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Volumn 76, Issue 1, 1998, Pages 28-31

Syndrome of alopecia totalis and 17b-hydroxysteroid dehydrogenase deficiency

Author keywords

17bHSD deficiency; Alopecia; Hypogonadism

Indexed keywords

ANDROSTENEDIONE; CHORIONIC GONADOTROPIN; CORTICOTROPIN; HYDROCORTISONE; HYDROXYPROGESTERONE; PRASTERONE SULFATE; PROGESTERONE; TESTOSTERONE; TESTOSTERONE 17BETA DEHYDROGENASE;

EID: 0032567903     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980226)76:1<28::AID-AJMG4>3.0.CO;2-L     Document Type: Article
Times cited : (2)

References (10)
  • 2
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    • (1973) J Pediatr , vol.82 , pp. 461-465
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  • 3
    • 0024578576 scopus 로고
    • The nature of the defect in male pseudohermaphroiditism in Arabs of Gaza
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  • 5
    • 0022447457 scopus 로고
    • Male pseudohermaphroditism due to 17b-hydroxysteroid dehydrogenase deficiency: Gender reassignment in early infancy
    • Gross D, Kohn G, Farkas A, Landau H, Elrayyes E, El-Shawwa R, Lasch EE, Rösler A (1986): Male pseudohermaphroditism due to 17b-hydroxysteroid dehydrogenase deficiency: Gender reassignment in early infancy. Acta Endocrinol 112:238-246.
    • (1986) Acta Endocrinol , vol.112 , pp. 238-246
    • Gross, D.1    Kohn, G.2    Farkas, A.3    Landau, H.4    Elrayyes, E.5    El-Shawwa, R.6    Lasch, E.E.7    Rösler, A.8
  • 6
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    • Normative data for adrenal steroidogenesis in a healthy pediatric population: Age- and sex-related changes after adrenocorticotropin stimulation
    • Lashansky G, Saenger P, Fishman K, Gautier T, Mayes D, Berg G, DiMaritino-Nardi J, Reiter E (1991): Normative data for adrenal steroidogenesis in a healthy pediatric population: Age- and sex-related changes after adrenocorticotropin stimulation. J Clin Endocrinol Metab 73:674-686.
    • (1991) J Clin Endocrinol Metab , vol.73 , pp. 674-686
    • Lashansky, G.1    Saenger, P.2    Fishman, K.3    Gautier, T.4    Mayes, D.5    Berg, G.6    Dimaritino-Nardi, J.7    Reiter, E.8
  • 7
    • 0027097126 scopus 로고
    • Steroid 17b-hydroxysteroid dehydrogenase deficiency in man: An inherited form of male pseudohermaphroditism
    • Rösler A (1992): Steroid 17b-hydroxysteroid dehydrogenase deficiency in man: An inherited form of male pseudohermaphroditism. J Steroid Biochem Molec Biol 43:989-1002.
    • (1992) J Steroid Biochem Molec Biol , vol.43 , pp. 989-1002
    • Rösler, A.1
  • 8
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    • Male pseudohermaphroditism due to 17b-hydroxysteroid dehydrogenase deficiency: Studies on the natural history of the defect and effect of androgens on gender role
    • Rösler A, Kohn G (1983): Male pseudohermaphroditism due to 17b-hydroxysteroid dehydrogenase deficiency: Studies on the natural history of the defect and effect of androgens on gender role. J Steroid Biochem 19:663-674.
    • (1983) J Steroid Biochem , vol.19 , pp. 663-674
    • Rösler, A.1    Kohn, G.2
  • 9
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    • A (R80Q) mutation in 17b-hydroxysteroid dehydrogenase type 3 gene among Arabs of Israel is associated with pseudohermaphroditism in males and normal asymptomatic females
    • Rösler A, Silverstein S, Abeliovich D (1996): A (R80Q) mutation in 17b-hydroxysteroid dehydrogenase type 3 gene among Arabs of Israel is associated with pseudohermaphroditism in males and normal asymptomatic females. J Clin Endoctrinol Metab 81:1827-1831.
    • (1996) J Clin Endoctrinol Metab , vol.81 , pp. 1827-1831
    • Rösler, A.1    Silverstein, S.2    Abeliovich, D.3
  • 10
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    • Woodhouse NJY, Sakati NA (1983): A syndrome of hypogonadism, alopecia, diabetes mellitus, mental retardation, deafness, and ECG abnormalities. J Med Genet 20:216-219.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.