PKD2-Related Autosomal Dominant Polycystic Kidney Disease: Prevalence, Clinical Presentation, Mutation Spectrum, and PrognosisÉmilie Cornec-Le Gall, Yannick Le Meur, P. Siohan et al.|American Journal of Kidney Diseases|2017Cited by 80
Spectrum and Prognosis of Noninfectious Renal Mixed Cryoglobulinemic GNMohamad Zaidan, Emmanuelle Plaisier, Benjamin Terrier et al.|Journal of the American Society of Nephrology|2015Cited by 61
Warfarin-related nephropathy induced by three different vitamin K antagonists: analysis of 13 biopsy-proven casesLéonard Golbin, T. Frouget, Cécile Vigneau et al.|Clinical Kidney Journal|2016Cited by 38
New clinical forms of hereditary apoA-I amyloidosis entail both glomerular and retinal amyloidosisMagali Colombat, Sophie Valleix, Jean‐Claude Aldigier et al.|Kidney International|2020Cited by 23
Diagnosis and risk factors for intracranial aneurysms in autosomal polycystic kidney disease: a cross-sectional study from the Genkyst cohortSiriane Lefèvre, Marie‐Pierre Audrézet, Jean‐Michel Halimi et al.|Nephrology Dialysis Transplantation|2022Cited by 22