New perspective on maintenance therapies for platinum- sensitive recurrent ovarian cancer in women with germline and somatic mutations in BRCA1 and BRCA2 genes

por Vergote, I, Bours, V, Blaumeiser, B, Baurain, J-F
Publicado 2016

HIDEA syndrome: A new case report highlighting similarities with ROHHAD syndrome

por Harvengt, J., Lumaka, A., Fasquelle, C., Caberg, J. H., Mastouri, M., Janssen, A., Palmeira, L., Bours, V.
Publicado 2023

A next-generation newborn screening pilot study: NGS on dried blood spots detects causal mutations in patients with inherited metabolic diseases

por Boemer, F., Fasquelle, C., d’Otreppe, S., Josse, C., Dideberg, V., Segers, K., Guissard, V., Capraro, V., Debray, FG., Bours, V.
Publicado 2017

Homologous recombination repair deficiency (HRD) testing in newly diagnosed advanced-stage epithelial ovarian cancer: A Belgian expert opinion

por Vergote, I, Denys, H, Altintas, S, Kerger, J, Baurain, J-F, Bours, V, Henry, S, Van de Vijver, K, Lambrechts, D, Gennigens, C
Publicado 2022