Publications and communications of Sandrine VAESSEN

Lumaka Zola, A., Fasquelle, C., Debray, F.-G., Alkan, S., Jacquinet, A., Harvengt, J., Boemer, F., Mulder, A., VAESSEN, S., Viellevoye, R., Gonon Rodrigues Palmeira, L., CHARLOTEAUX, B., Brysse, A., BULK, S., Rigo, V., & Bours, V. (16 February 2023). Rapid Whole Genome Sequencing Diagnoses and Guides Treatment in Critically Ill Children in Belgium in Less than 40 Hours. International Journal of Molecular Sciences, 24 (4), 4003. doi:10.3390/ijms24044003

DELBOS, M., Allington, N., VAESSEN, S., & Misson, J.-P. (November 2019). L'image du mois. Tibia arque chez le nouveau-ne. Revue Médicale de Liège, 74 (3), 117-119.

Gillis, N., BEX, A., Bex, V., Tebache, M., Michotte, A., PIETTE, C., VAESSEN, S., Defresne, A., & Lückers, O. (16 March 2019). A simple case of torticollis leads to the diagnosis of an infantile desmoplastic astrocytoma [Poster presentation]. Scientific meeting of Belgian Society of Neurosurgery.

BARREA, C., VAESSEN, S., BULK, S., HARVENGT, J., & Misson, J.-P. (2018). Phenotype-genotype correlation in children with neurofibromatosis type 1. Neuropediatrics. doi:10.1055/s-0037-1620239