-
1
-
-
0034308974
-
Familial nonmedullary thyroid cancer
-
Alsanea O (2000) Familial nonmedullary thyroid cancer. Curr Treat Options Oncol 1:345-351
-
(2000)
Curr Treat Options Oncol
, vol.1
, pp. 345-351
-
-
Alsanea, O.1
-
2
-
-
0029119781
-
Diversity of proto-oncogene mutations in familial and sporadic Hirschsprung disease
-
Attie T, Pelet A, Edery P et al. (1995) Diversity of proto-oncogene mutations in familial and sporadic Hirschsprung disease. Hum Mol Genet 4:1381-1386
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1381-1386
-
-
Attie, T.1
Pelet, A.2
Edery, P.3
-
3
-
-
85047682409
-
Guidelines for diagnosis and therapy of MEN type 1 and type 2
-
Brandi ML, Gagel RF, Angeli A et al. (2001) Guidelines for diagnosis and therapy of MEN type 1 and type 2. J Clin Endocrinol Metab 86:5658-5671
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 5658-5671
-
-
Brandi, M.L.1
Gagel, R.F.2
Angeli, A.3
-
4
-
-
0035992864
-
Papillary thyroid carcinoma in patients with RET proto-oncogene germline mutation
-
Brauckhoff M, Gimm O, Hinze R, Ukkat J, Brauckhoff K, Dralle H (2002) Papillary thyroid carcinoma in patients with RET proto-oncogene germline mutation. Thyroid 12:557-561
-
(2002)
Thyroid
, vol.12
, pp. 557-561
-
-
Brauckhoff, M.1
Gimm, O.2
Hinze, R.3
Ukkat, J.4
Brauckhoff, K.5
Dralle, H.6
-
5
-
-
16644397114
-
Multiple endocrine neoplasia 2B syndrome due to codon 918 mutation: Clinical manifestation and course in early and late onset disease
-
Brauckhoff M, Gimm O, Weiss C-L et al. (2004) Multiple endocrine neoplasia 2B syndrome due to codon 918 mutation: clinical manifestation and course in early and late onset disease. World J Surg 28:1305-1311
-
(2004)
World J Surg
, vol.28
, pp. 1305-1311
-
-
Brauckhoff, M.1
Gimm, O.2
Weiss, C.-L.3
-
7
-
-
0027977002
-
Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B
-
USA
-
Carlson KM, Dou S, Chi D et al. (1994) Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B. Proc Natl Acad Sci USA 91:1579-1583
-
(1994)
Proc Natl Acad Sci
, vol.91
, pp. 1579-1583
-
-
Carlson, K.M.1
Dou, S.2
Chi, D.3
-
8
-
-
0031964670
-
Hirschsprung disease in MEN 2A: Increased spectrum of RET Exon 10 genotypes and strong genotype-phenotype correlation
-
Decker RA, Peacock ML, Watson P (1998) Hirschsprung disease in MEN 2A: increased spectrum of RET Exon 10 genotypes and strong genotype-phenotype correlation. Hum Mol Genet 7:129-134
-
(1998)
Hum Mol Genet
, vol.7
, pp. 129-134
-
-
Decker, R.A.1
Peacock, M.L.2
Watson, P.3
-
9
-
-
0027303248
-
Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC
-
Donis-Keller H, Dou S, Chi D et al. (1993) Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC. Hum Mol Genet 2:851-856
-
(1993)
Hum Mol Genet
, vol.2
, pp. 851-856
-
-
Donis-Keller, H.1
Dou, S.2
Chi, D.3
-
10
-
-
15644377401
-
Prophylactic thyroidectomy in 75 children and adolescents with hereditary medullary thyroid carcinoma: German and Austrian experience
-
Dralle H, Gimm O, Simon D et al. (1998) Prophylactic thyroidectomy in 75 children and adolescents with hereditary medullary thyroid carcinoma: German and Austrian experience. World J Surg 22:744-751
-
(1998)
World J Surg
, vol.22
, pp. 744-751
-
-
Dralle, H.1
Gimm, O.2
Simon, D.3
-
11
-
-
0028314251
-
Compartment-oriented microdissection of regional lymph nodes in medullary thyroid carcinoma
-
Dralle H, Damm I, Scheumann GF et al. (2004) Compartment-oriented microdissection of regional lymph nodes in medullary thyroid carcinoma. Surg Today 24:112-121
-
(2004)
Surg Today
, vol.24
, pp. 112-121
-
-
Dralle, H.1
Damm, I.2
Scheumann, G.F.3
-
12
-
-
0029836333
-
Seminars in medicine of the Beth Israel Hospital, Boston. The RET proto-oncogene in multiple endocrine neoplasia type 2 and Hirschsprung's disease
-
Eng C (1996) Seminars in medicine of the Beth Israel Hospital, Boston. The RET proto-oncogene in multiple endocrine neoplasia type 2 and Hirschsprung's disease. N Engl J Med 335:943-951
-
(1996)
N Engl J Med
, vol.335
, pp. 943-951
-
-
Eng, C.1
-
13
-
-
4644256817
-
The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis
-
Eng C, Clayton D, Schuffenecker I et al. (1996) The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis. Jama 276:1575-1579
-
(1996)
Jama
, vol.276
, pp. 1575-1579
-
-
Eng, C.1
Clayton, D.2
Schuffenecker, I.3
-
14
-
-
11244327813
-
Management of patients with hereditary medullary thyroid carcinoma
-
Fitze G (2004) Management of patients with hereditary medullary thyroid carcinoma. Eur J Pediatr Surg 14:375-383
-
(2004)
Eur J Pediatr Surg
, vol.14
, pp. 375-383
-
-
Fitze, G.1
-
15
-
-
0027932274
-
Presymptomatic screening for medullary thyroid carcinoma in patients with multiple endocrine neoplasia type 2A
-
Frilling A, Röher H-D, Ponder BAJ (1994) Presymptomatic screening for medullary thyroid carcinoma in patients with multiple endocrine neoplasia type 2A. World J Surg 18:577-582
-
(1994)
World J Surg
, vol.18
, pp. 577-582
-
-
Frilling, A.1
Röher, H.-D.2
Ponder, B.A.J.3
-
16
-
-
0028807798
-
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 (1995) Presymptomatic DNA screening in families with multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma. Surgery 118:1099-1104
-
(1995)
Surgery
, vol.118
, pp. 1099-1104
-
-
Frilling, A.1
Dralle, H.2
Eng, C.3
Raue, F.4
Broelsch, C.E.5
-
17
-
-
8744227745
-
Germline RET V804 M mutation associated with multiple endocrine neoplasia type 2A
-
Gibelin H, Bezieau S, Misso C, Bouin-Pineau MH, Marechaud R, Kraimps JL (2004) Germline RET V804 M mutation associated with multiple endocrine neoplasia type 2A. Br J Surg 91:1458-1459
-
(2004)
Br J Surg
, vol.91
, pp. 1458-1459
-
-
Gibelin, H.1
Bezieau, S.2
Misso, C.3
Bouin-Pineau, M.H.4
Marechaud, R.5
Kraimps, J.L.6
-
18
-
-
0030722592
-
Germline dinucleotide mutation in codon 883 of the RET proto-oncogene in multiple endocrine neoplasia type 2B without codon 918 mutation
-
Gimm O, Marsh DJ, Andrew SD et al (1997) Germline dinucleotide mutation in codon 883 of the RET proto-oncogene in multiple endocrine neoplasia type 2B without codon 918 mutation. J Clin Endocrinol Metab 82:3902-3904
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 3902-3904
-
-
Gimm, O.1
Marsh, D.J.2
Andrew, S.D.3
-
19
-
-
0033729031
-
Multiple endocrine neoplasia type 2 and RET: From neoplasia to neurogenesis
-
Hansford JR, Mulligan LM (2000) Multiple endocrine neoplasia type 2 and RET: from neoplasia to neurogenesis. J Med Genet 37:817-827
-
(2000)
J Med Genet
, vol.37
, pp. 817-827
-
-
Hansford, J.R.1
Mulligan, L.M.2
-
20
-
-
0037270008
-
Surgical experience in children with differentiated thyroid carcinoma
-
Haveman JW, van Tol KM, Rouwe CW, Piers do A, Plukker JT (2003) Surgical experience in children with differentiated thyroid carcinoma. Ann Surg Oncol 10:15-20
-
(2003)
Ann Surg Oncol
, vol.10
, pp. 15-20
-
-
Haveman, J.W.1
Van Tol, K.M.2
Rouwe, C.W.3
Piers Do, A.4
Plukker, J.T.5
-
21
-
-
0032535770
-
A national cancer data base report on 53.856 cases of thyroid carcinoma treated in the U.S. 1985-1995
-
Hundahl SA, Fleming ID, Fremgen AM, Menck HR (1998) A national cancer data base report on 53.856 cases of thyroid carcinoma treated in the U.S. 1985-1995. Cancer 83:2638-2648
-
(1998)
Cancer
, vol.83
, pp. 2638-2648
-
-
Hundahl, S.A.1
Fleming, I.D.2
Fremgen, A.M.3
Menck, H.R.4
-
22
-
-
0028088256
-
Clinical screening as compared with DNA anlysis in families with multiple nedocrine neoplasia type 2A
-
Lips CJM, Landsvater RM, Höppener JWM et al. (1994) Clinical screening as compared with DNA anlysis in families with multiple nedocrine neoplasia type 2A. N Engl J Med 331:828-835
-
(1994)
N Engl J Med
, vol.331
, pp. 828-835
-
-
Lips, C.J.M.1
Landsvater, R.M.2
Höppener, J.W.M.3
-
23
-
-
0141940150
-
Early malignant progression of hereditary medullary thyroid cancer
-
Machens A, Niccoli-Sire P, Hoegel J et al. (2003) Early malignant progression of hereditary medullary thyroid cancer. N Engl J Med 349:1517-1525
-
(2003)
N Engl J Med
, vol.349
, pp. 1517-1525
-
-
Machens, A.1
Niccoli-Sire, P.2
Hoegel, J.3
-
24
-
-
12344335450
-
Advances in the management of hereditary medullary thyroid cancer
-
Machens A, Ukkat J, Brauckhoff M, Gimm O, Dralle H (2005) Advances in the management of hereditary medullary thyroid cancer. J Intern Med 257:50-59
-
(2005)
J Intern Med
, vol.257
, pp. 50-59
-
-
Machens, A.1
Ukkat, J.2
Brauckhoff, M.3
Gimm, O.4
Dralle, H.5
-
25
-
-
0023229266
-
A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10
-
Mathew CG, Chin KS, Easton DF et al. (1987) A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10. Nature 328:527-528
-
(1987)
Nature
, vol.328
, pp. 527-528
-
-
Mathew, C.G.1
Chin, K.S.2
Easton, D.F.3
-
26
-
-
0027231568
-
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
-
Mulligan LM, Kwok JB, Healey CS et al. (1993) Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A. Nature 363:458-460
-
(1993)
Nature
, vol.363
, pp. 458-460
-
-
Mulligan, L.M.1
Kwok, J.B.2
Healey, C.S.3
-
27
-
-
4444292985
-
Highly penetrant hereditary cancer syndromes
-
Nagy R, Sweet K, Eng C (2004) Highly penetrant hereditary cancer syndromes. Oncogene 23(38):6445-6470
-
(2004)
Oncogene
, vol.23
, Issue.38
, pp. 6445-6470
-
-
Nagy, R.1
Sweet, K.2
Eng, C.3
-
28
-
-
10744229656
-
When should thyroidectomy be performed in familial medullary thyroid carcinoma gene carriers with non-cysteine RET mutations?
-
Niccoli-Sire P, Murat A, Rohmer V et al. (2003) When should thyroidectomy be performed in familial medullary thyroid carcinoma gene carriers with non-cysteine RET mutations? Surgery 134:1029-1037
-
(2003)
Surgery
, vol.134
, pp. 1029-1037
-
-
Niccoli-Sire, P.1
Murat, A.2
Rohmer, V.3
-
29
-
-
0344406081
-
Polymorphisms G691S/S904S of RET as genetic modifiers of MEN 2A
-
Robledo M, Gil L, Pollan M et al. (2003) Polymorphisms G691S/S904S of RET as genetic modifiers of MEN 2A. Cancer Res 63:1814-1817
-
(2003)
Cancer Res
, vol.63
, pp. 1814-1817
-
-
Robledo, M.1
Gil, L.2
Pollan, M.3
-
30
-
-
0023204382
-
Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage
-
Simpson NE, Kidd KK, Goodfellow PJ, McDermid H et al. (1987) Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage. Nature 328:528-530
-
(1987)
Nature
, vol.328
, pp. 528-530
-
-
Simpson, N.E.1
Kidd, K.K.2
Goodfellow, P.J.3
McDermid, H.4
-
31
-
-
0022330363
-
Activation of a novel human transforming gene, ret, by DNA rearrangement
-
Takahashi M, Ritz J, Cooper GM (1985) Activation of a novel human transforming gene, ret, by DNA rearrangement. Cell 42:581-588
-
(1985)
Cell
, vol.42
, pp. 581-588
-
-
Takahashi, M.1
Ritz, J.2
Cooper, G.M.3
-
32
-
-
33744485019
-
Gene expression profiling in differentiated thyroid cancer - A viable strategy for the practice of genomic medicine?
-
in press
-
Weber F, Eng C (2005) Gene expression profiling in differentiated thyroid cancer - A viable strategy for the practice of genomic medicine? Future Oncol (in press)
-
(2005)
Future Oncol
-
-
Weber, F.1
Eng, C.2
-
33
-
-
21044448035
-
Genetic classification of benign and malignant thyroid follicular neoplasia based on a three-gene combination
-
Weber F, Shen L, Aldred MA et al. (2005) Genetic classification of benign and malignant thyroid follicular neoplasia based on a three-gene combination. J Clin Endocrinol Metab 90:2512-2521
-
(2005)
J Clin Endocrinol Metab
, vol.90
, pp. 2512-2521
-
-
Weber, F.1
Shen, L.2
Aldred, M.A.3
-
34
-
-
0028061726
-
Predictive DNA testing and prophylactic thyroidectomy in patients at risk for multiple endocrine neoplasia type 2A
-
Wells SA Jr, Chi DD, Toshima K et al. (1994) Predictive DNA testing and prophylactic thyroidectomy in patients at risk for multiple endocrine neoplasia type 2A. Ann Surg 220:237-250
-
(1994)
Ann Surg
, vol.220
, pp. 237-250
-
-
Wells Jr., S.A.1
Chi, D.D.2
Toshima, K.3
-
35
-
-
0344716605
-
Multiple endocrine neoplasia type 2: Evaluation of the genotype-phenotype relationship
-
Yip L, Cote GJ, Shapiro SE et al. (2003) Multiple endocrine neoplasia type 2: Evaluation of the genotype-phenotype relationship. Arch Surg 138:409-416
-
(2003)
Arch Surg
, vol.138
, pp. 409-416
-
-
Yip, L.1
Cote, G.J.2
Shapiro, S.E.3
|