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Pediatric Nephrology (Berlin, Germany)|January 22, 2013
Hereditary causes of kidney stones and chronic kidney diseaseVidar O Edvardsson, David S Goldfarb, John C Lieske, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|September 21, 2010
Transplantation outcomes in primary hyperoxaluriaE J Bergstralh, C G Monico, J C Lieske, et al.
Vascular and Endovascular Surgery|January 2, 2008
Renal artery intervention in pediatric and adolescent patients: a 20-year experienceYing Huang, Audra A Duncan, Michael A McKusick, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|May 7, 2014
Sustained pyridoxine response in primary hyperoxaluria type 1 recipients of kidney alone transplantE C Lorenz, J C Lieske, B M Seide, et al.
American Journal of Medical Quality : the Official Journal of the American College of Medical Quality|July 9, 2009
Quality: the Mayo Clinic approachStephen J Swensen, James A Dilling, Dawn S Milliner, et al.
The Journal of Pediatrics|August 1, 1993
Urinary oxalate and glycolate excretion patterns in the first year of life: a longitudinal studyB Z Morgenstern, D S Milliner, M E Murphy, et al.
Kidney International|March 23, 2007
Hyperoxaluric nephrolithiasis is a complication of Roux-en-Y gastric bypass surgeryM K Sinha, M L Collazo-Clavell, A Rule, et al.
Orphanet Journal of Rare Diseases|November 12, 2020
Specific populations of urinary extracellular vesicles and proteins differentiate type 1 primary hyperoxaluria patients without and with nephrocalcinosis or kidney stonesMuthuvel Jayachandran, Stanislav V Yuzhakov, Sanjay Kumar, et al.
Kidney International|February 26, 2020
Clinical features of genetically confirmed patients with primary hyperoxaluria identified by clinical indication versus familial screeningDavid J Sas, Felicity T Enders, Ramila A Mehta, et al.
Clinical Biochemistry|August 3, 2017
Plasma oxalate in relation to eGFR in patients with primary hyperoxaluria, enteric hyperoxaluria and urinary stone diseaseMajuran Perinpam, Felicity T Enders, Kristin C Mara, et al.
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