Academic title: Professor
Charge: Head reference lab centre hereditary anaemias - Clinical Chemistry
Link to personal website:
Which is your area of expertise for the "Disease/group of diseases"?
Specify your expertise for the "Disease/group of diseases" (eg SCT, Molecular diagnosis):
Molecular diagnosis, phenotypic diagnosis, genetic counselling.
Alpha- thalassaemia diseases Beta-thalassemia and related diseases Hemoglobinopathy (Other than THAL and SCD) Hereditary elliptocytosis Hereditary spherocytosis Hereditary stomatocytosis Porphyrias Rare constitutional hemolytic anemia due to an enzyme disorder (Other than PKD) Rare constitutional hemolytic anemia due to pyruvate kinase deficiency Sickle cell disease and related diseases
Which is your patient age coverage?
Scientific and Strategic Board member
|English name||Original name||Subnetworks of expertise||Healthcare provider|
|Department of Molecular Genetics||Centre of Human Genetics - ULB https://ulbgenetics.be/||Red blood cell defects, Bone marrow failure||CUB-Hôpital Erasme|
|Brussels Academic Hospital Laboratory||Laboratoire Hospitalier Universitaire de Bruxelles – Universitair Laboratorium Brussel||Myeloid malignancies, Red blood cell defects||CUB-Hôpital Erasme|
|University Laboratory department||LHUB-ULB https://LHUB-ULB.be||Red blood cell defects||CUB-Hôpital Erasme|