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Kidney International|February 12, 2004
Segment-specific expression of 2P domain potassium channel genes in human nephronDaniel I Levy, Heino Velazquez, Steve A N Goldstein, et al.
Pediatric Nephrology (Berlin, Germany)|May 28, 2011
Genetic testing in renal diseaseDetlef Bockenhauer, Alan J Medlar, Emma Ashton, et al.
Pediatric Nephrology (Berlin, Germany)|January 1, 2017
Hypomagnesemia and increased risk of new-onset diabetes mellitus after transplantation in pediatric renal transplant recipientsWesley Hayes, Sheila Boyle, Adrian Carroll, et al.
Clinical Journal of the American Society of Nephrology : CJASN|April 3, 2020
Inherited Tubulopathies of the Kidney: Insights from GeneticsMallory L Downie, Sergio C Lopez Garcia, Robert Kleta, et al.
Pediatric Nephrology (Berlin, Germany)|October 21, 2020
Novel insights in the genetics of steroid-sensitive nephrotic syndrome in childhoodStephanie Dufek-Kamperis, Robert Kleta, Detlef Bockenhauer, et al.
Nephron|July 1, 2021
Epidemiology of Distal Renal Tubular Acidosis: A Study Using Linked UK Primary Care and Hospital DataFlorence Bianic, Florent Guelfucci, Ludovic Robin, et al.
BMC Bioinformatics|February 10, 2018
OVAS: an open-source variant analysis suite with inheritance modellingMonika Mozere, Mehmet Tekman, Jameela Kari, et al.
Pediatric Nephrology (Berlin, Germany)|May 16, 2024
Antenatal presentation and early postnatal treatment of infantile hypercalcemia type 2Marcelien Verjans, An Hindryckx, Karen Rosier, et al.
Archives of Disease in Childhood|October 29, 2020
Hyponatraemia despite isotonic maintenance fluid therapy: a time series intervention studyMilan Chromek, Åsa Jungner, Niclas Rudolfson, et al.
Molecular Genetics & Genomic Medicine|September 22, 2016
Founder mutation in KCNJ10 in Pakistani patients with EAST syndromeOla Abdelhadi, Daniela Iancu, Mehmet Tekman, et al.
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