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Volumn 33, Issue 1, 2001, Pages 52-56

A large family with hereditary MTC: Role of RET genetic analysis in differential diagnosis between MEN 2A and FMTC

(9) Chiefari, E a Chiarella, R a Crocetti, U d Tardio, B c Arturi, F a Russo, D b Trischitta, V d Filetti, S a Zingrillo, M d

a Dipto di Med Sperim e Clinica (Italy)

b UNIVERSITY MAGNA GRAECIA OF CATANZARO (Italy)

c Divisione di Chirurgia Generale (Italy)

d CASA SOLLIEVO DELLA SOFFERENZA HOSPITAL (Italy)

Author keywords

Familial Medullary Thyroid Carcinoma (FMTC); Genetic analysis; Multiple Endocrine Neoplasia 2A (MEN 2A); Mutation; RET proto oncogene

Indexed keywords

CALCITONIN;

ARTICLE; DIFFERENTIAL DIAGNOSIS; FAMILIAL CANCER; GENE MUTATION; GENETIC ANALYSIS; HUMAN; HYPERPARATHYROIDISM; NEUROFIBROMATOSIS; PHENOTYPE; PHEOCHROMOCYTOMA; PRIORITY JOURNAL; PROGNOSIS; PROTO ONCOGENE; SIPPLE SYNDROME; THYROID MEDULLARY CARCINOMA; THYROIDECTOMY;

ADOLESCENT; ADULT; AGED; CARCINOMA, MEDULLARY; DIAGNOSIS, DIFFERENTIAL; DNA; FEMALE; GENOTYPE; HUMANS; MALE; MIDDLE AGED; MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A; PEDIGREE; PHENOTYPE; POINT MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; THYROID NEOPLASMS;

EID: 0035099911 PISSN: 00185043 EISSN: None Source Type: Journal
DOI: 10.1055/s-2001-12627 Document Type: Article

Times cited : (6)

References (15)

1
- 0021299457
- Genetic aspects of multiple endocrine neoplasia
- (1984) Ann Rev Med , vol.35 , pp. 25-31
- Schimke, R.N.¹

2
- 0014402822
- Syndrome of bilateral pheochromocytoma, medullary thyroid carcinoma and multiple neuromas: A possible regulatory defect in the differentiation of cromaffin tissue
- (1968) N Engl J Med , vol.279 , pp. 1-7
- Schimke, R.N.¹ Hartmann, W.H.² Prout, T.E.³ Rimoin, D.L.⁴

3
- 0022535165
- Familial medullary thyroid carcinoma without associated endocrinopathies: A distinct clinical entity
- (1986) Br J Surg , vol.73 , pp. 278-281
- Farndon, J.R.¹ Leight, G.S.² Dilley, W.G.³ Baylin, S.B.⁴ Smallridge, R.C.⁵ Harrison, T.S.⁶ Wells S.A., Jr.⁷

5
- 0033119329
- The phenotype associated with ret mutations in the Multiple Endocrine Neoplasia type 2 syndrome
- (1999) Cancer Res , vol.59 , Issue.SUPPL. , pp. 1736-1742
- Ponder, B.A.J.¹

6
- 0030437796
- Familial medullary thyroid carcinoma: Not a distinct entity? Genotype-phenotype correlation in a large family
- (1996) Am J Med , vol.101 , pp. 635-641
- Moers, A.M.¹ Landsvater, R.M.² Schaap, C.³ Jansen-Schillhorn van Veen, J.M.⁴ De Valk, I.A.⁵ Blijiham, J.H.⁶ Hoppener, J.W.⁷ Vroom, T.M.⁸ Van Amstel, H.K.⁹ Lips, C.J.¹⁰

7
- 0024208663
- Cloning and expression of the RET proto-oncogene encoding a tyrosine kinase with two potential transmembrane domains
- (1988) Oncogene , vol.3 , pp. 571-578
- Takahashi, M.¹ Buma, Y.² Iwamoto, T.³ Inaguma, Y.⁴ Ikeda, H.⁵ Hiai, H.⁶

8
- 0031850609
- Analysis of RET proto-oncogene abnormalities in patients with MEN 2A, MEN 2B, familial or sporadic medullary thyroid carcinoma
- (1998) J Endocrinol Invest , vol.21 , pp. 358-364
- Chiefari, E.¹ Russo, D.² Giuffrida, D.³ Zampa, G.A.⁴ Meringolo, D.⁵ Arturi, F.⁶ Chiodini, I.⁷ Bianchi, D.⁸ Attard, M.⁹ Trischitta, V.¹⁰ Bruno, R.¹¹ Giannasio, P.¹² Pontecorvi, A.¹³ Filetti, S.¹⁴

9
- 0030953350
- A case of metastatic medullary thyroid carcinoma: Early identification before surgery of a RET proto-oncogene somatic mutation in fine needle aspirate specimen
- (1997) J Clin Endocrinol Metab , vol.82 , pp. 3378-3382
- Russo, D.¹ Arturi, F.² Chiefari, E.³ Meringolo, D.⁴ Bianchi, D.⁵ Bellanova, B.⁶ Filetti, S.⁷

10
- 0030162739
- Comparison of octreotide scintigraphy and conventional imaging in medullary thyroid carcinoma
- (1996) J Nucl Med , vol.37 , pp. 912-916
- Baudin, E.¹ Lumbroso, J.² Schlumberger, M.³ Leclere, J.⁴ Giammarile, F.⁵ Gardet, P.⁶ Roche, A.⁷ Travagli, J.P.⁸ Parmentier, C.⁹

11
- 0005863784
- Disease of Sympathetic-Chromaffin System
- Felig P, Baxter JD, Frohman LA (III ed). New York McGraw Hill, Inc.
- (1997) Endocrinology and Metabolism
- Cryer, P.E.¹

12
- 0028785488
- The pratical management of multiple endocrine neoplasia
- (1995) Trends Endocrinol Metab , vol.6 , pp. 273-278
- Learoyd, D.L.¹ Twigg, S.M.² Marsh, D.J.³ Robinson, B.G.⁴

13
- 0032481129
- Dual effect on the RET receptor of MEN 2 mutations affecting specific extracytoplasmatic cysteines
- (1998) Oncogene , vol.17 , pp. 2851-2861
- Chappuis-Flament, S.¹ Pasini, A.² De Vita, G.³ Segouffin-Cariou, C.⁴ Fusco, A.⁵ Attie, T.⁶ Lenoir, G.M.⁷ Santoro, M.⁸ Billaud, M.⁹

14
- 0031916933
- Seventeen-year-long follow-up of a family affected by type 2A multiple endocrine neoplasia (MEN 2A)
- (1998) J Endocrinol Invest , vol.21 , pp. 87-92
- Libroia, A.¹ Verga, U.² Vecchi, G.³ Banfi, F.⁴ Zurleni, F.⁵ Quadro, L.⁶ Scurini, C.⁷ Fattoruso, O.⁸ Colantuoni, V.⁹

15
- 0030989728
- Unresolved issues in the genesis and management of multiple endocrine neoplasia type 2
- (1997) Horm Metab Res , vol.29 , pp. 135-137
- Gagel, R.F.¹

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