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Adrenal Hyperplasia, Congenital journal articles from PubMed MEDLINE database

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Michalakis K, Ilias I 
MEDICAL MANAGEMENT OF ADRENAL DISEASE: A NARRATIVE REVIEW. [JOURNAL ARTICLE]
Endocr Regul 2009; 43(3):127-135.
Abstract | Full Citation
Metherell LA, Naville D, Halaby G, et al. 
Nonclassic lipoid congenital adrenal hyperplasia masquerading as familial glucocorticoid deficiency. [Journal Article, Research Support, Non-U.S. Gov't]
J Clin Endocrinol Metab 2009 Oct; 94(10):3865-71.
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Kleinle S, Lang R, Fischer GF, et al. 
Duplications of the functional CYP21A2 gene are primarily restricted to Q318X alleles: evidence for a founder effect. [Journal Article]
J Clin Endocrinol Metab 2009 Oct; 94(10):3954-8.
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Skinningsrud B, Husebye ES, Gilfillan GD, et al. 
X-linked congenital adrenal hypoplasia with hypogonadotropic hypogonadism caused by an inversion disrupting a conserved noncoding element upstream of the NR0B1 (DAX1) gene. [Journal Article, Research Support, Non-U.S. Gov't]
J Clin Endocrinol Metab 2009 Oct; 94(10):4086-93.
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Khan AH, Aban M, Rameez-ul-Hassan , et al. 
Classic virilizing congenital adrenal hyperplasia presenting late: case series from Pakistan. [Journal Article, Research Support, Non-U.S. Gov't]
J Pak Med Assoc 2009 Sep; 59(9):643-6.
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Camanni D, Zaccara A, Capitanucci ML, et al. 
Bladder after total urogenital mobilization for congenital adrenal hyperplasia and cloaca--does it behave the same? [Journal Article]
J Urol 2009 Oct; 182(4 Suppl):1892-7.
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González R 
Editorial comment. [Comment, Editorial]
J Urol 2009 Oct; 182(4 Suppl):1897; discussion 1897.
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Gonçalves EM, de Lemos-Marini SH, de Mello MP, et al. 
Impairment in anthropometric parameters and body composition in females with classical 21-hydroxylase deficiency. [Journal Article, Research Support, Non-U.S. Gov't]
J Pediatr Endocrinol Metab 2009 Jun; 22(6):519-29.
Abstract | Full Citation
Liivak K, Tillmann V 
24-hour blood pressure profiles in children with congenital adrenal hyperplasia on two different hydrocortisone treatment regimens. [Journal Article]
J Pediatr Endocrinol Metab 2009 Jun; 22(6):511-7.
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Yao F, Qinjie T 
Novel human pathological mutations. Gene symbol: CYP17A1. Disease: 17alpha-hydroxylase/17,20-lyase deficiency. [Journal Article]
Hum Genet 2009 Aug; 126(2):340.
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