-
1
-
-
80052599580
-
Multiple endocrine neoplasia type 2: An overview
-
Moline J, Eng C 2011 Multiple endocrine neoplasia type 2: an overview. Genet Med 13: 755-764.
-
(2011)
Genet Med
, vol.13
, pp. 755-764
-
-
Moline, J.1
Eng, C.2
-
2
-
-
84890415609
-
Medullary thyroid carcinoma associated with RET mutations located in exon 8
-
Diamanti- Kandarakis E (ed), InTech, Rijeka, Croatia
-
Peppa Ma, Raptis SA 2011 Medullary thyroid carcinoma associated with RET mutations located in exon 8. In: Diamanti- Kandarakis E (ed) Contemporary Aspects of Endocrinology. InTech, Rijeka, Croatia, pp 271-280.
-
(2011)
Contemporary Aspects of Endocrinology
, pp. 271-280
-
-
Ma, P.1
Raptis, S.A.2
-
3
-
-
67749130797
-
Medullary thyroid cancer: Management guidelines of the American Thyroid Association
-
Kloos RT, Eng C, Evans DB, Francis GL, Gagel RF, Gharib H, Moley JF, Pacini F, Ringel MD, Schlumberger M, Wells SA Jr 2009 Medullary thyroid cancer: management guidelines of the American Thyroid Association. Thyroid 19: 565-612.
-
(2009)
Thyroid
, vol.19
, pp. 565-612
-
-
Kloos, R.T.1
Eng, C.2
Evans, D.B.3
Francis, G.L.4
Gagel, R.F.5
Gharib, H.6
Moley, J.F.7
Pacini, F.8
Ringel, M.D.9
Schlumberger, M.10
Wells Jr., S.A.11
-
4
-
-
0344442410
-
533Cys) in a Large Kindred with Familial Medullary Thyroid Carcinoma
-
DOI 10.1210/jc.2003-030997
-
Da Silva AM, Maciel RM, Da Silva MR, Toledo SR, De Carvalho MB, Cerutti JM 2003A novel germ-line point mutation in RET exon 8 (Gly(533)Cys) in a large kindred with familial medullary thyroid carcinoma. J Clin Endocrinol Metab 88: 5438-5443. (Pubitemid 37452751)
-
(2003)
Journal of Clinical Endocrinology and Metabolism
, vol.88
, Issue.11
, pp. 5438-5443
-
-
Alvares Da Silva, A.M.1
Maciel, R.M.B.2
Dias Da Silva, M.R.3
Toledo, S.R.C.4
De Carvalho, M.B.5
Cerutti, J.M.6
-
5
-
-
58149335397
-
Multiple endocrine neoplasia type 2A in two families with the familial medullary thyroid carcinoma associated G533C mutation of the RET proto-oncogene
-
Peppa M, Boutati E, Kamakari S, Pikounis V, Peros G, Panayiotides IG, Economopoulos T, Raptis SA, Hadjidakis D 2008 Multiple endocrine neoplasia type 2A in two families with the familial medullary thyroid carcinoma associated G533C mutation of the RET proto-oncogene. Eur J Endocrinol 159: 767-771.
-
(2008)
Eur J Endocrinol
, vol.159
, pp. 767-771
-
-
Peppa, M.1
Boutati, E.2
Kamakari, S.3
Pikounis, V.4
Peros, G.5
Panayiotides, I.G.6
Economopoulos, T.7
Raptis, S.A.8
Hadjidakis, D.9
-
6
-
-
33646015994
-
A rare RET gene exon 8 mutation is found in two Greek kindreds with familial medullary thyroid carcinoma: Implications for screening
-
Kaldrymides P, Mytakidis N, Anagnostopoulos T, Vassiliou M, Tertipi A, Zahariou M, Rampias T, Koutsodontis G, Konstantopoulou I, Ladopoulou A, Bei T, Yannoukakos D 2006A rare RET gene exon 8 mutation is found in two Greek kindreds with familial medullary thyroid carcinoma: implications for screening. Clin Endocrinol (Oxf) 64: 561-566.
-
(2006)
Clin Endocrinol (Oxf)
, vol.64
, pp. 561-566
-
-
Kaldrymides, P.1
Mytakidis, N.2
Anagnostopoulos, T.3
Vassiliou, M.4
Tertipi, A.5
Zahariou, M.6
Rampias, T.7
Koutsodontis, G.8
Konstantopoulou, I.9
Ladopoulou, A.10
Bei, T.11
Yannoukakos, D.12
-
7
-
-
34548653042
-
A newly detected mutation of the RET protooncogene in exon 8 as a cause of multiple endocrine neoplasia type 2A
-
Bethanis S, Koutsodontis G, Palouka T, Avgoustis C, Yannoukakos D, Bei T, Papadopoulos S, Linos D, Tsagarakis S 2007A newly detected mutation of the RET protooncogene in exon 8 as a cause of multiple endocrine neoplasia type 2A. Hormones 6: 152-156.
-
(2007)
Hormones
, vol.6
, pp. 152-156
-
-
Bethanis, S.1
Koutsodontis, G.2
Palouka, T.3
Avgoustis, C.4
Yannoukakos, D.5
Bei, T.6
Papadopoulos, S.7
Linos, D.8
Tsagarakis, S.9
-
8
-
-
80052486093
-
The RET PG533C mutation confers predisposition to multiple endocrine neoplasia type 2A in a Brazilian kindred and is able to induce a malignant phenotype in vitro and in vivo
-
Oliveira MN, Hemerly JP, Bastos AU, Tamanaha R, Latini FR, Camacho CP, Impellizzeri A, Maciel RM, Cerutti JM 2011 The RET p.G533C mutation confers predisposition to multiple endocrine neoplasia type 2A in a Brazilian kindred and is able to induce a malignant phenotype in vitro and in vivo. Thyroid 21: 975-985.
-
(2011)
Thyroid
, vol.21
, pp. 975-985
-
-
Oliveira, M.N.1
Hemerly, J.P.2
Bastos, A.U.3
Tamanaha, R.4
Latini, F.R.5
Camacho, C.P.6
Impellizzeri, A.7
Maciel, R.M.8
Cerutti, J.M.9
-
9
-
-
0033330662
-
A novel 9-base pair duplication in RET exon 8 in familial medullary thyroid carcinoma
-
Pigny P, Bauters C, Wemeau JL, Houcke ML, Crepin M, Caron P, Giraud S, Calender A, Buisine MP, Kerckaert JP, Porchet N 1999A novel 9-base pair duplication in RET exon 8 in familial medullary thyroid carcinoma. J Clin Endocrinol Metab 84: 1700-1704. (Pubitemid 30644279)
-
(1999)
Journal of Clinical Endocrinology and Metabolism
, vol.84
, Issue.5
, pp. 1700-1704
-
-
Pigny, P.1
Bauters, C.2
Wemeau, J.-L.3
Houcke, M.L.4
Crepin, M.5
Caron, P.6
Giraud, S.7
Calender, A.8
Buisine, M.-P.9
Kerckaert, J.-P.10
Porchet, N.11
-
10
-
-
84869035182
-
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 2012 High prevalence of exon 8 G533C mutation in apparently sporadic medullary thyroid carcinoma in Greece. Clin Endocrinol (Oxf) 77: 857-862.
-
(2012)
Clin Endocrinol (Oxf)
, vol.77
, pp. 857-862
-
-
Sarika, H.L.1
Papathoma, A.2
Garofalaki, M.3
Vasileiou, V.4
Vlassopoulou, B.5
Anastasiou, E.6
Alevizaki, M.7
-
11
-
-
22244480355
-
RET proto-oncogene: A review and update of genotype-phenotype correlations in hereditary medullary thyroid cancer and associated endocrine tumors
-
DOI 10.1089/thy.2005.15.531
-
Kouvaraki MA, Shapiro SE, Perrier ND, Cote GJ, Gagel RF, Hoff AO, Sherman SI, Lee JE, Evans DB 2005 RET proto-oncogene: a review and update of genotypephenotype correlations in hereditary medullary thyroid cancer and associated endocrine tumors. Thyroid 15: 531-544. (Pubitemid 40993726)
-
(2005)
Thyroid
, vol.15
, Issue.6
, pp. 531-544
-
-
Kouvaraki, M.A.1
Shapiro, S.E.2
Perrier, N.D.3
Cote, G.J.4
Gagel, R.F.5
Hoff, A.O.6
Sherman, S.I.7
Lee, J.E.8
Evans, D.B.9
-
12
-
-
66949149437
-
Evaluation of RET polymorphisms in a six-generation family with G533C RET mutation: Specific RET variants may modulate age at onset and clinical presentation
-
Tamanaha R, Camacho CP, Pereira AC, da Silva AM, Maciel RM, Cerutti JM 2009 Evaluation of RET polymorphisms in a six-generation family with G533C RET mutation: specific RET variants may modulate age at onset and clinical presentation. Clin Endocrinol (Oxf) 71: 56-64.
-
(2009)
Clin Endocrinol (Oxf)
, vol.71
, pp. 56-64
-
-
Tamanaha, R.1
Camacho, C.P.2
Pereira, A.C.3
Da Silva, A.M.4
Maciel, R.M.5
Cerutti, J.M.6
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