Clark AJL - Search Results

1

Adrenocorticotropin resistance syndromes.

Cooray SN, Chan L, Metherell L, Storr H, Clark AJL. Cooray SN, et al. Among authors: clark ajl. Endocr Dev. 2008;13:99-116. doi: 10.1159/000134828. Endocr Dev. 2008. PMID: 18493136 Review.

2

Adrenocorticotropin receptor gene mutations in familial glucocorticoid deficiency: relationships with clinical features in four families.

Weber A, Toppari J, Harvey RD, Klann RC, Shaw NJ, Ricker AT, Näntö-Salonen K, Bevan JS, Clark AJ. Weber A, et al. J Clin Endocrinol Metab. 1995 Jan;80(1):65-71. doi: 10.1210/jcem.80.1.7829641. J Clin Endocrinol Metab. 1995. PMID: 7829641

3

Familial glucocorticoid deficiency associated with point mutation in the adrenocorticotropin receptor.

Clark AJ, McLoughlin L, Grossman A. Clark AJ, et al. Lancet. 1993 Feb 20;341(8843):461-2. doi: 10.1016/0140-6736(93)90208-x. Lancet. 1993. PMID: 8094489

4

Expression of the mouse ACTH receptor gene and characterisation of its promoter.

Clark AJ, Cammas FM, Kapas S. Clark AJ, et al. Endocr Res. 1996 Nov;22(4):333-5. doi: 10.1080/07435809609043715. Endocr Res. 1996. PMID: 8969880 Review. No abstract available.

5

Familial glucocorticoid deficiency: one syndrome, but more than one gene.

Clark AJ, Cammas FM, Watt A, Kapas S, Weber A. Clark AJ, et al. J Mol Med (Berl). 1997 Jun;75(6):394-9. doi: 10.1007/s001090050124. J Mol Med (Berl). 1997. PMID: 9231879 Review.

6

Adrenocorticotropin insensitivity syndromes.

Clark AJ, Weber A. Clark AJ, et al. Endocr Rev. 1998 Dec;19(6):828-43. doi: 10.1210/edrv.19.6.0351. Endocr Rev. 1998. PMID: 9861547 Review. No abstract available.

7

Functional characterization of naturally occurring mutations of the human adrenocorticotropin receptor: poor correlation of phenotype and genotype.

Elias LL, Huebner A, Pullinger GD, Mirtella A, Clark AJ. Elias LL, et al. J Clin Endocrinol Metab. 1999 Aug;84(8):2766-70. doi: 10.1210/jcem.84.8.5924. J Clin Endocrinol Metab. 1999. PMID: 10443676

8

Tall stature in familial glucocorticoid deficiency.

Elias LL, Huebner A, Metherell LA, Canas A, Warne GL, Bitti ML, Cianfarani S, Clayton PE, Savage MO, Clark AJ. Elias LL, et al. Clin Endocrinol (Oxf). 2000 Oct;53(4):423-30. doi: 10.1046/j.1365-2265.2000.01122.x. Clin Endocrinol (Oxf). 2000. PMID: 11012566

9

The molecular pathogenesis of ACTH insensitivity syndromes.

Clark AJ, Metherell L, Swords FM, Elias LL. Clark AJ, et al. Ann Endocrinol (Paris). 2001 Apr;62(2):207-11. Ann Endocrinol (Paris). 2001. PMID: 11353896 Review.

10

Pseudoexon activation as a novel mechanism for disease resulting in atypical growth-hormone insensitivity.

Metherell LA, Akker SA, Munroe PB, Rose SJ, Caulfield M, Savage MO, Chew SL, Clark AJ. Metherell LA, et al. Am J Hum Genet. 2001 Sep;69(3):641-6. doi: 10.1086/323266. Epub 2001 Jul 20. Am J Hum Genet. 2001. PMID: 11468686 Free PMC article.

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