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Volumn 374, Issue 9691, 2009, Pages 756-

A reason to panic in pregnancy

Author keywords

[No Author keywords available]

Indexed keywords

CATECHOLAMINE; LABETALOL; PHENOXYBENZAMINE;

EID: 69149099536     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(09)61035-7     Document Type: Article
Times cited : (8)

References (5)
  • 1
    • 0035987952 scopus 로고    scopus 로고
    • Diagnosis and management of phaeochromocytoma in pregnancy
    • Manelli M., and Bemporad D. Diagnosis and management of phaeochromocytoma in pregnancy. J Endocrinol Invest 25 (2002) 567-572
    • (2002) J Endocrinol Invest , vol.25 , pp. 567-572
    • Manelli, M.1    Bemporad, D.2
  • 2
    • 0032709956 scopus 로고    scopus 로고
    • Phaeochromocytoma in pregnancy: Case report and review of the literature
    • Ahlawat S.K., Jain S., Kumari S., Varma S., and Sharma B.K. Phaeochromocytoma in pregnancy: Case report and review of the literature. Obstet Gynecol Surv 54 (1999) 728-737
    • (1999) Obstet Gynecol Surv , vol.54 , pp. 728-737
    • Ahlawat, S.K.1    Jain, S.2    Kumari, S.3    Varma, S.4    Sharma, B.K.5
  • 3
    • 0037139449 scopus 로고    scopus 로고
    • Biochemical diagnosis of pheochromocytoma: Which test is best?
    • Lenders J.W., Pacak K., Walther M.M., et al. Biochemical diagnosis of pheochromocytoma: Which test is best?. JAMA 287 (2002) 1427-1434
    • (2002) JAMA , vol.287 , pp. 1427-1434
    • Lenders, J.W.1    Pacak, K.2    Walther, M.M.3
  • 4
    • 0037046659 scopus 로고    scopus 로고
    • Germ-line mutations in nonsyndromic pheochromocytoma
    • Neumann H.P., Bausch B., McWhinney S.R., et al. 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.1    Bausch, B.2    McWhinney, S.R.3
  • 5
    • 4143105824 scopus 로고    scopus 로고
    • Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations
    • Neumann H.P., Pawlu C., Peczkowska M., et al. 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.1    Pawlu, C.2    Peczkowska, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.