The gene for X-linked hypophosphataemic rickets maps to a 200-300 kb region in Xp22.1, and is located on a single YAC containing a putative vitamin D response element (VDRE) von ROWE, P. S. N, GOULDING, J. N, WEISSENBACH, J, FRASER, W, DREZNER, M. K, DAVIES, K. E, O'RIORDAN, J. L. H, FRANCIS, F, OUDET, C, ECONS, M. J, HANAUER, A, LEHRACH, H, READ, A. P, MOUNTFORD, R. C, SUMMERFIELD, T

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Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysis von READ, A. P, THAKKER, R. V, MCGLADE, S, PEACOCK, C. J, SMITH, R, O'RIORDAN, J. L. H, DAVIES, K. E, MOUNTFORD, R. C, BRENTON, D. P, DAVIES, M, GLORIEUX, F, HARRIS, R, HENDY, G. N, KING, A

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Distribution of Mutations in the PEX Gene in Families with X-linked Hypophosphataemic Rickets (HYP) von Rowe, Peter S. N., Oudet, Claudine L., Francis, Fiona, Sinding, Christiane, Pannetier, Solange, Econs, Mike J., Strom, Tim M., Meitinger, Thomas, Garabedian, Michele, David, Albert, Macher, Marie-Alice, Questiaux, Elisabeth, Popowska, Ewa, Pronicka, Ewa, Read, Andrew P., Mokrzycki, Agnes, Glorieux, Francis H., Drezner, Marc K., Hanauer, Andre, Lehrach, Hans, Goulding, Johnathan N., O'Riordan, Jeffrey L. H.

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Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas von Eng, C, Crossey, P A, Mulligan, L M, Healey, C S, Houghton, C, Prowse, A, Chew, S L, Dahia, P L, O'Riordan, J L, Toledo, S P

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Refining the genetic map for the region flanking the X-linked hypophosphataemic rickets locus (Xp22.1-22.2) von ROWE, P. S. N, GOULDING, J, O'RIORDAN, J. L. H, READ, A, LEHRACH, H, FRANCIS, F, HANAUER, A, OUDET, C, BIANCALANA, V, KOOH, S. W, DAVIES, K. E

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Management of hyperparathyroidism in pregnancy von Gelister, J. S. K., Sanderson, J. D., Chapple, C. R., O'Riordan, J. L. H., Cowie, A. G. A., Milroy, E. J. G.

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Effect of Direction and Rate of Change of Calcium on Parathyroid Hormone Secretion in Uraemia von Cunningham, J., Altmann, P., Gleed, Janet H., Butter, K. C., Marsh, F. P., O'Riordan, J. L. H.

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Mutations in the vitamin D receptor gene in three kindreds associated with hereditary vitamin D resistant rickets von COCKERILL, F. J, HAWA, N. S, YOUSAF, N, HEWISON, M, O'RIORDAN, J. L. H, FARROW, S. M

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Vitamin D-dependent rickets type II: extreme end organ resistance to 1,25-dihydroxy vitamin D3 in a patient without alopecia von FRAHER, L. J, KARMALI, R, HINDE, F. R. J, HENDY, G. N, JANI, H, NICHOLSON, L, GRANT, D, O'RIORDAN, J. L. H

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Regulation of calcium absorption by 1,25,dihydroxy-vitamin D--studies of the effects of a bisphosphonate treatment von Adami, S, Frijlink, W B, Bijvoet, O L, O'Riordan, J L, Clemens, T L, Papapoulos, S E

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Association of Parathyroid Tumors in Multiple Endocrine Neoplasia Type 1 with Loss of Alleles on Chromosome 11 von Thakker, Rajesh V, Bouloux, Pierre, Wooding, Carol, Chotai, Kokila, Broad, Peter M, Spurr, Nigel K, Besser, Gordon M, O'Riordan, Jeffrey L.H

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Sir John David Nunes Nabarro   Edoardo Parma   Mary Veronica Porter (nee Burdett-Smith)   Anthony Watson Purdie   Rory Sadler   Norah Patricia Sherlock   Michael Edward Skinner   M... von O'Riordan, J L H, Caimi, V., Burdett-Smith, C B, Burdett-Smith, P, Caplan, H, Bennett, J. D C, Dickson, U., Enoch, P J, Taylor, S., Cash, J., Adams, A. K, Clark, A A

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The Amino-Acid Sequence of the Amino-Terminal 37 Residues of Human Parathyroid Hormone von Niall, H. D., Sauer, R. T., Jacobs, J. W., Keutmann, H. T., Segre, G. V., O'Riordan, J. L. H., Aurbach, G. D., Potts, J. T.

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Gene mapping of mineral metabolic disorders von Thakker, R. V., Davies, K. E., O'Riordan, J. L. H.

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Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies von THAKKER, R. V, DAVIES, K. E, WHYTE, M. P, WOODING, C, O'RIORDAN, J. L. H

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Dendritic cells from human tissues express receptors for the immunoregulatory vitamin D3 metabolite, dihydroxycholecalciferol von BRENNAN, A, KATZ, D. R, NUNN, J. D, BARKER, S, HEWISON, M, FRAHER, L. J, O'RIORDAN, J. L. H

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Translational regulation of parathyroid hormone gene expression and RNA: Protein interactions von Vadher, Shilpa, Hawa, Nigar S., O'Riordan, Jeffrey L. H., Farrow, Sheelagh M.

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Neonatal hyperparathyroidism von DEZATEUX, C. A, HYDE, J. C, HOEY, H. M. C. V, ÓRIORDAN, J. L. H, SPITZ, L, TAYLOR, G. W, GRANT, D. B

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Sir John David Nunes Nabarro von O'Riordan, J. L. H.

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Suppression Of Secondary Hyperparathyroidism In Uraemia: Acute And Chronic Studies von Muirhead, N., Catto, G. R. D., Edward, N., Adami, S., Manning, R. M., O'Riordan, J. L. H.

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