Niet alles wat piept bij kinderen is astma

Frans De Baets , Filomeen Haerynck
Tijdschrift Voor Geneeskunde 65 ( 13) 608 -611

2009
ABPA syndrome (ABPAs) in CF: FEV1 decline, infectious exacerbations and BMI before and after the year of diagnosis (index year), a case control study

Frans De Baets , Filomeen Haerynck , Petra Schelstraete , Sabine Van daele
European Respiratory Journal 44 1966

2014
2011
Malacia, inflammation and bacterial colonisation of the conducting airways in infants with persistent respiratory symptoms

Frans De Baets , Filomeen Haerynck , Petra Schelstraete , Sabine Van Daele
European Respiratory Journal 38 4277

2011
Limbic encephalitis as presentation of a SAP deficiency

Filomeen Haerynck , Rudy Van Coster , Genevieve Laureys , Helene Verhelst
Journal of Neuroimmunology 178 239 -239

2006
A putative tumor suppressor gene involved in Merkel cell carcinoma maps between p58 and D172

Franki Speleman , Nadine Van Roy , ML Geerts , Filomeen Haerynck
Cytogenetic and Genome Research 72 152 -152

1996
A missence mutation in complement factor I associated with recurrent aseptic meningoencephalitis

Filomeen Haerynck , Bart Loeys , F Mascart , J Vande Walle
Pediatric Nephrology 24 ( 9) 1847 -1847

2009
Acquired partial lipodystrophy : a rare clinical presentation of a complement deficiency

Filomeen Haerynck , Johan Vande Walle , Delfien Bogaert , Melissa Dullaers
16th Biennial meeting of the European Society for Immunodeficiencies (ESID) 34

2014
Clinical presentation of hyper-IgE syndrome in a family with impaired IL-22 production and STAT3 phosphorylation

Filomeen Haerynck , Delfien Bogaert , Elfride De Baere , Bart Lambrecht
16th Biennial meeting of the European Society for Immunodeficiencies (ESID) 34

2014
Recurrent cutaneous abscesses as the presenting manifestation of STAT1 gain-of-function mutation

Levi Hoste , Marieke De Bruyne , Delfien Bogaert , Elfride De Baere
17th Biennial meeting of the European Society for Immunodeficiencies (ESID 2016)

2016
The immunophenotypical landscape of patients with primary antibody deficiencies and their asymptomatic first-degree relatives : arguments for a multifactorial aetiology

Delfien Bogaert , Pauline Depuydt , Katleen De Preter , Carolien Bonroy
17th Biennial meeting of the European Society for Immunodeficiencies (ESID 2016)

2016
RC3H1 mutation with increased ICOS expression causes an autoinflammatory syndrome

Patrick Verloo , Filomeen Haerynck , Rudy Van Coster , Maria Bordon Cueto De Braem
17th Biennial meeting of the European Society for Immunodeficiencies (ESID 2016)

2016
A CARD9 Turkisch founder mutation disrupts NF-κB signaling by inhibiting Bcl10 recruitment

Marieke De Bruyne , Levi Hoste , Delfien Bogaert , Mélanie Migaud
Belgian Immunology Society, Annual scientific meeting, Abstracts

2017
2020
A novel STAT1 mutation in a patient with pneumocystis jiroveci and chronic mucocutaneous candidiasis

Karim Vermaelen , Filomeen Haerynck , Bart Lambrecht , Kathleen De Waele
43th Annual Meeting of the Belgian Society of Paediatrics

2015
Congenital defects of phagocytes

Filomeen Haerynck , Delfien Bogaert
Cellular primary immunodeficiencies

2021
Radiosensitivity analysis in patients with a primary immunodeficiency disease

Filomeen Haerynck , Carolien Bonroy , Victoria Bordon , Ans Baeyens
Focused Meeting of the European Society for Immunodeficiencies (ESID 2019)

2019
Assessment of radiation sensitivity in patients with a primary immunodeficiency disease

Filomeen Haerynck , Carolien Bonroy , Ans Baeyens , Stephanie Vermeulen
16th International Congress of Radiation Research (ICRR 2019)

2019
'Every sweet has its sour' : rare skin lesions in a boy with combined immunodeficiency

Delfien Bogaert , Margo Hagendorens , Marieke De Bruyne , Hilde Lapeere
47th Annual Meeting of the Belgian Society of Paediatrics, Abstracts

2019