Severe Prenatal Renal Anomalies Associated with Mutations in HNF1B or PAX2 GenesLeire Madariaga, Laurence Heidet, Vincent Morinière et al.|Clinical Journal of the American Society of Nephrology|2013Cited by 110
Treatment and long-term outcome in primary nephrogenic diabetes insipidusSergio Camilo Lopez-Garcia, Tanja Wlodkowski, B. C. Reynolds et al.|Nephrology Dialysis Transplantation|2020Cited by 26
Novel RRAGD Variants in Autosomal Dominant Kidney Hypomagnesemia and Therapeutic PerspectivesAnastasia Adella, Jeroen H. F. de Baaij, François Jouret et al.|Kidney International Reports|2025Cited by 4
Hypomagnesaemia with varying degrees of extrarenal symptoms as a consequence of heterozygous CNNM2 variantsWillem Bosman, Joost G.J. Hoenderop, Gijs A. C. Franken et al.|Scientific Reports|2024Cited by 3