Results 101 to 110 of about 7,704 (220)
Mechanisms of human kidney stone formation [PDF]
, 2014 The precise mechanisms of kidney stone formation and growth are not completely known, even though human stone disease appears to be one of the oldest diseases known to medicine.
Coe, Fredric L. +4 more
core +1 more source
Primary hyperoxaluria Type 1: organic aciduria diagnosed in plasma [PDF]
, 2013 Background: Primary hyperoxaluria Type 1 (PH1) is a rare autosomal recessive inborn error of glyoxylate metabolism, caused by a deficiency of the liver-specific peroxisomal enzyme alanine:glyoxylate aminotransferase.
Dias, Aureliano +3 more
core
Annals of the Academy of Medicine, Singapore, 2010 Niranjan, Khandelwal +3 more
openaire +3 more sources
Tamm-Horsfall protein in recurrent calcium kidney stone formers with positive family history: abnormalities in urinary excretion, molecular structure and function [PDF]
, 2018 Tamm-Horsfall protein (THP) powerfully inhibits calcium oxalate crystal aggregation, but structurally abnormal THPs from recurrent calcium stone formers may promote crystal aggregation.
Hess, Bernhard +3 more
core
BiomoleculesPrimary hyperoxalurias (PHs) are inherited metabolic disorders marked by enzymatic cascade disruption, leading to excessive oxalate production that is subsequently excreted in the urine.
Yueqi Huang +4 more
doaj +1 more source
CHRONIC RENAL FAILURE DUE TO HYPER OXALURIA IN PEDIATRIC PATIENTS
Turkish Journal of Nephrology, 2019 Primary hyperoxaluria is a rarely encountered disease characterised by recurrent urolithiasis, nephrocalcinosis, and oxalate deposition in almost all tissues, generally inherited in autosomal recessive fashion and the important complications of which can
Ali DELİBAŞ +5 more
doaj