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Case Reports in Medicine|August 28, 2020
Lactobacillus acidophilus Endocarditis Complicated by Pauci-Immune Necrotizing GlomerulonephritisVivian O Chukwurah, Comfort Takang, Chinelo Uche, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|July 23, 2013
Pregnancy-associated polyuria in familial renal glycosuriaHakan R Toka, Jun Yang, Chloe A Zera, et al.Clinical Case Reports|June 8, 2026
Hypokalemic Periodic Paralysis in a Young Woman With Mast Cell Activation Syndrome: A Case Report of an Atypical Presentation Associated With an Ultra-Rare CACNA1S VariantAli Moradi, Yasmin Aboutaleb, Saba Noreen, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 9, 2024
Vadadustat Three Times Weekly in Patients With Anemia Due to Dialysis-Dependent CKDHakan R Toka, Marializa Bernardo, Steven K Burke, et al.Pediatric Research|February 23, 2019
Multisite measurement of regional oxygen saturation in Fontan patients with and without protein-losing enteropathy at rest and during exerciseSimon Schröer, Fabian B Fahlbusch, Frank Münch, et al.Journal of the American Society of Nephrology : JASN|March 29, 2014
Mutations in PAX2 associate with adult-onset FSGSMoumita Barua, Emilia Stellacci, Lorenzo Stella, et al.Hypertension (Dallas, Tex. : 1979)|December 19, 2007
Inversion region for hypertension and brachydactyly on chromosome 12p features multiple splicing and noncoding RNASylvia Bähring, Martin Kann, Yvette Neuenfeld, et al.Proceedings of the National Academy of Sciences of the United States of America|April 5, 2017
Parathyroid hormone controls paracellular Ca2+ transport in the thick ascending limb by regulating the tight-junction protein Claudin14Tadatoshi Sato, Marie Courbebaisse, Noriko Ide, et al.Journal of the American Society of Nephrology : JASN|September 22, 2012
Deficiency of the calcium-sensing receptor in the kidney causes parathyroid hormone-independent hypocalciuriaHakan R Toka, Khaldoun Al-Romaih, Jacob M Koshy, et al.Science (New York, N.Y.)|October 23, 2004
A cluster of metabolic defects caused by mutation in a mitochondrial tRNAFrederick H Wilson, Ali Hariri, Anita Farhi, et al.Pageof 3