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Hormone Research

Volumn 53, Issue 5, 2000, Pages 260-266

Apparent cortisone reductase deficiency: A rare cause of hyperandrogenemia and hypercortisolism

(4) Biason Lauber, Anna a Suter, Stephan L b Shackleton, Cedric H L c Zachmann, Milo a

a UNIVERSITY OF ZURICH (Switzerland)

b Children's Hospital ^*

c CHILDREN S HOSPITAL OAKLAND (United States)

Author keywords

11 Hydroxysteroid dehydrogenase type 1; Adrenal hyperandrogenism; Gas chromatography mass spectrometric steroid profile; Hypercortisolism

Indexed keywords

11BETA HYDROXYSTEROID DEHYDROGENASE; 3ALPHA(OR 20BETA) HYDROXYSTEROID DEHYDROGENASE; ANDROGEN; CONJUGATED ESTROGEN; CYPROTERONE ACETATE; HYDROCORTISONE; HYDROXYPROGESTERONE; PREDNISONE; PREGNANEDIOL; PREGNANETRIOL; SPIRONOLACTONE; TESTOSTERONE; TETRAHYDROCORTISOL; TETRAHYDROCORTISONE;

ADULT; ARTICLE; CASE REPORT; CLINICAL FEATURE; DIAGNOSTIC IMAGING; DIFFERENTIAL DIAGNOSIS; DRUG EFFICACY; ENZYME ACTIVITY; ENZYME DEFICIENCY; FEMALE; HIRSUTISM; HUMAN; HYPERANDROGENISM; HYPERCORTISOLISM; HYPERPLASIA; KIDNEY; LIPID OXIDATION; MALE TYPE ALOPECIA; OVARY TUMOR; PRIORITY JOURNAL; STEROID 21 MONOOXYGENASE DEFICIENCY; STEROID BLOOD LEVEL; STEROID URINE LEVEL; SYMPTOM; TERATOMA; TREATMENT OUTCOME;

EID: 0033679530 PISSN: 03010163 EISSN: None Source Type: Journal
DOI: 10.1159/000023577 Document Type: Article

Times cited : (33)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.