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Acta Gastro-Enterologica Belgica|November 23, 2011
The genetics of familial adenomatous polyposis (FAP) and MutYH-associated polyposis (MAP)Kathleen Claes, Karin Dahan, S Tejpar, et al.The Journal of Cell Biology|June 14, 2024
Dipeptidyl peptidases and E3 ligases of N-degron pathways cooperate to regulate protein stabilityAdi Shimshon, Karin Dahan, Mor Israel-Gueta, et al.Gastroenterology|May 6, 2003
Frequent mutations of hepatocyte nuclear factor 1 in colorectal cancer with microsatellite instabilityPierre Laurent-Puig, Olivier Plomteux, Olivier Bluteau, et al.Kidney International Reports|June 2, 2018
Genotype and Outcome After Kidney Transplantation in Alport SyndromeValentine Gillion, Karin Dahan, Jean-Pierre Cosyns, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 13, 2008
Evaluating PVALB as a candidate gene for SLC12A3-negative cases of Gitelman's syndromeEva Riveira-Munoz, Olivier Devuyst, Hendrica Belge, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 15, 2021
Genetic testing in the diagnosis of chronic kidney disease: recommendations for clinical practiceNine Knoers, Corinne Antignac, Carsten Bergmann, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 26, 2011
Impact of polymorphism of Multidrug Resistance-associated Protein 1 (ABCC1) gene on the severity of cystic fibrosisAndrea Mafficini, Myriam Ortombina, Isabelle Sermet-Gaudelius, et al.Diabetes|February 28, 2003
The focal form of persistent hyperinsulinemic hypoglycemia of infancy: morphological and molecular studies show structural and functional differences with insulinomaChristine Sempoux, Yves Guiot, Karin Dahan, et al.Kidney International|March 5, 2015
Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management--A KDIGO consensus reportKai-Uwe Eckardt, Seth L Alper, Corinne Antignac, et al.Human Mutation|October 28, 2014
An augmented ABCA4 screen targeting noncoding regions reveals a deep intronic founder variant in Belgian Stargardt patientsMiriam Bauwens, Julie De Zaeytijd, Nicole Weisschuh, et al.Pageof 8