Search Results - "Timbaldi, M."

Clinical relevance of hemochromatosis-related HFE C282Y/H63D gene mutations in patients on chronic dialysis by Canavese, C, Bergamo, D, Barbieri, S, Timbaldi, M, Thea, A, Martina, G, Damiani, D, Fenoglio, R, Donati-Marella, B, Priolo, G

“…The actual prevalence and the clinical relevance of gene mutations of HFE (which are linked to hemochromatosis) have not yet been established in patients on…”
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Acid-base / electrolytes / nephrolithiasis by Haller, M., Van Biesen, W., Webster, A. C., Vanholder, R., Nagler, E. V., Lee, J. E., Kim, S. K., Park, S. K., Yun, G. Y., Choi, H. Y., Ha, S.-K., Park, H. C., Hernandez-Sevillano, B., Rodriguez, J. R., Perez del Valle, K., de Lorenzo, A., Salas, P., Bienvenido, M., Sanchez-Heras, M., Basterrechea, M. A., Tallon, S., de Arriba, G., Greenberg, A., Verbalis, J., Burst, V., Haymann, J.-P., Poch, E., Chiodo, J., Vanmassenhove, J., van der Veer, S. N., Nistor, I., Pignataro, A., Alfieri, V., Cesano, G., Timbaldi, M., Torta, E., Boero, R., Haller, M. C., Cucchiari, D., Podesta, M., Merizzoli, E., Angelini, C., Badalamenti, S., Alves, M. T., Moyses, R. M., Jorgetti, V., Heilberg, I., Menon, V., Lhotta, K., Muendlein, A., Meusburger, E., Zitt, E., Bijarnia, R., Pasch, A., Hwang, S. W., Lee, C. H., Kim, G.-H., Leckstrom, D., Pereira, C., Bultitude, M., McGrath, A., Goldsmith, D. J., Vasquez, D., Fernandez, B., Palomo, S., Aller, C., Gordillo, R., Perez, V., Bustamante, J., Coca, A., Vitale, C., Bagnis, C., Tricerri, A., Gallo, L., Dutto, F., Migliardi, M., Marangella, M., Outerelo, C., Figueiredo, P., Freitas, J., Teixeira Costa, F., Ramos, A., Rambod, M., Melikterminas, E., Atallah, H., Saadi, M., Connery, S., Mulla, Z., Tolouian, R., Cristofaro, R., Masola, V., Ceol, M., Priante, G., Familiari, A., Gambaro, G., Anglani, F.

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