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Kidney International|February 17, 2024
A Neanderthal haplotype introgressed into the human genome confers protection against membranous nephropathyCătălin D Voinescu, Monika Mozere, Giulio Genovese, et al.
Nephron. Physiology|August 19, 2011
KCNJ10 mutations disrupt function in patients with EAST syndromeBernard Freudenthal, Duvaraka Kulaveerasingam, Lokesh Lingappa, et al.
Kidney International Reports|March 20, 2023
Machine Learning to Identify Genetic Salt-Losing Tubulopathies in Hypokalemic PatientsElizabeth R Wan, Daniela Iancu, Emma Ashton, et al.
Kidney International|May 29, 2016
Chromosome 17q12 microdeletions but not intragenic HNF1B mutations link developmental kidney disease and psychiatric disorderRhian L Clissold, Charles Shaw-Smith, Peter Turnpenny, et al.
Kidney International Reports|September 14, 2019
ADPedKD: A Global Online Platform on the Management of Children With ADPKDStéphanie De Rechter, Detlef Bockenhauer, Lisa M Guay-Woodford, et al.
Nature Reviews. Nephrology|January 30, 2021
Management of congenital nephrotic syndrome: consensus recommendations of the ERKNet-ESPN Working GroupOlivia Boyer, Franz Schaefer, Dieter Haffner, et al.
Physiological Reports|December 27, 2021
Quantification of FAM20A in human milk and identification of calcium metabolism proteinsVaksha Patel, Enriko Klootwijk, Gail Whiting, et al.
Kidney & Blood Pressure Research|June 20, 2024
RRAGD-Associated Autosomal Dominant Kidney Hypomagnesemia with Cardiomyopathy: A Review on the Clinical Manifestations and Therapeutic OptionsFrancesco Trepiccione, Irene Sambri, Barbara Ruggiero, et al.
Journal of the American Society of Nephrology : JASN|September 24, 2016
Risk Factors for Severe Renal Disease in Bardet-Biedl SyndromeElizabeth Forsythe, Kathryn Sparks, Sunayna Best, et al.
Pediatric Nephrology (Berlin, Germany)|June 7, 2014
Clinico-pathological correlations of congenital and infantile nephrotic syndrome over twenty yearsJameela A Kari, Giovanni Montini, Detlef Bockenhauer, et al.
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