Show
Sort by
-
Rare skin lesions in a boy with activated phosphoinositide 3-kinase delta syndrome
-
'Every sweet has its sour' : rare skin lesions in a boy with combined immunodeficiency
-
A novel IKAROS haploinsufficiency kindred with unexpectedly late and variable B-cell maturation defects
-
To B or not to B matured : a novel IKAROS haploinsufficiency kindred with unexpectedly late and variable B cell maturation defects
-
To B or not to B matured : a novel IKAROS haploinsufficiency kindred with incomplete penetrance both at clinical and cellular level
-
- Journal Article
- A1
- open access
Early-onset primary antibody deficiency resembling common variable immunodeficiency challenges the diagnosis of Wiedeman-Steiner and Roifman syndromes
-
Early-onset common variable immunodeficiency as a cardinal manifestation challenges the diagnosis of Wiedemann-Steiner and Roifman syndromes
-
When two rare diseases coincide : Kartagener Syndrome and Familial Mediterranean Fever
-
CVID, isolated IgG deficiency and isolated IgG subclass deficiency : clinical features and B cell maturation of the Ghent cohort
(2016) -
JAK2 deficiency as a novel cause of impaired Th17 immunity