Search Results - Helene Verhelst

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    Severe congenital microcephaly with AP4M1 mutation, a case report by Sarah Duerinckx, Helene Verhelst, Camille Perazzolo, Philippe David, Laurence Desmyter, Isabelle Pirson, Marc Abramowicz

    Published 2017
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    Blood transcriptomics to facilitate diagnosis and stratification in pediatric rheumatic diseases - a proof of concept study by My Kieu Ha, Esther Bartholomeus, Luc Van Os, Julie Dandelooy, Julie Leysen, Olivier Aerts, Vasiliki Siozopoulou, Eline De Smet, Jan Gielen, Khadija Guerti, Michel De Maeseneer, Nele Herregods, Bouchra Lechkar, Ruth Wittoek, Elke Geens, Laura Claes, Mahmoud Zaqout, Wendy Dewals, Annelies Lemay, David Tuerlinckx, David Weynants, Koen Vanlede, Gerlant van Berlaer, Marc Raes, Helene Verhelst, Tine Boiy, Pierre Van Damme, Anna C. Jansen, Marije Meuwissen, Vito Sabato, Guy Van Camp, Arvid Suls, Jutte Van der Werff ten Bosch, Joke Dehoorne, Rik Joos, Kris Laukens, Pieter Meysman, Benson Ogunjimi

    Published 2022
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