메뉴 건너뛰기




Volumn 4, Issue 2, 2008, Pages 111-115

Extra-adrenal and adrenal pheochromocytomas associated with a germline SDHC mutation

Author keywords

Head and neck paraganglioma; Paraganglioma syndromes; Pheochromocytoma; Succinate dehydrogenase subunit genes

Indexed keywords

(3 IODOBENZYL)GUANIDINE I 123;

EID: 38549134313     PISSN: 17458366     EISSN: 17458374     Source Type: Journal    
DOI: 10.1038/ncpendmet0726     Document Type: Article
Times cited : (91)

References (19)
  • 2
    • 0036920488 scopus 로고    scopus 로고
    • The molecular pathogenesis of hereditary and sporadic adrenocortical and adrenomedullary tumors
    • Koch CA et al. (2002) The molecular pathogenesis of hereditary and sporadic adrenocortical and adrenomedullary tumors. J Clin Endocrinol Metab 87: 5367-5384
    • (2002) J Clin Endocrinol Metab , vol.87 , pp. 5367-5384
    • Koch, C.A.1
  • 4
    • 33750592253 scopus 로고    scopus 로고
    • Pheochromocytoma: Presentation, diagnosis and treatment
    • Reisch N et al. (2006) Pheochromocytoma: presentation, diagnosis and treatment. J Hypertens 24: 2331-2339
    • (2006) J Hypertens , vol.24 , pp. 2331-2339
    • Reisch, N.1
  • 5
    • 33845875992 scopus 로고    scopus 로고
    • Cancer phenomics: RET and PTEN as illustrative models
    • Zbuk KM and Eng C (2007) Cancer phenomics: RET and PTEN as illustrative models. Nat Rev Cancer 7: 35-45
    • (2007) Nat Rev Cancer , vol.7 , pp. 35-45
    • Zbuk, K.M.1    Eng, C.2
  • 6
    • 33748755275 scopus 로고    scopus 로고
    • Comprehensive mutation scanning of NF1 in apparently sporadic cases of pheochromocytoma
    • Bausch B et al. (2006) Comprehensive mutation scanning of NF1 in apparently sporadic cases of pheochromocytoma. J Clin Endocrinol Metab 91: 3478-3481
    • (2006) J Clin Endocrinol Metab , vol.91 , pp. 3478-3481
    • Bausch, B.1
  • 7
    • 0034602950 scopus 로고    scopus 로고
    • Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma
    • Baysal BE 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
  • 8
    • 0033767445 scopus 로고    scopus 로고
    • Mutations in SDHC cause autosomal dominant paraganglioma, type 3
    • Niemann S and 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
  • 9
    • 0034964421 scopus 로고    scopus 로고
    • Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma
    • Astuti D 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
  • 10
    • 0034671551 scopus 로고    scopus 로고
    • Somatic and occult germline mutations in SDHD, a mitochondrial complex II gene, in non-familial pheochromocytoma
    • Gimm O et al. (2000) Somatic and occult germline mutations in SDHD, a mitochondrial complex II gene, in non-familial pheochromocytoma. Cancer Res 60: 6822-6825
    • (2000) Cancer Res , vol.60 , pp. 6822-6825
    • Gimm, O.1
  • 11
    • 0037364314 scopus 로고    scopus 로고
    • A role for mitochondrial enzymes in inherited neoplasia and beyond
    • Eng C et al. (2003) A role for mitochondrial enzymes in inherited neoplasia and beyond. Nat Rev Cancer 3: 193-202
    • (2003) Nat Rev Cancer , vol.3 , pp. 193-202
    • Eng, C.1
  • 12
    • 0037046659 scopus 로고    scopus 로고
    • Germ-line mutations in nonsyndromic pheochromocytoma
    • Neumann HPH et al. (2002) Germ-line mutations in nonsyndromic pheochromocytoma. N Engl J Med 346: 1459-1466
    • (2002) N Engl J Med , vol.346 , pp. 1459-1466
    • Neumann, H.P.H.1
  • 13
    • 4143105824 scopus 로고    scopus 로고
    • Distinct clinical features characterize paraganglioma syndromes associated with SDHB and SDHD gene mutations
    • Neumann HPH et al. (2004) Distinct clinical features characterize paraganglioma syndromes associated with SDHB and SDHD gene mutations. JAMA 292: 943-951
    • (2004) JAMA , vol.292 , pp. 943-951
    • Neumann, H.P.H.1
  • 14
    • 27244446452 scopus 로고    scopus 로고
    • Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene
    • Schiavi F et al. (2005) Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene. JAMA 294: 2057-2063
    • (2005) JAMA , vol.294 , pp. 2057-2063
    • Schiavi, F.1
  • 15
    • 31344478803 scopus 로고    scopus 로고
    • Mutation analysis of SDHB and SDHC: Novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma
    • Bayley JP et al. (2006) Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma. BMC Med Genet 11: 1
    • (2006) BMC Med Genet , vol.11 , pp. 1
    • Bayley, J.P.1
  • 16
    • 34548830453 scopus 로고    scopus 로고
    • Genetic screening for pheochromocytoma: Should SDHC gene analysis be included?
    • Mannelli M et al. (2007) Genetic screening for pheochromocytoma: should SDHC gene analysis be included? J Med Genet 44: 586-587
    • (2007) J Med Genet , vol.44 , pp. 586-587
    • Mannelli, M.1
  • 18
    • 0034948451 scopus 로고    scopus 로고
    • Somatostatin receptor imaging: Current status and future perspectives
    • Bohuslavizki KH (2001) Somatostatin receptor imaging: current status and future perspectives. J Nucl Med 42: 1057-1058
    • (2001) J Nucl Med , vol.42 , pp. 1057-1058
    • Bohuslavizki, K.H.1
  • 19
    • 33646597235 scopus 로고    scopus 로고
    • Laparoscopic and retroperitoneoscopic treatment of pheochromocytomas and retroperitoneal paragangliomas: Results of 161 tumors in 126 patients
    • Walz MK et al. (2006) Laparoscopic and retroperitoneoscopic treatment of pheochromocytomas and retroperitoneal paragangliomas: results of 161 tumors in 126 patients. World J Surg 30: 1-10
    • (2006) World J Surg , vol.30 , pp. 1-10
    • Walz, M.K.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.