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Clinical Journal of the American Society of Nephrology : CJASN|August 25, 2022
Arterial Stiffness and Chronic Kidney Disease Progression in ChildrenKarolis Azukaitis, Marietta Kirchner, Anke Doyon, et al.Journal of Molecular Biology|August 6, 2014
Molecular analysis of two novel missense mutations in the GDF5 proregion that reduce protein activity and are associated with brachydactyly type CKatja Stange, Tino Thieme, Karen Hertel, et al.Genes|July 29, 2023
SLC5A1 Variants in Turkish Patients with Congenital Glucose-Galactose MalabsorptionFerda Ö Hoşnut, Andreas R Janecke, Gülseren Şahin, et al.American Journal of Hypertension|May 7, 2015
Aortic Pulse Wave Velocity in Healthy Children and Adolescents: Reference Values for the Vicorder Device and Modifying FactorsDaniela Thurn, Anke Doyon, Betul Sözeri, et al.American Journal of Physiology. Renal Physiology|August 15, 2008
Magnesium stimulates renal phosphate reabsorptionJulia Thumfart, Susanne Jung, Salah Amasheh, et al.Scientific Reports|March 30, 2018
Chronic kidney disease induces a systemic microangiopathy, tissue hypoxia and dysfunctional angiogenesisHans-Ulrich Prommer, Johannes Maurer, Karoline von Websky, et al.JIMD Reports|February 23, 2013
MNGIE Syndrome: Liver Cirrhosis Should Be Ruled Out Prior to Bone Marrow TransplantationArmin Finkenstedt, Melanie Schranz, Sylvia Bösch, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 28, 2006
A randomized crossover trial comparing sevelamer with calcium acetate in children with CKDAnne-Kathrin Pieper, Dieter Haffner, Bernd Hoppe, et al.American Journal of Human Genetics|December 17, 2009
Loss of dermatan-4-sulfotransferase 1 function results in adducted thumb-clubfoot syndromeMunis Dündar, Thomas Müller, Qi Zhang, et al.The Journal of Pediatrics|October 17, 2012
Homozygous SALL1 mutation causes a novel multiple congenital anomaly-mental retardation syndromeJulia Vodopiutz, Heinz Zoller, Aimée L Fenwick, et al.Pageof 25