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Endocrinology AND Amenorrhea, primary, etiology journal articles from PubMed MEDLINE database

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Gokce C, Atabek EM, Kaynar L, et al. 
Achondroplasia associated with gonadal dysgenesis. [Journal Article]
J Int Med Res 2008 May-Jun; 36(3):605-8.
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Zirilli L, Rochira V, Diazzi C, et al. 
Human models of aromatase deficiency. [JOURNAL ARTICLE]
J Steroid Biochem Mol Biol 2008 Mar 20.
Abstract | Full Citation
Bhangoo A, Aisenberg J, Chartoffe A, et al. 
Novel mutation in cytochrome P450c17 causes complete combined 17alpha-hydroxylase/17,20-lyase deficiency. [Journal Article, Research Support, Non-U.S. Gov't]
J Pediatr Endocrinol Metab 2008 Feb; 21(2):185-90.
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Jarzabek K, Philibert P, Koda M, et al. 
Primary amenorrhea in a young Polish woman with complete androgen insensitivity syndrome and Sertoli-Leydig cell tumor: Identification of a new androgen receptor gene mutation and evidence of aromatase hyperactivity and apoptosis dysregulation within the tumor. [JOURNAL ARTICLE]
Gynecol Endocrinol 2007 Aug 6.:1-6.
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Gianotti L, Lanfranco F, Ramunni J, et al. 
GH/IGF-I axis in anorexia nervosa. [Journal Article, Research Support, Non-U.S. Gov't]
Eat Weight Disord 2002 Jun; 7(2):94-105.
Abstract | Full Citation
Mattle V, Bilgyicildirim A, Hadziomerovic D, et al. 
Polycystic ovarian disease unmasked by pulsatile GnRH therapy in a subgroup of women with hypothalamic amenorrhea. [JOURNAL ARTICLE]
Fertil Steril 2007 Jun 19.
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Paris F, Philibert P, Lumbroso S, et al. 
Primary amenorrhea in a 46,XY adolescent girl with partial gonadal dysgenesis: identification of a new SRY gene mutation. [JOURNAL ARTICLE]
Fertil Steril 2007 May 9.
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Scott EC, Greenberg TS, Arndt S, et al. 
Complete androgen insensitivity syndrome in a black South African family: a clinical and molecular investigation. [Journal Article, Research Support, Non-U.S. Gov't]
Endocr Pract 2006 Nov-Dec; 12(6):664-9.
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Bieniasz J, Zak T, Laskowska-Zietek A, et al. 
[Causes of menstrual disorders in adolescent girls - a retrospective study.] [Journal Article]
Endokrynol Diabetol Chor Przemiany Materii Wieku Rozw 2006; 12(3):205-10.
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Goulis DG, Iliadou PK, Papanikolaou A, et al. 
R831X mutation of the androgen receptor gene in an adolescent with Complete Androgen Insensitivity Syndrome and bilateral testicular hamartomata. [JOURNAL ARTICLE]
Hormones (Athens) 2006 Jul; 5(3):200-204.
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