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Journal of the American Society of Nephrology : JASN|September 11, 2025
Fifty Shades of Risk: Population Studies and the Genetic Architecture of Kidney DiseasesOmid Sadeghi-Alavijeh, Melanie M Y Chan, Horia Stanescu, et al.
Pediatric Nephrology (Berlin, Germany)|July 8, 2022
Mendelian steroid resistant nephrotic syndrome in childhood: is it as common as reported?Zainab Arslan, Hazel Webb, Emma Ashton, et al.
Nature Reviews. Nephrology|April 4, 2023
The pathophysiology of distal renal tubular acidosisCarsten A Wagner, Robert Unwin, Sergio C Lopez-Garcia, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 11, 2017
Genetics of membranous nephropathySanjana Gupta, Anna Köttgen, Elion Hoxha, et al.
Archives of Disease in Childhood|January 30, 2023
Burosumab in management of X-linked hypophosphataemia: a retrospective cohort study of growth and serum phosphate levelsEmma Yi Xiu Walker, Timothy Alexander James Lindsay, Jeremy Allgrove, et al.
Hormone Research in Paediatrics|June 2, 2016
Hepatocyte Nuclear Factor-4 Alfa Mutation Associated with Hyperinsulinaemic Hypoglycaemia and Atypical Renal Fanconi Syndrome: Expanding the Clinical PhenotypeNicola Improda, Pratik Shah, Maria Güemes, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 31, 2016
Tolvaptan is successful in treating inappropriate antidiuretic hormone secretion in infantsDaniela Marx-Berger, David V Milford, Meenakshi Bandhakavi, et al.
Pflugers Archiv : European Journal of Physiology|January 12, 2011
The salt-wasting phenotype of EAST syndrome, a disease with multifaceted symptoms linked to the KCNJ10 K+ channelSascha Bandulik, Katharina Schmidt, Detlef Bockenhauer, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 14, 2011
A family with hyponatremia and the nephrogenic syndrome of inappropriate antidiuresisDetlef Bockenhauer, Michael D Penney, David Hampton, et al.
Pediatric Nephrology (Berlin, Germany)|May 29, 2016
Genetic causes of hypomagnesemia, a clinical overviewDaan H H M Viering, Jeroen H F de Baaij, Stephen B Walsh, et al.
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