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Volumn 58, Issue 4, 2005, Pages 439-442

Recurrent severe hyperandrogenism during pregnancy: A case report

Author keywords

[No Author keywords available]

Indexed keywords

ANDROGEN; ANDROSTENEDIONE; AROMATASE; ORAL CONTRACEPTIVE AGENT; PRASTERONE SULFATE; SEX HORMONE BINDING GLOBULIN; TESTOSTERONE;

EID: 17144424282     PISSN: 00219746     EISSN: None     Source Type: Journal    
DOI: 10.1136/jcp.2004.018382     Document Type: Article
Times cited : (21)

References (14)
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    • Stillman SC, Evans BAJ, Hughes IA. Aromatase activity in genital skin fibroblasts from normal and androgen-insensitive individuals. J Endocrinol 1990;127:177-83.
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  • 5
    • 0017836471 scopus 로고
    • Differential maternal-fetal response to androgenizing luteoma or hyperreactio luteinalis
    • Hensleigh PA, Woodruff JD. Differential maternal-fetal response to androgenizing luteoma or hyperreactio luteinalis. Obstet Gynecol Surv 1978;33:262-71.
    • (1978) Obstet Gynecol Surv , vol.33 , pp. 262-271
    • Hensleigh, P.A.1    Woodruff, J.D.2
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    • Luteoma of pregnancy: Recurrent or persistent?
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  • 7
    • 0015320809 scopus 로고
    • Bilateral luteomas of pregnancy with virilization. A case report
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    • Thomas, E.1    Mestman, J.2    Henneman, C.3
  • 8
    • 0023621243 scopus 로고
    • Recurrent androgenicity in pregnancy: A case report and literature review
    • Shortle BE, Warren MP, Tsin D. Recurrent androgenicity in pregnancy: a case report and literature review. Obstet Gynecol 1987;70:462-6.
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  • 9
    • 0026441461 scopus 로고
    • Recurrent maternal virilization during pregnancy caused by benign androgen-producing ovarian lesions
    • VanSlooten AJ, Rechner SF, Dodds WG. Recurrent maternal virilization during pregnancy caused by benign androgen-producing ovarian lesions. Am J Obstet Gynecol 1992;167:1342-3.
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    • Steroid studies in a case of ovarian hyperluteinization with virilism in two consecutive pregnancies
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    • Aromatase deficiency in male and female siblings caused by a novel mutation and the physiological role of estrogens
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    • Normal female infants born of mothers with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.