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 session presented at 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