Cécile Boulanger
5PUBLICATIONS
42CO-AUTHORS
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Publications (5)
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|Jan 15, 2025
Mutations disrupting the kinase domain of IKKα lead to immunodeficiency and immune dysregulation in humans.Quentin Riller, Boris Sorin, Charline Courteille
|May 04, 2022
Successful use of empagliflozin to treat neutropenia in two G6PC3-deficient children: Impact of a mutation in SGLT5.Cécile Boulanger, Xavier Stephenne, Jennifer Diederich
|Mar 31, 2022
Osteoid osteoma mimicking refractory juvenile arthritis in a pediatric patient.C A Baert, J Shoelinck, C Galant
|Jan 20, 2021
Atypical phenotype? The answer's in the genotype: AGS caused by a novel RNASEH2C variant combined with XLA caused by a BTK deficiency.Cécile Boulanger, Olga Chatzis, Delphine Nolf
|Nov 19, 2019
DNAJB1-PRKACA-positive metastatic fibrolamellar carcinoma with unknown primary in a pediatric patient.Samuel Balbeur, Adeline Dumortier, Julien Mergen
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Frequent Collaborators
1 joint publications
C A Baert
1 joint publications
C Galant
1 joint publications
Samuel Balbeur
1 joint publications
Maelle de Ville de Goyet
1 joint publications
Xavier Stephenne
1 joint publications
Alina Ferster
1 joint publications
Emile Van Schaftingen
1 joint publications
Maria Veiga-da-Cunha
1 joint publications
Quentin Riller
1 joint publications
Boris Sorin
