Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Samuel Dembi Samba"'
Autor:
Tatjana Welzel, Samuel Dembi Samba, Johannes N. van den Anker, Reinhild Klein, Jasmin B Kuemmerle-Deschner
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 605, p 605 (2021)
Journal of Clinical Medicine
Volume 10
Issue 4
Journal of Clinical Medicine
Volume 10
Issue 4
COVID-19 disease increases interleukin (IL)-1β release. Anti-IL-1-treatment is effective in IL-1-mediated autoinflammatory diseases (AID). This case series presents COVID-19 in patients with IL-1-mediated and unclassified AID with immunosuppressive
Autor:
Ilias Tsiflikas, Susanne Schlipf, Xiao Liu, Samuel Dembi Samba, Tatjana Welzel, Alexander N.R. Weber, Sandra Hansmann, Jasmin B Kuemmerle-Deschner, Susanne M. Benseler, Konstanze Hoertnagel, Andreas Griesinger, Anton Hospach
Publikováno v:
Rheumatology (Oxford, England). 59(11)
Objective To report a chronic recurrent multifocal osteomyelitis (CRMO)-like clinical phenotype with multisystem inflammation associated with a novel gene variant in the spectrum of IL-1-mediated diseases. Methods A 3-year-old boy presented with recu
Autor:
Susanne M. Benseler, Norbert Deschner, Samuel Dembi Samba, Isabelle Marie, Pascal N. Tyrrell, Isabelle Koné-Paut, Jasmin B Kuemmerle-Deschner
Publikováno v:
Arthritis Care & Research. 66:765-772
Objective The diagnosis of Muckle-Wells syndrome (MWS) remains challenging due to the clinical heterogeneity and lack of diagnostic criteria. The aims of this study were to describe key elements of the diagnostic evaluation process in MWS and compare
Autor:
Jasmin B, Kuemmerle-Deschner, Samuel, Dembi Samba, Pascal N, Tyrrell, Isabelle, Koné-Paut, Isabelle, Marie, Norbert, Deschner, Susanne M, Benseler
Publikováno v:
Arthritis careresearch. 66(5)
The diagnosis of Muckle-Wells syndrome (MWS) remains challenging due to the clinical heterogeneity and lack of diagnostic criteria. The aims of this study were to describe key elements of the diagnostic evaluation process in MWS and compare identifie
Autor:
Susanne M. Benseler, Isabelle Marie, Theodoros Xenitidis, Sandra Hansmann, Samuel Dembi Samba, Isabelle Koné-Paut, Jasmin B Kuemmerle-Deschner, Katharina Gramlich
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 10, Iss Suppl 1, p A88 (2012)
Pediatric Rheumatology Online Journal
Pediatric Rheumatology Online Journal
Purpose Muckle-Wells syndrome (MWS) is a rare inherited autoinflammatory disease. Patients may present with fever, rash, arthralgia, or conjunctivitis. Effective treatment of MWS has become available with the advance of IL-1 inhibition preventing dis