullary thyroid carcinoma. Chiefari E; Russo D; Giuffrida D; Zampa GA; Meringolo D; Arturi F; Chiodini I; Bianchi D; Attard M; Trischitta V; Bruno R; Giannasio P; Pontecorvi A; Filetti S J Endocrinol Invest; 1998 Jun; 21(6):358-64. PubMed ID: 9699127 [TBL] [Abstract][Full Text] [Related]
16. [The direct gene test in familial medullary thyroid gland carcinoma and in MEN syndromes. Detection of mutations in the ret proto-oncogene saves screening studies]. Stuhrmann M Fortschr Med; 1995 Dec; 113(35-36):503-6. PubMed ID: 8582691 [TBL] [Abstract][Full Text] [Related]
17. [Early diagnosis of multiple endocrine neoplasia type 2 (MEN 2) by detection of mutated RET proto-oncogene carriers]. Sansó G; Domené HM; Iorcansky S; Barontini M Medicina (B Aires); 1998; 58(2):179-84. PubMed ID: 9706252 [TBL] [Abstract][Full Text] [Related]
18. Mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2. Ponder BA Cancer Surv; 1995; 25():195-205. PubMed ID: 8718519 [No Abstract] [Full Text] [Related]
19. Genetic testing for familial cancer. Consequences of RET proto-oncogene mutation analysis in multiple endocrine neoplasia, type 2. Learoyd DL; Marsh DJ; Richardson AL; Twigg SM; Delbridge L; Robinson BG Arch Surg; 1997 Sep; 132(9):1022-5. PubMed ID: 9301617 [TBL] [Abstract][Full Text] [Related]
20. "Cold" single-strand conformational variants for mutation analysis of the RET protooncogene. Musholt PB; Musholt TJ; Goodfellow PJ; Zehnbauer BA; Wells SA; Moley JF Surgery; 1997 Aug; 122(2):363-70; discussion 370-1. PubMed ID: 9288142 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]