Articles dans des revues avec comité de lecture (148)
142.
Gerard, C., Lefort, A., Abramowicz, M., Libert, F., & Christophe, D. (1989). Transcriptional regulation of thyroglobulin and thyroperoxydase genes by cAMP: evidence for distinct mechanisms. Annales d'Endocrinologie, 50, 164.143.
Reuse, C., Leeman, M., Degaute, J.-P., Abramowicz, M., Prost, J.-F., & Naeije, R. (1988). Preserved renal perfusion during beta blockade by tertatolol with and without cyclooxygenase inhibition in normal humans. Journal of clinical pharmacology, 28(4), 312-316. doi:10.1002/j.1552-4604.1988.tb03149.x144.
Degaute, J.-P., Naeije, R., Abramowicz, M., Leeman, M., Schoutens, A., & Prost, J.-F. (1988). Acute effects of tertatolol and nadolol on systemic and renal hemodynamics in patients with essential hypertension. American journal of hypertension, 1(3 III), 263S-268S.145.
Sobolski, J., Kornitzer, M., De Backer, G., Dramaix Wilmet, M., Abramowicz, M., Degré, S., & Denolin, H. (1987). Protection against ischemic heart disease in the Belgian physical fitness study: physical fitness rather than physical activity? American journal of epidemiology, 125, 601-610.148.
Goldman, M., Kinnaert, P., Fuss, M., Abramowicz, M., Van Geertruyden, J., & Toussaint, C. (1986). Parathyroid adenoma causing persistent hypercalcaemia after rhabdomyolysis-induced acute renal failure. Nephrology, dialysis, transplantation, 1(1), 50-52. Communications publiées lors de congrès ou colloques nationaux et internationaux (1)
Rapports de recherche, comptes rendus, lettres à l'éditeur, working papers (3)
1.
Massart, A., Ghisdal, L., Viklicky, O., Naesens, M., Abramowicz, D., & Abramowicz, M. (2018). Reply to Hernandez et al. - GWAS of acute renal graft rejection. American Journal of Transplantation, 18(8), 2098-2099. doi:10.1111/ajt.14877 Participations à des congrès et colloques internationaux (21)
1.
Remiche, G., Abramowicz, M., Sternberg, D., Baudin, P., Buon, C., Praline, J., Aure, K., & Nicole, S. (2017). Trifunctional protein beta subunit (HADHB) mutations associated with periodic paralysis phenotype. Neuromuscular disorders,(27), P.228.