DELANNOY, P., NECHIFOR - POTORAC, I., & Beckers, A. (2022). Nouveautés dans le diagnostic et la prise en charge des complications en lien avec l'acromégalie. Vaisseaux, Coeur, Poumons, 27 (3), 14-20. |
DELANNOY, P., NECHIFOR - POTORAC, I., & Beckers, A. (2021). Multiple Endocrine Neoplasia Type 1 in Clinical Practice. In Endocrinology. Springer International Publishing. doi:10.1007/978-3-319-89497-3_19 |
Lousberg, L., Collignon, J., Troisfontaine, F., PAULUS, A., VAILLANT, F., DELANNOY, P., Petignot, S., Petrossians, P., Rohmer, V., Jadoul, A., & Beckers, A. (2021). Néoplasies neuroendocrines : une nouvelle ère a l’apogée de la multidisciplinarité ! Revue Médicale de Liège, 76 (5-6), 425-431. |
DELANNOY, P., VRANKEN, L., CAVALIER, E., & VALDES SOCIN, H. G. (2020). Carence en vitamine B12 : diagnostic et prise en charge. Tempo Médical, 24-28. |
DELANNOY, P., GRANDFILS, S., LEBRETHON, M.-C., CHANTRAINE, F., VAN LINTHOUT, C., BECKERS, A., & VALDES SOCIN, H. G. (2019). A series of 9 pregnancies with hyperthyroidism and Graves disease : fetal and maternal follow up. In Abstract book : Annual congress of the Belgian Society of Internal Medicine. |
VALDES SOCIN, H. G., VRANKEN, L., Schoneveld, L., DELANNOY, P., Le Goff, C., Beckers, A., & CAVALIER, E. (2019). Vitamin B12 deficiency prevalence and associated biomarkers in type 2 Diabetes (T2DM) treated with metformin : biochemical assessment in a series of 106 patients. In Endocrine Abstracts - ECE 2019. |
DELANNOY, P., Debray, F.-G., Verloes, A., Beckers, A., & VALDES SOCIN, H. G. (2017). How to recognize Cowden syndrome: A novel PTEN mutation description. Annales d'Endocrinologie. doi:10.1016/j.ando.2017.01.001 |
DELANNOY, P., DEBRAY, F.-G., BECKERS, A., & VALDES SOCIN, H. G. (2014). Cowden Syndrome: a novel PTEN mutation description and how to recognize a not so rare hereditary cancer syndrome. Acta Clinica Belgica, 69 (suppl 3), 16. |