A novel mutatioin in the PSTPIP1 gene is associated with an autoinflammatory disease distinct from classical PAPA syndrome

Por Holzinger, D, Austermann, J, Lohse, P, Aksentijevich, I, Holland, S, Gattorno, M, Rodríguez-Gallego, C, Fessatou, S, Isidor, B, Tokio, S, Bernstein, J, Sampson, B, Sunderkoetter, C, Roth, J
Publicado em 2011

PW02-018 - Impact of PSTPIP1 mutaions on clinical phenotype

Por Holzinger, D, Lohse, P, Faßl, S, Austermann, J, Vogl, T, de Jager, W, Holland, S, Gattorno, M, Rodriguez-Gallego, C, Arostegui, J, Fessatou, S, Isidor, B, Ito, K, Epple, H-J, Bernstein, J, Jeng, M, Lionetti, G, Ong, P, Hinze, C, Sampson, B, Sunderkoetter, C, Foell, D, Chae, J, Ombrello, A, Brady, J, Aksentijevich, I, Roth, J
Publicado em 2013

The registry of the German Network for Systemic Scleroderma: frequency of disease subsets and patterns of organ involvement

Por Hunzelmann, N., Genth, E., Krieg, T., Lehmacher, W., Melchers, I., Meurer, M., Moinzadeh, P., Müller-Ladner, U., Pfeiffer, C., Riemekasten, G., Schulze-Lohoff, E., Sunderkoetter, C., Weber, M., Worm, M., Klaus, P., Rubbert, A., Steinbrink, K., Grundt, B., Hein, R., Scharffetter-Kochanek, K., Hinrichs, R., Walker, K., Szeimies, R.-M., Karrer, S., Müller, A., Seitz, C., Schmidt, E., Lehmann, P., Foeldvári, I., Reichenberger, F., Gross, W.L., Kuhn, A., Haust, M., Reich, K., Böhm, M., Saar, P., Fierlbeck, G., Kötter, I., Lorenz, H.-M., Blank, N., Gräfenstein, K., Juche, A., Aberer, E., Bali, G., Fiehn, C., Stadler, R., Bartels, V.
Publicado em 2008