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Kidney International|May 3, 2021
Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variantsKathrin Burgmaier, Leonie Brinker, Florian Erger, et al.
Nature Communications|September 5, 2019
Defects in t<sup>6</sup>A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndromeChristelle Arrondel, Sophia Missoury, Rozemarijn Snoek, et al.
Pediatric Nephrology (Berlin, Germany)|January 23, 2025
Survey of legislative frameworks and national recommendations governing paediatric maintenance haemodialysis in EuropeEnzo Vedrine, Claus Peter Schmitt, Johan Vande Walle, et al.
Arthritis and Rheumatism|May 14, 2013
Protein kinase cδ deficiency causes mendelian systemic lupus erythematosus with B cell-defective apoptosis and hyperproliferationAlexandre Belot, Paul R Kasher, Eleanor W Trotter, et al.
The Journal of Clinical Investigation|October 16, 2019
Human C-terminal CUBN variants associate with chronic proteinuria and normal renal functionMathilda Bedin, Olivia Boyer, Aude Servais, et al.
Journal of the American Society of Nephrology : JASN|June 2, 2017
Long-Term Outcome of Steroid-Resistant Nephrotic Syndrome in ChildrenAgnes Trautmann, Sven Schnaidt, Beata S Lipska-Ziętkiewicz, et al.
Journal of the American Society of Nephrology : JASN|March 9, 2019
Effects of Hemodiafiltration versus Conventional Hemodialysis in Children with ESKD: The HDF, Heart and Height StudyRukshana Shroff, Colette Smith, Bruno Ranchin, et al.
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