Evaluation of vertebral fracture assessment by dual X-ray absorptiometry in a multicenter setting von Fuerst, T, Wu, C, Genant, H. K, von Ingersleben, G, Chen, Y, Johnston, C, Econs, M. J, Binkley, N, Vokes, T. J, Crans, G, Mitlak, B. H

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FGF-23 Is Elevated by Chronic Hyperphosphatemia von Gupta, A., Winer, K., Econs, M. J., Marx, S. J., Collins, M. T.

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Race and sex differences in bone mineral density and geometry at the femur von Peacock, M, Buckwalter, K.A, Persohn, S, Hangartner, T.N, Econs, M.J, Hui, S

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Effect of raloxifene after recombinant teriparatide [hPTH(1–34)] treatment in postmenopausal women with osteoporosis von Adami, S., San Martin, J., Muñoz-Torres, M., Econs, M. J., Xie, L., Dalsky, G. P., McClung, M., Felsenberg, D., Brown, J. P., Brandi, M. L., Sipos, A.

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Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosis von KOLLER, D. L, ECONS, M. J, PEACOCK, M, JOHNSTON, C. C, FOROUD, T, MORIN, P. A, CHRISTIAN, J. C, HUI, S. L, PARRY, P, CURRAN, M. E, RODRIGUEZ, L. A, CONNEALLY, P. M, JOSLYN, G

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MEPE, a New Gene Expressed in Bone Marrow and Tumors Causing Osteomalacia von Rowe, Peter S.N, de Zoysa, Priyal A, Dong, Rong, Wang, Huei Rong, White, Kenneth E, Econs, Michael J, Oudet, Claudine L

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Resolution of severe, adolescent-onset hypophosphatemic rickets following resection of an FGF-23-producing tumour of the distal ulna von Ward, L.M, Rauch, F, White, K.E, Filler, G, Matzinger, M.A, Letts, M, Travers, R, Econs, M.J, Glorieux, F.H

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Autosomal Dominant Hypophosphatemic Rickets/Osteomalacia: Clinical Characterization of a Novel Renal Phosphate-Wasting Disorder von Econs, Michael J, McEnery, Paul T

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Pex Gene Deletions in Gy and Hyp Mice Provide Mouse Models for X-Linked Hypophosphatemia von Strom, Tim M., Francis, Fiona, Lorenz, Bettina, Böddrich, Annett, Lehrach, Hans, Econs, Michael J., Meitinger, Thomas

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Linkage of a QTL Contributing to Normal Variation in Bone Mineral Density to Chromosome 11q12–13 von Koller, D. L., Rodriguez, L. A., Christian, J. C., Slemenda, C. W., Econs, M. J., Hui, S. L., Morin, P., Conneally, P. M., Joslyn, G., Curran, M. E., Peacock, M., Johnston, C. C., Foroud, T.

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Osteoglophonic dysplasia: A 'common' mutation in a rare disease von Sow, AJ, Ramli, R, Latiff, ZA, Ichikawa, S, Gray, AK, Nordin, R, Abd Jabar, MN, Primuharsa Putra, SHA, Siar, CH, Econs, MJ

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Association studies of ALOX5 and bone mineral density in healthy adults von Foroud, T., Ichikawa, S., Koller, D., Lai, D., Curry, L., Xuei, X., Edenberg, H. J., Hui, S., Peacock, M., Econs, M. J.

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Identification of a quantitative trait locus on rat chromosome 4 that is strongly linked to femoral neck structure and strength von Alam, I., Sun, Q., Liu, L., Koller, D.L., Fishburn, T., Carr, L.G., Econs, M.J., Foroud, T., Turner, C.H.

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Polymorphisms in the bone morphogenetic protein 2 (BMP2) gene do not affect bone mineral density in white men or women von ICHIKAWA, S, JOHNSON, M. L, KOLLER, D. L, LAI, D, XUEI, X, EDENBERG, H. J, HUI, S. L, FOROUD, T. M, PEACOCK, M, ECONS, M. J

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Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23 von White, Kenneth E., Carn, Gwenaelle, Lorenz-Depiereux, Bettina, Benet-Pages, Anna, Strom, Tim M., Econs, Michael J.

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New insights into the pathogenesis of inherited phosphate wasting disorders von Econs, M.J.

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Tumor-Induced Osteomalacia -- Unveiling a New Hormone von Econs, Michael J, Drezner, Marc K

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Linkage of Structure at the Proximal Femur to Chromosomes 3, 7, 8, and 19 von Koller, Dl, White, Ke, Liu, G, Hui, Sl, Conneally, Pm, Johnston, Cc, Econs, Mj, Foroud, T, Peacock, M

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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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A PHEX gene mutation is responsible for adult-onset vitamin D-resistant hypophosphatemic osteomalacia : Evidence that the disorder is not a distinct entity from X-linked hypophosph... von ECONS, M. J, FRIEDMAN, N. E, BERGEN, H, ROWE, P. S. N, SPEER, M. C, FRANCIS, F, STROM, T. M, OUDET, C, SMITH, J. A, NINOMIYA, J. T, LEE, B. E

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