  | Schellekens, P., Verjans, M., Janssens, P., Dachy, A., De Rechter, S., Breysem, L., Allegaert, K., Bammens, B., Vennekens, R., Vermeersch, P., Pottel, H., & Mekahli, D. (September 2023). Low agreement between various eGFR formulae in pediatric and young adult ADPKD patients. Pediatric Nephrology, 38 (9), 3043 - 3053. doi:10.1007/s00467-023-05926-w  Peer Reviewed verified by ORBi |
 | Dachy, A., Van Loo, L., & Mekahli, D. (May 2023). Autosomal Dominant Polycystic Kidney Disease in Children and Adolescents: Assessing and Managing Risk of Progression. Advances in Kidney Disease and Health, 30 (3), 236 - 244. doi:10.1053/j.akdh.2023.01.007 Peer reviewed |
 | De Groof, J., Dachy, A., Breysem, L., & Mekahli, D. (May 2023). Cystic kidney diseases in children. Archives de Pédiatrie, 30 (4), 240 - 246. doi:10.1016/j.arcped.2023.02.005 Peer Reviewed verified by ORBi |
 | Breysem, L., De Keyzer, F., Schellekens, P., Dachy, A., De Rechter, S., Janssens, P., Vennekens, R., Bammens, B., Irazabal, M. V., Van Ongeval, C., Harris, P. C., Mekahli, D., & CRISP Consortium. (17 February 2023). Risk Severity Model for Pediatric Autosomal Dominant Polycystic Kidney Disease Using 3D Ultrasound Volumetry. Clinical Journal of the American Society of Nephrology, 18 (5), 581-591. doi:10.2215/CJN.0000000000000122 Peer Reviewed verified by ORBi |
 | Dachy, A., Decuypere, J.-P., Vennekens, R., Jouret, F., & Mekahli, D. (September 2022). Correction to: Is autosomal dominant polycystic kidney disease an early sweet disease? Pediatric Nephrology, 37 (9), 2223-2224. doi:10.1007/s00467-022-05624-z Editorial reviewed |
 | Tusseau, M., Lovšin, E., Samaille, C., Pescarmona, R., Mathieu, A.-L., Maggio, M.-C., Selmanović, V., Debeljak, M., Dachy, A., Novljan, G., Janin, A., Januel, L., Gibier, J.-B., Chopin, E., Rouvet, I., Goncalves, D., Fabien, N., Rice, G. I., Lesca, G., ... Belot, A. (August 2022). DNASE1L3 deficiency, new phenotypes, and evidence for a transient type I IFN signaling. Journal of Clinical Immunology, 42 (6), 1310-1320. doi:10.1007/s10875-022-01287-5 Peer Reviewed verified by ORBi |
  | Dachy, A., Decuypère, J.-P., Vennekens, R., Jouret, F., & mekahli, D. (2022). Is autosomal dominant polycystic kidney disease an early sweet disease? Pediatric Nephrology. doi:10.1007/s00467-021-05406-z Peer Reviewed verified by ORBi |
DACHY, A., De Rechter, S., L.M, G.-W., A.J., M., Tess, H., Detlef, B., Franz, S., Max Christophe, L., Djalila, M., & on behalf of the ADPedKD consortium. (16 September 2021). ADPedKD: A global online platform to explore the childhood phenotype of Autosomal Dominant Polycystic Kidney Disease [Poster presentation]. European Society of Pediatric Nephrology, 53rd Congress, 2021. |
DACHY, A., De Rechter, S., L.M, G.-W., Andrew.J., M., Tess, H., Detlef, B., Franz, S., Max. C., L., & Djalila, M. (05 June 2021). ADPedKD: A global online platform to explore the childhood phenotype of Autosomal Dominant Polycystic Kidney Disease [Paper presentation]. 58th ERA-EDTA Congress. |
DACHY, A., De Rechter, S., Djalila, M., & On behalf of the AdPedKD consortium. (27 May 2021). ADPedKD: A global online platform to explore the childhood phenotype of Autosomal Dominant Polycystic Kidney Disease [Paper presentation]. Annual Meeting of the Belgian Society of Nephrology 2021. |
DACHY, A., DE RECHTER, S., Guay-Woodford, L. M., Mallet, A., Harris, T., Bockenhauer, D., Schaefer, F., Liebau, M., & Mekahli, D. (18 March 2021). ADPedKD: A global online platform to explore the childhood phenotype of Autosomal Dominant Polycystic Kidney Disease [Paper presentation]. 49e congrès annuel de la Société Belge de Pédiatrie. |
DACHY, A., De Rechter, S., Mekahli, D., & on behalf of the ADPedKD consortium. (29 January 2021). ADPedKD : A global online platform to explore the childhood phenotype of autosomal dominant polycystic kidney disease [Paper presentation]. Congrès de la Société de Néphrologie Pédiatrique (SNP) 2021. |
DACHY, A., DE RECHTER, S., Guay-Woodford, L., Mallet, A. J., Harris, T., Bockenhauer, D., Schaefer, F., Liebau, M., & Mekahli, D. (2021). ADPedKD: A global online platform to explore the childhood phenotype of Autosomal Dominant Polycystic Kidney Disease [Poster presentation]. World Congress of Nephrology 2021. |
 | Dachy, A., Bacchetta, J., Sellier-Leclerc, A.-L., Bertholet-Thomas, A., Demède, D., Cochat, P., Nobili, F., & Ranchin, B. (December 2020). Long-term outcomes of peritoneal dialysis started in infants below 6 months of age: An experience from two tertiary centres. Nephrologie & therapeutique, 16 (7), 424-430. doi:10.1016/j.nephro.2020.08.002 Peer reviewed |
 | Dachy, A., Collard, L., Krzesinski, J.-M., Seghaye, M.-C., Ghuysen, M.-S., Mekhali, D., & Jouret, F. (December 2020). Polykystose rénale autosomique dominante : perspective pédiatrique. Revue Médicale de Liège, 75 (12), 775-780. Peer reviewed |
 | DACHY, A., EIRAS DA SILVA, S., THELEN, A., COLLARD, L., GHUYSEN, M.-S., LOMBET, J., MAQUET, J., & PHILIPPET, P. (19 May 2016). Oral treatment of febrile urinary tract infection in children: Feasibility and follow-up. Archives de Pédiatrie, 23 (6), 642-643. doi:10.1016/j.arcped.2016.03.046 |
 | Dachy, A., Paquot, F., Debray, F.-G., Bovy, C., Christensen, E. I., Collard, L., & Jouret, F. (2015). In-depth phenotyping of a Donnai-Barrow patient helps clarify proximal tubule dysfunction. Pediatric Nephrology, 30 (6), 1027-31. doi:10.1007/s00467-014-3037-7 Peer Reviewed verified by ORBi |
 | Dachy, A., & Battisti, O. (2014). Comment j'explore...les infections nosocomiales en néonatologie. Revue Médicale de Liège. Peer reviewed |
 | Dachy, A., Lefèbvre, P., & Battisti, O. (2013). comment j'explore une otite séromuqueuse chez l'enfant. Revue Médicale de Liège, 68, 542-547. Peer reviewed |
