Ectopic hormone productionCLARK, A. J. L.Baillière's clinical endocrinology and metabolism. 1989, Vol 2, Num 4, pp 967-986, issn 0950-351XArticle

Oil pollution of a groundwater source = Pollution par hydrocarbure d'une nappe d'eau souterraineCLARK, A. J. L.Journal of the Institution of Water Engineers and Scientists. 1986, Vol 40, Num 1, pp 17-28, issn 0309-1600Article

TPIT mutations are associated with early-onset, but not late-onset isolated ACTH deficiencyMETHERELL, L. A; SAVAGE, M. O; DATTANI, M et al.European journal of endocrinology. 2004, Vol 151, Num 4, pp 463-465, issn 0804-4643, 3 p.Article

Functional characterization of naturally occurring mutations of the human adrenocorticotropin receptor : Poor correlation of phenotype and genotypeELIAS, L. L. K; HUEBNER, A; PULLINGER, G. D et al.The Journal of clinical endocrinology and metabolism. 1999, Vol 84, Num 8, pp 2766-2770, issn 0021-972XArticle

The broad spectrum of inherited growth hormone insensitivity syndrome growth hormone insensitivity syndromeJOHNSTON, L. B; WOODS, K. A; ROSE, S. J et al.Trends in endocrinology and metabolism. 1998, Vol 9, Num 6, pp 228-232, issn 1043-2760Article

Adrenocorticotropin insensitivity syndromesCLARK, A. J. L; WEBER, A.Endocrine reviews. 1998, Vol 19, Num 6, pp 828-843, issn 0163-769XArticle

Phenotype: Genotype relationships in growth hormone insensitivity syndromeWOODS, K. A; DASTOT, F; PREECE, M. A et al.The Journal of clinical endocrinology and metabolism. 1997, Vol 82, Num 11, pp 3529-3535, issn 0021-972XArticle

Adrenomedullin acts via stimulation of cyclic AMP and not via calcium signalling in vascular cells in cultureBARKER, S; KAPAS, S; CORDER, R et al.Journal of human hypertension. 1996, Vol 10, Num 6, pp 421-423, issn 0950-9240Conference Paper

Molecular cloning of the canine angiotensin II receptor : an AT1-like receptor with reduced affinity for DuP753BURNS, L; CLARK, K. L; BRADLEY, J et al.FEBS letters. 1994, Vol 343, Num 2, pp 146-150, issn 0014-5793Article

d3-GHR genotype does not explain heterogeneity in GH responsiveness in hypopituitary adultsMOYES, V. J; WALKER, D. M; OWUSU-ANTWI, S et al.Clinical endocrinology (Oxford. Print). 2010, Vol 72, Num 6, pp 807-813, issn 0300-0664, 7 p.Article

Clinical features, diagnosis, treatment and molecular studies in paediatric Cushing's syndrome due to primary nodular adrenocortical hyperplasiaSTORR, H. L; MITCHELL, H; GROSSMAN, A. B et al.Clinical endocrinology (Oxford. Print). 2004, Vol 61, Num 5, pp 553-559, issn 0300-0664, 7 p.Article

Exclusion of the adrenocorticotropin (ACTH) receptor (MC2R) locus in some families with ACTH resistance but no mutations of the MC2R coding sequence (familial glucocorticoid deficiency type 2)NAVILLE, D; WEBER, A; GENIN, E et al.The Journal of clinical endocrinology and metabolism. 1998, Vol 83, Num 10, pp 3592-3596, issn 0021-972XArticle

Relations phénotype-génotype dans l'insensibilité à l'hormone de croissance = Phenotype heterogeneity in inherited growth hormone insensitivitySAVANE, M. O; WOODS, K. A; CLARK, A. J. L et al.Archives de pédiatrie (Paris). 1998, Vol 5, pp 364s-370s, issn 0929-693X, SUP4Conference Paper

Adrenocorticotropin receptor gene mutationsin familial glucocorticoid deficiency : rleationships with clinical features in four familiesWEBER, A; TOPPARI, J; HARVEY, R. D et al.The Journal of clinical endocrinology and metabolism. 1995, Vol 80, Num 1, pp 65-71, issn 0021-972XArticle

Mutations of the ACTH receptor gene are only one cause of familial glucocorticoid deficiencyWEBER, A; CLARK, A. J. L.Human molecular genetics (Print). 1994, Vol 3, Num 4, pp 585-588, issn 0964-6906Article

Familial glucocorticoid deficiency associated with point mutation in the adrenocorticotropin receptorCLARK, A. J. L; MCLOUGHLIN, L; GROSSMAN, A et al.Lancet (British edition). 1993, Vol 341, Num 8843, pp 461-462, issn 0140-6736Article

Cloning and expression of a novel angiotensin II receptor subtypeSANDBERG, K; HONG JI; CLARK, A. J. L et al.The Journal of biological chemistry (Print). 1992, Vol 267, Num 14, pp 9455-9458, issn 0021-9258Article

In vitro and in vivo analysis of the processing and fate of the peptide products of the short proopiomelanocortin mRNACLARK, A. J. L; LAVENDER, P. M; COATES, P et al.Molecular endocrinology (Baltimore, Md.). 1990, Vol 4, Num 11, pp 1737-1743, issn 0888-8809, 7 p.Article

Pro-opiomelanocortin mRNA size heterogeneity in ACTH-dependent Cushing's syndromeCLARK, A. J. L; LAVENDER, P. M; BESSER, G. M et al.Journal of molecular endocrinology. 1989, Vol 2, Num 1, pp 3-9, issn 0952-5041, 7 p.Article

The Majority of Adrenocorticotropin Receptor (Melanocortin 2 Receptor) Mutations Found in Familial Glucocorticoid Deficiency Type 1 Lead to Defective Trafficking of the Receptor to the Cell SurfaceCHUNG, T. T; WEBB, T. R; CHAN, L. F et al.The Journal of clinical endocrinology and metabolism. 2008, Vol 93, Num 12, pp 4948-4954, issn 0021-972X, 7 p.Article

Growth hormone (GH) insensitivity syndrome due to a GH receptor truncated after Box1, resulting in isolated failure of STAT 5 signal transductionMILWARD, A; METHERELL, L; WEBB, S. M et al.The Journal of clinical endocrinology and metabolism. 2004, Vol 89, Num 3, pp 1259-1266, issn 0021-972X, 8 p.Article

The molecular pathogenesis of ACTH insensitivity syndromesCLARK, A. J. L; METHERELL, L; SWORDS, F. M et al.Annales d'endocrinologie. 2001, Vol 62, Num 2, pp 207-211, issn 0003-4266Conference Paper

DNA methylation and silencing of gene expressionNEWELL-PRICE, J; CLARK, A. J. L; KING, P et al.Trends in endocrinology and metabolism. 2000, Vol 11, Num 4, pp 142-148, issn 1043-2760Article

Intrauterine growth retardation and postnatal growth failure associated with deletion of the insulin-like growth factor I geneWOODS, K. A; CAMACHO-HÜBNER, C; SAVAGE, M. O et al.The New England journal of medicine. 1996, Vol 335, Num 18, pp 1363-1367, issn 0028-4793Article

Angiotensinogen in human essential hypertensionCAULFIELD, M; LAVENDER, P; NEWELL-PRICE, J et al.Hypertension (Dallas, Tex. 1979). 1996, Vol 28, Num 6, pp 1123-1125, issn 0194-911XConference Paper