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Volumn 59, Issue SUPPL. 1, 2003, Pages 56-61

Clinical and genetic aspects of phaeochromocytoma

Author keywords

Chromosome 1; Genetics; Phaeochromocytoma

Indexed keywords

(3 IODOBENZYL)GUANIDINE I 123; ALPHA ADRENERGIC RECEPTOR BLOCKING AGENT; BETA ADRENERGIC RECEPTOR BLOCKING AGENT; CALCIUM ANTAGONIST; METADRENALIN; NORMETADRENALIN;

EID: 0037262032     PISSN: 03010163     EISSN: None     Source Type: Journal    
DOI: 10.1159/000067846     Document Type: Conference Paper
Times cited : (25)

References (24)
  • 2
    • 0033394457 scopus 로고    scopus 로고
    • Pheochromocytoma in Italy: A multicentric retrospective study
    • Mannelli M, Ianni L, Cilotti A, Conti A: Pheochromocytoma in Italy: A multicentric retrospective study. Eur J Endocrinol 1999;141:619-624.
    • (1999) Eur J Endocrinol , vol.141 , pp. 619-624
    • Mannelli, M.1    Ianni, L.2    Cilotti, A.3    Conti, A.4
  • 3
    • 0035037534 scopus 로고    scopus 로고
    • Factors associated with perioperative morbidity and mortality in patients with pheochromocytoma: Analysis of 165 operations at a single centre
    • Plouin P-F, Duclos J-M, Soppelsa F, Boublil G, Chatellier G: Factors associated with perioperative morbidity and mortality in patients with pheochromocytoma: Analysis of 165 operations at a single centre. J Clin Endocrinol Metab 2001;86:1480-1486.
    • (2001) J Clin Endocrinol Metab , vol.86 , pp. 1480-1486
    • Plouin, P.-F.1    Duclos, J.-M.2    Soppelsa, F.3    Boublil, G.4    Chatellier, G.5
  • 5
    • 0032138226 scopus 로고    scopus 로고
    • Multiple endocrine neoplasia - Syndrome of the twentieth century
    • Thakker RV: Multiple endocrine neoplasia - syndrome of the twentieth century [editorial]. J Clin Endocrinol Metab 1998;83:2617-2620.
    • (1998) J Clin Endocrinol Metab , vol.83 , pp. 2617-2620
    • Thakker, R.V.1
  • 7
    • 0030896614 scopus 로고    scopus 로고
    • Molecular diagnosis of von Hippel-Lindau disease in a kindred with a predominance of familial phaeochromocytoma
    • Garcia A, Matias-Guiu X, Cabezas R, Chico A, Prat J, Baiget M, De Leiva A: Molecular diagnosis of von Hippel-Lindau disease in a kindred with a predominance of familial phaeochromocytoma. Clin Endocrinol 1997;46:359-363.
    • (1997) Clin Endocrinol , vol.46 , pp. 359-363
    • Garcia, A.1    Matias-Guiu, X.2    Cabezas, R.3    Chico, A.4    Prat, J.5    Baiget, M.6    De Leiva, A.7
  • 8
    • 0027379865 scopus 로고
    • An analysis of variation in expression in neurofibromatosis (NF) type 1 (NF1): Evidence for modifying genes
    • Easton DF, Ponder MA, Huson SM, Ponder BAJ: An analysis of variation in expression in neurofibromatosis (NF) type 1 (NF1): evidence for modifying genes. Am J Hum Genet 1993;53:305-313.
    • (1993) Am J Hum Genet , vol.53 , pp. 305-313
    • Easton, D.F.1    Ponder, M.A.2    Huson, S.M.3    Ponder, B.A.J.4
  • 9
    • 0029035747 scopus 로고
    • Neurofibromatosis type 1: Pathology, clinical features and molecular genetics
    • von Deimling A, Krone W, Menon AG: Neurofibromatosis type 1: pathology, clinical features and molecular genetics. Brain Pathol 1995;5:153-162.
    • (1995) Brain Pathol , vol.5 , pp. 153-162
    • Von Deimling, A.1    Krone, W.2    Menon, A.G.3
  • 10
    • 0035724034 scopus 로고    scopus 로고
    • Paraganglioma genes
    • Chew SL: Paraganglioma genes. Clin Endocrinol 2001;54:573-574.
    • (2001) Clin Endocrinol , vol.54 , pp. 573-574
    • Chew, S.L.1
  • 11
    • 0034671551 scopus 로고    scopus 로고
    • Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma
    • Gimm O, Armanios M, Dziema H, Neumann HP, Eng C: Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma. Cancer Res 2000;60:6822-6825.
    • (2000) Cancer Res , vol.60 , pp. 6822-6825
    • Gimm, O.1    Armanios, M.2    Dziema, H.3    Neumann, H.P.4    Eng, C.5
  • 12
    • 0034977649 scopus 로고    scopus 로고
    • Analysis of the SDHD gene, the susceptibility gene for familial paraganglioma syndrome (PGL1), in pheochromocytomas
    • Aguiar RC, Cox G, Pomeroy SL, Dahia PL: Analysis of the SDHD gene, the susceptibility gene for familial paraganglioma syndrome (PGL1), in pheochromocytomas. J Clin Endocrinol Metab 2001;86:2890-2894.
    • (2001) J Clin Endocrinol Metab , vol.86 , pp. 2890-2894
    • Aguiar, R.C.1    Cox, G.2    Pomeroy, S.L.3    Dahia, P.L.4
  • 16
    • 0031298741 scopus 로고    scopus 로고
    • Sporadic phaeochromocytomas are rarely associated with germline mutations in the von Hippel-Lindau and RET genes
    • Bar M, Friedman E, Jakobovitz O, Leibowitz G, Lerer I, Abeliovich D, Gross DJ: Sporadic phaeochromocytomas are rarely associated with germline mutations in the von Hippel-Lindau and RET genes. Clin Endocrinol 1997;47:707-712.
    • (1997) Clin Endocrinol , vol.47 , pp. 707-712
    • Bar, M.1    Friedman, E.2    Jakobovitz, O.3    Leibowitz, G.4    Lerer, I.5    Abeliovich, D.6    Gross, D.J.7
  • 17
    • 0017073848 scopus 로고
    • Clonal origin or inherited medullary thyroid carcinoma and pheochromocytoma
    • Baylin SB, Gann DS, Hsu SH: Clonal origin or inherited medullary thyroid carcinoma and pheochromocytoma. Science 1976;193:321-323.
    • (1976) Science , vol.193 , pp. 321-323
    • Baylin, S.B.1    Gann, D.S.2    Hsu, S.H.3
  • 18
    • 0017182358 scopus 로고
    • Adrenal medullary disease in multiple endocrine neoplasia type 2: Pheochromocytoma and its precursor
    • Carney JA, Sizemore GM, Tyre GM: Adrenal medullary disease in multiple endocrine neoplasia type 2: Pheochromocytoma and its precursor. Am J Clin Pathol 1976;66:279-290.
    • (1976) Am J Clin Pathol , vol.66 , pp. 279-290
    • Carney, J.A.1    Sizemore, G.M.2    Tyre, G.M.3
  • 19
    • 0025865768 scopus 로고
    • Loss of heterozygosity suggests multiple genetic alterations in pheochromocytomas and medullary thyroid carcinomas
    • Khosla S, Patel VM, Hay ID, Schaid DJ, Grant CS, Van Heerden JA, Thibodeau SN: Loss of heterozygosity suggests multiple genetic alterations in pheochromocytomas and medullary thyroid carcinomas. J Clin Invest 1991;87:1691-1699.
    • (1991) J Clin Invest , vol.87 , pp. 1691-1699
    • Khosla, S.1    Patel, V.M.2    Hay, I.D.3    Schaid, D.J.4    Grant, C.S.5    Van Heerden, J.A.6    Thibodeau, S.N.7
  • 20
    • 0026548844 scopus 로고
    • Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes
    • Moley JF, Brother MB, Fong C, White PS, Baylin SB, Nelkin B, Wells SA, Brodeur GM: Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes. Cancer Res 1992;52:770-774.
    • (1992) Cancer Res , vol.52 , pp. 770-774
    • Moley, J.F.1    Brother, M.B.2    Fong, C.3    White, P.S.4    Baylin, S.B.5    Nelkin, B.6    Wells, S.A.7    Brodeur, G.M.8
  • 22
    • 0030907932 scopus 로고    scopus 로고
    • Loss of heterozygosity on the short arm of chromosomes 1 and 3 in sporadic pheochromocytoma and extra-adrenal paraganglioma
    • Vargas MP, Zhuang Z, Wang C, Vortmeyer A, Linehan MW, Merino MJ: Loss of heterozygosity on the short arm of chromosomes 1 and 3 in sporadic pheochromocytoma and extra-adrenal paraganglioma. Hum Pathol 1997;28:411-415.
    • (1997) Hum Pathol , vol.28 , pp. 411-415
    • Vargas, M.P.1    Zhuang, Z.2    Wang, C.3    Vortmeyer, A.4    Linehan, M.W.5    Merino, M.J.6
  • 24
    • 0029057487 scopus 로고
    • Loss of heterozygosity on the short arm of chromosome 3 in sporadic, von Hippel-Lindau disease-associated, and familial pheochromocytoma
    • Zeiger MA, Zbar B, Keiser H, Linehan MW, Gnarra JR: Loss of heterozygosity on the short arm of chromosome 3 in sporadic, von Hippel-Lindau disease-associated, and familial pheochromocytoma. Genes Chromosomes Cancer 1995;13:151-156.
    • (1995) Genes Chromosomes Cancer , vol.13 , pp. 151-156
    • Zeiger, M.A.1    Zbar, B.2    Keiser, H.3    Linehan, M.W.4    Gnarra, J.R.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.