El Kheir, A., CALMES, D., Poirrier, A.-L., Harvengt, J., Docampo, E., KUKOR, L., Bricmont, N., & Kempeneers, C. (December 2025). Les soins pour les bronchiectasies et la dyskinésie ciliaire chez l'enfant. Percentile, 30 (6), 12-19. |
Chatelain, C., KUKOR, L., Bailleux, S., Bours, V., Bulk, S., & Docampo Martínez, E. (February 2025). Shprintzen - Goldberg syndrome without intellectual disability: A clinical report and review of literature. European Journal of Medical Genetics, 73, 104985. doi:10.1016/j.ejmg.2024.104985 |
Chatelain, C., KUKOR, L., BULK, S., Bours, V., & Docampo Martínez, E. (12 April 2024). SKI missense variant c.539C>T p.(Thr180Met), a recurrent variant in Shprintzen-Goldberg syndrome: a case report and review of literature [Poster presentation]. Annual Symposium : Single cells, to care or not to care?, Leuven, Belgium. |
KUKOR, L., GESTER, F., Guiot, J., Bours, V., & Docampo Martínez, E. (2024). Genetic counseling of the idiopatic pulmonary fibrosis in the University Hospital of Liège [Poster presentation]. Belgian Society of Human Genetics annual meeting, Leuven, Belgium. |
Kukor, L., BERTOLI, S., CREVECOEUR, J., Bours, V., & BULK, S. (21 April 2022). What does a Genetic Counsellor do in the University Hospital of Liège ? [Poster presentation]. BeSHG/NVHG Annual Genetics Symposium 2022. |
KUKOR, L., BERTOLI, S., Bours, V., BULK, S., & DOCAMPO MARTINEZ, E. (16 February 2018). Ehlers-Danlos syndrome in the University Hospital of Liege [Poster presentation]. Meeting of the Belgian Society for Human Genetics (BeSHG) : "The Epigenome in development and disease", Ghent, Belgium. |