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The genes that control calcium homeostasisHENDY, G. N; O'RIORDAN, J. L. H.Clinical endocrinology (Oxford. Print). 1984, Vol 21, Num 4, pp 465-470, issn 0300-0664Article

Gene mapping of mineral metabolic disordersTHAKKER, R. V; DAVIES, K. E; O'RIORDAN, J. L. H et al.Journal of inherited metabolic disease. 1989, Vol 12, Num 1, pp 231-246, issn 0141-8955, 16 p.Article

An investigation of the biological activity of parathyroid hormone in pseudohypoparathyroidism: comparison with vitamin D deficiencyALLGROVE, J; CHAYEN, J; JAYAWEERA, P et al.Clinical endocrinology (Oxford. Print). 1984, Vol 20, Num 5, pp 503-513, issn 0300-0664Article

Binding of 1,25-dihydroxyvitamin D3 receptors to the 5'-flanking region of the bovine parathyroid hormone geneHAWA, N. S; O'RIORDAN, J. L. H; FARROW, S. M et al.Journal of endocrinology. 1994, Vol 142, Num 1, pp 53-60, issn 0022-0795Article

Construction of a high-resolution linkage map for Xp22.1-p22.2 and refinement of the genetic localization of the Coffin-Lowry syndrome geneBIANCALANA, V; TRIVIER, E; WEBER, C et al.Genomics (San Diego, Calif.). 1994, Vol 22, Num 3, pp 617-625, issn 0888-7543Article

New markers for linkage analysis of X-linked hypophosphataemic ricketsROWE, P. S. N; GOULDING, J; O'RIORDAN, J. L. H et al.Human genetics. 1993, Vol 91, Num 6, pp 571-575, issn 0340-6717Article

Three DNA markers for hypophosphataemic ricketsROWE, P. S. N; READ, A. P; MOUNTFORD, R et al.Human genetics. 1992, Vol 89, Num 5, pp 539-542, issn 0340-6717Article

Regulation of human tonsillar T-cell proliferation by the active metabolite of vitamin D3NUNN, J. D; KATZ, D. R; BARKER, S et al.Immunology (Oxford). 1986, Vol 59, Num 4, pp 479-484, issn 0019-2805Article

The effect of hemodialysis, vitamin D metabolites and renal transplantation on the skeletal demineralization associated with renal osteodystrophy: a computerized histomorphometric analysisMAIN, J; VELASCO, N; CATTO, G. R. D et al.Clinical nephrology. 1986, Vol 26, Num 6, pp 279-287, issn 0301-0430Article

Distribution of mutations in the PEX gene in families with X-linked hypophosphataemic rickets (HYP)ROWE, P. S. N; OUDET, C. L; MACHER, M.-A et al.Human molecular genetics (Print). 1997, Vol 6, Num 4, pp 539-549, issn 0964-6906Article

Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomasENG, C; CROSSEY, P. A; SMITH, D. P et al.Journal of medical genetics. 1995, Vol 32, Num 12, pp 934-937, issn 0022-2593Article

Binding of the receptor for 1,25-dihydroxyvitamin D3 to the 5'-flanking region of the bovine parathyroid hormone geneFARROW, S. M; HAWA, N. S; KARMALI, R et al.Journal of endocrinology. 1990, Vol 126, Num 3, pp 355-359, issn 0022-0795, 7 p.Article

Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studiesTHAKKER, R. V; DAVIES, K. E; WHYTE, M. P et al.The Journal of clinical investigation. 1990, Vol 86, Num 1, pp 40-45, issn 0021-9738Article

Effect of direction and rate of change of calcium on parathyroid hormone secretion in uraemiaCUNNINGHAM, J; ALTMANN, P; GLEED, J. H et al.Nephrology, dialysis, transplantation (Print). 1989, Vol 4, Num 5, pp 339-344, issn 0931-0509Article

Controlled trial of calcitriol in hemodialysis patientsBAKER, L. R. I; MUIR, J. W; HATTERSLEY, L. A et al.Clinical nephrology. 1986, Vol 26, Num 4, pp 185-191, issn 0301-0430Article

Hypomagnesaemia: studies of parathyroid hormone secretion and functionALLGROVE, J; ADAMI, S; FRAHER, L et al.Clinical endocrinology (Oxford. Print). 1984, Vol 21, Num 4, pp 435-449, issn 0300-0664Article

Identification of a novel mutation in hereditary vitamin D resistant rickets causing exons skippingHAWA, N. S; COCKERILL, F. J; VADHER, S et al.Clinical endocrinology (Oxford. Print). 1996, Vol 45, Num 1, pp 85-92, issn 0300-0664Article

A YAC contig spanning the hypophosphatemic rickets disease gene (HYP) candidate regionFRANCIS, F; ROWE, P. S. N; ECONS, M. J et al.Genomics (San Diego, Calif.). 1994, Vol 21, Num 1, pp 229-237, issn 0888-7543Article

Tissue resistance to 1,25-dihydroxyvitamin D without a mutation of the vitamin D receptor geneHEWISON, M; RUT, A. R; KRISTJANSSON, K et al.Clinical endocrinology (Oxford. Print). 1993, Vol 39, Num 6, pp 663-670, issn 0300-0664Article

Early regulation of C-myc mRNA by 1,25-dihydroxyvitamin D3 in human myelomonocytic U937 cellsKARMALI, R; BHALLA, A. K; FARROW, S. M et al.Journal of molecular endocrinology. 1989, Vol 3, Num 1, pp 43-48, issn 0952-5041, 6 p.Article

Autocrine regulation of 1,25-dihydroxycholecalciferol metabolism in myelomonocytic cellsHEWISON, M; BARKER, S; BRENNAN, A et al.Immunology (Oxford). 1989, Vol 68, Num 2, pp 247-252, issn 0019-2805Article

Effects of 1,25-dihydroxyvitamin D3 and cortisol on bovine and human parathyroid cellsKARMALI, R; FARROW, S; HEWISON, M et al.Journal of endocrinology. 1989, Vol 123, Num 1, pp 137-142, issn 0022-0795Article

Evidence for extrarenal metabolism of 25-hydroxyvitamin D3 in manFRAHER, L. J; ADAMI, S; PAPAPOULOS, S. E et al.Clinical science (1979). 1986, Vol 71, Num 1, pp 89-95, issn 0143-5221Article

Comparison of intravenous (3-amino-1-hydroxypropylidene)-1, 1-biphosphonate and volume repletion in tumour-induced hypercalcemia = Comparaison entre le (3-amino-1-hydroxypropylidène)-1 et le 1-bisphosphonate en I-V et la diminution de l'importance de l'hypercalcémie induite par les tumeursSLEEBOOM, H. P; BIJUDET, O. L. M; VAN OOSTEROM, A. T et al.Lancet (British edition). 1983, Num 8344, pp 239-243, issn 0140-6736Article

Mutations in the vitamin D receptor gene in three kindreds associated with hereditary vitamin D resistant ricketsCOCKERILL, F. J; HAWA, N. S; YOUSAF, N et al.The Journal of clinical endocrinology and metabolism. 1997, Vol 82, Num 9, pp 3156-3160, issn 0021-972XArticle

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