메뉴 건너뛰기




Volumn , Issue , 2005, Pages 251-264

Genetic syndromes associated with adrenal tumors

Author keywords

[No Author keywords available]

Indexed keywords


EID: 70349877798     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1007/3-540-26861-8_25     Document Type: Chapter
Times cited : (4)

References (98)
  • 1
    • 0033619201 scopus 로고    scopus 로고
    • Dehy-droepiandrosterone replacement in women with adrenal insufficiency
    • Arlt W, Callies F, van Vlijmen JC, et al (1999) Dehy-droepiandrosterone replacement in women with adrenal insufficiency. N Engl J Med 341:1013-1020
    • (1999) N Engl J Med , vol.341 , pp. 1013-1020
    • Arlt, W.1    Callies, F.2    Van Vlijmen, J.C.3
  • 2
    • 0035857957 scopus 로고    scopus 로고
    • Germline SDHD mutation in familial phaeochromocytoma
    • Astuti D, Douglas F, Lennard TWJ, et al (2001) Germline SDHD mutation in familial phaeochromocytoma. Lancet 357:1181-1182
    • (2001) Lancet , vol.357 , pp. 1181-1182
    • Astuti, D.1    Douglas, F.2    Lennard, T.W.J.3
  • 3
    • 0034964421 scopus 로고    scopus 로고
    • Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma
    • Astuti D, Latif F, Dallol A., et al (2001) Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. Am J Hum Genet 69:49-54
    • (2001) Am J Hum Genet , vol.69 , pp. 49-54
    • Astuti, D.1    Latif, F.2    Dallol, A.3
  • 4
    • 0036274254 scopus 로고    scopus 로고
    • Pheo-chromocytomas and paragangliomas in von hippel-lin-dau disease. A role for laparoscopic and cortical-sparing surgery
    • Baghai M, Thompson GB, Young W.F., et al (2002) Pheo-chromocytomas and paragangliomas in von Hippel-Lin-dau disease. A role for laparoscopic and cortical-sparing surgery. Arch Surg 137:682-689
    • (2002) Arch Surg , vol.137 , pp. 682-689
    • Baghai, M.1    Thompson, G.B.2    Young, W.F.3
  • 5
    • 0036712593 scopus 로고    scopus 로고
    • Hereditary paraganglioma targets diverse paraganglia
    • Baysal BE (2002) Hereditary paraganglioma targets diverse paraganglia. J Med Genet 39:617-622
    • (2002) J Med Genet , vol.39 , pp. 617-622
    • Baysal, B.E.1
  • 6
    • 0034602950 scopus 로고    scopus 로고
    • Mutations in SDHD, a mitochondrial complex II gene in hereditary paraganglioma
    • Baysal BE, Ferrell RE, Willett-Brozick JE, et al (2000) Mutations in SDHD, a mitochondrial complex II gene in hereditary paraganglioma. Science 287:848-851
    • (2000) Science , vol.287 , pp. 848-851
    • Baysal, B.E.1    Ferrell, R.E.2    Willett-Brozick, J.E.3
  • 7
    • 0034803010 scopus 로고    scopus 로고
    • Pheno-typic dichotomy in mitochondrial complex II genetic disorders
    • Baysal BE, Rubinstein WS, Taschner PEM (2001) Pheno-typic dichotomy in mitochondrial complex II genetic disorders. J Mol Med 79:495-503
    • (2001) J Mol Med , vol.79 , pp. 495-503
    • Baysal, B.E.1    Rubinstein, W.S.2    Taschner, P.E.M.3
  • 8
    • 0000077851 scopus 로고
    • Macroglossia, omphalocoele, adrenal cytomegaly, gigantism and hyperplastic visceromegaly
    • Beckwith JB (1969) Macroglossia, omphalocoele, adrenal cytomegaly, gigantism and hyperplastic visceromegaly. Birth Defects 5:188-196
    • (1969) Birth Defects , vol.5 , pp. 188-196
    • Beckwith, J.B.1
  • 9
    • 0037422207 scopus 로고    scopus 로고
    • Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas
    • Benn DE, Croxson MS, Tucker K, et al (2003) Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas. Oncogene 22:1358-1364
    • (2003) Oncogene , vol.22 , pp. 1358-1364
    • Benn, D.E.1    Croxson, M.S.2    Tucker, K.3
  • 10
    • 0030781576 scopus 로고    scopus 로고
    • Sporadic pheochromocytomas are rarely associated with germline mutations in the VHL tumor suppressor gene or the RET protooncogene
    • Brauch H, Hoppner W, Jahnig H., et al (1997) Sporadic pheochromocytomas are rarely associated with germline mutations in the VHL tumor suppressor gene or the RET protooncogene. J Clin Endocrinol Metab 82:4101-4104
    • (1997) J Clin Endocrinol Metab , vol.82 , pp. 4101-4104
    • Brauch, H.1    Hoppner, W.2    Jahnig, H.3
  • 11
    • 0030018392 scopus 로고    scopus 로고
    • Laparoscopic adrenalectomy compared to open adrenalectomy for benign adrenal neoplasms
    • Brunt LM, Doherty GM, Norton J.A., et al (1996) Laparoscopic adrenalectomy compared to open adrenalectomy for benign adrenal neoplasms. J Am Coll Surg 183:1-10
    • (1996) J Am Coll Surg , vol.183 , pp. 1-10
    • Brunt, L.M.1    Doherty, G.M.2    Norton, J.A.3
  • 12
    • 0036240747 scopus 로고    scopus 로고
    • Adrenalectomy for familial pheochromocytoma in the laparoscopic era
    • Brunt LM, Lairmore TC, Doherty G.M., et al (2001) Adrenalectomy for familial pheochromocytoma in the laparoscopic era. Ann Surg 235:713-721
    • (2001) Ann Surg , vol.235 , pp. 713-721
    • Brunt, L.M.1    Lairmore, T.C.2    Doherty, G.M.3
  • 13
    • 0029900871 scopus 로고    scopus 로고
    • Adrenal lesions in a large kindred with multiple endocrine neoplasia type 1
    • Burgess JR, Harle RA, Tucker P, et al (1996) Adrenal lesions in a large kindred with multiple endocrine neoplasia type 1. Arch Surg 131:699-702
    • (1996) Arch Surg , vol.131 , pp. 699-702
    • Burgess, J.R.1    Harle, R.A.2    Tucker, P.3
  • 14
    • 0025217744 scopus 로고
    • Somato-statin-producing duodenal carcinoids in patients with von recklinghausen's neurofibromatosis. A predilection for black patients
    • Burke AP, Sobin LH, Shekitka K.M., et al (1990) Somato-statin-producing duodenal carcinoids in patients with von Recklinghausen's neurofibromatosis. A predilection for black patients. Cancer 65:1591-1595
    • (1990) Cancer , vol.65 , pp. 1591-1595
    • Burke, A.P.1    Sobin, L.H.2    Shekitka, K.M.3
  • 15
    • 0022054926 scopus 로고
    • Multiple endocrine neoplasia type IIa
    • Cance WG, Wells SA Jr (1985) Multiple endocrine neoplasia type IIa. Curr Probl Surg 22:1-56
    • (1985) Curr Probl Surg , vol.22 , pp. 1-56
    • Cance, W.G.1    Wells Jr., S.A.2
  • 16
    • 0027977002 scopus 로고
    • Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B
    • 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 USA , vol.91 , pp. 1579-1583
    • Carlson, K.M.1    Dou, S.2    Chi, D.3
  • 17
    • 0017182358 scopus 로고
    • Adrenal medullary disease in multiple endocrine neoplasia type 2: Pheochromocytoma and its precursors
    • Carney JA, Sizemore GW, Sheps S.G. (1976) Adrenal medullary disease in multiple endocrine neoplasia type 2: pheochromocytoma and its precursors. Am J Clin Pathol 66:279-290
    • (1976) Am J Clin Pathol , vol.66 , pp. 279-290
    • Carney, J.A.1    Sizemore, G.W.2    Sheps, S.G.3
  • 18
    • 0016427998 scopus 로고
    • Bilateral adrenal medullary hyperplasia in multiple endocrine neoplasia, type 2: The precursor of bilateral pheochromocytoma
    • Carney JA, Sizemore GW, Tyce G.M. (1975) Bilateral adrenal medullary hyperplasia in multiple endocrine neoplasia, type 2: the precursor of bilateral pheochromocytoma. Mayo Clin Proc 50:3-10
    • (1975) Mayo Clin Proc , vol.50 , pp. 3-10
    • Carney, J.A.1    Sizemore, G.W.2    Tyce, G.M.3
  • 19
    • 0027297690 scopus 로고
    • Phaeochromocytoma in multiple endocrine neoplasia type 2A: Survey of 100 cases
    • Casanova S, Rosenberg-Bourgin M, Farkas D., et al (1993) Phaeochromocytoma in multiple endocrine neoplasia type 2A: survey of 100 cases. Clin Endocrinol 38:531-537
    • (1993) Clin Endocrinol , vol.38 , pp. 531-537
    • Casanova, S.1    Rosenberg-Bourgin, M.2    Farkas, D.3
  • 20
    • 0035724034 scopus 로고    scopus 로고
    • Paraganglioma genes
    • Chew SL (2001) Paraganglioma genes. Clin Endocrinol 54:573-574
    • (2001) Clin Endocrinol , vol.54 , pp. 573-574
    • Chew, S.L.1
  • 22
    • 0027303248 scopus 로고
    • 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
  • 23
    • 0024569718 scopus 로고
    • The clinical and screening age-at-onset distribution for the MEN-2 syndrome
    • Easton DF, Ponder MA, Cummings T, et al (1989) The clinical and screening age-at-onset distribution for the MEN-2 syndrome. Am J Hum Genet 44:208-215
    • (1989) Am J Hum Genet , vol.44 , pp. 208-215
    • Easton, D.F.1    Ponder, M.A.2    Cummings, T.3
  • 24
    • 0033577985 scopus 로고    scopus 로고
    • Plasma normetanephrine and metanephrine for detecting pheochromocytoma in von hippel-lindau disease and multiple endocrine neoplasia type 2
    • Eisenhofer G, Lenders JW, Linehan W.M., et al (1999) Plasma normetanephrine and metanephrine for detecting pheochromocytoma in von Hippel-Lindau disease and multiple endocrine neoplasia type 2. N Engl J Med 340: 1872-1879
    • (1999) N Engl J Med , vol.340 , pp. 1872-1879
    • Eisenhofer, G.1    Lenders, J.W.2    Linehan, W.M.3
  • 25
    • 0028788184 scopus 로고
    • Mutations in the RET proto-oncogene and the von hippel-lindau disease tumor suppressor gene in sporadic and syndromic pheochromocytomas
    • Eng C, Crossey PA, Mulligan L.M., et al (1995) Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumor suppressor gene in sporadic and syndromic pheochromocytomas. J Med Genet 32:934-937
    • (1995) J Med Genet , vol.32 , pp. 934-937
    • Eng, C.1    Crossey, P.A.2    Mulligan, L.M.3
  • 26
    • 0022535165 scopus 로고
    • Familial medullary thyroid carcinoma without associated en-docrinopathies: A distinct clinical entity
    • Farndon JR, Leight GS, Dilley W.G., et al (1986) Familial medullary thyroid carcinoma without associated en-docrinopathies: a distinct clinical entity. Br J Surg 73: 278-281
    • (1986) Br J Surg , vol.73 , pp. 278-281
    • Farndon, J.R.1    Leight, G.S.2    Dilley, W.G.3
  • 27
    • 0030966414 scopus 로고    scopus 로고
    • Type 1 neurofibromatosis: A descriptive analysis of the disorder in 1, 728 patients
    • Friedman JM, Birch P.H. (1997) Type 1 neurofibromatosis: a descriptive analysis of the disorder in 1, 728 patients. Am J Med Genet 70:138-143
    • (1997) Am J Med Genet , vol.70 , pp. 138-143
    • Friedman, J.M.1    Birch, P.H.2
  • 28
    • 0033569787 scopus 로고    scopus 로고
    • Von hippel-lindau syndrome. A pleomorphic condition
    • Friedrich CA (1999) Von Hippel-Lindau syndrome. A pleomorphic condition. Cancer 86:2478-2482
    • (1999) Cancer , vol.86 , pp. 2478-2482
    • Friedrich, C.A.1
  • 29
    • 0035054565 scopus 로고    scopus 로고
    • Genotype-phenotype correlation in von hippel-lindau syndrome
    • Friedrich CA (2001) Genotype-phenotype correlation in von Hippel-Lindau syndrome. Hum Mol Genet 10: 763-767
    • (2001) Hum Mol Genet , vol.10 , pp. 763-767
    • Friedrich, C.A.1
  • 30
    • 0026645968 scopus 로고
    • Laparoscopic adrenalectomy in cushing's syndrome and pheochromocytoma
    • Gagner M, Lacroix A, Bolte E. (1992) Laparoscopic adrenalectomy in Cushing's syndrome and pheochromocytoma. N Engl J Med 327:1033
    • (1992) N Engl J Med , vol.327 , pp. 1033
    • Gagner, M.1    Lacroix, A.2    Bolte, E.3
  • 31
    • 0034671551 scopus 로고    scopus 로고
    • Somatic and occult germline mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma
    • Gimm O, Armanios M, Dziema H., et al (2000) Somatic and occult germline mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma. Cancer Res 60:6822-6825
    • (2000) Cancer Res , vol.60 , pp. 6822-6825
    • Gimm, O.1    Armanios, M.2    Dziema, H.3
  • 32
    • 0030957310 scopus 로고    scopus 로고
    • The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2
    • Gutmann DH, Aylsworth A, Carey J.C., et al (1997) The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2. JAMA 278:51-57
    • (1997) JAMA , vol.278 , pp. 51-57
    • Gutmann, D.H.1    Aylsworth, A.2    Carey, J.C.3
  • 33
    • 0018225331 scopus 로고
    • Measurement of urinary epinephrine in screening for pheochromocytoma in multiple endocrine neoplasia type II
    • Hamilton BP, Landsberg L, Levine R.J. (1978) Measurement of urinary epinephrine in screening for pheochromocytoma in multiple endocrine neoplasia type II. Am J Med 65:1027-1032
    • (1978) Am J Med , vol.65 , pp. 1027-1032
    • Hamilton, B.P.1    Landsberg, L.2    Levine, R.J.3
  • 34
    • 0033729031 scopus 로고    scopus 로고
    • Multiple endocrine neoplasia type 2 (MEN 2) and RET: From neoplasia to neurogenesis
    • Hansford JR, Mulligan L.M. (2000) Multiple endocrine neoplasia type 2 (MEN 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
  • 36
    • 0025738681 scopus 로고
    • Uniparental paternal disomy in a genetic cancer-predisposing syndrome
    • Henry I, Bonaiti-Pellie C, Chehensse V., et al (1991) Uniparental paternal disomy in a genetic cancer-predisposing syndrome. Nature 351:665-667
    • (1991) Nature , vol.351 , pp. 665-667
    • Henry, I.1    Bonaiti-Pellie, C.2    Chehensse, V.3
  • 37
    • 0028174024 scopus 로고
    • A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma
    • Hofstra RM, Landsvater RM, Ceccherini I, et al (1994) A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma. Nature 367:375-376
    • (1994) Nature , vol.367 , pp. 375-376
    • Hofstra, R.M.1    Landsvater, R.M.2    Ceccherini, I.3
  • 38
    • 0027136050 scopus 로고
    • Prevalence of pheochromocytoma and hyperparathyroidism in multiple endocrine neoplasia type 2A: Results of long-term follow-up
    • Howe JR, Norton JA, Wells SA Jr (1993) Prevalence of pheochromocytoma and hyperparathyroidism in multiple endocrine neoplasia type 2A: results of long-term follow-up. Surgery 114:1070-1077
    • (1993) Surgery , vol.114 , pp. 1070-1077
    • Howe, J.R.1    Norton, J.A.2    Wells Jr., S.A.3
  • 39
    • 0033675895 scopus 로고    scopus 로고
    • Pheochromocytoma: Inherited associations, bilaterality, and cortex preservation
    • Inabnet W, Caragliano P, Pertsemlidis D. (2000) Pheochromocytoma: inherited associations, bilaterality, and cortex preservation. Surgery 128:1007-1012
    • (2000) Surgery , vol.128 , pp. 1007-1012
    • Inabnet, W.1    Caragliano, P.2    Pertsemlidis, D.3
  • 40
    • 0033935327 scopus 로고    scopus 로고
    • Laparoscopic partial adrenalectomy in patients with hereditary forms of pheochromocytoma
    • Janetschek G, Finkenstedt G, Gasser R., et al (1998) Laparoscopic partial adrenalectomy in patients with hereditary forms of pheochromocytoma. J Urol 164:14-17
    • (1998) J Urol , vol.164 , pp. 14-17
    • Janetschek, G.1    Finkenstedt, G.2    Gasser, R.3
  • 41
    • 0034693757 scopus 로고    scopus 로고
    • The RET protooncogene in human cancers
    • Jhiang SM (2000) The RET protooncogene in human cancers. Oncogene 19:5590-5597
    • (2000) Oncogene , vol.19 , pp. 5590-5597
    • Jhiang, S.M.1
  • 42
    • 0021043434 scopus 로고
    • Carcinoid tumour of ampulla of vater associated with viscero-cuta-neous neurofibromatosis
    • Kapur BM, Sarin SK, Anand C.S., et al (1983) Carcinoid tumour of ampulla of Vater associated with viscero-cuta-neous neurofibromatosis. Postgrad Med 59:734-735
    • (1983) Postgrad Med , vol.59 , pp. 734-735
    • Kapur, B.M.1    Sarin, S.K.2    Anand, C.S.3
  • 43
    • 0038207881 scopus 로고    scopus 로고
    • 11C-metomidate PET imaging of adrenocortical cancer
    • Khan TS, Sundin A, Juhlin C., et al (2003) 11C-metomidate PET imaging of adrenocortical cancer. Eur J Nucl Med Mol Imaging 30:403-410
    • (2003) Eur J Nucl Med Mol Imaging , vol.30 , pp. 403-410
    • Khan, T.S.1    Sundin, A.2    Juhlin, C.3
  • 44
    • 0000671591 scopus 로고    scopus 로고
    • Genetic Abnormalities in multiple endocrine neoplasia type 2
    • Doherty GM, Skogseid B (eds) Lippincott Williams & Wilkins, Philadelphia
    • Kikumori T, Evans D, Lee J.E., et al (2001) Genetic abnormalities in multiple endocrine neoplasia type 2. In: Doherty GM, Skogseid B (eds) Surgical endocrinology. Lippincott Williams & Wilkins, Philadelphia, pp 531-540
    • (2001) Surgical Endocrinology , pp. 531-540
    • Kikumori, T.1    Evans, D.2    Lee, J.E.3
  • 45
    • 0033812849 scopus 로고    scopus 로고
    • Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the carney complex
    • Kirschner LS, Carney JA, Pack S.D., et al (2000) Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex. Nat Genet 26:89-92
    • (2000) Nat Genet , vol.26 , pp. 89-92
    • Kirschner, L.S.1    Carney, J.A.2    Pack, S.D.3
  • 47
    • 0035986364 scopus 로고    scopus 로고
    • Pheochromocytoma in von hippel-lindau disease: Distinct histopathologic phenotype compared to pheochromo cytoma in multiple endocrine neoplasia type 2
    • Koch C, Mauro D, McClellan M.W., et al (2002) Pheochromocytoma in von Hippel-Lindau disease: distinct histopathologic phenotype compared to pheochromo cytoma in multiple endocrine neoplasia type 2. Endocrine Pathol 13:17-27
    • (2002) Endocrine Pathol , vol.13 , pp. 17-27
    • Koch, C.1    Mauro, D.2    McClellan, M.W.3
  • 48
    • 0031015524 scopus 로고    scopus 로고
    • Octreotide scintigraphy and catecholamine response to an octreotide challenge in Malignant phaeochromocytoma
    • Kopf D, Bockisch A, Steinert H., et al (1997) Octreotide scintigraphy and catecholamine response to an octreotide challenge in malignant phaeochromocytoma. Clin Endocrinol 46:39-44
    • (1997) Clin Endocrinol , vol.46 , pp. 39-44
    • Kopf, D.1    Bockisch, A.2    Steinert, H.3
  • 49
    • 0033674591 scopus 로고    scopus 로고
    • Malignancy in neurofibromatosis type 1
    • Korf BR (2000) Malignancy in neurofibromatosis type 1. The Oncologist 5:477-485
    • (2000) The Oncologist , vol.5 , pp. 477-485
    • Korf, B.R.1
  • 50
    • 0027238246 scopus 로고
    • Management of pheochromocytomas in patients with multiple endocrine neoplasia type 2 syndromes
    • Lairmore TC, Ball DW, Baylin S.B., et al (1993) Management of pheochromocytomas in patients with multiple endocrine neoplasia type 2 syndromes. Ann Surg 217: 595-603
    • (1993) Ann Surg , vol.217 , pp. 595-603
    • Lairmore, T.C.1    Ball, D.W.2    Baylin, S.B.3
  • 51
    • 0029906124 scopus 로고    scopus 로고
    • Cortical-sparing adrenalectomy for patients with bilateral pheochromocytoma
    • Lee JE, Curley SA, Gagel R.F., et al (1996) Cortical-sparing adrenalectomy for patients with bilateral pheochromocytoma. Surgery 120:1064-1071
    • (1996) Surgery , vol.120 , pp. 1064-1071
    • Lee, J.E.1    Curley, S.A.2    Gagel, R.F.3
  • 52
    • 0014587529 scopus 로고
    • Soft-tissue sarcomas, breast cancer, and other neoplasms: A familial syndrome?
    • Li FP, Fraumeni J.F. (1969) Soft-tissue sarcomas, breast cancer, and other neoplasms: a familial syndrome? Ann Int Med 71:747-752
    • (1969) Ann Int Med , vol.71 , pp. 747-752
    • Li, F.P.1    Fraumeni, J.F.2
  • 53
    • 0019522340 scopus 로고
    • Bilateral occurrence of pheochromocytoma in patients with the multiple endocrine neoplasia syndrome type 2A (Sipple's syndrome)
    • Lips KJ, Van der Sluys Veer J, Struyvenberg A, et al. (1981) Bilateral occurrence of pheochromocytoma in patients with the multiple endocrine neoplasia syndrome type 2A (Sipple's syndrome). Am J Med 70:1051-1060
    • (1981) Am J Med , vol.70 , pp. 1051-1060
    • Lips, K.J.1    Van Der Sluys Veer, J.2    Struyvenberg, A.3
  • 54
    • 0025741681 scopus 로고
    • Von hippel-lindau disease: A genetic study
    • Maher ER, Iselius L, Yates J.R., et al (1991) Von Hippel-Lindau disease: a genetic study. J Med Genet 28:443-447
    • (1991) J Med Genet , vol.28 , pp. 443-447
    • Maher, E.R.1    Iselius, L.2    Yates, J.R.3
  • 55
    • 0026530299 scopus 로고
    • Germline mutations of the p53 tumor-suppressor gene in children and young adults with second Malignant neoplasms
    • Malkin D, Jolly KW, Barbier N, et al (1992) Germline mutations of the p53 tumor-suppressor gene in children and young adults with second malignant neoplasms. N Engl J Med 326:1309-1315
    • (1992) N Engl J Med , vol.326 , pp. 1309-1315
    • Malkin, D.1    Jolly, K.W.2    Barbier, N.3
  • 56
    • 0030792719 scopus 로고    scopus 로고
    • Adrenal masses in patients with familial adenomatous polyposis
    • Marchesa P, Fazio VW, Church J.M., et al (1997) Adrenal masses in patients with familial adenomatous polyposis. Dis Colon Rectum 40:1023-1028
    • (1997) Dis Colon Rectum , vol.40 , pp. 1023-1028
    • Marchesa, P.1    Fazio, V.W.2    Church, J.M.3
  • 57
    • 0028783824 scopus 로고
    • Pheochromocytoma in multiple endocrine neoplasia type 2: European study
    • Modigliani E, Vasen HM, Raue K, et al (1995) Pheochromocytoma in multiple endocrine neoplasia type 2: European study. J Internal Med 238:363-367
    • (1995) J Internal Med , vol.238 , pp. 363-367
    • Modigliani, E.1    Vasen, H.M.2    Raue, K.3
  • 58
    • 0038360493 scopus 로고    scopus 로고
    • Medullary thyroid carcinoma and the multiple endocrine neoplasia type 2 syndromes
    • Doherty GM, Skogseid B (eds) Lippincott Williams & Wilkins, Philadelphia
    • Moley JF, Albinson C. (2001) Medullary thyroid carcinoma and the multiple endocrine neoplasia type 2 syndromes. In: Doherty GM, Skogseid B (eds) Surgical endocrinology. Lippincott Williams & Wilkins, Philadelphia, pp 541-557
    • (2001) Surgical Endocrinology , pp. 541-557
    • Moley, J.F.1    Albinson, C.2
  • 59
    • 0027231568 scopus 로고
    • Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
    • Mulligan LM, Kwok JB, Healey C.S., 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
  • 60
    • 0023530559 scopus 로고
    • A case of von recklinghausen's disease associated with pheochromo-cytoma and papillary carcinoma of the thyroid gland
    • Nakamura H, Koga M, Higa S., et al (1987) A case of von Recklinghausen's disease associated with pheochromo-cytoma and papillary carcinoma of the thyroid gland. Endocrinol Jpn 34:545-551
    • (1987) Endocrinol Jpn , vol.34 , pp. 545-551
    • Nakamura, H.1    Koga, M.2    Higa, S.3
  • 61
    • 0027508442 scopus 로고
    • Pheochromocytomas, multiple endocrine neoplasia type 2, and von hippel-lindau disease
    • Neumann HPH, Berger DP, Sigmund G, et al (1993) Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease. N Engl J Med 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
  • 62
    • 84885783005 scopus 로고
    • Erratum
    • Erratum (1994) N Engl J Med 331: 1535
    • (1994) N Engl J Med , vol.331 , pp. 1535
  • 63
    • 0029090153 scopus 로고
    • Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia type 2
    • Neumann HPH, Eng C, Mulligan L.M., et al (1995) Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia type 2. JAMA 274:1149-1151
    • (1995) JAMA , vol.274 , pp. 1149-1151
    • Neumann, H.P.H.1    Eng, C.2    Mulligan, L.M.3
  • 64
    • 0032893034 scopus 로고    scopus 로고
    • Adrenal-sparing surgery for phaeochromocytoma
    • Neumann HPH, Bender BU, Reincke M, et al (1999) Adrenal-sparing surgery for phaeochromocytoma. Br J Surg 86:94-97
    • (1999) Br J Surg , vol.86 , pp. 94-97
    • Neumann, H.P.H.1    Bender, B.U.2    Reincke, M.3
  • 65
    • 0037046659 scopus 로고    scopus 로고
    • Germ-line mutations in nonsyndromic pheochromocy-toma
    • Neumann HPH, Bausch B, McWhinney S.R., et al (2002) Germ-line mutations in nonsyndromic pheochromocy-toma. N Engl J Med 346:1459-1466
    • (2002) N Engl J Med , vol.346 , pp. 1459-1466
    • Neumann, H.P.H.1    Bausch, B.2    McWhinney, S.R.3
  • 67
    • 0035151026 scopus 로고    scopus 로고
    • Pheochromocytoma in multiple endocrine neoplasia type 2: A prospective study
    • Nguyen L, Niccoli-Sire P, Caron P., et al (2001) Pheochromocytoma in multiple endocrine neoplasia type 2: a prospective study. Eur J Endocrinol 144:37-44
    • (2001) Eur J Endocrinol , vol.144 , pp. 37-44
    • Nguyen, L.1    Niccoli-Sire, P.2    Caron, P.3
  • 68
    • 0033767445 scopus 로고    scopus 로고
    • Mutations in SDHC cause autosomal dominant paraganglioma, type 3
    • Niemann S, Müller U (2000) Mutations in SDHC cause autosomal dominant paraganglioma, type 3. Nat Genet 26:268-270
    • (2000) Nat Genet , vol.26 , pp. 268-270
    • Niemann, S.1    Müller, U.2
  • 69
    • 0028850669 scopus 로고
    • Multiple endocrine neoplasia type 2B: More than an endocrine disorder
    • O'Riordain D.S., O'Brien T, Crotty TB, et al (1995) Multiple endocrine neoplasia type 2B: more than an endocrine disorder. Surgery 118:936-942
    • (1995) Surgery , vol.118 , pp. 936-942
    • O'Riordain, D.S.1    O'Brien, T.2    Crotty, T.B.3
  • 70
    • 0031657522 scopus 로고    scopus 로고
    • Neurofibromatosis type 1 (NF1): A protein truncation assay yielding identification of mutations in 73% of patients
    • Park VM, Pivnick E.K. (1998) Neurofibromatosis type 1 (NF1): A protein truncation assay yielding identification of mutations in 73% of patients. J Med Genet 35:813-820
    • (1998) J Med Genet , vol.35 , pp. 813-820
    • Park, V.M.1    Pivnick, E.K.2
  • 71
    • 0031889547 scopus 로고    scopus 로고
    • Differences between sporadic and multiple endocrine neoplasia type 2A phaeochromocytoma
    • Pomares FJ, Canas R, Rodriguez J.M., et al (1998) Differences between sporadic and multiple endocrine neoplasia type 2A phaeochromocytoma. Clin Endocrinol 48:195-200
    • (1998) Clin Endocrinol , vol.48 , pp. 195-200
    • Pomares, F.J.1    Canas, R.2    Rodriguez, J.M.3
  • 72
    • 0026876355 scopus 로고
    • Neurofibromatosis: From gene to phe-notype
    • Ponder BA (1992) Neurofibromatosis: from gene to phe-notype. Semin Cancer Biol 3:115-120
    • (1992) Semin Cancer Biol , vol.3 , pp. 115-120
    • Ponder, B.A.1
  • 73
    • 0028149096 scopus 로고
    • Pheochromocytoma as the first manifestation of von hippel-lindau disease
    • Richard S, Beigelman C, Duclos J.M., et al (1994) Pheochromocytoma as the first manifestation of von Hippel-Lindau disease. Surgery 116:1076-1081
    • (1994) Surgery , vol.116 , pp. 1076-1081
    • Richard, S.1    Beigelman, C.2    Duclos, J.M.3
  • 74
    • 0026695967 scopus 로고
    • PET scanning with hydroxyephedrine: An approach to the localization of pheochromocytoma
    • Shulkin BL, Wieland DM, Schwaiger M, et al (1992) PET scanning with hydroxyephedrine: an approach to the localization of pheochromocytoma. J Nucl Med 33: 1125-1131
    • (1992) J Nucl Med , vol.33 , pp. 1125-1131
    • Shulkin, B.L.1    Wieland, D.M.2    Schwaiger, M.3
  • 75
    • 0035683789 scopus 로고    scopus 로고
    • Von hippel-lindau disease: Gene to bedside
    • Sims KB (2001) Von Hippel-Lindau disease: gene to bedside. Curr Opin Neurol 14:695-703
    • (2001) Curr Opin Neurol , vol.14 , pp. 695-703
    • Sims, K.B.1
  • 76
    • 0001251788 scopus 로고
    • The association of pheochromocytoma with carcinoma of the thyroid gland
    • Sipple JH (1961) The association of pheochromocytoma with carcinoma of the thyroid gland. Am J Med 31:163-166
    • (1961) Am J Med , vol.31 , pp. 163-166
    • Sipple, J.H.1
  • 77
    • 0019417415 scopus 로고
    • Scintigraphic localization of pheochromocytoma
    • Sisson JC, Frager MS, Valk T.W., et al (1981) Scintigraphic localization of pheochromocytoma. N Engl J Med 305: 12-17
    • (1981) N Engl J Med , vol.305 , pp. 12-17
    • Sisson, J.C.1    Frager, M.S.2    Valk, T.W.3
  • 78
    • 0026762788 scopus 로고
    • Clinical and genetic features of adrenocortical lesions in multiple endocrine neoplasia type 1
    • Skogseid B, Larsson C, Lindgren P.G., et al (1992) Clinical and genetic features of adrenocortical lesions in multiple endocrine neoplasia type 1. J Clin Endocrinol Metab 75:76-81
    • (1992) J Clin Endocrinol Metab , vol.75 , pp. 76-81
    • Skogseid, B.1    Larsson, C.2    Lindgren, P.G.3
  • 79
    • 0028806115 scopus 로고
    • Adrenal lesion in multiple endocrine neoplasia type 1
    • Skogseid B, Rastad J, Gobl A., et al (1995) Adrenal lesion in multiple endocrine neoplasia type 1. Surgery 118: 1077-1082
    • (1995) Surgery , vol.118 , pp. 1077-1082
    • Skogseid, B.1    Rastad, J.2    Gobl, A.3
  • 80
    • 0031938588 scopus 로고    scopus 로고
    • A family with hereditary extra-adrenal paragangliomas without evidence for mutations in the von hippel-lindau disease or ret genes
    • Sköldberg F., Grimelius L, Woodward E.R., et al (1998) A family with hereditary extra-adrenal paragangliomas without evidence for mutations in the von Hippel-Lindau disease or ret genes. Clin Endocrinol 48:11-16
    • (1998) Clin Endocrinol , vol.48 , pp. 11-16
    • Sköldberg, F.1    Grimelius, L.2    Woodward, E.R.3
  • 81
    • 0025648762 scopus 로고
    • Germ-line transmission of a mutated p53 gene in a cancer-prone family with li-fraumeni syndrome
    • Srivastava S, Zou Z, Pirollo K., et al (1990) Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome. Nature 348:747-749
    • (1990) Nature , vol.348 , pp. 747-749
    • Srivastava, S.1    Zou, Z.2    Pirollo, K.3
  • 82
    • 0035001830 scopus 로고    scopus 로고
    • Clinical genetics of multiple endocrine neoplasias, carney complex and related syndromes
    • Stratakis CA (2001) Clinical genetics of multiple endocrine neoplasias, Carney complex and related syndromes. J Endocrinol Invest 24:370-383
    • (2001) J Endocrinol Invest , vol.24 , pp. 370-383
    • Stratakis, C.A.1
  • 83
    • 0034853288 scopus 로고    scopus 로고
    • Genetics of endocrine disease. Clinical and molecular features of the carney complex: Diagnostic criteria and recommendations for patient evaluation
    • Stratakis CA, Kirschner LS, Carney J.A. (2001) Genetics of endocrine disease. Clinical and molecular features of the Carney complex: diagnostic criteria and recommendations for patient evaluation. J Clin Endocrinol Metab 86:4041-4046
    • (2001) J Clin Endocrinol Metab , vol.86 , pp. 4041-4046
    • Stratakis, C.A.1    Kirschner, L.S.2    Carney, J.A.3
  • 84
    • 0001926360 scopus 로고    scopus 로고
    • A refined genetic, radiation hybrid, and physical map of the carney complex (CNC) locus on chromosome 2p16; evidence for genetic heterogeneity in the syndrome
    • Taymans SE, Macrae CA, Casey M, et al (1997) A refined genetic, radiation hybrid, and physical map of the Carney complex (CNC) locus on chromosome 2p16; evidence for genetic heterogeneity in the syndrome. Am J Hum Genet 61 Suppl A84.
    • (1997) Am J Hum Genet , vol.61 , Issue.SUPPL. A84
    • Taymans, S.E.1    Macrae, C.A.2    Casey, M.3
  • 85
    • 0028817229 scopus 로고
    • Comparison of radiolabeled octreotide and meta-iodobenzylguanidine (MIBG) scintigraphy in Malignant pheochromocytoma
    • Tenenbaum F, Lumbroso J, Schlumberger M., et al (1995) Comparison of radiolabeled octreotide and meta-iodobenzylguanidine (MIBG) scintigraphy in malignant pheochromocytoma. J Nucl Med 36:1-6
    • (1995) J Nucl Med , vol.36 , pp. 1-6
    • Tenenbaum, F.1    Lumbroso, J.2    Schlumberger, M.3
  • 86
    • 0031444499 scopus 로고    scopus 로고
    • Laparoscopic versus open posterior adrenalectomy: A case-control study of 100 patients
    • Thompson GB, Grant CS, van Heerden JA, et al (1997) Laparoscopic versus open posterior adrenalectomy: a case-control study of 100 patients. Surgery 122:1132-1136
    • (1997) Surgery , vol.122 , pp. 1132-1136
    • Thompson, G.B.1    Grant, C.S.2    Van Heerden, J.A.3
  • 87
    • 0020568781 scopus 로고
    • Unilateral versus bilateral adrenalectomy in multiple endocrine neoplasia IIA
    • Tibblin S, Dymling JF, Ingemansson S, et al (1983) Unilateral versus bilateral adrenalectomy in multiple endocrine neoplasia IIA. World J Surg 7:201-208
    • (1983) World J Surg , vol.7 , pp. 201-208
    • Tibblin, S.1    Dymling, J.F.2    Ingemansson, S.3
  • 88
    • 0021604045 scopus 로고
    • Surgical management of the adrenal glands in the multiple endocrine neoplasia type II syndrome
    • van Heerden J.A., Sizemore GW, Carney J.A., et al (1984) Surgical management of the adrenal glands in the multiple endocrine neoplasia type II syndrome. World J Surg 8:612-621
    • (1984) World J Surg , vol.8 , pp. 612-621
    • Van Heerden, J.A.1    Sizemore, G.W.2    Carney, J.A.3
  • 89
    • 0022335261 scopus 로고
    • Bilateral subtotal adrenal resection for bilateral pheochromocytomas in multiple endocrine neoplasia, type IIa: A case report
    • van Heerden J.A., Sizemore GW, Carney J.A., et al (1985) Bilateral subtotal adrenal resection for bilateral pheochromocytomas in multiple endocrine neoplasia, type IIa: a case report. Surgery 98:363-365
    • (1985) Surgery , vol.98 , pp. 363-365
    • Van Heerden, J.A.1    Sizemore, G.W.2    Carney, J.A.3
  • 90
    • 0027985697 scopus 로고
    • High frequency of germline p53 mutations in childhood adrenocortical cancer
    • Wagner J, Portwine C, Rabin K., et al (1994) High frequency of germline p53 mutations in childhood adrenocortical cancer. J Natl Cancer Inst 86:1707-1710
    • (1994) J Natl Cancer Inst , vol.86 , pp. 1707-1710
    • Wagner, J.1    Portwine, C.2    Rabin, K.3
  • 91
    • 0032825694 scopus 로고    scopus 로고
    • Von recklinghausen's disease and pheochromocytomas
    • Walther MM, Herring J, Enquist E., et al (1999) Von Recklinghausen's disease and pheochromocytomas. J Urol 162:1582-1586
    • (1999) J Urol , vol.162 , pp. 1582-1586
    • Walther, M.M.1    Herring, J.2    Enquist, E.3
  • 92
    • 6544234532 scopus 로고    scopus 로고
    • Clinical and genetic characterization of pheochromocytoma in von hippel-lindau families: Comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytoma
    • Walther MM, Reiter R, Keiser H.R., et al (1999) Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families: comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytoma. J Urol 162:659-664
    • (1999) J Urol , vol.162 , pp. 659-664
    • Walther, M.M.1    Reiter, R.2    Keiser, H.R.3
  • 93
    • 0033935327 scopus 로고    scopus 로고
    • Laparoscopic partial adrenalectomy in patients with hereditary forms of pheochromocytoma
    • Walther MM, Herring J, Choyke P.L., et al (2000) Laparoscopic partial adrenalectomy in patients with hereditary forms of pheochromocytoma. J Urol 164:14-17
    • (2000) J Urol , vol.164 , pp. 14-17
    • Walther, M.M.1    Herring, J.2    Choyke, P.L.3
  • 94
    • 33745819042 scopus 로고    scopus 로고
    • Von hippel-lindau disease and von recklinghausen's disease
    • Doherty GM, Skogseid B (eds) Lip-pincott Williams & Wilkins, Philadelphia
    • Walther MM, Linehan WM, Libutti S.K. (2001) von Hippel-Lindau disease and von Recklinghausen's disease. In: Doherty GM, Skogseid B (eds) Surgical endocrinology. Lip-pincott Williams & Wilkins, Philadelphia, pp 581-591
    • (2001) Surgical Endocrinology , pp. 581-591
    • Walther, M.M.1    Linehan, W.M.2    Libutti, S.K.3
  • 95
    • 0037024513 scopus 로고    scopus 로고
    • New therapeutic and surgical approaches for sporadic and hereditary pheochromocy-toma
    • Walther MM (2002) New therapeutic and surgical approaches for sporadic and hereditary pheochromocy-toma. Ann N Y Acad Sci 970:41-53
    • (2002) Ann N y Acad Sci , vol.970 , pp. 41-53
    • Walther, M.M.1
  • 96
    • 0031947929 scopus 로고    scopus 로고
    • Subtotal adrenalectomy by the posterior retroperitoneoscopic approach
    • Walz MK, Peitgen K, Saller B., et al (1998) Subtotal adrenalectomy by the posterior retroperitoneoscopic approach. World J Surg 22:621-627
    • (1998) World J Surg , vol.22 , pp. 621-627
    • Walz, M.K.1    Peitgen, K.2    Saller, B.3
  • 97
    • 0022896381 scopus 로고
    • The association of neurofibromatosis, pheochromocytoma, and somatostatinrich duodenal carcinoid tumor
    • Wheeler MH, Curley IR, Williams E.D. (1986) The association of neurofibromatosis, pheochromocytoma, and somatostatinrich duodenal carcinoid tumor. Surgery 100: 1163-1169
    • (1986) Surgery , vol.100 , pp. 1163-1169
    • Wheeler, M.H.1    Curley, I.R.2    Williams, E.D.3
  • 98
    • 76549164702 scopus 로고
    • Complex malformatif familial avec hernie ombilicale et macroglossie-Un syndrome nouveau?
    • Wiedemann HR (1964) Complex malformatif familial avec hernie ombilicale et macroglossie-un syndrome nouveau? J Genet Hum 13:223-232
    • (1964) J Genet Hum , vol.13 , pp. 223-232
    • Wiedemann, H.R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.