Results 91 to 100 of about 13,710 (218)
Basic studies on the cause of urolithiasis. I. Stone producing substances and experimental stone formation with administration of drugs [PDF]
1) Vitamin D, oxalic acid and CAI (carbonic anhydrase inhibitor) were administered to Wistar strain rats as stone producing substances. Although nephrocalcinosis was observed in the experimental animals, results did not come to formation of urolithiasis.
松尾, 光雄
core
BackgroundPrimary hyperoxaluria type 1 (PH1) is a genetic disorder resulting in overproduction of hepatic oxalate, potentially leading to recurrent kidney stones, nephrocalcinosis, chronic kidney disease, and kidney failure.
Yaacov Frishberg +10 more
doaj +1 more source
Lecture: New light on the role of claudins in the kidney [PDF]
The physiology of paracellular permeation of ions and solutes in the kidney is pivotally important but poorly understood. Claudins are the key components of the paracellular pathway.
Hou, Jianghui
core +2 more sources
Long-term nephrocalcinosis leads to kidney injury, fibrosis, and even chronic kidney disease (CKD). Macrophage-to-myofibroblast transition (MMT) has been identified as a new mechanism in CKD, however, the effect of MMT in calcium oxalate (CaOx)-induced ...
Yuqi Xia +15 more
doaj +1 more source
Histopathological patterns of nephrocalcinosis: a phosphate type can be distinguished from a calcium type [PDF]
Background. The etiology of nephrocalcinosis is variable. In this study, we wanted to elucidate whether the histopathological appearance of calcium phosphate deposits provides information about possible etiology. Methods.
Banyai-Falger, Susanne +7 more
core
Inference of gene-phenotype associations via protein-protein interaction and orthology [PDF]
published_or_final_versio
Lai, WF +6 more
core +3 more sources
Modalities of Vitamin D Administration to Preterm Infants: Impact on 25 OH Vitamin D Levels
Acta Paediatrica, Volume 115, Issue 4, Page 985-987, April 2026.
Sophie Laborie +3 more
wiley +1 more source
Nephrolithiasis Associated with Nephrocalcinosis Is Primarily Composed of Carbonate Apatite
Introduction: This study was designed to determine the mineral composition of calculi in nephrocalcinosis with nephrolithiasis, diagnose the underlying disease, and monitor the course of renal function in patients with nephrocalcinosis-nephrolithiasis ...
Teresa Antonia Kiener +6 more
doaj +1 more source
A role for OCRL in glomerular function and disease [PDF]
Background: Lowe syndrome and Dent-2 disease are caused by mutations in the OCRL gene, which encodes for an inositol 5-phosphatase. The renal phenotype associated with OCRL mutations typically comprises a selective proximal tubulopathy, which can ...
Bierzynska, Agnieszka +6 more
core +4 more sources
Nephrocalcinosis Infantum [PDF]
R A, SHANKS, A M, MACDONALD
openaire +2 more sources

