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Pediatric Nephrology (Berlin, Germany)|February 12, 2017
Clinical and molecular aspects of distal renal tubular acidosis in childrenMartine T P Besouw, Marc Bienias, Patrick Walsh, et al.Kidney International Reports|February 23, 2023
Shockwaves and the Rolling Stones: An Overview of Pediatric Stone DiseaseNaima Smeulders, Alexander Cho, Abdulelah Alshaiban, et al.Pediatric Transplantation|April 12, 2019
Plasma electrolyte imbalance in pediatric kidney transplant recipientsWesley Hayes, Catherine Longley, Nicola Scanlon, et al.Hormone Research in Paediatrics|June 8, 2020
Co-Existence of Congenital Adrenal Hyperplasia and Bartter Syndrome due to Maternal Uniparental Isodisomy of HSD3B2 and CLCNKB MutationsDinesh Giri, Detlef Bockenhauer, Charu Deshpande, et al.The Journal of Clinical Endocrinology and Metabolism|May 18, 2006
Unusual clinical presentation and possible rescue of a novel claudin-16 mutationDominik Müller, P Jaya Kausalya, Detlef Bockenhauer, et al.Clinical Kidney Journal|June 27, 2018
Clinical and diagnostic features of Bartter and Gitelman syndromesPatrick R Walsh, Yincent Tse, Emma Ashton, et al.Clinical Kidney Journal|January 4, 2021
Erratum: Long-term outcome in inherited nephrogenic diabetes insipidusSonia Sharma, Emma Ashton, Daniela Iancu, et al.Clinical Kidney Journal|April 13, 2019
Long-term outcome in inherited nephrogenic diabetes insipidusSonia Sharma, Emma Ashton, Daniela Iancu, et al.Disease Models & Mechanisms|March 9, 2013
Generation and validation of a zebrafish model of EAST (epilepsy, ataxia, sensorineural deafness and tubulopathy) syndromeFahad Mahmood, Monika Mozere, Anselm A Zdebik, et al.Pediatric Nephrology (Berlin, Germany)|July 19, 2023
Tolvaptan and urea in paediatric hyponatraemiaFaidra Veligratli, Demitra Alexandrou, Sarit Shah, et al.Pageof 20