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Biochimica Et Biophysica Acta|May 27, 2008
Caenorhabditis elegans as a model for lysosomal storage disordersGert de Voer, Dorien Peters, Peter E M TaschnerTrends in Cardiovascular Medicine|October 24, 2006
Cardiovascular polycystins: insights from autosomal dominant polycystic kidney disease and transgenic animal modelsDelphine Bichet, Dorien Peters, Amanda Jane Patel, et al.European Journal of Human Genetics : EJHG|May 12, 2016
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTSJohannes G Dauwerse, Martine van Belzen, Arie van Haeringen, et al.Journal of the American Society of Nephrology : JASN|October 24, 2008
Unified criteria for ultrasonographic diagnosis of ADPKDYork Pei, James Obaji, Annie Dupuis, et al.Journal of the American Society of Nephrology : JASN|May 8, 2016
Stat3 Controls Tubulointerstitial Communication during CKDFrank Bienaimé, Mordi Muorah, Lucie Yammine, et al.Journal of Nephrology|November 7, 2022
Urinary epidermal growth factor/monocyte chemotactic peptide 1 ratio as non-invasive predictor of Mayo clinic imaging classes in autosomal dominant polycystic kidney diseaseMaria Teresa Rocchetti, Francesco Pesce, Silvia Matino, et al.Journal of the American Society of Nephrology : JASN|April 23, 2003
Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney diseaseRiccardo Magistroni, Ning He, Kairong Wang, et al.Pageof 1