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Volumn 160, Issue 2, 2009, Pages 227-231

Should genetic testing be performed in each patient with sporadic pheochromocytoma at presentation?

Author keywords

[No Author keywords available]

Indexed keywords

GUANOSINE; NEUROFIBROMIN; PROTEIN RET; SUCCINATE DEHYDROGENASE; SUCCINATE DEHYDROGENASE B; SUCCINATE DEHYDROGENASE C; SUCCINATE DEHYDROGENASE D; THYMIDINE; UNCLASSIFIED DRUG; VON HIPPEL LINDAU PROTEIN;

EID: 61449266628     PISSN: 08044643     EISSN: 1479683X     Source Type: Journal    
DOI: 10.1530/EJE-08-0574     Document Type: Article
Times cited : (25)

References (12)
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    • 33646709396 scopus 로고    scopus 로고
    • Evolving concepts in pheochromocytoma and paraganglioma
    • Dahia PL. Evolving concepts in pheochromocytoma and paraganglioma. Current Opinion in Oncology 2006 18 1-8.
    • (2006) Current Opinion in Oncology , vol.18 , pp. 1-8
    • Dahia, P.L.1
  • 7
    • 29144484161 scopus 로고    scopus 로고
    • The SDH mutation database: An online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency
    • Bayley JP, Deville 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 Medical Genetics 2005 6 39.
    • (2005) BMC Medical Genetics , vol.6 , pp. 39
    • Bayley, J.P.1    Deville, P.2    Taschner, P.E.3
  • 8
    • 43049095689 scopus 로고    scopus 로고
    • Ser80Ile mutation and a concurrent Pro25Leu variant of the VHL gene in an extented Hungarian von Hippel-Lindau family
    • Patocs A, Gergics P, Balogh K, Toth M, Fazakas F, Liko O & Racz K. Ser80Ile mutation and a concurrent Pro25Leu variant of the VHL gene in an extented Hungarian von Hippel-Lindau family. BMC Medical Genetics 2008 9 29.
    • (2008) BMC Medical Genetics , vol.9 , pp. 29
    • Patocs, A.1    Gergics, P.2    Balogh, K.3    Toth, M.4    Fazakas, F.5    Liko, O.6    Racz, K.7
  • 9
    • 65549161244 scopus 로고    scopus 로고
    • Synthèse Nationale de L'évolution de L'activité D'oncogénétique 2003-2006. Institut National du Cancer, Mars 2008.
    • Synthèse Nationale de L'évolution de L'activité D'oncogénétique 2003-2006. Institut National du Cancer, Mars 2008.
  • 10
    • 33747638645 scopus 로고    scopus 로고
    • Should patients with apparently sporadic pheochromocytomas or paragangliomas be screened for hereditary syndromes?
    • Jimenez C, Cote G, Arnold A & Gagel RF. Should patients with apparently sporadic pheochromocytomas or paragangliomas be screened for hereditary syndromes? Journal of Clinical Endocrinology and Metabolism 2006 91 2851-2858.
    • (2006) Journal of Clinical Endocrinology and Metabolism , vol.91 , pp. 2851-2858
    • Jimenez, C.1    Cote, G.2    Arnold, A.3    Gagel, R.F.4
  • 11
    • 33846432718 scopus 로고    scopus 로고
    • Pacak K, Eisenhofer G, Ahlman H, Bornstein SR, Gimenez Roqueplo AP, Grossman AB, Kimura N, Mannelli M, McNicol AM & Tischler AS. Pheochromocytoma: recommendations for clinical practice from the first International Symposium. Nature Clinical Practice. Endocrinology & Metabolism 2007 3 92-102.
    • Pacak K, Eisenhofer G, Ahlman H, Bornstein SR, Gimenez Roqueplo AP, Grossman AB, Kimura N, Mannelli M, McNicol AM & Tischler AS. Pheochromocytoma: recommendations for clinical practice from the first International Symposium. Nature Clinical Practice. Endocrinology & Metabolism 2007 3 92-102.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.