180 related articles for article (PubMed ID: 9379517)
1. A case of multiple endocrine neoplasia type 2B.
Ohta M; Tokuda Y; Suzuki Y; Kuge S; Okumura A; Kubota M; Tajima T; Osamura RY; Mitomi T
Jpn J Clin Oncol; 1997 Aug; 27(4):268-73. PubMed ID: 9379517
[TBL] [Abstract][Full Text] [Related]
2. Multiple endocrine neoplasia type 2B.
Nakata S; Okugi H; Saitoh Y; Takahashi H; Shimizu K
Int J Urol; 2001 Jul; 8(7):398-400. PubMed ID: 11442663
[TBL] [Abstract][Full Text] [Related]
3. Relationship of familial prominent corneal nerves and lesions of the tongue resembling neuromas to multiple endocrine neoplasia type 2B.
Dennehy PJ; Feldman GL; Kambouris M; O'Malley ER; Sanders CY; Jackson CE
Am J Ophthalmol; 1995 Oct; 120(4):456-61. PubMed ID: 7573303
[TBL] [Abstract][Full Text] [Related]
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
[TBL] [Abstract][Full Text] [Related]
5. Multiple endocrine neoplasia type 2B (mucosal neuroma syndrome, Wagenmann-Froboese syndrome).
Morrison PJ; Nevin NC
J Med Genet; 1996 Sep; 33(9):779-82. PubMed ID: 8880581
[TBL] [Abstract][Full Text] [Related]
6. Pediatric medullary carcinoma of the thyroid with point mutation of RET proto-oncogene associated with multiple endocrine neoplasia and initially diagnosed by fine-needle aspiration biopsy.
Chai C; Lemos LB; Kaelbling M; Baliga M
South Med J; 2003 Mar; 96(3):287-90. PubMed ID: 12659362
[TBL] [Abstract][Full Text] [Related]
7. De novo RET proto-oncogene mutation in a patient with multiple endocrine neoplasia type 2B.
Chang TJ; Wu SL; Chang TC; Huang SH; Chang TJ
J Formos Med Assoc; 1999 Oct; 98(10):692-7. PubMed ID: 10575840
[TBL] [Abstract][Full Text] [Related]
8. Multiple endocrine neoplasia type 2B mutation in human RET oncogene induces medullary thyroid carcinoma in transgenic mice.
Acton DS; Velthuyzen D; Lips CJ; Höppener JW
Oncogene; 2000 Jun; 19(27):3121-5. PubMed ID: 10871866
[TBL] [Abstract][Full Text] [Related]
9. RET protooncogene mutational analysis in multiple endocrine neoplasia syndrome type 2B: case report and review of the literature.
Kahn MA; Cote GJ; Gagel RF
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 1996 Sep; 82(3):288-94. PubMed ID: 8884827
[TBL] [Abstract][Full Text] [Related]
10. No mutation at codon 918 of the RET gene in a family with multiple endocrine neoplasia type 2B.
Toogood AA; Eng C; Smith DP; Ponder BA; Shalet SM
Clin Endocrinol (Oxf); 1995 Dec; 43(6):759-62. PubMed ID: 8736281
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. [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]
13. 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]
14. Germ line mutation in the RET proto-oncogene associated with familial multiple endocrine neoplasia type 2B: a case report.
Ishida O; Zeki K; Morimoto I; Yamamoto S; Fujihira T; Eto S
Jpn J Clin Oncol; 1995 Jun; 25(3):104-8. PubMed ID: 7596047
[TBL] [Abstract][Full Text] [Related]
15. [Hereditary medullary thyroid carcinoma--genotype-phenotype characterization].
Frank-Raue K; Heimbach C; Rondot S; Usadel KH; Meng W; Varma C; Fuchs-Hammoser R; Höppner W; Schulze E; Raue F
Dtsch Med Wochenschr; 2003 Sep; 128(39):1998-2002. PubMed ID: 14508694
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. Somatic mutations of the ret protooncogene in sporadic medullary thyroid carcinoma are not restricted to exon 16 and are associated with tumor recurrence.
Romei C; Elisei R; Pinchera A; Ceccherini I; Molinaro E; Mancusi F; Martino E; Romeo G; Pacini F
J Clin Endocrinol Metab; 1996 Apr; 81(4):1619-22. PubMed ID: 8636377
[TBL] [Abstract][Full Text] [Related]
20. Aggressive medullary thyroid carcinoma in a ten-year-old patient with multiple endocrine neoplasia 2B due to the A883F mutation.
Mathiesen JS; Stochholm K; Poulsen PL; Vestergaard EM; Christiansen P; Vestergaard P
Thyroid; 2015 Jan; 25(1):139-40. PubMed ID: 25244518
[No Abstract] [Full Text] [Related]
[Next] [New Search]
