PSY108 - Population Preferences for Rare Diseases in Spain von de Sola-Morales, O, Knebelman, N

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Population Preferences for Rare Diseases in Spain von de Sola-Morales, O, Knebelman, N

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Social Preferences for Rare Diseases in Spain von Reyes, M, Camps, B, Knebelman, N, de Solà-Morales, O

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PSY109 - Social Preferences for Rare Diseases in Spain von Reyes, M, Camps, B, Knebelman, N, de Solà-Morales, O

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Advances and unmet needs in genetic, basic and clinical science in Alport syndrome: report from the 2015 International Workshop on Alport Syndrome von Gross, Oliver, Kashtan, Clifford E, Rheault, Michelle N, Flinter, Frances, Savige, Judith, Miner, Jeffrey H, Torra, Roser, Ars, Elisabet, Deltas, Constantinos, Savva, Isavella, Perin, Laura, Renieri, Alessandra, Ariani, Francesca, Mari, Francesca, Baigent, Colin, Judge, Parminder, Knebelman, Bertrand, Heidet, Laurence, Lagas, Sharon, Blatt, Dave, Ding, Jie, Zhang, Yanqin, Gale, Daniel P, Prunotto, Marco, Xue, Yong, Schachter, Asher D, Morton, Lori C G, Blem, Jacqui, Huang, Michael, Liu, Shiguang, Vallee, Sebastien, Renault, Daniel, Schifter, Julia, Skelding, Jules, Gear, Susie, Friede, Tim, Turner, A Neil, Lennon, Rachel

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L’amylose inflammatoire (AA) de causes multiples existe-t-elle ? À propos de 61 cas issus de la cohorte française de 290 patients avec amylose AA von Delplanque, M., Bourguiba, R., Lea, S., Audard, V., Knebelman, B., Karras, A., Boffa, J.J., Grateau, G., Buob, D., Georgin-Lavialle, S.

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Anaemia in CKD 1-5 von Woodburn, K., Holmes, C., Fong, K.-L., Sloneker, S., Strzemienski, P., Solon, E., Ryckelynck, J.- P., Lang, P., Bataille, P., Choukroun, G., Esnault, V., Knebelman, B., Laville, M., Fellous, M., Legrand, E., Portoles, J., Vega, N. J., Fernandez-Fresnedo, G., Perez, A., Bea, S., Camba, M. J., Leistikow, F., Heidenreich, S., Cases, A., Calls, J., Martinez Castelao, A., Sanchez-Guisande, D., Espinel, E., Carreno, A., Campistol, J. M., Arias, M., Morales, J. M., Pallardo, L., Franco, A., Shestakova, M., Tsubakihara, Y., Bessho, M., Suzuki, M., Correa-Rotter, R., Niihata, K., Tomosugi, N., Uehata, T., Shoji, T., Sonoda, M., Kawabata, H., Sakaguchi, Y., Suzuki, A., Okada, N., Kuragano, T., Shimonaka, Y., Kida, A., Kitamura, R., Furuta, M., Yahiro, M., Otaki, Y., Nisihara, F., Nonoguchi, H., Nakanishi, T., Mircescu, G., Stancu, S., Stanciu, A., Viasu, L., Capusa, C., Petrescu, L., Zugravu, A., Aydin, Z., Gursu, M., Uzun, S., Karadag, S., Tatli, E., Sumnu, A., Doventas, Y., Koldas, M., Ozturk, S., Kazancioglu, R., Malyszko, Y., Levin-Iaina, N., Malyszko, J., Kozminski, P., Koc-Zorawska, E., Mysliwiec, M., Hara, M., Ando, M., Tsuchiya, K., Nitta, K., Mirescu, G., Deray, G., Garneata, L., Goldsmith, D., Gorriz Teruel, J. L., Martin, P. Y., Mitchell, D., Mori, C., Schafer, R., Guerin, A., Addison, J., Bridges, I., Di Giulio, S., Farouk, M., Winearls, C.

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SFP PC-73 – Données clinico-biologiques des patients homozygotes et hétérozygotes mutés pour CYP24A1 von Figueres, M., Allain-Launay, E., Roussey-Kesler, G., Bienaimé, F., Linglart, A., Isidor, B., Knebelman, B., Kury, S., Lambert, A., Nathanson, S., Prier, D., Ryckwaert, A., Souberbielle, J., Kottler, M., Hourmant, M.

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Advances and unmet needs in genetic, basic and clinical science in Alport syndrome : report from the 2015 International Workshop on Alport Syndrome von Gross, Oliver, Kashtan, Clifford E, Rheault, Michelle N, Flinter, Frances, Savige, Judith, Miner, Jeffrey H, Torra Balcells, Roser, Ars, Elisabet, Deltas, Constantinos, Savva, Isavella, Perin, Laura, Renieri, Alessandra, Ariani, Francesca, Mari, Francesca, Baigent, Colin, Judge, Parminder, Knebelman, Bertrand, Heidet, Laurence, Lagas, Sharon, Blatt, Dave, Ding, Jie, Zhang, Yanqin, Gale, Daniel P, Prunotto, Marco, Xue, Yong, Schachter, Asher D, Morton, Lori C. G, Blem, Jacqui, Huang, Michael, Liu, Shiguang, Vallee, Sebastien, Renault, Daniel, Schifter, Julia, Skelding, Jules, Gear, Susie, Friede, Tim, Turner, A. Neil, Lennon, Rachel, Universitat Autònoma de Barcelona

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Advances and unmet needs in genetic, basic and clinical science in Alport syndrome : report from the 2015 International Workshop on Alport Syndrome von Gross, Oliver, Kashtan, Clifford E, Rheault, Michelle N, Flinter, Frances, Savige, Judith, Miner, Jeffrey H, Torra Balcells, Roser, Ars, Elisabet, Deltas, Constantinos, Savva, Isavella, Perin, Laura, Renieri, Alessandra, Ariani, Francesca, Mari, Francesca, Baigent, Colin, Judge, Parminder, Knebelman, Bertrand, Heidet, Laurence, Lagas, Sharon, Blatt, Dave, Ding, Jie, Zhang, Yanqin, Gale, Daniel, Prunotto, Marco, Xue, Yong, Schachter, Asher D, Morton, Lori C. G, Blem, Jacqui, Huang, Michael, Liu, Shiguang, Vallee, Sebastien, Renault, Daniel, Schifter, Julia, Skelding, Jules, Gear, Susie, Friede, Tim, Turner, A. Neil, Lennon, Rachel, Universitat Autònoma de Barcelona

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Mesure échographique du volume rénal au cours de la phase initiale de la polykystose autosomique dominante : comparaison aux mesures tomodensitométriques von Hammoud, S., Tissier, A.-M., Elie, C., Pousset, M., Knebelman, B., Joly, D., Hélénon, O., Correas, J.-M.

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Trigonometry von Knebelman, M. S.

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Classroom Notes von Scholomiti, N. C., Hill, R. G., Poliferno, M. J., Garner, Jackie B., Barrett, Louis C., Firey, W. J., Knebelman, M. S.

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Recent Publications von Knebelman, M. S., Swain, Robert L., Bush, K. A., Sagan, Hans, Feld, J. M., Bradt, R. N., Calloway, Jean M., Arnold, B. H., Good, R. A., Keeping, E. S., Danese, Arthur E., Sanger, Ralph G., Allen, Bess E., Carlton, Virginia, Dekker, David B., Kattsoff, Louis O.

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