-
1
-
-
33846964878
-
Predictive value of serum calcitonin levels for preoperative diagnosis of medullary thyroid carcinoma in a cohort of 5817 consecutive patients with thyroid nodules
-
Costante G, Meringolo D, Durante C, Bianchi D, Nocera M, Tumino S, Crocetti U, Attard M, Maranghi M, Torlontano M & Filetti S. Predictive value of serum calcitonin levels for preoperative diagnosis of medullary thyroid carcinoma in a cohort of 5817 consecutive patients with thyroid nodules. Journal of Clinical Endocrinology and Metabolism 2007 92 450-455.
-
(2007)
Journal of Clinical Endocrinology and Metabolism
, vol.92
, pp. 450-455
-
-
Costante, G.1
Meringolo, D.2
Durante, C.3
Bianchi, D.4
Nocera, M.5
Tumino, S.6
Crocetti, U.7
Attard, M.8
Maranghi, M.9
Torlontano, M.10
Filetti, S.11
-
2
-
-
85047682409
-
Guidelines for diagnosis and therapy of MEN type 1 and type 2
-
Brandi ML, Gagel RF, Angeli A, Bilezikian J, Beck-Peccoz P, Bordi C, Cont-Devolx B, Falchetti A, Gionata Gheri R, Libraia A, Lips CJM, Lombardi G, Mannelli M, Pacini F, Ponder BAJ, Raue F, Skogseid B, Tamburano G, Thakker RV, Thompson NW, Tomassetti P, Tonelli F, Wells S Jr & Marx SJ. Guidelines for diagnosis and therapy of MEN type 1 and type 2. Journal of Clinical Endocrinology and Metabolism 2001 86 5658-5671.
-
(2001)
Journal of Clinical Endocrinology and Metabolism
, vol.86
, pp. 5658-5671
-
-
Brandi, M.L.1
Gagel, R.F.2
Angeli, A.3
Bilezikian, J.4
Beck-Peccoz, P.5
Bordi, C.6
Cont-Devolx, B.7
Falchetti, A.8
Gionata Gheri, R.9
Libraia, A.10
Lips, C.J.M.11
Lombardi, G.12
Mannelli, M.13
Pacini, F.14
Ponder, B.A.J.15
Raue, F.16
Skogseid, B.17
Tamburano, G.18
Thakker, R.V.19
Thompson, N.W.20
Tomassetti, P.21
Tonelli, F.22
Wells Jr, S.23
Marx, S.J.24
more..
-
3
-
-
0344716605
-
Multiple endocrine neoplasia type 2: Evaluation of the genotype-phenotype relationship
-
Yip L, Cote GJ, Shapiro SE, Ayers GD, Herzog CE, Sellin RV, Sherman SI, Gagel RF, Lee JE & Evans DB. Multiple endocrine neoplasia type 2: evaluation of the genotype-phenotype relationship. Archives of Surgery 2003 138 409-416.
-
(2003)
Archives of Surgery
, vol.138
, pp. 409-416
-
-
Yip, L.1
Cote, G.J.2
Shapiro, S.E.3
Ayers, G.D.4
Herzog, C.E.5
Sellin, R.V.6
Sherman, S.I.7
Gagel, R.F.8
Lee, J.E.9
Evans, D.B.10
-
4
-
-
0036156121
-
Multigenerational familial medullary throid cancer (FMTC): Evidence for FMTC phenocopies and association with papillary thyroid cancer
-
Fugazzola L, Cerutti N, Mannavola D, Ghilardi G, Alberti L, Romoli R & Beck-Peccoz P. Multigenerational familial medullary throid cancer (FMTC): evidence for FMTC phenocopies and association with papillary thyroid cancer. Clinical Endocrinology 2002 56 53-63.
-
(2002)
Clinical Endocrinology
, vol.56
, pp. 53-63
-
-
Fugazzola, L.1
Cerutti, N.2
Mannavola, D.3
Ghilardi, G.4
Alberti, L.5
Romoli, R.6
Beck-Peccoz, P.7
-
5
-
-
9444272942
-
Minireview RET: Normal and abnormal functions
-
Santoro M, Melillo RM, Carlomagno F, Vecchio G & Fusco A. Minireview RET: normal and abnormal functions. Endocrinology 2004 145 5448-5451.
-
(2004)
Endocrinology
, vol.145
, pp. 5448-5451
-
-
Santoro, M.1
Melillo, R.M.2
Carlomagno, F.3
Vecchio, G.4
Fusco, A.5
-
8
-
-
34547791796
-
Histopathological and molecular studies in patients with goiter and hypercalcitoninemia: Reactive or neoplastic C-cell hyperplasia?
-
Verga U, Ferrero S, Vicentini L, Brambilla T, Cirelio, V, Muzza M, Beck-Peccoz P & Fugazzola L. Histopathological and molecular studies in patients with goiter and hypercalcitoninemia: reactive or neoplastic C-cell hyperplasia? Endocrine-Related Cancer 2007 14 393-403.
-
(2007)
Endocrine-Related Cancer
, vol.14
, pp. 393-403
-
-
Verga, U.1
Ferrero, S.2
Vicentini, L.3
Brambilla, T.4
Cirelio, V.5
Muzza, M.6
Beck-Peccoz, P.7
Fugazzola, L.8
-
9
-
-
0031026236
-
Sex-related C-cell hyperplasia in the normal human thyroid: A quantitative autopsy study
-
Guyetant S, Rousselet MC, Durigon M, Chappard D, Franc B & Guerin O. Sex-related C-cell hyperplasia in the normal human thyroid: a quantitative autopsy study. Journal of Clinical Endocrinology and Metabolism 1997 82 42-47.
-
(1997)
Journal of Clinical Endocrinology and Metabolism
, vol.82
, pp. 42-47
-
-
Guyetant, S.1
Rousselet, M.C.2
Durigon, M.3
Chappard, D.4
Franc, B.5
Guerin, O.6
-
10
-
-
1442352328
-
Frequency and relevance of elevated calcitonin levels in patients with neoplastic and nonneoplastic thyroid disease and in healthy subjects
-
Karanikas G, Moameni A, Poetzi C, Zettinig G, Kaserer K, Bieglmayer C, Niederle B, Dudczak R & Pirich C. Frequency and relevance of elevated calcitonin levels in patients with neoplastic and nonneoplastic thyroid disease and in healthy subjects. Journal of Clinical Endocrinology and Metabolism 2004 89 515-519.
-
(2004)
Journal of Clinical Endocrinology and Metabolism
, vol.89
, pp. 515-519
-
-
Karanikas, G.1
Moameni, A.2
Poetzi, C.3
Zettinig, G.4
Kaserer, K.5
Bieglmayer, C.6
Niederle, B.7
Dudczak, R.8
Pirich, C.9
-
11
-
-
10744223544
-
Impact of routine measurement of serum calcitonin on the diagnosis and outcome of medullary thyroid cancer: Experience in 10864 patients with nodular thyroid disorders
-
Elisei R, Bottici V, Luchetti F, Di Coscio G, Romei C, Grasso L, Miccoli P, Iacconi P, Basolo F, Pinchera A & Pacini F. Impact of routine measurement of serum calcitonin on the diagnosis and outcome of medullary thyroid cancer: experience in 10864 patients with nodular thyroid disorders. Journal of Clinical Endocrinology and Metabolism 2004 89 163-168.
-
(2004)
Journal of Clinical Endocrinology and Metabolism
, vol.89
, pp. 163-168
-
-
Elisei, R.1
Bottici, V.2
Luchetti, F.3
Di Coscio, G.4
Romei, C.5
Grasso, L.6
Miccoli, P.7
Iacconi, P.8
Basolo, F.9
Pinchera, A.10
Pacini, F.11
-
12
-
-
0034086880
-
Cytologic diagnosis of medullary carcinoma of the thyroid gland
-
Papaparaskeva K, Nagel H & Droese M. Cytologic diagnosis of medullary carcinoma of the thyroid gland. Diagnostic Cytopathology 2000 22 351-358.
-
(2000)
Diagnostic Cytopathology
, vol.22
, pp. 351-358
-
-
Papaparaskeva, K.1
Nagel, H.2
Droese, M.3
-
13
-
-
24944433989
-
Medullary thyroid carcinoma: Pitfalls in diagnosis by fine needle aspiration cytology and relationship of cytomorphology to RET proto-oncogene mutations
-
Chang TC, Wu SL & Hsiao YL. Medullary thyroid carcinoma: pitfalls in diagnosis by fine needle aspiration cytology and relationship of cytomorphology to RET proto-oncogene mutations. Acta Cytologica 2005 49 477-482.
-
(2005)
Acta Cytologica
, vol.49
, pp. 477-482
-
-
Chang, T.C.1
Wu, S.L.2
Hsiao, Y.L.3
-
15
-
-
4544274825
-
Familial melanoma, pancreatic cancer and germline CDKN2A mutations
-
Goldstein AM. Familial melanoma, pancreatic cancer and germline CDKN2A mutations. Human Mutation 2004 23 630.
-
(2004)
Human Mutation
, vol.23
, pp. 630
-
-
Goldstein, A.M.1
-
16
-
-
32144446457
-
Calcitonin measurements for early detection of medullary thyroid carcinoma or its premalignant conditions in Hashimoto's thyroiditis
-
Schuetz M, Beheshti M, Oczer S, Novotny C, Paul M, Hofmann A, Bieglmayer C, Niederle B, Kletter K, Dudczak R, Karanikas G & Pirich C. Calcitonin measurements for early detection of medullary thyroid carcinoma or its premalignant conditions in Hashimoto's thyroiditis. Anticancer Research 2006 26 723-728.
-
(2006)
Anticancer Research
, vol.26
, pp. 723-728
-
-
Schuetz, M.1
Beheshti, M.2
Oczer, S.3
Novotny, C.4
Paul, M.5
Hofmann, A.6
Bieglmayer, C.7
Niederle, B.8
Kletter, K.9
Dudczak, R.10
Karanikas, G.11
Pirich, C.12
-
17
-
-
0031729019
-
Papillary thyroid carcinoma, parathyroid adenoma, and unexplained hypercalcitoninemia: An unusual presentation of multiple endocrine neoplasia typ2 2A?
-
Rone JK, Lane AG & Grinkemeyer MD. Papillary thyroid carcinoma, parathyroid adenoma, and unexplained hypercalcitoninemia: an unusual presentation of multiple endocrine neoplasia typ2 2A? Thyroid 1998 8 781-785.
-
(1998)
Thyroid
, vol.8
, pp. 781-785
-
-
Rone, J.K.1
Lane, A.G.2
Grinkemeyer, M.D.3
-
18
-
-
0033973161
-
Incidence of RET mutations in Hirschsprung's disease patients
-
Sancandi M, Ceccherini I, Costa M, Fava M, Chen B, Wu Y, Hofstra R, Laurie T, Griffiths M, Burge D & Tam PK. Incidence of RET mutations in Hirschsprung's disease patients. Journal of Pediatric Surgery 2000 35 139-142.
-
(2000)
Journal of Pediatric Surgery
, vol.35
, pp. 139-142
-
-
Sancandi, M.1
Ceccherini, I.2
Costa, M.3
Fava, M.4
Chen, B.5
Wu, Y.6
Hofstra, R.7
Laurie, T.8
Griffiths, M.9
Burge, D.10
Tam, P.K.11
-
19
-
-
33644815947
-
Haplotypes of the human RET proto-oncogene associated with Hirschsprung disease in the Italian population derive from a single ancestral combination of alleles
-
Lantieri F, Griseri P, Puppo F, Campus R, Martucciello, G, Ravazzolo R, Devoto M & Ceccherini I. Haplotypes of the human RET proto-oncogene associated with Hirschsprung disease in the Italian population derive from a single ancestral combination of alleles. Annals of Human Genetics 2006 70 12-26.
-
(2006)
Annals of Human Genetics
, vol.70
, pp. 12-26
-
-
Lantieri, F.1
Griseri, P.2
Puppo, F.3
Campus, R.4
Martucciello, G.5
Ravazzolo, R.6
Devoto, M.7
Ceccherini, I.8
-
20
-
-
33748750438
-
Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma
-
Ghiorzo P, Gargiulo S, Pastorino L, Nasti S, Cusano R, Bruno W, Gliori S, Sertoli MR, Burroni A, Savarino V, Gensini F, Sestini R, Queirolo P, Goldstein AM & Scarra GB. Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma. Human Molecular Genetics 2006 15 2682-2689.
-
(2006)
Human Molecular Genetics
, vol.15
, pp. 2682-2689
-
-
Ghiorzo, P.1
Gargiulo, S.2
Pastorino, L.3
Nasti, S.4
Cusano, R.5
Bruno, W.6
Gliori, S.7
Sertoli, M.R.8
Burroni, A.9
Savarino, V.10
Gensini, F.11
Sestini, R.12
Queirolo, P.13
Goldstein, A.M.14
Scarra, G.B.15
-
21
-
-
0030063766
-
Physiologic versus neoplastic C-cell hyperplasia of the thyroid: Separation of distinct histologic and biologic entities
-
Perry A, Molberg K & Albores-Saavedra J. Physiologic versus neoplastic C-cell hyperplasia of the thyroid: separation of distinct histologic and biologic entities. Cancer 1996 77 750-756.
-
(1996)
Cancer
, vol.77
, pp. 750-756
-
-
Perry, A.1
Molberg, K.2
Albores-Saavedra, J.3
-
22
-
-
10744228150
-
C-cell, hyperplasia and medullary thryoid carcinoma, clinicopathological and genetic correlations in 66 consecutive patients
-
Guyetant S, Josselin N, Savagner F, Rohmer V, Michalak S & Saint-André JP. C-cell, hyperplasia and medullary thryoid carcinoma, clinicopathological and genetic correlations in 66 consecutive patients. Modern Pathologyy 2003 16 756-763.
-
(2003)
Modern Pathologyy
, vol.16
, pp. 756-763
-
-
Guyetant, S.1
Josselin, N.2
Savagner, F.3
Rohmer, V.4
Michalak, S.5
Saint-André, J.P.6
-
23
-
-
0034886423
-
Germline RET634 mutation positive MEN 2A-related C-cell hyperplasias have genetic features consistent with intraepithelial neoplasia
-
Diaz-Cano SJ, de Miguel M, Blanes A, Tashjian R & Wolfe HJ. Germline RET634 mutation positive MEN 2A-related C-cell hyperplasias have genetic features consistent with intraepithelial neoplasia. Journal of Clinical Endocrinology and Metabolism 2001 86 3948-3957.
-
(2001)
Journal of Clinical Endocrinology and Metabolism
, vol.86
, pp. 3948-3957
-
-
Diaz-Cano, S.J.1
de Miguel, M.2
Blanes, A.3
Tashjian, R.4
Wolfe, H.J.5
-
24
-
-
34247855133
-
Absence of RET gene point mutations in sporadic thyroid C-cell hyperplasia
-
Saggiorato E, Rapa I, Garino F, Bussolati G, Orlandi F, Papotti MN & Volante M. Absence of RET gene point mutations in sporadic thyroid C-cell hyperplasia. Journal of Molecular Diagnostics 2007 9 214-219.
-
(2007)
Journal of Molecular Diagnostics
, vol.9
, pp. 214-219
-
-
Saggiorato, E.1
Rapa, I.2
Garino, F.3
Bussolati, G.4
Orlandi, F.5
Papotti, M.N.6
Volante, M.7
-
25
-
-
21244479769
-
Germline homozygous mutations at codon 804 in the RET proto-oncogene in medullary thyroid carcinoma/ multiple endocrine neoplasia type 2A patients
-
Lesueur F, Cebrian A, Cranston A, Leyland J, Faid TM, Clements MR, Robledo M, Whittaker J & Ponder BA. Germline homozygous mutations at codon 804 in the RET proto-oncogene in medullary thyroid carcinoma/ multiple endocrine neoplasia type 2A patients. Journal of Clinical Endocrinology and Metabolism 2005 90 3454-3457.
-
(2005)
Journal of Clinical Endocrinology and Metabolism
, vol.90
, pp. 3454-3457
-
-
Lesueur, F.1
Cebrian, A.2
Cranston, A.3
Leyland, J.4
Faid, T.M.5
Clements, M.R.6
Robledo, M.7
Whittaker, J.8
Ponder, B.A.9
-
26
-
-
28844445630
-
Experience of prophylactic thyroidectomy in multiple endocrine neoplasia type 2A kindreds with RET codon 804 mutations
-
Learoyd DL, Gosnell J, Elston MS, Saurine TJ, Richardson AL, Delbridge LW, Aglen JV & Robinson BG. Experience of prophylactic thyroidectomy in multiple endocrine neoplasia type 2A kindreds with RET codon 804 mutations. Clinical Endocrinology 2005 63 636-641.
-
(2005)
Clinical Endocrinology
, vol.63
, pp. 636-641
-
-
Learoyd, D.L.1
Gosnell, J.2
Elston, M.S.3
Saurine, T.J.4
Richardson, A.L.5
Delbridge, L.W.6
Aglen, J.V.7
Robinson, B.G.8
-
27
-
-
0033670409
-
Update on the MEN 2A c804 RET mutation: Is prophylactic thyroidectomy indicated?
-
Frohnauer MK & Decker PA. Update on the MEN 2A c804 RET mutation: is prophylactic thyroidectomy indicated? Surgery 2000 128 1052-1058.
-
(2000)
Surgery
, vol.128
, pp. 1052-1058
-
-
Frohnauer, M.K.1
Decker, P.A.2
-
28
-
-
34250723400
-
Asymptomatic bilateral adrenal pheocromocytorna in a patient with a germline V804M mutation in the RET protooncogene
-
Recasens M, Oriola J, Fernddnez-Real JM, Roig J, Rodriguez-Hermosa JI, Font JA, Galofre P, López-Bermejo A & Ricart W. Asymptomatic bilateral adrenal pheocromocytorna in a patient with a germline V804M mutation in the RET protooncogene. Clinical Endocrinology 2007 67 29-33.
-
(2007)
Clinical Endocrinology
, vol.67
, pp. 29-33
-
-
Recasens, M.1
Oriola, J.2
Fernddnez-Real, J.M.3
Roig, J.4
Rodriguez-Hermosa, J.I.5
Font, J.A.6
Galofre, P.7
López-Bermejo, A.8
Ricart, W.9
-
29
-
-
27744559793
-
Polymorphisms in the initiators of RET (rearranged during transfection) signalling pathway and susceptibility to sporadic medullary thryoid carcinoma
-
Cebrian A, Lesueue F, Martin S, Leyland J, Ahmed S, Luccarini C, Smith PL, Luben R, Whittaker J, Pharoah PD, Dunning AM & Ponder BA. Polymorphisms in the initiators of RET (rearranged during transfection) signalling pathway and susceptibility to sporadic medullary thryoid carcinoma. Journal of Clinical Endocrinology and Metabolism 2005 90 6268-6274.
-
(2005)
Journal of Clinical Endocrinology and Metabolism
, vol.90
, pp. 6268-6274
-
-
Cebrian, A.1
Lesueue, F.2
Martin, S.3
Leyland, J.4
Ahmed, S.5
Luccarini, C.6
Smith, P.L.7
Luben, R.8
Whittaker, J.9
Pharoah, P.D.10
Dunning, A.M.11
Ponder, B.A.12
-
30
-
-
3242694881
-
RET exon 11 (G691S) polymorphism is significantly more frequent in sporadic medullary thyroid carcinoma than in the general population
-
Elisei R, Cosci B, Romei C, Bottici V, Sculli M, Lari R, Barale R, Pacini F & Pinchera A. RET exon 11 (G691S) polymorphism is significantly more frequent in sporadic medullary thyroid carcinoma than in the general population. Journal of Clinical Endocrinology and Metabolism 2005 89 3579-3584.
-
(2005)
Journal of Clinical Endocrinology and Metabolism
, vol.89
, pp. 3579-3584
-
-
Elisei, R.1
Cosci, B.2
Romei, C.3
Bottici, V.4
Sculli, M.5
Lari, R.6
Barale, R.7
Pacini, F.8
Pinchera, A.9
-
31
-
-
27744453187
-
Polymorphisms in exon 13 and intron 14 of the RET proto-oncogene: Genetic modifiers of medullary carcinoma?
-
Baumgartner-Parzer SM, Lang R, Wagner L, Heinze G, Niederle B, Kaserer K, Waldhausl W & Vierhaper H. Polymorphisms in exon 13 and intron 14 of the RET proto-oncogene: genetic modifiers of medullary carcinoma? Journal of Clinical Endocrinology and Metabolism 2005 90 6232-6236.
-
(2005)
Journal of Clinical Endocrinology and Metabolism
, vol.90
, pp. 6232-6236
-
-
Baumgartner-Parzer, S.M.1
Lang, R.2
Wagner, L.3
Heinze, G.4
Niederle, B.5
Kaserer, K.6
Waldhausl, W.7
Vierhaper, H.8
-
32
-
-
33846556213
-
Significance of the RET protooncogene polymorphism in Turkish sporadic medullary thyroid carcinoma patients
-
Gursoy A, Erdogan MF & Erdogan G. Significance of the RET protooncogene polymorphism in Turkish sporadic medullary thyroid carcinoma patients. Journal of Endocrinological Investigation 2006 29 858-862.
-
(2006)
Journal of Endocrinological Investigation
, vol.29
, pp. 858-862
-
-
Gursoy, A.1
Erdogan, M.F.2
Erdogan, G.3
-
33
-
-
31544434233
-
Polymorphism in RET and its coreceptors and ligands as genetic modifiers of multiple endocrine neoplasia type 2A
-
Lesucur E Cebrian A, Robeldo M, Niccoli-Sire P, Svensson KA, Pinson S, Leyland J, Whittaker J, Pharoah P & Ponder BAJ. Polymorphism in RET and its coreceptors and ligands as genetic modifiers of multiple endocrine neoplasia type 2A. Cancer Research 2006 66 1177-1180.
-
(2006)
Cancer Research
, vol.66
, pp. 1177-1180
-
-
Lesucur, E.1
Cebrian, A.2
Robeldo, M.3
Niccoli-Sire, P.4
Svensson, K.A.5
Pinson, S.6
Leyland, J.7
Whittaker, J.8
Pharoah, P.9
Ponder, B.A.J.10
-
34
-
-
26844496309
-
RET polymorphism and a sporadic medullary thyroid carcinoma in a Portuguese population
-
Costa P, Domingues R, Sobrinho LG & Bugalho MJ. RET polymorphism and a sporadic medullary thyroid carcinoma in a Portuguese population. Endocrine 2005 27 239-243.
-
(2005)
Endocrine
, vol.27
, pp. 239-243
-
-
Costa, P.1
Domingues, R.2
Sobrinho, L.G.3
Bugalho, M.J.4
-
35
-
-
0035860135
-
CDKN2A and CDK4 mutation analysis in Italian mclanoma-prone families: Functional characterization of a novel CDKN2A germ line mutation
-
Della Torre G, Pasini B, Frigerio S, Donghi R, Rovini D, Delia D, Peters G, Huot TJ, Bianchi-Scarra G, Lantieri F, Rodolfo M, Parmiani G & Pierotti MA. CDKN2A and CDK4 mutation analysis in Italian mclanoma-prone families: functional characterization of a novel CDKN2A germ line mutation. British Journal of Cancer 2001 85 836-844.
-
(2001)
British Journal of Cancer
, vol.85
, pp. 836-844
-
-
Della Torre, G.1
Pasini, B.2
Frigerio, S.3
Donghi, R.4
Rovini, D.5
Delia, D.6
Peters, G.7
Huot, T.J.8
Bianchi-Scarra, G.9
Lantieri, F.10
Rodolfo, M.11
Parmiani, G.12
Pierotti, M.A.13
-
36
-
-
13544259887
-
-
Mantelli M, Pastorino L, Ghiorzo P, Barile M, Bruno W, Gargiulo S, Sormani MP, Gliori S, Vecchio S, Ciotti P, Sertoli MR, Queirolo P, Goldstein AM, Bianchi-Scarra G & Italian Melanoma Intergroup. Early onset may predict G101W CDKN2A founder mutation carrier status in Ligurian melanoma patients. Melanoma Research 2004 14 443-448.
-
Mantelli M, Pastorino L, Ghiorzo P, Barile M, Bruno W, Gargiulo S, Sormani MP, Gliori S, Vecchio S, Ciotti P, Sertoli MR, Queirolo P, Goldstein AM, Bianchi-Scarra G & Italian Melanoma Intergroup. Early onset may predict G101W CDKN2A founder mutation carrier status in Ligurian melanoma patients. Melanoma Research 2004 14 443-448.
-
-
-
-
37
-
-
33646195732
-
The P48T germline mutation and polymorphism in the CDKN2A gene of patients with melanoma
-
Huber J & Ramos ES. The P48T germline mutation and polymorphism in the CDKN2A gene of patients with melanoma. Brazilian Journal of Medical and Biological Research 2006 39 237-241.
-
(2006)
Brazilian Journal of Medical and Biological Research
, vol.39
, pp. 237-241
-
-
Huber, J.1
Ramos, E.S.2
-
38
-
-
34447570751
-
First detection of the melanoma-predisposing praline-48-threonine mutation of p 16 in Hungarians: Was there a common founder either in Italy or in Hungary?
-
Szell M, Balogh K, Bobozy A, Kemeny L & Olah J. First detection of the melanoma-predisposing praline-48-threonine mutation of p 16 in Hungarians: was there a common founder either in Italy or in Hungary? Melanoma Research 2007 17 251-254.
-
(2007)
Melanoma Research
, vol.17
, pp. 251-254
-
-
Szell, M.1
Balogh, K.2
Bobozy, A.3
Kemeny, L.4
Olah, J.5
-
39
-
-
33750567811
-
-
Goldstein AM, Chan M, Harland M, Gillanders EM, Hayward NK, Avril MV, Azizi E, Bianchi-Scarra G, Bishop DT, Bressac-de Paillerets B, Bruno W, Calista D, Cannon Albright LA, Demenais E Elder DE, Ghiorzo P, Gruis NA, Hansson J, Hogg D, Holland EA, Kanetsky PA, Kefford RE Landi MT, Lang J, Leachman SA, Mackie RM, Magnusson V, Mann GJ, Niendorf K, Newton Bishop J, Palmer JM, Puig S, Puig-Butille 1A, de Snoo FA, Stark M, Tsao H, Tucker MA, Whitaker L, Yakobson E & Melanoma Genetics Consortium (GenoMEL). High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL. Cancer Research 2006 66 9818-9828.
-
Goldstein AM, Chan M, Harland M, Gillanders EM, Hayward NK, Avril MV, Azizi E, Bianchi-Scarra G, Bishop DT, Bressac-de Paillerets B, Bruno W, Calista D, Cannon Albright LA, Demenais E Elder DE, Ghiorzo P, Gruis NA, Hansson J, Hogg D, Holland EA, Kanetsky PA, Kefford RE Landi MT, Lang J, Leachman SA, Mackie RM, Magnusson V, Mann GJ, Niendorf K, Newton Bishop J, Palmer JM, Puig S, Puig-Butille 1A, de Snoo FA, Stark M, Tsao H, Tucker MA, Whitaker L, Yakobson E & Melanoma Genetics Consortium (GenoMEL). High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL. Cancer Research 2006 66 9818-9828.
-
-
-
-
40
-
-
0034323678
-
A novel germline mutation, P48T, in the CDKN2A/p16 gene in a patient with pancreatic carcinoma
-
Moore PS, Zamboni G, Falconi M, Bassi C & Scarpa A. A novel germline mutation, P48T, in the CDKN2A/p16 gene in a patient with pancreatic carcinoma. Human Mutation 2000 16 447-448.
-
(2000)
Human Mutation
, vol.16
, pp. 447-448
-
-
Moore, P.S.1
Zamboni, G.2
Falconi, M.3
Bassi, C.4
Scarpa, A.5
-
41
-
-
0030045908
-
Infrequent CDKN2 mutation in human differentiated thyroid cancers
-
Tung WS, Shevlin DW, Bartsch D, Norton JA, Wells SA Jr & Godfellow PJ. Infrequent CDKN2 mutation in human differentiated thyroid cancers. Molecular Carcinogenesis 1996 15 5-10.
-
(1996)
Molecular Carcinogenesis
, vol.15
, pp. 5-10
-
-
Tung, W.S.1
Shevlin, D.W.2
Bartsch, D.3
Norton, J.A.4
Wells Jr, S.A.5
Godfellow, P.J.6
|