Results 111 to 120 of about 6,717 (218)
Niranjan, Khandelwal +3 more
openaire +2 more sources
Primary hyperoxaluria is a group of rare inherited diseases characterized by impaired oxalate metabolism with the early manifestation of urolithiasis and the development of the chronic kidney disease.
Azova M.M. +11 more
core
Primary hyperoxaluria type 1 (PH1) is a rare autosomal recessive inborn error of the glyoxylate metabolism that is based on absence, deficiency or mislocalization of the liver-specific peroxisomal enzyme alanine:glyoxylate aminotransferase. Hyperoxaluria
Velibor Tasic +5 more
core
Baolin Zhang,1 Ting Li,2 Ziyang Qiang,1 Lan Ma,3 Xiangfeng Kong,1 Shuang Chen1 1Department of Urology, Qinghai University Affiliated Hospital, Xining, Qinghai, 810000, People’s Republic of China; 2School of Pharmacy, Medical College of Qinghai University,
Zhang B +5 more
doaj
Prevalence of hyperoxaluria in idiopathic calcium oxalate kidney stone disease.
Urinary excretion of oxalate, calcium and urate has been investigated in 88 patients affected by idiopathic calcium oxalate stone disease and in 20 normal subjects. Of these ions, only oxalate was found significantly higher in stone formers.
Favaro S +3 more
core
Comparison of Risk Profiles, Nutrient Intake, and Kidney Function of Calcium Oxalate Stone Formers with and without Enteric Hyperoxaluria. A Matched Case-Control Study. [PDF]
Ernsten C, Spuck N, Hesse A, Siener R.
europepmc +1 more source
Treatment of enteric hyperoxaluria [PDF]
J, Harper, M A, Mansell
openaire +2 more sources
Urinary biomarkers of urolithiasis risk in Crohn's disease: hyperoxaluria, hypocitraturia, and hypomagnesuria in patients with and without ileocolic resection. [PDF]
Navratil V +6 more
europepmc +1 more source
Metabolic origins of hyperoxaluria: the critical role of precursors and vitamin B6 status in rats. [PDF]
Ogawa Y.
europepmc +1 more source

