메뉴 건너뛰기




Volumn 4, Issue 1, 2005, Pages 25-36

Multiple endocrine neoplasia type 2

Author keywords

Medullary thyroid carcinoma; MEN 2; Pheochromocytoma; RET

Indexed keywords

(3 IODOBENZYL)GUANIDINE I 131; ALPHA ADRENERGIC RECEPTOR BLOCKING AGENT; AZELASTINE; BETA ADRENERGIC RECEPTOR BLOCKING AGENT; CYSTEINE; DACARBAZINE; IMATINIB; MEMBRANE PROTEIN; METIROSINE; OCTREOTIDE; PROTEIN RET; PROTEIN TYROSINE KINASE; PROTEIN TYROSINE KINASE INHIBITOR; SUCCINATE DEHYDROGENASE; VON HIPPEL LINDAU PROTEIN;

EID: 19944424474     PISSN: 13899600     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10689-005-0656-y     Document Type: Review
Times cited : (40)

References (109)
  • 1
    • 0023229266 scopus 로고
    • A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10
    • CGP Mathew KS Chin DF Easton 1987 A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10 Nature 128 527 30
    • (1987) Nature , vol.128 , pp. 527-30
    • Mathew, C.G.P.1    Chin, K.S.2    Easton, D.F.3
  • 2
    • 0029836333 scopus 로고    scopus 로고
    • The RET proto-oncogene in multiple endocrine neoplasia type 2 and Hirschsprung's disease
    • C Eng 1996 The RET proto-oncogene in multiple endocrine neoplasia type 2 and Hirschsprung's disease N Engl J Med 335 943 51
    • (1996) N Engl J Med , vol.335 , pp. 943-51
    • Eng, C.1
  • 3
    • 0037262032 scopus 로고    scopus 로고
    • Clinical and genetic aspects of pheochromocytoma
    • G Opocher F Sciavi P Conton 2003 Clinical and genetic aspects of pheochromocytoma Horn Res 59(Suppl 1) 56 61
    • (2003) Horn Res , vol.591 , pp. 56-61
    • Opocher, G.1    Sciavi, F.2    Conton, P.3
  • 4
    • 0027508442 scopus 로고
    • Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease
    • HPH Neumann DP Berger G Sigmund 1993 Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease N Engl J Med 329 1531 8
    • (1993) N Engl J Med , vol.329 , pp. 1531-8
    • Neumann, H.P.H.1    Berger, D.P.2    Sigmund, G.3
  • 5
    • 0035126870 scopus 로고    scopus 로고
    • Genetic testing for cancer predisposition
    • C Eng H Hampel A de la Chapelle 2000 Genetic testing for cancer predisposition Ann Rev Med 52 371 400
    • (2000) Ann Rev Med , vol.52 , pp. 371-400
    • Eng, C.1    Hampel, H.2    De La Chapelle, A.3
  • 6
    • 0036240262 scopus 로고    scopus 로고
    • Gastrointestinal manifestations of multiple endocrine neoplasia type 2
    • MS Cohen JE Phay C Albinson 2002 Gastrointestinal manifestations of multiple endocrine neoplasia type 2 Ann Surg 235 648 55
    • (2002) Ann Surg , vol.235 , pp. 648-55
    • Cohen, M.S.1    Phay, J.E.2    Albinson, C.3
  • 7
    • 0035223922 scopus 로고    scopus 로고
    • Multiple endocrine neoplasia type 2: Clinical aspects
    • O Gimm 2001 Multiple endocrine neoplasia type 2: clinical aspects Front Horm Res 28 103 30
    • (2001) Front Horm Res , vol.28 , pp. 103-30
    • Gimm, O.1
  • 8
    • 85047682409 scopus 로고    scopus 로고
    • Consensus. Guidelines for diagnosis and therapy of MEN type 1 and type 2
    • ML Brandi RF Gagel A Angeli 2001 Consensus. Guidelines for diagnosis and therapy of MEN type 1 and type 2 J Clin Endocrinol Metab 86 5658 71
    • (2001) J Clin Endocrinol Metab , vol.86 , pp. 5658-71
    • Brandi, M.L.1    Gagel, R.F.2    Angeli, A.3
  • 9
    • 0027297690 scopus 로고
    • Pheochromocytoma in multiple endocrine neoplasia type 2A: Survey of 100 cases
    • S Casanova M Rosenberg-Bourgin D Farkas 1993 Pheochromocytoma in multiple endocrine neoplasia type 2A: survey of 100 cases Clin Endocrinol 38 531 7
    • (1993) Clin Endocrinol , vol.38 , pp. 531-7
    • Casanova, S.1    Rosenberg-Bourgin, M.2    Farkas, D.3
  • 10
    • 0035088195 scopus 로고    scopus 로고
    • Long-term biochemical results after operative treatment of primary hyperparathyroidism associated with multiple endocrine neoplasia type I and IIa: Is a more or less extended operation essential
    • C Dotzenrath K Cupisti PE Goretzki 2001 Long-term biochemical results after operative treatment of primary hyperparathyroidism associated with multiple endocrine neoplasia type I and IIa: is a more or less extended operation essential Eur J Surg 167 173 8
    • (2001) Eur J Surg , vol.167 , pp. 173-8
    • Dotzenrath, C.1    Cupisti, K.2    Goretzki, P.E.3
  • 11
    • 15144343501 scopus 로고    scopus 로고
    • Risk and penetrance of primary hyperparathyroidism in multiple endocrine neoplasia type 2A families with mutations at codon 634 of the RET proto-oncogene
    • I Schuffenecker M Virally-Monod R Brohet 1998 Risk and penetrance of primary hyperparathyroidism in multiple endocrine neoplasia type 2A families with mutations at codon 634 of the RET proto-oncogene J Clin Endocrinol Metab 83 487 91
    • (1998) J Clin Endocrinol Metab , vol.83 , pp. 487-91
    • Schuffenecker, I.1    Virally-Monod, M.2    Brohet, R.3
  • 12
    • 0028838578 scopus 로고
    • Mutation of codon 918 in the RET proto-oncogene correlate to poor prognosis in sporadic medullary thyroid carcinomas
    • J Zedenius C Larsson U Bergholm 1995 Mutation of codon 918 in the RET proto-oncogene correlate to poor prognosis in sporadic medullary thyroid carcinomas J Clin Endocrinol Metab 80 3088 90
    • (1995) J Clin Endocrinol Metab , vol.80 , pp. 3088-90
    • Zedenius, J.1    Larsson, C.2    Bergholm, U.3
  • 13
    • 0036143710 scopus 로고    scopus 로고
    • Medullary thyroid carcinoma as part of a multiple endocrine neoplasia type 2B syndrome. Influence on the stage on the clinical course
    • S Leboulleux JP Travagli B Caillou 2002 Medullary thyroid carcinoma as part of a multiple endocrine neoplasia type 2B syndrome. Influence on the stage on the clinical course Cancer 94 44 50
    • (2002) Cancer , vol.94 , pp. 44-50
    • Leboulleux, S.1    Travagli, J.P.2    Caillou, B.3
  • 14
    • 0035048305 scopus 로고    scopus 로고
    • Genotype-phenotype correlations in hereditary medullary thyroid carcinoma: Oncological features and biochemical properties
    • A Machens O Gimm R Hinze 2001 Genotype-phenotype correlations in hereditary medullary thyroid carcinoma: Oncological features and biochemical properties J Clin Endocrinol Metab 86 1104 9
    • (2001) J Clin Endocrinol Metab , vol.86 , pp. 1104-9
    • MacHens, A.1    Gimm, O.2    Hinze, R.3
  • 15
    • 0028199074 scopus 로고
    • Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC
    • LM Mulligan C Eng CS Healey 1994 Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC Nat Genet 6 70 4
    • (1994) Nat Genet , vol.6 , pp. 70-4
    • Mulligan, L.M.1    Eng, C.2    Healey, C.S.3
  • 17
    • 0028881998 scopus 로고
    • Genotype-phenotype correlation in multiple endocrine neoplasia type 2: Report of the International RET mutation Consortium
    • LM Mulligan DJ Marsh BG Robinson 1995 Genotype-phenotype correlation in multiple endocrine neoplasia type 2: report of the International RET mutation Consortium J Intern Med 238 343 6
    • (1995) J Intern Med , vol.238 , pp. 343-6
    • Mulligan, L.M.1    Marsh, D.J.2    Robinson, B.G.3
  • 18
    • 4644256817 scopus 로고    scopus 로고
    • The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET Mutation Consortium analysis
    • C Eng D Clayton I Schuffenecker 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 9
    • (1996) JAMA , vol.276 , pp. 1575-9
    • Eng, C.1    Clayton, D.2    Schuffenecker, I.3
  • 19
    • 0028006092 scopus 로고
    • Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours
    • 2
    • C Eng DP Smith LM Mulligan 1994 Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours Human Mol Genet 3 2 237 41
    • (1994) Human Mol Genet , vol.3 , pp. 237-41
    • Eng, C.1    Smith, D.P.2    Mulligan, L.M.3
  • 20
    • 0027231568 scopus 로고
    • Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
    • LM Mulligan JBJ Kwok CS Healey 1993 Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A Nature 363 458 60
    • (1993) Nature , vol.363 , pp. 458-60
    • Mulligan, L.M.1    Kwok, J.B.J.2    Healey, C.S.3
  • 21
    • 0344442410 scopus 로고    scopus 로고
    • A novel germ-line point mutation in RET exon 8 (gly(533)cys) in a large kindred with familial medullary thyroid carcinoma
    • AM Alvares Da Silva RM Maciel MR Dias Da Silva 2003 A 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 43
    • (2003) J Clin Endocrinol Metab , vol.88 , pp. 5438-43
    • Alvares Da Silva, A.M.1    MacIel, R.M.2    Dias Da Silva, M.R.3
  • 22
    • 0031964670 scopus 로고    scopus 로고
    • Hirschsprung disease in MEN 2A: Increased spectrum of RET exon 10 genotypes and strong genotype-phenotype correlation
    • 1
    • RA Decker ML Peacock P Watson 1998 Hirschsprung disease in MEN 2A: increased spectrum of RET exon 10 genotypes and strong genotype-phenotype correlation Human Mol Genet 7 1 129 34
    • (1998) Human Mol Genet , vol.7 , pp. 129-34
    • Decker, R.A.1    Peacock, M.L.2    Watson, P.3
  • 23
    • 0029896244 scopus 로고    scopus 로고
    • Diagnosis of multiple endocrine neoplasia [MEN] 2A, 2B and familial medullary thyroid cancer [FMTC] by multiplex PCR and heteroduplex analyses of RET proto-oncogene mutations
    • M Kambouris CE Jackson GL Feldman 1996 Diagnosis of multiple endocrine neoplasia [MEN] 2A, 2B and familial medullary thyroid cancer [FMTC] by multiplex PCR and heteroduplex analyses of RET proto-oncogene mutations Hum Mut 8 64 70
    • (1996) Hum Mut , vol.8 , pp. 64-70
    • Kambouris, M.1    Jackson, C.E.2    Feldman, G.L.3
  • 24
    • 0028033474 scopus 로고
    • RET proto-oncogene mutations in inherited and sporadic medullary thyroid cancer
    • JE Blaugrund MM Johns YJ Eby 1994 RET proto-oncogene mutations in inherited and sporadic medullary thyroid cancer Hum Mol Genet 3 1895 7
    • (1994) Hum Mol Genet , vol.3 , pp. 1895-7
    • Blaugrund, J.E.1    Johns, M.M.2    Eby, Y.J.3
  • 25
    • 9344234978 scopus 로고    scopus 로고
    • Mutations of the ret protooncogene in German multiple endocrine neoplasia families: Relation between genotype and phenotype
    • K Frank-Raue W Höppner A Frilling 1996 Mutations of the ret protooncogene in German multiple endocrine neoplasia families: relation between genotype and phenotype J Clin Endocrinol Metab 81 1780 3
    • (1996) J Clin Endocrinol Metab , vol.81 , pp. 1780-3
    • Frank-Raue, K.1    Höppner, W.2    Frilling, A.3
  • 26
    • 0034830378 scopus 로고    scopus 로고
    • Molecular genetic diagnosis program of multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma syndrome in Hungary
    • I Klein O Erik V Homolya 2001 Molecular genetic diagnosis program of multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma syndrome in Hungary J Endocrinol 170 661 6
    • (2001) J Endocrinol , vol.170 , pp. 661-6
    • Klein, I.1    Erik, O.2    Homolya, V.3
  • 27
    • 18444398955 scopus 로고    scopus 로고
    • Occurrence of pheochromocytoma in a MEN 2A family with codon 609 mutation of the RET proto-oncogene
    • P Igaz A Patocs K Racz 2002 Occurrence of pheochromocytoma in a MEN 2A family with codon 609 mutation of the RET proto-oncogene J Clin Endocrinol Metab 87 2994
    • (2002) J Clin Endocrinol Metab , vol.87 , pp. 2994
    • Igaz, P.1    Patocs, A.2    Racz, K.3
  • 28
    • 19944406892 scopus 로고
    • Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC
    • H Donis-Keller S Dou D Chi 1994 Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC Hum Mol Genet 3 237 41
    • (1994) Hum Mol Genet , vol.3 , pp. 237-41
    • Donis-Keller, H.1    Dou, S.2    Chi, D.3
  • 29
    • 0030060475 scopus 로고    scopus 로고
    • Mutation analysis of the RET proto-oncogene in Duth families with MEN 2A, MEN 2B and FMTC: Two novel mutations and one de novo mutation for MEN 2A
    • RM Landsvater RP Jansen RM Hofstra 1996 Mutation analysis of the RET proto-oncogene in Duth families with MEN 2A, MEN 2B and FMTC: two novel mutations and one de novo mutation for MEN 2A Hum Genet 97 11 4
    • (1996) Hum Genet , vol.97 , pp. 11-4
    • Landsvater, R.M.1    Jansen, R.P.2    Hofstra, R.M.3
  • 30
    • 0031802249 scopus 로고    scopus 로고
    • Novel point mutation in exon 10 of the RET proto-oncogene in a family with medullary thyroid carcinoma
    • J Oriola C Paramo I Halperin 1998 Novel point mutation in exon 10 of the RET proto-oncogene in a family with medullary thyroid carcinoma Am J Med Genet 78 271 3
    • (1998) Am J Med Genet , vol.78 , pp. 271-3
    • Oriola, J.1    Paramo, C.2    Halperin, I.3
  • 31
    • 0038074416 scopus 로고    scopus 로고
    • Cys611Ser mutation in RET proto-oncogene in a kindred with medullary thyroid carcinoma and Hirschsprung disease
    • M Nishikawa Y Murakumo T Imai 2003 Cys611Ser mutation in RET proto-oncogene in a kindred with medullary thyroid carcinoma and Hirschsprung disease Eur J Hum Genet 11 364 8
    • (2003) Eur J Hum Genet , vol.11 , pp. 364-8
    • Nishikawa, M.1    Murakumo, Y.2    Imai, T.3
  • 32
    • 0028095123 scopus 로고
    • A rapid screening method for the detection of mutations in RET proto-oncogene in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma families
    • DJ Marsh BG Robinson S Andrew 1994 A rapid screening method for the detection of mutations in RET proto-oncogene in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma families Genomics 23 477 9
    • (1994) Genomics , vol.23 , pp. 477-9
    • Marsh, D.J.1    Robinson, B.G.2    Andrew, S.3
  • 33
    • 0036220980 scopus 로고    scopus 로고
    • RET mutation profile and variable clinical manifestations in a family with multiple endocrine neoplasia type 2A and Hirschsprung disease
    • B Pasini R Rossi MR Ambrosio 2002 RET mutation profile and variable clinical manifestations in a family with multiple endocrine neoplasia type 2A and Hirschsprung disease Surgery 131 372 81
    • (2002) Surgery , vol.131 , pp. 372-81
    • Pasini, B.1    Rossi, R.2    Ambrosio, M.R.3
  • 34
    • 0029119781 scopus 로고
    • Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease
    • T Attie A Pelet P Edery 1995 Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease Hum Mol Genet 4 1381 6
    • (1995) Hum Mol Genet , vol.4 , pp. 1381-6
    • Attie, T.1    Pelet, A.2    Edery, P.3
  • 35
    • 0030896418 scopus 로고    scopus 로고
    • Mutations of the RET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and Hirschsprung disease
    • C Eng LM Mulligan 1997 Mutations of the RET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and Hirschsprung disease Hum Mutat 9 97 109
    • (1997) Hum Mutat , vol.9 , pp. 97-109
    • Eng, C.1    Mulligan, L.M.2
  • 36
    • 0028027543 scopus 로고
    • RET proto-oncogene mutations in French MEN 2A and FMTC families
    • I Schuffenecker M Billaud A Calender 1994 RET proto-oncogene mutations in French MEN 2A and FMTC families Hum Mol Genet 3 1939 43
    • (1994) Hum Mol Genet , vol.3 , pp. 1939-43
    • Schuffenecker, I.1    Billaud, M.2    Calender, A.3
  • 37
    • 8544224970 scopus 로고    scopus 로고
    • Novel germline RET proto-oncogene mutations associated with medullary thyroid carcinoma (MTC): Mutation analysis in Japanese patients with MTC
    • Y Kitamura PJ Goodfellow K Shimizu 1997 Novel germline RET proto-oncogene mutations associated with medullary thyroid carcinoma (MTC): mutation analysis in Japanese patients with MTC Oncogene 14 3103 6
    • (1997) Oncogene , vol.14 , pp. 3103-6
    • Kitamura, Y.1    Goodfellow, P.J.2    Shimizu, K.3
  • 38
    • 0043167812 scopus 로고    scopus 로고
    • Frequent association between MEN 2A and cutaneous lichen amyloidosis
    • U Verga L Fugazzola S Cambiaghi 2003 Frequent association between MEN 2A and cutaneous lichen amyloidosis Clin Endocrinol 59 156 61
    • (2003) Clin Endocrinol , vol.59 , pp. 156-61
    • Verga, U.1    Fugazzola, L.2    Cambiaghi, S.3
  • 39
    • 0028196667 scopus 로고
    • Direct, non-radioactive detection of mutations in multiple endocrine neoplasia type 2A families
    • R McMahon LM Mulligan CS Healey 1994 Direct, non-radioactive detection of mutations in multiple endocrine neoplasia type 2A families Hum Mol Genet 3 643 6
    • (1994) Hum Mol Genet , vol.3 , pp. 643-6
    • McMahon, R.1    Mulligan, L.M.2    Healey, C.S.3
  • 40
    • 0030939501 scopus 로고    scopus 로고
    • A cys 634gly substitution of the RET proto-oncogene in a family with recurrence of multiple endocrine neoplasia type 2A and cutaneous lichen amyloidosis
    • M Seri I Celli N Betsos 1997 A cys 634gly substitution of the RET proto-oncogene in a family with recurrence of multiple endocrine neoplasia type 2A and cutaneous lichen amyloidosis Clin Genet 51 86 90
    • (1997) Clin Genet , vol.51 , pp. 86-90
    • Seri, M.1    Celli, I.2    Betsos, N.3
  • 41
    • 0028838075 scopus 로고
    • A novel point mutation in the tyrosine kinase domain of the RET proto-oncogene in sporadic medullary thyroid carcinoma and in a family with FMTC
    • C Eng DP Smith LM Mulligan 1995 A novel point mutation in the tyrosine kinase domain of the RET proto-oncogene in sporadic medullary thyroid carcinoma and in a family with FMTC Oncogene 10 509 13
    • (1995) Oncogene , vol.10 , pp. 509-13
    • Eng, C.1    Smith, D.P.2    Mulligan, L.M.3
  • 42
    • 0036605120 scopus 로고    scopus 로고
    • A novel germline point mutation, c2304->T, in codon 768 of the RET proto-oncogene in a patient with medullar thyroid carcinoma
    • G Antinolo I Marcos RM Fernandez 2002 A novel germline point mutation, c2304->T, in codon 768 of the RET proto-oncogene in a patient with medullar thyroid carcinoma Am J Med Genet 110 85 7
    • (2002) Am J Med Genet , vol.110 , pp. 85-7
    • Antinolo, G.1    Marcos, I.2    Fernandez, R.M.3
  • 43
    • 0036691404 scopus 로고    scopus 로고
    • Prospective trial of unilateral surgery for nonhereditary medullary thyroid carcinoma in patients without germline RET mutations
    • A Miyauchi F Matsuzuka K Hirai 2002 Prospective trial of unilateral surgery for nonhereditary medullary thyroid carcinoma in patients without germline RET mutations World J Surg 26 1023 8
    • (2002) World J Surg , vol.26 , pp. 1023-8
    • Miyauchi, A.1    Matsuzuka, F.2    Hirai, K.3
  • 44
    • 0036067046 scopus 로고    scopus 로고
    • A new indentified germline mutation of the RET proto-oncogene responsible for familial medullary carcinoma in co-existence with a hyperfunctioning autonomous nodule
    • W Mashek R Pichler R Rieger 2002 A new indentified germline mutation of the RET proto-oncogene responsible for familial medullary carcinoma in co-existence with a hyperfunctioning autonomous nodule Clin Endocrinol 56 823
    • (2002) Clin Endocrinol , vol.56 , pp. 823
    • Mashek, W.1    Pichler, R.2    Rieger, R.3
  • 45
    • 0031765304 scopus 로고    scopus 로고
    • A new hot spot for mutations in the ret proto-oncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A
    • I Berndt M Reuter B Saller 1998 A new hot spot for mutations in the ret proto-oncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A J Clin Endocrinol Metab 83 770 4
    • (1998) J Clin Endocrinol Metab , vol.83 , pp. 770-4
    • Berndt, I.1    Reuter, M.2    Saller, B.3
  • 46
    • 0036919493 scopus 로고    scopus 로고
    • RET proto-oncogene mutations affecting codon 790/791: A mild form of multiple endocrine neoplasia type 2A syndrome
    • O Gimm BE Niederle T Weber 2002 RET proto-oncogene mutations affecting codon 790/791: a mild form of multiple endocrine neoplasia type 2A syndrome Surgery 132 952 9
    • (2002) Surgery , vol.132 , pp. 952-9
    • Gimm, O.1    Niederle, B.E.2    Weber, T.3
  • 47
    • 0029002147 scopus 로고
    • RET mutations in exons 13 and 14 of FMTC patients
    • A Bolino I Schuffenecker Y Luo 1995 RET mutations in exons 13 and 14 of FMTC patients Oncogene 10 2415 9
    • (1995) Oncogene , vol.10 , pp. 2415-9
    • Bolino, A.1    Schuffenecker, I.2    Luo, Y.3
  • 48
    • 0033526365 scopus 로고    scopus 로고
    • Adrenal and extra-adrenal pheochromocytomas in a family with germline RET V804L mutation
    • O Nilsson LE Tisell S Jansson 1999 Adrenal and extra-adrenal pheochromocytomas in a family with germline RET V804L mutation JAMA 281 1587
    • (1999) JAMA , vol.281 , pp. 1587
    • Nilsson, O.1    Tisell, L.E.2    Jansson, S.3
  • 49
    • 0029848352 scopus 로고    scopus 로고
    • Distinction between sporadic and hereditary medullary thyroid carcinoma (MTC) by mutation analysis of the RET proto-oncogene. 'Study Group Multiple Endocrine Neoplasia Austria (SMENA)'
    • M Fink A Wienhusel B Niederle OA Haas 1996 Distinction between sporadic and hereditary medullary thyroid carcinoma (MTC) by mutation analysis of the RET proto-oncogene. 'Study Group Multiple Endocrine Neoplasia Austria (SMENA)' Int J Cancer 69 312 6
    • (1996) Int J Cancer , vol.69 , pp. 312-6
    • Fink, M.1    Wienhusel, A.2    Niederle, B.3    Haas, O.A.4
  • 50
    • 0035320931 scopus 로고    scopus 로고
    • A rare variant, I852M, of the RET proto-oncogene in a patient with medullary thyroid carcinoma at age 20 years
    • R Demeester J Parma P Cochaux 2001 A rare variant, I852M, of the RET proto-oncogene in a patient with medullary thyroid carcinoma at age 20 years Hum Mutat 17 354
    • (2001) Hum Mutat , vol.17 , pp. 354
    • Demeester, R.1    Parma, J.2    Cochaux, P.3
  • 51
    • 0030722592 scopus 로고    scopus 로고
    • Germline dinucleotide mutation in codon 883 of the RET proto-oncogene in multiple endocrine neoplasia type 2B without codon 918 mutation
    • O Gimm DJ Marsh SD Andrew 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 4
    • (1997) J Clin Endocrinol Metab , vol.82 , pp. 3902-4
    • Gimm, O.1    Marsh, D.J.2    Andrew, S.D.3
  • 52
    • 0030819689 scopus 로고    scopus 로고
    • A novel point mutation in the intracellular domain of the ret protoncogene in a family with medullary thyroid carcinoma
    • RM Hofsra O Fatturoso L Quadro 1997 A novel point mutation in the intracellular domain of the ret protoncogene in a family with medullary thyroid carcinoma J Clin Endocrinol Metab 82 4176 8
    • (1997) J Clin Endocrinol Metab , vol.82 , pp. 4176-8
    • Hofsra, R.M.1    Fatturoso, O.2    Quadro, L.3
  • 53
    • 4043122025 scopus 로고    scopus 로고
    • Pheochromocytoma and medullary thyroid carcinoma: A new genotype-phenotype correlation of the RET protooncogene 891 germline mutation
    • C Jimenez MA Habra SC Huang 2004 Pheochromocytoma and medullary thyroid carcinoma: a new genotype-phenotype correlation of the RET protooncogene 891 germline mutation J Clin Endocrinol Metab 89 4142 5
    • (2004) J Clin Endocrinol Metab , vol.89 , pp. 4142-5
    • Jimenez, C.1    Habra, M.A.2    Huang, S.C.3
  • 54
    • 3242729164 scopus 로고    scopus 로고
    • A novel point mutation of the RET protooncogene involving the second intracellular tyrosine kinase domain in a family with medullary thyroid carcinoma
    • C Jimenez GT Dang PN Schultz 2004 A novel point mutation of the RET protooncogene involving the second intracellular tyrosine kinase domain in a family with medullary thyroid carcinoma J Clin Endocrinol Metab 89 3521 6
    • (2004) J Clin Endocrinol Metab , vol.89 , pp. 3521-6
    • Jimenez, C.1    Dang, G.T.2    Schultz, P.N.3
  • 55
    • 0027977002 scopus 로고
    • Single missense mutation in tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B
    • KM Carlson S Dou D Chi 1994 Single missense mutation in tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B Proc Natl Acad Sci USA 91 1579 83
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 1579-83
    • Carlson, K.M.1    Dou, S.2    Chi, D.3
  • 56
    • 0028787248 scopus 로고
    • Two maternally derived missense mutations in the tyrosine kinase domain of the RET protooncogene in a patient with de novo MEN 2B
    • Y Kitamura N Scavarda Jr SA Wells 1995 Two maternally derived missense mutations in the tyrosine kinase domain of the RET protooncogene in a patient with de novo MEN 2B Hum Mol Genet 4 1987 8
    • (1995) Hum Mol Genet , vol.4 , pp. 1987-8
    • Kitamura, Y.1    Scavarda, N.2    Wells Jr., S.A.3
  • 57
    • 0033330662 scopus 로고    scopus 로고
    • A novel 9-base pair duplication in RET exon 8 in familial medullary thyroid carcinoma
    • P Pigny C Bauters JL Wemeau 1999 A novel 9-base pair duplication in RET exon 8 in familial medullary thyroid carcinoma J Clin Endocrinol Metab 84 1700 4
    • (1999) J Clin Endocrinol Metab , vol.84 , pp. 1700-4
    • Pigny, P.1    Bauters, C.2    Wemeau, J.L.3
  • 58
    • 0030981891 scopus 로고    scopus 로고
    • A duplication of 12 bp in the critical cysteine rich domain of the RET proto-oncogene results in a distinct phenotype of multiple endocrine neoplasia type 2A
    • W Hoppner MM Ritter 1997 A duplication of 12 bp in the critical cysteine rich domain of the RET proto-oncogene results in a distinct phenotype of multiple endocrine neoplasia type 2A HumMol Genet 6 587 90
    • (1997) HumMol Genet , vol.6 , pp. 587-90
    • Hoppner, W.1    Ritter, M.M.2
  • 59
    • 0031984908 scopus 로고    scopus 로고
    • Duplication of 9 base pairs in the critical cysteine rich domain of the RET proto-oncogene causes of multiple endocrine neoplasia type 2A
    • Hoppner W, Dralle H, Brabant G. Duplication of 9 base pairs in the critical cysteine rich domain of the RET proto-oncogene causes of multiple endocrine neoplasia type 2A. Hum Mutat 1998; (Suppl. 1): S128-S30
    • (1998) Hum Mutat , Issue.1 SUPPL.
    • Hoppner, W.1    Dralle, H.2    Brabant, G.3
  • 60
    • 0033304922 scopus 로고    scopus 로고
    • A novel case of multiple endocrine neoplasia type 2A associated with two de novo mutations of the RET protooncogene
    • A Tessitore AA Sinisi MC Pasquali 1999 A novel case of multiple endocrine neoplasia type 2A associated with two de novo mutations of the RET protooncogene J Clin Endocrinol Metab 84 3522 7
    • (1999) J Clin Endocrinol Metab , vol.84 , pp. 3522-7
    • Tessitore, A.1    Sinisi, A.A.2    Pasquali, M.C.3
  • 61
    • 0036882138 scopus 로고    scopus 로고
    • A novel Val648Ile substitution in RET protooncogene observed in a Cys634Arg multiple endocrine neoplasia type 2A kindred presenting with an adrenocorticotropin-producing pheochromocytoma
    • AB Nunes MCL Ezabella AC Pereira 2002 A novel Val648Ile substitution in RET protooncogene observed in a Cys634Arg multiple endocrine neoplasia type 2A kindred presenting with an adrenocorticotropin-producing pheochromocytoma J Clin Endocrinol Metab 87 5658 61
    • (2002) J Clin Endocrinol Metab , vol.87 , pp. 5658-61
    • Nunes, A.B.1    Ezabella, M.C.L.2    Pereira, A.C.3
  • 62
    • 0033045514 scopus 로고    scopus 로고
    • Two Germline missense mutations at codon 804 and 806 of the RET proto-oncogene in the same allele in a patient with multiple endocrine neoplasia type 2B without 918 mutation
    • A Miyauchi H Futami N Hai 1999 Two Germline missense mutations at codon 804 and 806 of the RET proto-oncogene in the same allele in a patient with multiple endocrine neoplasia type 2B without 918 mutation Jpn J Cancer Res 90 1 5
    • (1999) Jpn J Cancer Res , vol.90 , pp. 1-5
    • Miyauchi, A.1    Futami, H.2    Hai, N.3
  • 63
    • 0034766527 scopus 로고    scopus 로고
    • Familial medullary thyroid carcinoma and prominent corneal nerves associated with the germline V804M and V778I mutations on the same allele of RET
    • L Kasprzak S Nolet L Gaboury 2001 Familial medullary thyroid carcinoma and prominent corneal nerves associated with the germline V804M and V778I mutations on the same allele of RET J Med Genet 38 784 7
    • (2001) J Med Genet , vol.38 , pp. 784-7
    • Kasprzak, L.1    Nolet, S.2    Gaboury, L.3
  • 64
    • 0036148536 scopus 로고    scopus 로고
    • Atypical MEN type 2B associated with two germline RET mutations on the same allele not involving codon 918
    • FH Menko RB van der Luijt IAJ de Valk 2002 Atypical MEN type 2B associated with two germline RET mutations on the same allele not involving codon 918 J Clin Endocrinol Metab 87 393 7
    • (2002) J Clin Endocrinol Metab , vol.87 , pp. 393-7
    • Menko, F.H.1    Van Der Luijt, R.B.2    De Valk, I.A.J.3
  • 65
    • 0034014147 scopus 로고    scopus 로고
    • A RET double mutation in the germline of the kindred with FMTC
    • DK Bartsch C Hasse C Schug 2000 A RET double mutation in the germline of the kindred with FMTC Exp Clin Endocrinol Diabetes 108 128 32
    • (2000) Exp Clin Endocrinol Diabetes , vol.108 , pp. 128-32
    • Bartsch, D.K.1    Hasse, C.2    Schug, C.3
  • 66
    • 0036798174 scopus 로고    scopus 로고
    • The pressure rises: Update on genetics of phaeochromocytoma
    • ER Maher C Eng 2003 The pressure rises: update on genetics of phaeochromocytoma Human Mol Genet 11 2347 54
    • (2003) Human Mol Genet , vol.11 , pp. 2347-54
    • Maher, E.R.1    Eng, C.2
  • 67
    • 0344716605 scopus 로고    scopus 로고
    • Multiple endocrine neoplasia type 2. Evaluation of the genotype-phenotype relationship
    • L Yip GJ Cote SE Shapiro 2003 Multiple endocrine neoplasia type 2. Evaluation of the genotype-phenotype relationship Arch Surg 138 409 16
    • (2003) Arch Surg , vol.138 , pp. 409-16
    • Yip, L.1    Cote, G.J.2    Shapiro, S.E.3
  • 68
    • 0037629965 scopus 로고    scopus 로고
    • RET codon 634 mutations in multiple endocrine neoplasia type 2A - Variable clinical features and clinical outcome
    • 6
    • MK Punales H Graf JL Gross AL Maia 2003 RET codon 634 mutations in multiple endocrine neoplasia type 2A - variable clinical features and clinical outcome J Clin Endocrinol Metab 88 6 2644 9
    • (2003) J Clin Endocrinol Metab , vol.88 , pp. 2644-9
    • Punales, M.K.1    Graf, H.2    Gross, J.L.3    Maia, A.L.4
  • 69
    • 0029090153 scopus 로고
    • Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia, type II
    • HPH Neumann C Eng LM Mulligan 1995 Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia, type II JAMA 274 1149 51
    • (1995) JAMA , vol.274 , pp. 1149-51
    • Neumann, H.P.H.1    Eng, C.2    Mulligan, L.M.3
  • 70
    • 17944370976 scopus 로고    scopus 로고
    • Familial medullary thyroid carcinoma with noncysteine RET mutations: Phenotype-genotype relationship in a large series of patients
    • 8
    • P Niccoli-Sire A Murat V Rohmer 2001 Familial medullary thyroid carcinoma with noncysteine RET mutations: phenotype-genotype relationship in a large series of patients J Clin Endocrinol Metab 86 8 3746 53
    • (2001) J Clin Endocrinol Metab , vol.86 , pp. 3746-53
    • Niccoli-Sire, P.1    Murat, A.2    Rohmer, V.3
  • 71
    • 0031759421 scopus 로고    scopus 로고
    • Germ line mutation analysis in families with multiple endocrine neoplasia type 2A or familial medullary thyroid carcinoma
    • HJ Karga MK Karayianni DA Linos 1998 Germ line mutation analysis in families with multiple endocrine neoplasia type 2A or familial medullary thyroid carcinoma Eur J Endocrinol 139 410 5
    • (1998) Eur J Endocrinol , vol.139 , pp. 410-5
    • Karga, H.J.1    Karayianni, M.K.2    Linos, D.A.3
  • 72
    • 0030949872 scopus 로고    scopus 로고
    • RET proto-oncogene mutations in multiple endocrine neoplasia type 2 and medullary thyroid carcinoma
    • 4-6
    • DJ Marsh LM Mulligan C Eng 1997 RET proto-oncogene mutations in multiple endocrine neoplasia type 2 and medullary thyroid carcinoma Horm Res 47 4-6 168 78
    • (1997) Horm Res , vol.47 , pp. 168-78
    • Marsh, D.J.1    Mulligan, L.M.2    Eng, C.3
  • 73
    • 0031018680 scopus 로고    scopus 로고
    • Prevalence and parental origin of de novo RET mutations in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma
    • I Schuffenecker N Ginet D Goldgar 1997 Prevalence and parental origin of de novo RET mutations in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma Am J Hum Genet 60 233 7
    • (1997) Am J Hum Genet , vol.60 , pp. 233-7
    • Schuffenecker, I.1    Ginet, N.2    Goldgar, D.3
  • 74
    • 0033388487 scopus 로고    scopus 로고
    • Germline V804M mutation in the RET proto-oncogene in two apparently sporadic cases of MTC presenting in the seventh decade of life
    • KE Shannon O Gimm R Hinze 1999 Germline V804M mutation in the RET proto-oncogene in two apparently sporadic cases of MTC presenting in the seventh decade of life J Endocr Genet 1 39 45
    • (1999) J Endocr Genet , vol.1 , pp. 39-45
    • Shannon, K.E.1    Gimm, O.2    Hinze, R.3
  • 75
    • 0034603172 scopus 로고    scopus 로고
    • Transforming ability of MEN2A-RET requires activation of the phosphatidylinositol 3-kinase/AKT signaling pathway
    • 5
    • C Segouffin-Cariou M Billaud 2000 Transforming ability of MEN2A-RET requires activation of the phosphatidylinositol 3-kinase/AKT signaling pathway J Biol Chem 275 5 3568 76
    • (2000) J Biol Chem , vol.275 , pp. 3568-76
    • Segouffin-Cariou, C.1    Billaud, M.2
  • 76
    • 18444380535 scopus 로고    scopus 로고
    • Familial medullary thyroid carcinoma: Clinical variability and low aggressiveness associated with RET mutation at codon 804
    • F Lombardo E Baudin E Chiefari 2002 Familial medullary thyroid carcinoma: clinical variability and low aggressiveness associated with RET mutation at codon 804 J Clin Endocrinol Metab 87 1674 80
    • (2002) J Clin Endocrinol Metab , vol.87 , pp. 1674-80
    • Lombardo, F.1    Baudin, E.2    Chiefari, E.3
  • 77
    • 0033526365 scopus 로고    scopus 로고
    • Adrenal and extra-adrenal pheochromocytomas in a family with germline RET V804L mutation
    • 17
    • O Nilsson LE Tisell S Jansson 1999 Adrenal and extra-adrenal pheochromocytomas in a family with germline RET V804L mutation JAMA 281 17 1587 88
    • (1999) JAMA , vol.281 , pp. 1587-88
    • Nilsson, O.1    Tisell, L.E.2    Jansson, S.3
  • 78
    • 0141940150 scopus 로고    scopus 로고
    • Early malignant progression of hereditary medullary thyroid carcinoma
    • A Machens P Niccoli-Sire J Hoegel 2003 Early malignant progression of hereditary medullary thyroid carcinoma N Engl J Med 349 1517 27
    • (2003) N Engl J Med , vol.349 , pp. 1517-27
    • MacHens, A.1    Niccoli-Sire, P.2    Hoegel, J.3
  • 79
    • 0141974809 scopus 로고    scopus 로고
    • Lessons learned from management of a rare genetic cancer
    • J Cote RF Gagel 2003 Lessons learned from management of a rare genetic cancer N Engl J Med 349 1566 68
    • (2003) N Engl J Med , vol.349 , pp. 1566-68
    • Cote, J.1    Gagel, R.F.2
  • 80
    • 0344406081 scopus 로고    scopus 로고
    • Polymorphism G691S/S904S of RET asgenetic modifiers of MEN 2A
    • M Robledo L Gil M Pollan 2003 Polymorphism G691S/S904S of RET asgenetic modifiers of MEN 2A Cancer Res 63 1814 19
    • (2003) Cancer Res , vol.63 , pp. 1814-19
    • Robledo, M.1    Gil, L.2    Pollan, M.3
  • 81
    • 0036842406 scopus 로고    scopus 로고
    • Presurgical assessment of the tumor burden of familial medullary thyroid carcinoma by calcitonin testing
    • FJ Pomares JM Rodriguez F Nicolas 2002 Presurgical assessment of the tumor burden of familial medullary thyroid carcinoma by calcitonin testing J Am Coll Surg 195 630 4
    • (2002) J Am Coll Surg , vol.195 , pp. 630-4
    • Pomares, F.J.1    Rodriguez, J.M.2    Nicolas, F.3
  • 82
    • 0038695856 scopus 로고    scopus 로고
    • Surgical treatment of medullary thyroid carcinoma
    • MS Cohen JF Moley 2003 Surgical treatment of medullary thyroid carcinoma J Int Med 253 616 26
    • (2003) J Int Med , vol.253 , pp. 616-26
    • Cohen, M.S.1    Moley, J.F.2
  • 83
    • 0036109088 scopus 로고    scopus 로고
    • Molecular and biochemical screening for the diagnosis and management of medullary thyroid carcinoma in multiple endocrine neoplasia type 2A
    • AEF Viera MP Mello LLK Elias 2002 Molecular and biochemical screening for the diagnosis and management of medullary thyroid carcinoma in multiple endocrine neoplasia type 2A Horm Metab Res 34 202 6
    • (2002) Horm Metab Res , vol.34 , pp. 202-6
    • Viera, A.E.F.1    Mello, M.P.2    Elias, L.L.K.3
  • 84
    • 0033498338 scopus 로고    scopus 로고
    • Surgical strategy for treatment of medullary thyroid carcinoma
    • JB Fleming JE Lee M Bouvet 1999 Surgical strategy for treatment of medullary thyroid carcinoma Ann Surg 230 697 707
    • (1999) Ann Surg , vol.230 , pp. 697-707
    • Fleming, J.B.1    Lee, J.E.2    Bouvet, M.3
  • 85
    • 0034163301 scopus 로고    scopus 로고
    • Medullary thyroid carcinoma. Clinical characteristic, treatment, prognostic factors, and a comparison of staging systems
    • E Kebebew PHG Ituarte AE Siperstein 2000 Medullary thyroid carcinoma. Clinical characteristic, treatment, prognostic factors, and a comparison of staging systems Cancer 88 1139 48
    • (2000) Cancer , vol.88 , pp. 1139-48
    • Kebebew, E.1    Ituarte, P.H.G.2    Siperstein, A.E.3
  • 86
    • 0037313426 scopus 로고    scopus 로고
    • Review of multiple endocrine neoplasia type 2A in children: Therapeutic results of early thyroidectomy and prognostic value of codon analysis
    • G Szinnai C Meier P Komminoth UW Zumsteg 2003 Review of multiple endocrine neoplasia type 2A in children: therapeutic results of early thyroidectomy and prognostic value of codon analysis Pediatrics 111 132 9
    • (2003) Pediatrics , vol.111 , pp. 132-9
    • Szinnai, G.1    Meier, C.2    Komminoth, P.3    Zumsteg, U.W.4
  • 87
    • 0037080134 scopus 로고    scopus 로고
    • Very early detection of RET proto-oncogene mutation is crucial for preventive thyroidectomy in multiple endocrine neoplasia type 2 children
    • GE Sanso HM Domene MC Garcia Rudaz 2002 Very early detection of RET proto-oncogene mutation is crucial for preventive thyroidectomy in multiple endocrine neoplasia type 2 children Cancer 94 323 30
    • (2002) Cancer , vol.94 , pp. 323-30
    • Sanso, G.E.1    Domene, H.M.2    Garcia Rudaz, M.C.3
  • 88
    • 0031926082 scopus 로고    scopus 로고
    • Determinative factors of biochemical cure after primary and reoperative surgery for sporadic medullary carcinoma
    • O Gimm J Ukkat H Dralle 1998 Determinative factors of biochemical cure after primary and reoperative surgery for sporadic medullary carcinoma World J Surg 22 562 8
    • (1998) World J Surg , vol.22 , pp. 562-8
    • Gimm, O.1    Ukkat, J.2    Dralle, H.3
  • 89
    • 0036330820 scopus 로고    scopus 로고
    • Prophylactic thyroidectomy in MEN 2A syndrome: Experience in a single center
    • JMR Gonzales MD Balsalobre F Pomares 2002 Prophylactic thyroidectomy in MEN 2A syndrome: experience in a single center J Am Coll Surg 195 159 66
    • (2002) J Am Coll Surg , vol.195 , pp. 159-66
    • Gonzales, J.M.R.1    Balsalobre, M.D.2    Pomares, F.3
  • 90
    • 0038651140 scopus 로고    scopus 로고
    • Acceptable age for prophylactic surgery in children with multiple endocrine neoplasia type 2a
    • T de Kahraman JWB Groot C Rouwe 2002 Acceptable age for prophylactic surgery in children with multiple endocrine neoplasia type 2a EJSO 29 331 5
    • (2002) EJSO , vol.29 , pp. 331-5
    • De Kahraman, T.1    Groot, J.W.B.2    Rouwe, C.3
  • 92
    • 0035987665 scopus 로고    scopus 로고
    • Multiple endocrine neoplasia type 2A syndrome: Surgical management
    • S Simon M Pavel J Hensen 2002 Multiple endocrine neoplasia type 2A syndrome: surgical management J Pediatr Surg 37 897 900
    • (2002) J Pediatr Surg , vol.37 , pp. 897-900
    • Simon, S.1    Pavel, M.2    Hensen, J.3
  • 93
    • 15644377401 scopus 로고    scopus 로고
    • Prophylactic thyroidectomy in 75 children and adolescents with hereditary medullary thyroid carcinoma: German and Austrian experience
    • H Dralle O Gimm D Simon 1998 Prophylactic thyroidectomy in 75 children and adolescents with hereditary medullary thyroid carcinoma: German and Austrian experience World J Surg 22 744 51
    • (1998) World J Surg , vol.22 , pp. 744-51
    • Dralle, H.1    Gimm, O.2    Simon, D.3
  • 94
    • 0037046659 scopus 로고    scopus 로고
    • Germ-line mutations in nonsyndromic pheochromocytoma
    • HPH Neumann B Bausch SR McWhinney 2002 Germ-line mutations in nonsyndromic pheochromocytoma N Engl J Med 346 1459 66
    • (2002) N Engl J Med , vol.346 , pp. 1459-66
    • Neumann, H.P.H.1    Bausch, B.2    McWhinney, S.R.3
  • 95
    • 0011874462 scopus 로고    scopus 로고
    • Pheochromocytoma (with a preface about incidental adrenal masses)
    • Williams and Wilkins Baltimore, MD
    • NM Kaplan 1998 Pheochromocytoma (with a preface about incidental adrenal masses) NM Kaplan Clinical Hypertension. Williams and Wilkins Baltimore, MD 345 64
    • (1998) Clinical Hypertension. , pp. 345-64
    • Kaplan, N.M.1    Kaplan, N.M.2
  • 96
    • 0028783824 scopus 로고
    • Pheochromocytoma in multiple endocrine neoplasia type 2: European study
    • E Modigliani HM Vasen K Raue 1995 Pheochromocytoma in multiple endocrine neoplasia type 2: European study J Intern Med. 238 363 7
    • (1995) J Intern Med. , vol.238 , pp. 363-7
    • Modigliani, E.1    Vasen, H.M.2    Raue, K.3
  • 97
    • 0037125450 scopus 로고    scopus 로고
    • Imaging vs. biochemical testing for pheochromocytoma
    • HP Neumann 2002 Imaging vs. biochemical testing for pheochromocytoma JAMA 288 314 5
    • (2002) JAMA , vol.288 , pp. 314-5
    • Neumann, H.P.1
  • 98
    • 0037323423 scopus 로고    scopus 로고
    • A comparison of biochemical tests for pheochromocytoma: Measurement of fractionated plasma metanephrines compared with the combination of 24-hour urinary metanephrines and catecholamines
    • 2
    • AM Sawka R Jaeschke RJ Singh WF Young 2003 A comparison of biochemical tests for pheochromocytoma: measurement of fractionated plasma metanephrines compared with the combination of 24-hour urinary metanephrines and catecholamines J Clin Endocrinol Metab 88 2 553 8
    • (2003) J Clin Endocrinol Metab , vol.88 , pp. 553-8
    • Sawka, A.M.1    Jaeschke, R.2    Singh, R.J.3    Young, W.F.4
  • 99
    • 0037329062 scopus 로고    scopus 로고
    • Editorial: Biochemical diagnosis of pheochromocytoma - Is it time to switch to plasma-free metanephrines
    • 2
    • G Eisenhofer 2003 Editorial: Biochemical diagnosis of pheochromocytoma - is it time to switch to plasma-free metanephrines J Clin Endocrinol Metab 88 2 550 2
    • (2003) J Clin Endocrinol Metab , vol.88 , pp. 550-2
    • Eisenhofer, G.1
  • 100
    • 0033577985 scopus 로고    scopus 로고
    • Plasma normetanephrine and metanephrines for pheochromocytoma in von Hippel - Lindau disease and multiple endocrine neoplasia type 2
    • G Eisenhofer JW Lenders WM Linehan 1999 Plasma normetanephrine and metanephrines for pheochromocytoma in von Hippel - Lindau disease and multiple endocrine neoplasia type 2 N Engl J Med 340 1872 9
    • (1999) N Engl J Med , vol.340 , pp. 1872-9
    • Eisenhofer, G.1    Lenders, J.W.2    Linehan, W.M.3
  • 101
    • 0034706422 scopus 로고    scopus 로고
    • Diagnostic efficacy of unconjugated plasma metanephrines for the detection of pheochromocytoma
    • W Raber W Raffesberg M Bischof 2000 Diagnostic efficacy of unconjugated plasma metanephrines for the detection of pheochromocytoma Arch Intern Med 160 2957 63
    • (2000) Arch Intern Med , vol.160 , pp. 2957-63
    • Raber, W.1    Raffesberg, W.2    Bischof, M.3
  • 102
    • 0035013938 scopus 로고    scopus 로고
    • Lessons from an unpleasant surprise: A biochemical strategy for the diagnosis of pheochromocytoma
    • V Gardet B Gatta G Simonnet 2001 Lessons from an unpleasant surprise: a biochemical strategy for the diagnosis of pheochromocytoma J Hypertens 19 1029 35
    • (2001) J Hypertens , vol.19 , pp. 1029-35
    • Gardet, V.1    Gatta, B.2    Simonnet, G.3
  • 103
    • 16744366177 scopus 로고    scopus 로고
    • Clinical experience over 48 years with pheochromocytoma
    • RE Goldstein JA O'Neill GW Holcomb 1999 Clinical experience over 48 years with pheochromocytoma Ann Surg 229 755 66
    • (1999) Ann Surg , vol.229 , pp. 755-66
    • Goldstein, R.E.1    O'Neill, J.A.2    Holcomb, G.W.3
  • 104
    • 0035528831 scopus 로고    scopus 로고
    • 18F]Fluorodopamine positron emission tomographic (PET) scanning for diagnostic localization of pheochromocytoma.
    • 18F]Fluorodopamine positron emission tomographic (PET) scanning for diagnostic localization of pheochromocytoma. Hypertension 38 6 8
    • (2001) Hypertension , vol.38 , pp. 6-8
    • Pacak, K.1    Eisenhofer, G.2    Carasquillo, J.A.3
  • 105
    • 0036007324 scopus 로고    scopus 로고
    • Pheochromocytomas: Detection with 18F DOPA whole-body PET - Initial results
    • S Hoegerle E Nitzsche C Altehoefer 2003 Pheochromocytomas: detection with 18F DOPA whole-body PET - initial results Radiology 222 507 12
    • (2003) Radiology , vol.222 , pp. 507-12
    • Hoegerle, S.1    Nitzsche, E.2    Altehoefer, C.3
  • 106
    • 0029906124 scopus 로고    scopus 로고
    • Cortical-sparing adrenalectomy for patients with bilateral pheochromocytoma
    • JE Lee SA Curley RF Gagel 1996 Cortical-sparing adrenalectomy for patients with bilateral pheochromocytoma Surgery 120 1064 71
    • (1996) Surgery , vol.120 , pp. 1064-71
    • Lee, J.E.1    Curley, S.A.2    Gagel, R.F.3
  • 107
  • 108
    • 0036419547 scopus 로고    scopus 로고
    • Effects of slow-release octerotide on urinary metanephrine excretion and plasma chromogranin a and catecholamine levels in patients with malignant or recurrent phaeochromocytoma
    • 5
    • M Lamarre-Cliche AP Gimenez-Roqueplo E Billaud 2002 Effects of slow-release octerotide on urinary metanephrine excretion and plasma chromogranin A and catecholamine levels in patients with malignant or recurrent phaeochromocytoma Clin Endocrinol 57 5 629 34
    • (2002) Clin Endocrinol , vol.57 , pp. 629-34
    • Lamarre-Cliche, M.1    Gimenez-Roqueplo, A.P.2    Billaud, E.3
  • 109
    • 0034764571 scopus 로고    scopus 로고
    • Management of malignant pheochromocytoma: A retrospective review of the use of MIBG and chemotherapy in the West Midlands
    • A Hartley D Spooner AM Brunt 2001 Management of malignant pheochromocytoma: a retrospective review of the use of MIBG and chemotherapy in the West Midlands Clin Oncol 13 361 6
    • (2001) Clin Oncol , vol.13 , pp. 361-6
    • Hartley, A.1    Spooner, D.2    Brunt, A.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.