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    Case Reports 1. A Late Presentation of Loeys-Dietz Syndrome: Beware of TGF  Receptor Mutations in Benign Joint Hypermobility by Mehta, P., Holder, S., Fisher, B., Vincent, T., Nadesalingam, K., Maciver, H., Shingler, W., Bakshi, J., Hassan, S., D'Cruz, D., Chan, A., Litwic, A. E., McCrae, F., Seth, R., Nandagudi, A., Jury, E., Isenberg, D., Karjigi, U., Paul, A., Rees, F., O'Dowd, E., Kinnear, W., Johnson, S., Lanyon, P., Stevens, R., Narayan, N., Marguerie, C., Robinson, H., Ffolkes, L., Worsnop, F., Ostlere, L., Kiely, P., Dharmapalaiah, C., Hassan, N., Bharadwaj, A., Skibinska, M., Gendi, N., Davies, E. J., Akil, M., Kilding, R., Ramachandran Nair, J., Walsh, M., Farrar, W., Thompson, R. N., Borukhson, L., McFadyen, C., Singh, D., Rajagopal, V., Chan, A. M. L., Wearn Koh, L., Christie, J. D., Croot, L., Gayed, M., Disney, B., Singhal, S., Grindulis, K., Reynolds, T. D., Conway, K., Williams, D., Quin, J., Dean, G., Churchill, D., Walker-Bone, K. E., Goff, I., Reynolds, G., Grove, M., Patel, P., Lazarus, M. N., Roncaroli, F., Gabriel, C., Kinderlerer, A. R., Nikiphorou, E., Hall, F. C., Bruce, E., Gray, L., Krutikov, M., Wig, S., Bruce, I., D'Agostino, M. A., Wakefield, R., Berner Hammer, H., Vittecoq, O., Galeazzi, M., Balint, P., Filippucci, E., Moller, I., Iagnocco, A., Naredo, E., Ostergaard, M., Gaillez, C., Kerselaers, W., Van Holder, K., Le Bars, M., Stone, M. A., Williams, F., Wolber, L., Karppinen, J., Maatta, J., Thompson, B., Atchia, I.

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