Similar articles for PMID: 18631007

Year	Number of Results
1997	1
1999	1
2002	1
2003	2
2004	3
2005	8
2006	8
2007	7
2008	6
2009	10
2010	7
2011	6
2012	2
2013	2
2015	2
2017	2
2018	2
2019	1
2020	2
2021	2
2022	1
2023	1
2024	0

1

A new germline point mutation in Ret exon 8 (cys515ser) in a family with medullary thyroid carcinoma.

Fazioli F, Piccinini G, Appolloni G, Bacchiocchi R, Palmonella G, Recchioni R, Pierpaoli E, Silvetti F, Scarpelli M, Bruglia M, Melillo RM, Santoro M, Boscaro M, Taccaliti A. Fazioli F, et al. Thyroid. 2008 Jul;18(7):775-82. doi: 10.1089/thy.2007.0365. Thyroid. 2008. PMID: 18631007

2

The oncogenic activity of RET point mutants for follicular thyroid cells may account for the occurrence of papillary thyroid carcinoma in patients affected by familial medullary thyroid carcinoma.

Melillo RM, Cirafici AM, De Falco V, Bellantoni M, Chiappetta G, Fusco A, Carlomagno F, Picascia A, Tramontano D, Tallini G, Santoro M. Melillo RM, et al. Am J Pathol. 2004 Aug;165(2):511-21. doi: 10.1016/S0002-9440(10)63316-0. Am J Pathol. 2004. PMID: 15277225 Free PMC article.

3

A novel germ-line point mutation in RET exon 8 (Gly(533)Cys) in a large kindred with familial medullary thyroid carcinoma.

Da Silva AM, Maciel RM, Da Silva MR, Toledo SR, De Carvalho MB, Cerutti JM. Da Silva AM, et al. J Clin Endocrinol Metab. 2003 Nov;88(11):5438-43. doi: 10.1210/jc.2003-030997. J Clin Endocrinol Metab. 2003. PMID: 14602786

4

Exon 5 of the RET proto-oncogene: a newly detected risk exon for familial medullary thyroid carcinoma, a novel germ-line mutation Gly321Arg.

Dvorakova S, Vaclavikova E, Duskova J, Vlcek P, Ryska A, Bendlova B. Dvorakova S, et al. J Endocrinol Invest. 2005 Nov;28(10):905-9. doi: 10.1007/BF03345322. J Endocrinol Invest. 2005. PMID: 16419493

5

Clinical case seminar: in vivo and in vitro characterization of a novel germline RET mutation associated with low-penetrant nonaggressive familial medullary thyroid carcinoma.

D'Aloiso L, Carlomagno F, Bisceglia M, Anaganti S, Ferretti E, Verrienti A, Arturi F, Scarpelli D, Russo D, Santoro M, Filetti S. D'Aloiso L, et al. J Clin Endocrinol Metab. 2006 Mar;91(3):754-9. doi: 10.1210/jc.2005-2338. Epub 2005 Dec 29. J Clin Endocrinol Metab. 2006. PMID: 16384843

6

New mutations in the RET protooncogene-L881V - associated with medullary thyroid carcinoma and -R770Q - in a patient with mixed medullar/follicular thyroid tumour.

Frank-Raue K, Döhring J, Scheumann G, Rondot S, Lorenz A, Schulze E, Dralle H, Raue F, Leidig-Bruckner G. Frank-Raue K, et al. Exp Clin Endocrinol Diabetes. 2010 Aug;118(8):550-3. doi: 10.1055/s-0029-1241851. Epub 2009 Dec 11. Exp Clin Endocrinol Diabetes. 2010. PMID: 20013610

7

Familial medullary carcinoma prevention, risk evaluation, and RET in children of families with MEN2.

Moore SW, Appfelstaedt J, Zaahl MG. Moore SW, et al. J Pediatr Surg. 2007 Feb;42(2):326-32. doi: 10.1016/j.jpedsurg.2006.10.005. J Pediatr Surg. 2007. PMID: 17270543

8

High prevalence of exon 8 G533C mutation in apparently sporadic medullary thyroid carcinoma in Greece.

Sarika HL, Papathoma A, Garofalaki M, Vasileiou V, Vlassopoulou B, Anastasiou E, Alevizaki M. Sarika HL, et al. Clin Endocrinol (Oxf). 2012 Dec;77(6):857-62. doi: 10.1111/j.1365-2265.2012.04462.x. Clin Endocrinol (Oxf). 2012. PMID: 22676047

9

An in-frame complex germline mutation in the juxtamembrane intracellular domain causing RET activation in familial medullary thyroid carcinoma.

Cordella D, Muzza M, Alberti L, Colombo P, Travaglini P, Beck-Peccoz P, Fugazzola L, Persani L. Cordella D, et al. Endocr Relat Cancer. 2006 Sep;13(3):945-53. doi: 10.1677/erc.1.01144. Endocr Relat Cancer. 2006. PMID: 16954442

10

RET genetic screening in patients with medullary thyroid cancer and their relatives: experience with 807 individuals at one center.

Elisei R, Romei C, Cosci B, Agate L, Bottici V, Molinaro E, Sculli M, Miccoli P, Basolo F, Grasso L, Pacini F, Pinchera A. Elisei R, et al. J Clin Endocrinol Metab. 2007 Dec;92(12):4725-9. doi: 10.1210/jc.2007-1005. Epub 2007 Sep 25. J Clin Endocrinol Metab. 2007. PMID: 17895320

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