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simple premature pubarche相关文献:
Premature pubarche, ovarian hyperandrogenism, hyperinsulinism and the polycystic ovary syndrome: from a complex constellation to a simple sequence of prenatal onset.
Ibáñez L, de Zegher F, Potau N.
J Endocrinol Invest. 1998 Oct;21(9):558-66. doi: 10.1007/BF03350781.
PMID:9856410
Mutation detection of CYP21A2 gene in nonclassical congenital adrenal hyperplasia patients with premature pubarche.
Kolahdouz M, Hashemipour M, Khanahmad H, Rabbani B, Salehi M, Rabbani A, Ansari A, Naseri MM.
Adv Biomed Res. 2016 Mar 16;5:33. doi: 10.4103/2277-9175.178794. eCollection 2016.
PMID:27099846
Is anti-Mullerian hormone an indicator of potential polycystic ovary syndrome in prepubertal girls with simple obesity?
Korkmaz Ö, Gökşen D, Özen S, Darcan Ş.
Turk J Pediatr. 2016;58(4):406-412. doi: 10.24953/turkjped.2016.04.010.
PMID:28276214
Adrenarche in Prader-Willi syndrome appears not related to insulin sensitivity and serum adiponectin.
Unanue N, Bazaes R, Iñiguez G, Cortés F, Avila A, Mericq V.
Horm Res. 2007;67(3):152-8. doi: 10.1159/000096742. Epub 2006 Nov 2.
PMID:17085944
Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia.
Dolzan V, Sólyom J, Fekete G, Kovács J, Rakosnikova V, Votava F, Lebl J, Pribilincova Z, Baumgartner-Parzer SM, Riedl S, Waldhauser F, Frisch H, Stopar-Obreza M, Krzisnik C, Battelino T.
Eur J Endocrinol. 2005 Jul;153(1):99-106. doi: 10.1530/eje.1.01944.
PMID:15994751
[Hirsutism and light forms of congenital adrenogenital syndrome with 21- and 11-beta hydroxylase defect].
Zachmann M.
Schweiz Med Wochenschr. 1986 Mar 29;116(13):408-12.
PMID:3486468
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