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Volumn 13, Issue 2, 2007, Pages 151-154

A Chinese family with familial paraganglioma syndrome due to succinate dehydrogenase deficiency

Author keywords

Paraganglioma; Phaeochromocytoma; Succinate dehydrogenase

Indexed keywords

LANSOPRAZOLE;

EID: 34147099624     PISSN: 10242708     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (9)

References (15)
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    • Hereditary paraganglioma/ pheochromocytoma and inherited succinate dehydrogenase deficiency
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  • 3
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    • On the association of succinate dehydrogenase mutations with hereditary paraganglioma
    • Baysal BE. On the association of succinate dehydrogenase mutations with hereditary paraganglioma. Trends Endocrinol Metab 2003;14:453-9.
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    • Baysal, B.E.1
  • 4
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    • Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma
    • Baysal BE, Ferrell RE, Willett-Brozick JE, et al. Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. Science 2000;287:848-51.
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    • Baysal, B.E.1    Ferrell, R.E.2    Willett-Brozick, J.E.3
  • 5
    • 0028855025 scopus 로고
    • A patient with co-existing bronchial carcinoid tumour and bilateral phaeochromocytoma
    • Chan HH, Yeung VT, Chow CC, Ko GT, Cockram CS. A patient with co-existing bronchial carcinoid tumour and bilateral phaeochromocytoma. Postgrad Med J 1995;71:102-3.
    • (1995) Postgrad Med J , vol.71 , pp. 102-103
    • Chan, H.H.1    Yeung, V.T.2    Chow, C.C.3    Ko, G.T.4    Cockram, C.S.5
  • 6
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    • Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene
    • Taschner PE, Jansen JC, Baysal BE, et al. Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene. Genes Chromosomes Cancer 2001;31:274-81.
    • (2001) Genes Chromosomes Cancer , vol.31 , pp. 274-281
    • Taschner, P.E.1    Jansen, J.C.2    Baysal, B.E.3
  • 8
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    • The SDH mutation database: An online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency
    • Bayley JP, Devilee P, Taschner PE. The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency. BMC Med Genet 2005;6:39.
    • (2005) BMC Med Genet , vol.6 , pp. 39
    • Bayley, J.P.1    Devilee, P.2    Taschner, P.E.3
  • 9
    • 0035213138 scopus 로고    scopus 로고
    • The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathway
    • Gimenez-Roqueplo AP, Favier J, Rustin P, et al. The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathway. Am J Hum Genet 2001;69:1186-97.
    • (2001) Am J Hum Genet , vol.69 , pp. 1186-1197
    • Gimenez-Roqueplo, A.P.1    Favier, J.2    Rustin, P.3
  • 10
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    • Germ-line mutations in nonsyndromic pheochromocytoma
    • Neumann HP, Bausch B, McWhinney SR, et al. Germ-line mutations in nonsyndromic pheochromocytoma. N Engl J Med 2002;346:1459-66.
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  • 12
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    • Hereditary paraganglioma due to the SDHD M1I mutation in a second Chinese family: A founder effect?
    • Lee SC, Chionh SB, Chong SM, Taschner PE. Hereditary paraganglioma due to the SDHD M1I mutation in a second Chinese family: a founder effect? Laryngoscope 2003;113:1055-8.
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    • Lee, S.C.1    Chionh, S.B.2    Chong, S.M.3    Taschner, P.E.4
  • 13
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    • Benn, D.E.1    Gimenez-Roqueplo, A.P.2    Reilly, J.R.3
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    • (1986) Acta Pathol Microbiol Immunol Scand [A] , vol.94 , pp. 229-235
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.