NLRP3 E311K mutation in a large family with Muckle-Wells syndrome - description of a heterogeneous phenotype and response to treatment

por Kuemmerle-Deschner, Jasmin B, Lohse, Peter, Koetter, Ina, Dannecker, Guenther E, Reess, Fabian, Ummenhofer, Katharina, Koch, Silvia, Tzaribachev, Nikolay, Bialkowski, Anja, Benseler, Susanne M
Publicado 2011

Early detection of sensorineural hearing loss in Muckle-Wells-syndrome

por Kuemmerle-Deschner, Jasmin B., Koitschev, Assen, Tyrrell, Pascal N., Plontke, Stefan K., Deschner, Norbert, Hansmann, Sandra, Ummenhofer, Katharina, Lohse, Peter, Koitschev, Christiane, Benseler, Susanne M.
Publicado 2015

Treatment of Muckle-Wells syndrome: analysis of two IL-1-blocking regimens

por Kuemmerle-Deschner, Jasmin B, Wittkowski, Helmut, Tyrrell, Pascal N, Koetter, Ina, Lohse, Peter, Ummenhofer, Katharina, Reess, Fabian, Hansmann, Sandra, Koitschev, Assen, Deuter, Christoph, Bialkowski, Anja, Foell, Dirk, Benseler, Susanne M
Publicado 2013