Similar articles for PMID: 11502806

Year	Number of Results
1970	4
1975	2
1976	2
1977	4
1978	3
1979	2
1980	2
1981	4
1982	1
1983	2
1984	1
1986	1
1987	2
1988	2
1989	1
1990	4
1992	1
1993	2
1994	8
1995	12
1996	15
1997	23
1998	21
1999	13
2000	20
2001	33
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2003	19
2004	11
2005	5
2006	3
2007	3
2008	4
2009	8
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2011	8
2012	6
2013	5
2014	8
2015	4
2016	9
2017	4
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2019	9
2020	12
2021	8
2022	9
2023	7
2024	1

1

Familial medullary thyroid carcinoma with noncysteine ret mutations: phenotype-genotype relationship in a large series of patients.

Niccoli-Sire P, Murat A, Rohmer V, Franc S, Chabrier G, Baldet L, Maes B, Savagner F, Giraud S, Bezieau S, Kottler ML, Morange S, Conte-Devolx B; French Calcitonin Tumors Group (GETC). Niccoli-Sire P, et al. J Clin Endocrinol Metab. 2001 Aug;86(8):3746-53. doi: 10.1210/jcem.86.8.7767. J Clin Endocrinol Metab. 2001. PMID: 11502806

2

When should thyroidectomy be performed in familial medullary thyroid carcinoma gene carriers with non-cysteine RET mutations?

Niccoli-Sire P, Murat A, Rohmer V, Gibelin H, Chabrier G, Conte-Devolx B, Visset J, Ronceray J, Jaeck D, Henry JF, Proye C, Carnaille B, Kraimps JL; Groupe D'étude Des Tumeurs Endocrines. Niccoli-Sire P, et al. Surgery. 2003 Dec;134(6):1029-36; discussion 1036-7. doi: 10.1016/j.surg.2003.07.019. Surgery. 2003. PMID: 14668737

3

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. Romei C, et al. J Clin Endocrinol Metab. 1996 Apr;81(4):1619-22. doi: 10.1210/jcem.81.4.8636377. J Clin Endocrinol Metab. 1996. PMID: 8636377

4

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. Sanso GE, et al. Cancer. 2002 Jan 15;94(2):323-30. doi: 10.1002/cncr.10228. Cancer. 2002. PMID: 11900218 Free article.

5

Recommendations for reporting C cell pathology of the thyroid.

Kaserer K, Scheuba C, Neuhold N, Weinhäusel A, Vierhapper H, Niederle B. Kaserer K, et al. Wien Klin Wochenschr. 2002 Apr 15;114(7):274-8. Wien Klin Wochenschr. 2002. PMID: 12089863

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. Komminoth P. Verh Dtsch Ges Pathol. 1995;79:L-LV. Verh Dtsch Ges Pathol. 1995. PMID: 8600671

7

Variable expressivity of familial medullary thyroid carcinoma (FMTC) due to a RET V804M (GTG-->ATG) mutation.

Feldman GL, Edmonds MW, Ainsworth PJ, Schuffenecker I, Lenoir GM, Saxe AW, Talpos GB, Roberson J, Petrucelli N, Jackson CE. Feldman GL, et al. Surgery. 2000 Jul;128(1):93-8. doi: 10.1067/msy.2000.107103. Surgery. 2000. PMID: 10876191

8

Presentation of a kindred with familial medullary thyroid carcinoma and Cys611Phe mutation of the RET proto-oncogene demonstrating low grade malignancy.

Siggelkow H, Melzer A, Nolte W, Karsten K, Hoppner W, Hufner M. Siggelkow H, et al. Eur J Endocrinol. 2001 May;144(5):467-73. doi: 10.1530/eje.0.1440467. Eur J Endocrinol. 2001. PMID: 11331212

9

Somatic mutations in the RET proto-oncogene in sporadic medullary thyroid carcinoma.

Marsh DJ, Learoyd DL, Andrew SD, Krishnan L, Pojer R, Richardson AL, Delbridge L, Eng C, Robinson BG. Marsh DJ, et al. Clin Endocrinol (Oxf). 1996 Mar;44(3):249-57. doi: 10.1046/j.1365-2265.1996.681503.x. Clin Endocrinol (Oxf). 1996. PMID: 8729519

10

Presymptomatic DNA screening in families with multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma.

Frilling A, Dralle H, Eng C, Raue F, Broelsch CE. Frilling A, et al. Surgery. 1995 Dec;118(6):1099-103; discussion 1103-4. doi: 10.1016/s0039-6060(05)80120-5. Surgery. 1995. PMID: 7491529

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