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Volumn 132, Issue 3, 2005, Pages 467-470

Paragangliomas in patients with mutations of the SDHD gene

Author keywords

[No Author keywords available]

Indexed keywords

FLUORO DOPA F 18; ISOENZYME; RADIOPHARMACEUTICAL AGENT; SUCCINATE DEHYDROGENASE D; UNCLASSIFIED DRUG;

EID: 14744274616     PISSN: 01945998     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.otohns.2004.09.024     Document Type: Article
Times cited : (20)

References (12)
  • 1
    • 0032709254 scopus 로고    scopus 로고
    • Paraganglioma as a systemic syndrome: Pitfalls and strategies
    • W. Maier, N. Marangos, R. Laszig Paraganglioma as a systemic syndrome pitfalls and strategies J Laryngol Otol 113 1999 978 982
    • (1999) J Laryngol Otol , vol.113 , pp. 978-982
    • Maier, W.1    Marangos, N.2    Laszig, R.3
  • 3
    • 0036712593 scopus 로고    scopus 로고
    • Hereditary paraganglioma targets diverse paraganglia
    • B.E. Baysal Hereditary paraganglioma targets diverse paraganglia J Med Genet 39 2002 617 622
    • (2002) J Med Genet , vol.39 , pp. 617-622
    • Baysal, B.E.1
  • 4
    • 0036468725 scopus 로고    scopus 로고
    • National cancer data base report on malignant paragangliomas of the head and neck
    • J.H. Lee, F. Barich, L.H. Karnell National cancer data base report on malignant paragangliomas of the head and neck Cancer 94 2002 730 737
    • (2002) Cancer , vol.94 , pp. 730-737
    • Lee, J.H.1    Barich, F.2    Karnell, L.H.3
  • 5
    • 0037046659 scopus 로고    scopus 로고
    • Germ-line mutations in nonsyndromic pheochromocytoma
    • H.P.H. Neumann, B. Bausch, S.R. McWhinney Germ-line mutations in nonsyndromic pheochromocytoma N Engl J Med 346 2002 1459 1466
    • (2002) N Engl J Med , vol.346 , pp. 1459-1466
    • Neumann, H.P.H.1    Bausch, B.2    McWhinney, S.R.3
  • 7
    • 0042566135 scopus 로고    scopus 로고
    • Altitude is a phenotypic modifier in hereditary paraganglioma type 1: Evidence for an oxygen-sensing defect
    • K. Astrom, J.E. Cohen, J.E. Willett-Brozick Altitude is a phenotypic modifier in hereditary paraganglioma type 1 evidence for an oxygen-sensing defect Hum Genet 113 2003 228 237
    • (2003) Hum Genet , vol.113 , pp. 228-237
    • Astrom, K.1    Cohen, J.E.2    Willett-Brozick, J.E.3
  • 8
    • 0034602950 scopus 로고    scopus 로고
    • Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma
    • B.E. Baysal, R.E. Ferrell, J.E. Willett-Brozick Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma Science 287 2000 848 851
    • (2000) Science , vol.287 , pp. 848-851
    • Baysal, B.E.1    Ferrell, R.E.2    Willett-Brozick, J.E.3
  • 9
    • 4143105824 scopus 로고    scopus 로고
    • Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations
    • H.P.H. Neumann, C. Pawlu, M. Peczkowska Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations JAMA 292 2004 943 951
    • (2004) JAMA , vol.292 , pp. 943-951
    • Neumann, H.P.H.1    Pawlu, C.2    Peczkowska, M.3
  • 10
    • 0037307412 scopus 로고    scopus 로고
    • A novel mutation in the SDHD gene in a family with inherited paragangliomas--implications of genetic diagnosis for follow up and treatment
    • L. Renard, C. Godfraind, L.M. Boon A novel mutation in the SDHD gene in a family with inherited paragangliomas--implications of genetic diagnosis for follow up and treatment Head Neck 25 2003 146 151
    • (2003) Head Neck , vol.25 , pp. 146-151
    • Renard, L.1    Godfraind, C.2    Boon, L.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.