068061/Wellcome Trust/United Kingdom[Grant Number] - Search Results

Year	Number of Results
2003	1
2004	4
2005	5
2006	5
2007	2
2022	0

1

The adrenal.

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

2

The role of SF1/DAX1 in adrenal and reproductive function.

Achermann JC. Achermann JC. Ann Endocrinol (Paris). 2005 Jun;66(3):233-9. doi: 10.1016/s0003-4266(05)81755-x. Ann Endocrinol (Paris). 2005. PMID: 15988384 Review. No abstract available.

3

SF1 in the development of the adrenal gland and gonads.

Ozisik G, Achermann JC, Meeks JJ, Jameson JL. Ozisik G, et al. Horm Res. 2003;59 Suppl 1:94-8. doi: 10.1159/000067831. Horm Res. 2003. PMID: 12566727 Review.

4

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. Fertil Steril. 2005 May;83(5):1548-51. doi: 10.1016/j.fertnstert.2004.11.063. Fertil Steril. 2005. PMID: 15866602 Review.

5

Inherited adrenal hypoplasia: not just for kids!

Lin L, Achermann JC. Lin L, et al. 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.

6

IMAGe association and congenital adrenal hypoplasia: no disease-causing mutations found in the ACD gene.

Hutz JE, Krause AS, Achermann JC, Vilain E, Tauber M, Lecointre C, McCabe ER, Hammer GD, Keegan CE. Hutz JE, et al. Mol Genet Metab. 2006 May;88(1):66-70. doi: 10.1016/j.ymgme.2006.01.006. Epub 2006 Feb 28. Mol Genet Metab. 2006. PMID: 16504561

7

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. 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.

8

Homozygous disruption of P450 side-chain cleavage (CYP11A1) is associated with prematurity, complete 46,XY sex reversal, and severe adrenal failure.

Hiort O, Holterhus PM, Werner R, Marschke C, Hoppe U, Partsch CJ, Riepe FG, Achermann JC, Struve D. Hiort O, et al. J Clin Endocrinol Metab. 2005 Jan;90(1):538-41. doi: 10.1210/jc.2004-1059. Epub 2004 Oct 26. J Clin Endocrinol Metab. 2005. PMID: 15507506

9

Two novel missense mutations in g protein-coupled receptor 54 in a patient with hypogonadotropic hypogonadism.

Semple RK, Achermann JC, Ellery J, Farooqi IS, Karet FE, Stanhope RG, O'rahilly S, Aparicio SA. Semple RK, et al. J Clin Endocrinol Metab. 2005 Mar;90(3):1849-55. doi: 10.1210/jc.2004-1418. Epub 2004 Dec 14. J Clin Endocrinol Metab. 2005. PMID: 15598687 Free article.

10

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. 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.

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