Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Willem Roosens"'
Autor:
Willem Roosens, Frederik Staels, Sien Van Loo, Stephanie Humblet-Baron, Isabelle Meyts, Hadewijch De Samblanx, Chris Verslype, Hannah van Malenstein, Schalk van der Merwe, Wim Laleman, Rik Schrijvers
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Common variable immunodeficiency (CVID) associated liver disease is an underrecognized and poorly studied non-infectious complication that lacks an established treatment. We describe a CVID patient with severe multiorgan complications, including non-
Externí odkaz:
https://doaj.org/article/e21d3fdefa9b4e7db721bc3581145977
Autor:
Frederik Staels, Willem Roosens, Simone Giovannozzi, Leen Moens, Jan Bogaert, Cecilia Iglesias-Herrero, Rik Gijsbers, Xavier Bossuyt, Glynis Frans, Adrian Liston, Stephanie Humblet-Baron, Isabelle Meyts, Lucas Van Aelst, Rik Schrijvers
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Autosomal dominant Signal transducer and activator of transcription 1 (STAT1) gain-of-function (GOF) mutations result in an inborn error of immunity characterized by chronic mucocutaneous candidiasis, recurrent viral and bacterial infections, and div
Externí odkaz:
https://doaj.org/article/061572d412a24b048567c236fa13b3dd
Autor:
Willem Roosens, Frederik Staels, Cecilia Iglesias Herrero, Rik Gijsbergs, Leen Moens, Xavier Bossuyt, Jan Bogaert, Isabelle Meyts, Lucas Van Aelst, Rik Schrijvers
Publikováno v:
Clinical Immunology. 250:109417
Autor:
Willem Roosens, Pieter Schellekens, Bert Bammens, Rudi Vennekens, Isabelle Meyts, Djalila Mekahli
Publikováno v:
Pediatric nephrology (Berlin, Germany). 36(11)
Autosomal dominant polycystic kidney disease (ADPKD) is associated with distinct cytopenias in observational studies; the most consistent and strongest association is seen with alternations in the lymphocytic lineages. Although the underlying mechani