Enzyme Replacement Therapy Prevents Dental Defects in a Model of Hypophosphatasia von McKee, M.D., Nakano, Y., Masica, D.L., Gray, J.J., Lemire, I., Heft, R., Whyte, M.P., Crine, P., Millán, J.L.

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Periodontal Defects in the A116T Knock-in Murine Model of Odontohypophosphatasia von Foster, B.L., Sheen, C.R., Hatch, N.E., Liu, J., Cory, E., Narisawa, S., Kiffer-Moreira, T., Sah, R.L., Whyte, M.P., Somerman, M.J., Millán, J.L.

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Hypophosphatasia von Whyte, M.P

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Cementum and Dentin in Hypophosphatasia von van den Bos, T., Handoko, G., Niehof, A., Ryan, L.M., Coburn, S.P., Whyte, M.P., Beertsen, W.

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Enzyme replacement therapy (ENB-0040) in hypophosphatasia improves functional outcome and decreases TNSALP substrates in adolescents and adults von Whyte, M.P, Greenberg, C.R, Kishnani, P, Madson, K, Mhanni, A, Weber, T.J, Mack, K, Reeves, A, Plotkin, H, Kreher, N.C, Landy, H

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Enzyme replacement therapy (ERT) for murine hypophosphatasia von Millan, J.L, Lemire, I, Narisawa, S, Loisel, T.P, Boileau, G, Leonard, P, McKee, M.D, Crine, P, Whyte, M.P

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ENB-0040, a bone-targeted human recombinant tissue nonspecific alkaline phosphatase (TNSALP) fusion protein, in the treatment of infants and adults with hypophosphatasia von Whyte, M.P, Landy, H, Edgar, T, Weber, T, Kishnani, P, Wenkert, D, McAlister, W.H, Bauer, M.L, Van Sickle, B.J, Salman, N, Hamdan, M, Rockman-Greenberg, C

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Distinct OI phenotype caused by COL1 C-proteinase site mutations von Barnes, A.M, Lindahl, K, Whyte, M.P, Hefferan, T, Rubin, C, Kindmark, A, McAlister, W, Mumm, S, Ljunggren, O, Marini, J.C

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X-linked hypophosphatemia: Normal renal function despite medullary nephrocalcinosis 25 years after transient vitamin D2-Induced renal azotemia von EDDY, M. C, MCALISTER, W. H, WHYTE, M. P

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A Missense Mutation in the Human Liver/Bone/Kidney Alkaline Phosphatase Gene Causing a Lethal Form of Hypophosphatasia von Weiss, Mitchell J., David E. C. Cole, Ray, Kunal, Whyte, Michael P., Lafferty, Mary Ann, Mulivor, Richard A., Harris, Harry

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Rhumatologie - Une nouvelle approche thérapeutique de l’ostéoporose von Mc Clung, M.R., Whyte, M.P.

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Asfotase alfa for infants and young children with hypophosphatasia: 7 year outcomes of a single-arm, open-label, phase 2 extension trial von Whyte, M.P, Simmons, J.H, Moseley, S, Fujita, K.P, Bishop, N, Salman, N.J, Taylor, J, Phillips, D, McGinn, M, McAlister, W.H

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X-linked hypophosphatemia: Normal renal function despite medullary nephrocalcinosis 25 years after transient vitamin D 2-induced renal azotemia von Eddy, M.C., McAlister, W.H., Whyte, M.P.

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New markers for linkage analysis of X-linked hypophosphataemic rickets von ROWE, P. S. N, GOULDING, J, O'RIORDAN, J. L. H, READ, A, MOUNTFORD, R, HANAUER, A, OUDET, C, WHYTE, M. P, MEIER-EWERT, S, LEHRACH, H, DAVIES, K. E

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Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families von Thakker, R.V., Davies, K.E., Read, A.P., Tippett, P., Wooding, C., Flint, T., Woob, S., Kruse, T.A., Whyte, M.P., O'Riordan, J.L.H.

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Normal activity of nucleoside triphosphate pyrophosphatase in fibroblasts derived from patients with infantile hypophosphatasia von Caswell, A.M., Whyte, M.P., Russell, R.G.G.

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Assessment of calcitriol and inorganic phosphate therapy before cure of oncogenous osteomalacia by resection of a mixed mesenchymal tumor von Taylor, H.C., Santa-Cruz, D., Teitelbaum, S.L., Bergfeld, M.A., Whyte, M.P.

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Intermittent radiographic changes of rickets without defective trabecular bone mineralization in a case of spondylometaphyseal dysplasia von Kim, G.S., McAlister, W.H., Whyte, M.P.

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OLD SCOTTISH BALLAD, “LOGIE O' BUCHAN” von Bayne, Thomas

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