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Volumn 50, Issue 3, 1999, Pages 343-346

No overrepresentation of congenital adrenal hyperplasia in patients with adrenocortical tumours

Author keywords

[No Author keywords available]

Indexed keywords

ADRENALIN; ALDOSTERONE; HYDROCORTISONE; NORADRENALIN; PRASTERONE SULFATE; STEROID 21 MONOOXYGENASE; TESTOSTERONE;

EID: 0032946872     PISSN: 03000664     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2265.1999.00655.x     Document Type: Article
Times cited : (29)

References (18)
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    • (1997) Hormone Research , vol.47 , pp. 279-283
    • Angeli, A.1    Osella, G.2    Ali, A.3    Terzolo, M.4
  • 4
    • 0014326195 scopus 로고
    • On the prevalence of adrenocortical adenomas in an autopsy material in relation to hypertension and diabetes
    • Hedeland, H., Östberg, G. & Hökfelt, B. (1968) On the prevalence of adrenocortical adenomas in an autopsy material in relation to hypertension and diabetes. Acta Medica Scandcinavica, 184, 211-214.
    • (1968) Acta Medica Scandcinavica , vol.184 , pp. 211-214
    • Hedeland, H.1    Östberg, G.2    Hökfelt, B.3
  • 6
    • 0023915848 scopus 로고
    • Evidence for Frequent Gene Conversion in the Steroid 21-Hydroxylase P-450 (C21) gene: Implications for Steroid 21-Hydroxylase Deficiency
    • Higashi, Y.,Tanae, A., Inoue, H. & Fujii-Kuriyaraa, Y. (1988) Evidence for Frequent Gene Conversion in the Steroid 21-Hydroxylase P-450 (C21) Gene: Implications for Steroid 21-Hydroxylase Deficiency. American Journal of Human Genetics, 42, 17-25.
    • (1988) American Journal of Human Genetics , vol.42 , pp. 17-25
    • Higashi, Y.1    Tanae, A.2    Inoue, H.3    Fujii-Kuriyaraa, Y.4
  • 9
    • 0023258576 scopus 로고
    • Molecular and clinical advances in congenital adrenal hyperplasia
    • Miller, W.L. & Levine, L.S. (1987) Molecular and clinical advances in congenital adrenal hyperplasia. Journal of Pediatrics, 111, 1-17.
    • (1987) Journal of Pediatrics , vol.111 , pp. 1-17
    • Miller, W.L.1    Levine, L.S.2
  • 10
    • 0024808985 scopus 로고
    • The molecular genetics of 21-hydroxylase deficiency
    • Miller, W.L. & Morel, Y. (1989) The molecular genetics of 21-hydroxylase deficiency. Annual Review of Genetics, 23, 371-393.
    • (1989) Annual Review of Genetics , vol.23 , pp. 371-393
    • Miller, W.L.1    Morel, Y.2
  • 11
    • 0015336316 scopus 로고
    • Adrenal cortical adenomas and hypertension. A clinical pathologic analysis of 690 cases with matched controls and a review of the literature
    • Russell, R., Masi, A. & Richter, E. (1972) Adrenal cortical adenomas and hypertension. A clinical pathologic analysis of 690 cases with matched controls and a review of the literature. Medicine, 51, 211-225.
    • (1972) Medicine , vol.51 , pp. 211-225
    • Russell, R.1    Masi, A.2    Richter, E.3
  • 13
    • 0023933536 scopus 로고
    • Molecular genetic analysis of nonclassical steroid 21-hydroxylase deficiency associated with HLA-B14, DR1
    • Speiser, P.W., New, M.I. & White, P.C. (1988) Molecular genetic analysis of nonclassical steroid 21-hydroxylase deficiency associated with HLA-B14, DR1. New England Journal of Medicine, 319, 19-23.
    • (1988) New England Journal of Medicine , vol.319 , pp. 19-23
    • Speiser, P.W.1    New, M.I.2    White, P.C.3
  • 14
    • 0027159735 scopus 로고
    • Steroid 21-hydroxylase deficiency: Two additional mutations in salt-wasting disease and rapid screening of disease-causing mutations
    • Wedell, A. & Luthman, H. (1993) Steroid 21-hydroxylase deficiency: two additional mutations in salt-wasting disease and rapid screening of disease-causing mutations. Human Molecular Genetics, 2, 499-504.
    • (1993) Human Molecular Genetics , vol.2 , pp. 499-504
    • Wedell, A.1    Luthman, H.2
  • 15
    • 0028208951 scopus 로고
    • Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: Implications for genetic diagnosis and association with disease manifestation
    • Wedell, A., Thilen, A., Ritzen, E., Stengler, B. & Luthman, H. (1994) Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: implications for genetic diagnosis and association with disease manifestation. Journal of Clinical Endocrinology and Metabolism, 78, 1145-1152.
    • (1994) Journal of Clinical Endocrinology and Metabolism , vol.78 , pp. 1145-1152
    • Wedell, A.1    Thilen, A.2    Ritzen, E.3    Stengler, B.4    Luthman, H.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.