메뉴 건너뛰기




Volumn 115, Issue 11, 2000, Pages 405-409

Distinctive clinic features of pheochromocytoma in the setting of multiple endocrine neoplasia 2A;Feocromocitoma asociado a neoplasia endocrina múltiple 2A y esporádico: Características diferenciales

Author keywords

Adrenal; Catecholamines; Hypertension; Multiple endocrine neoplasia 2A; Pheochromocytoma

Indexed keywords

CATECHOLAMINE; VANILMANDELIC ACID;

EID: 0034618972     PISSN: 00257753     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0025-7753(00)71575-2     Document Type: Article
Times cited : (2)

References (26)
  • 3
    • 0027437581 scopus 로고
    • Pheochromocytoma: Current diagnosis and management
    • Manger WM, Gifford RW. Pheochromocytoma: current diagnosis and management. Clev Clin J Med 1993; 60: 365-378.
    • (1993) Clev Clin J Med , vol.60 , pp. 365-378
    • Manger, W.M.1    Gifford, R.W.2
  • 4
    • 0027508442 scopus 로고
    • Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease
    • Neumann HPH, Berger DP, Sigmund G, Blum U, Schmidt D, Parmer RJ et al. Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease. N Engl J Med 1993; 329: 1531-1538.
    • (1993) N Engl J Med , vol.329 , pp. 1531-1538
    • Neumann, H.P.H.1    Berger, D.P.2    Sigmund, G.3    Blum, U.4    Schmidt, D.5    Parmer, R.J.6
  • 5
    • 0028851141 scopus 로고
    • Genetic testing in the diagnosis and management of multiple endocrine neoplasia type II
    • Ledger GA, Khosla S, Lindor NM, Thibodeau SN, Gharib H. Genetic testing in the diagnosis and management of multiple endocrine neoplasia type II. Ann Intern Med 1995; 122: 118-124.
    • (1995) Ann Intern Med , vol.122 , pp. 118-124
    • Ledger, G.A.1    Khosla, S.2    Lindor, N.M.3    Thibodeau, S.N.4    Gharib, H.5
  • 8
    • 0028261916 scopus 로고
    • Advances in genetic screening for multiple endocrine neoplasia type 2 and the implications for management of children at risk
    • Thomas PM, Gagel RF. Advances in genetic screening for multiple endocrine neoplasia type 2 and the implications for management of children at risk. Endocrinologist 1994; 4: 140-146.
    • (1994) Endocrinologist , vol.4 , pp. 140-146
    • Thomas, P.M.1    Gagel, R.F.2
  • 12
    • 85031470096 scopus 로고
    • Conferencia clinicopatológica: Cefalea, tetania y síndrome diarreico en una paciente con MEN II
    • Conferencia clinicopatológica: cefalea, tetania y síndrome diarreico en una paciente con MEN II. Endocrinología 1992; 39: 30-42.
    • (1992) Endocrinología , vol.39 , pp. 30-42
  • 14
    • 0040226103 scopus 로고    scopus 로고
    • Alteraciones moleculares del protooncogén RET en familias con neoplasia endocrina múltiple 2A
    • Barc
    • Biarnés J, Miranda M, Corral J, Gabau E, Matías-Guiu X, Matilla A et al. Alteraciones moleculares del protooncogén RET en familias con neoplasia endocrina múltiple 2A. Med Clin (Barc) 1996; 107: 321-325.
    • (1996) Med Clin , vol.107 , pp. 321-325
    • Biarnés, J.1    Miranda, M.2    Corral, J.3    Gabau, E.4    Matías-Guiu, X.5    Matilla, A.6
  • 16
    • 0033561989 scopus 로고    scopus 로고
    • Análisis genético de las mutaciones de RET en las familias con neoplasia endocrina múltiple tipo 2 de la comunidad de Murcia
    • Barc
    • Pomares FJ, Bernabé MJ, Matías-Guiu X, Rodríguez JM, Soriano J, Sola J et al. Análisis genético de las mutaciones de RET en las familias con neoplasia endocrina múltiple tipo 2 de la comunidad de Murcia. Med Clin (Barc) 1999; 112: 646-650.
    • (1999) Med Clin , vol.112 , pp. 646-650
    • Pomares, F.J.1    Bernabé, M.J.2    Matías-Guiu, X.3    Rodríguez, J.M.4    Soriano, J.5    Sola, J.6
  • 19
    • 0021764576 scopus 로고
    • Pheochromocytoma: Diagnosis, localization and management
    • Bravo EL, Gifford RW. Pheochromocytoma: diagnosis, localization and management. N Engl J Med 1984; 311: 1298-1303.
    • (1984) N Engl J Med , vol.311 , pp. 1298-1303
    • Bravo, E.L.1    Gifford, R.W.2
  • 20
    • 0025978264 scopus 로고
    • A simplified diagnostic approach to pheochromocytoma. A review of the literature and report of one institution's experience
    • Baltimore
    • Stein PP, Black HR. A simplified diagnostic approach to pheochromocytoma. A review of the literature and report of one institution's experience. Medicine (Baltimore) 1990; 70: 46-66.
    • (1990) Medicine , vol.70 , pp. 46-66
    • Stein, P.P.1    Black, H.R.2
  • 21
    • 0026042570 scopus 로고
    • Diagnosis of pheochromocytoma. Reflections on a controversy
    • Bravo EL. Diagnosis of pheochromocytoma. Reflections on a controversy. Hypertension 1991; 17: 742-744.
    • (1991) Hypertension , vol.17 , pp. 742-744
    • Bravo, E.L.1
  • 22
    • 0023896984 scopus 로고
    • Molecular cloning of cDNA and chromosomal assignment of the gene for human phenylethanolamine N-methyltransferase, the enzyme for epinephrine biosynthesis
    • Kaneda N, Ichinose H, Kohayashi K, Oka K, Kishi F, Nakazawa A et al. Molecular cloning of cDNA and chromosomal assignment of the gene for human phenylethanolamine N-methyltransferase, the enzyme for epinephrine biosynthesis. J Biol Chem 1988; 263: 7672.
    • (1988) J Biol Chem , vol.263 , pp. 7672
    • Kaneda, N.1    Ichinose, H.2    Kohayashi, K.3    Oka, K.4    Kishi, F.5    Nakazawa, A.6
  • 23
    • 85031469772 scopus 로고
    • Feocromocitoma: Diagnóstico de localización mediante métodos no invasivos
    • Simó R. Feocromocitoma: diagnóstico de localización mediante métodos no invasivos. Endocrinologia 1991; 38: 51-56.
    • (1991) Endocrinologia , vol.38 , pp. 51-56
    • Simó, R.1
  • 24
    • 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
    • Eng C, Clayton D, Schuffenecker I, Lenoir G, Cote G, Gagel RF et al. The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis. JAMA 1996; 276: 1575-1579.
    • (1996) JAMA , vol.276 , pp. 1575-1579
    • Eng, C.1    Clayton, D.2    Schuffenecker, I.3    Lenoir, G.4    Cote, G.5    Gagel, R.F.6
  • 25
    • 9344234978 scopus 로고    scopus 로고
    • Mutations of the RET protooncogene in German multiple endocrine neoplasia families: Relation between genotype and phenotype. German Medullary Thyroid Carcinoma Study Group
    • Frank-Raue K, Hoppner W, Frilling A, Kotzerke J, Dralle H, Haase R et al. Mutations of the RET protooncogene in German multiple endocrine neoplasia families: relation between genotype and phenotype. German Medullary Thyroid Carcinoma Study Group. J Clin Endocrinol Metab 1996; 81; 1780-1783.
    • (1996) J Clin Endocrinol Metab , vol.81 , pp. 1780-1783
    • Frank-Raue, K.1    Hoppner, W.2    Frilling, A.3    Kotzerke, J.4    Dralle, H.5    Haase, R.6
  • 26
    • 0030739287 scopus 로고    scopus 로고
    • Biological properties of RET with cysteine mutations correlate with multiple endocrine neoplasia type 2A, familial medullary thyroid carcinoma, and Hirschsprung's disease phenotype
    • Ito S, Iwashita T, Asai N, Murakami H, Iwata Y, Sobue G et al. Biological properties of RET with cysteine mutations correlate with multiple endocrine neoplasia type 2A, familial medullary thyroid carcinoma, and Hirschsprung's disease phenotype. Cancer Res 1997; 57: 2870-2872.
    • (1997) Cancer Res , vol.57 , pp. 2870-2872
    • Ito, S.1    Iwashita, T.2    Asai, N.3    Murakami, H.4    Iwata, Y.5    Sobue, G.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.