Achermann JC - Search Results

1

Steroidogenic factor-1 (SF-1) and its relevance to pediatric endocrinology.

de-Souza BF, Lin L, Achermann JC. de-Souza BF, et al. Among authors: achermann jc. Pediatr Endocrinol Rev. 2006 Jun;3(4):359-64. Pediatr Endocrinol Rev. 2006. PMID: 16816804 Review.

2

Gonadal determination and adrenal development are regulated by the orphan nuclear receptor steroidogenic factor-1, in a dose-dependent manner.

Achermann JC, Ozisik G, Ito M, Orun UA, Harmanci K, Gurakan B, Jameson JL. Achermann JC, et al. J Clin Endocrinol Metab. 2002 Apr;87(4):1829-33. doi: 10.1210/jcem.87.4.8376. J Clin Endocrinol Metab. 2002. PMID: 11932325

3

Inherited adrenal hypoplasia: not just for kids!

Lin L, Achermann JC. Lin L, et al. Among authors: achermann jc. Clin Endocrinol (Oxf). 2004 May;60(5):529-37. doi: 10.1111/j.1365-2265.2004.01988.x. Clin Endocrinol (Oxf). 2004. PMID: 15104553 Review. No abstract available.

4

The adrenal.

Lin L, Achermann JC. Lin L, et al. Among authors: achermann jc. Horm Res. 2004;62 Suppl 3:22-9. doi: 10.1159/000080495. Horm Res. 2004. PMID: 15539795 Review.

5

Isolated 17,20-lyase (desmolase) deficiency in a 46,XX female presenting with delayed puberty.

Simsek E, Ozdemir I, Lin L, Achermann JC. Simsek E, et al. Among authors: achermann jc. Fertil Steril. 2005 May;83(5):1548-51. doi: 10.1016/j.fertnstert.2004.11.063. Fertil Steril. 2005. PMID: 15866602 Free article. Review.

6

A novel point mutation in P450c17 (CYP17) causing combined 17alpha-hydroxylase/17,20-lyase deficiency.

Brooke AM, Taylor NF, Shepherd JH, Gore ME, Ahmad T, Lin L, Rumsby G, Papari-Zareei M, Auchus RJ, Achermann JC, Monson JP. Brooke AM, et al. Among authors: achermann jc. J Clin Endocrinol Metab. 2006 Jun;91(6):2428-31. doi: 10.1210/jc.2005-2653. Epub 2006 Mar 28. J Clin Endocrinol Metab. 2006. PMID: 16569739

7

Analysis of DAX1 (NR0B1) and steroidogenic factor-1 (NR5A1) in children and adults with primary adrenal failure: ten years' experience.

Lin L, Gu WX, Ozisik G, To WS, Owen CJ, Jameson JL, Achermann JC. Lin L, et al. Among authors: achermann jc. J Clin Endocrinol Metab. 2006 Aug;91(8):3048-54. doi: 10.1210/jc.2006-0603. Epub 2006 May 9. J Clin Endocrinol Metab. 2006. PMID: 16684822 Free PMC article.

8

Nonclassic congenital lipoid adrenal hyperplasia: a new disorder of the steroidogenic acute regulatory protein with very late presentation and normal male genitalia.

Baker BY, Lin L, Kim CJ, Raza J, Smith CP, Miller WL, Achermann JC. Baker BY, et al. Among authors: achermann jc. J Clin Endocrinol Metab. 2006 Dec;91(12):4781-4785. doi: 10.1210/jc.2006-1565. Epub 2006 Sep 12. J Clin Endocrinol Metab. 2006. PMID: 16968793 Free PMC article.

9

A homozygous R262Q mutation in the gonadotropin-releasing hormone receptor presenting as constitutional delay of growth and puberty with subsequent borderline oligospermia.

Lin L, Conway GS, Hill NR, Dattani MT, Hindmarsh PC, Achermann JC. Lin L, et al. Among authors: achermann jc. J Clin Endocrinol Metab. 2006 Dec;91(12):5117-21. doi: 10.1210/jc.2006-0807. Epub 2006 Sep 12. J Clin Endocrinol Metab. 2006. PMID: 16968799 Free PMC article.

10

Variable phenotypes associated with aromatase (CYP19) insufficiency in humans.

Lin L, Ercan O, Raza J, Burren CP, Creighton SM, Auchus RJ, Dattani MT, Achermann JC. Lin L, et al. Among authors: achermann jc. J Clin Endocrinol Metab. 2007 Mar;92(3):982-90. doi: 10.1210/jc.2006-1181. Epub 2006 Dec 12. J Clin Endocrinol Metab. 2007. PMID: 17164303 Free PMC article.

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