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Kidney international, ISSN 0085-2538, 03/2018, Volume 93, Issue 3, pp. 656 - 669
Primary/secondary hyperoxalurias involve nephrocalcinosis-related chronic kidney disease (CKD) leading to end-stage kidney disease. Mechanistically, intrarenal... 
beta-hydroxybutyrate | necroinflammation | fibrosis | crystal nephropathy | NALP3 | Life Sciences & Biomedicine | Urology & Nephrology | Science & Technology | Cell Plasticity - drug effects | Inflammasomes - metabolism | Kidney - pathology | Nephrocalcinosis - immunology | Kidney - immunology | Hyperoxaluria - metabolism | Male | CARD Signaling Adaptor Proteins - genetics | Hyperoxaluria - drug therapy | NLR Family, Pyrin Domain-Containing 3 Protein - genetics | Renal Insufficiency, Chronic - metabolism | CARD Signaling Adaptor Proteins - metabolism | Kidney - metabolism | Nephrocalcinosis - metabolism | Butylene Glycols - pharmacology | Inflammasomes - drug effects | Interleukin-1 - immunology | Nephrocalcinosis - prevention & control | Female | Macrophages - immunology | Disease Models, Animal | Fibroblasts - metabolism | Interleukin-1 - metabolism | Renal Insufficiency, Chronic - immunology | Macrophages - pathology | Signal Transduction | NLR Family, Pyrin Domain-Containing 3 Protein - metabolism | Mice, Inbred C57BL | Cells, Cultured | NLR Family, Pyrin Domain-Containing 3 Protein - antagonists & inhibitors | Fibroblasts - pathology | Inflammasomes - genetics | Hyperoxaluria - pathology | Mice, Knockout | Renal Insufficiency, Chronic - pathology | Renal Insufficiency, Chronic - prevention & control | Macrophages - metabolism | Nephrocalcinosis - pathology | Phenotype | Animals | NLR Family, Pyrin Domain-Containing 3 Protein - immunology | Receptors, Transforming Growth Factor beta - metabolism | Inflammasomes - immunology | Fibroblasts - immunology | Macrophages - drug effects | Hyperoxaluria - immunology | End-stage renal disease | Phenotypes | CD11b antigen | Kidneys | Interleukin 1 receptor antagonist | Therapeutic applications | CX3CR1 protein | Inflammation | Macrophages | CD45 antigen | Atrophy | Signal transduction | Calcium oxalate | Oxalic acid | Calcinosis | Interleukin 1 | Fibrosis | Fibroblasts | Hyperoxaluria | Kidney diseases | Index Medicus
Journal Article
Journal Article
Pediatric nephrology (Berlin, West), ISSN 1432-198X, 12/2008, Volume 25, Issue 3, pp. 403 - 413
Journal Article
Pediatric nephrology (Berlin, West), ISSN 1432-198X, 05/2016, Volume 32, Issue 7, pp. 1123 - 1135
Magnesium is essential to the proper functioning of numerous cellular processes. Magnesium ion (Mg2+) deficits, as reflected in hypomagnesemia, can cause... 
Homeostasis | Thick ascending limb of Henle’s loop | Magnesium | Hereditary | Distal convoluted tubule | Kidney | Pediatrics | Life Sciences & Biomedicine | Urology & Nephrology | Science & Technology | Seizures - blood | Hypokalemia - blood | Kidney Tubules, Distal - physiology | Humans | Renal Tubular Transport, Inborn Errors - genetics | Renal Reabsorption - genetics | Nephrocalcinosis - complications | Renal Tubular Transport, Inborn Errors - blood | Hypercalciuria - blood | Magnesium Deficiency - genetics | Magnesium Deficiency - complications | Renal Reabsorption - drug effects | Hypokalemia - drug therapy | Magnesium - physiology | Magnesium Deficiency - drug therapy | Hypercalciuria - genetics | Membrane Proteins - metabolism | Child | Hypokalemia - etiology | Renal Tubular Transport, Inborn Errors - drug therapy | Membrane Proteins - genetics | Nephrocalcinosis - drug therapy | Arrhythmias, Cardiac - etiology | Mitochondria - metabolism | Loop of Henle - physiology | Renal Tubular Transport, Inborn Errors - complications | Magnesium - therapeutic use | Mineralocorticoid Receptor Antagonists - therapeutic use | Hypercalciuria - complications | Hypercalciuria - drug therapy | Phenotype | Renal Elimination - genetics | Nephrocalcinosis - genetics | Epithelial Sodium Channel Blockers - therapeutic use | Seizures - etiology | Nephrocalcinosis - blood | Arrhythmias, Cardiac - blood | Mutation | Recommended Dietary Allowances | Hypokalemia - genetics | Magnesium - blood | Homeostasis - genetics | Complications and side effects | Care and treatment | Kidney failure | Arrhythmia | Gene mutations | Research | Magnesium deficiency diseases | Index Medicus | Review
Journal Article
Journal Article
Journal Article
Pediatric nephrology (Berlin, West), ISSN 1432-198X, 01/2013, Volume 28, Issue 10, pp. 1923 - 1942
Adenine phosphoribosyltransferase (APRT) deficiency, cystinuria, Dent disease, familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC), and... 
Pediatrics | Nephrocalcinosis | Dent disease | Hereditary disorders | Crystalline nephropathy | Nephrolithiasis | Cystinuria | Familial hypomagnesemia with hypercalciuria and nephrocalcinosis | Kidney failure | Medicine & Public Health | Adenine phosphoribosyltransferase deficiency | Primary hyperoxaluria | 2,8-dihydroxyadeninuria | Life Sciences & Biomedicine | Urology & Nephrology | Science & Technology | Hypercalciuria - epidemiology | Humans | Dent Disease - therapy | Renal Insufficiency, Chronic - epidemiology | Renal Insufficiency, Chronic - therapy | Dent Disease - genetics | Renal Insufficiency, Chronic - genetics | Renal Insufficiency, Chronic - diagnosis | Dent Disease - epidemiology | Child | Cystinuria - diagnosis | Genetic Predisposition to Disease | Adenine Phosphoribosyltransferase - genetics | Risk Factors | Heredity | Nephrocalcinosis - therapy | Hyperoxaluria, Primary - epidemiology | Hyperoxaluria, Primary - genetics | Metabolism, Inborn Errors - diagnosis | Phenotype | Kidney Calculi - therapy | Nephrocalcinosis - genetics | Cystinuria - epidemiology | Nephrocalcinosis - diagnosis | Kidney Calculi - genetics | Urolithiasis - genetics | Cystinuria - therapy | Prognosis | Hyperoxaluria, Primary - diagnosis | Nephrocalcinosis - epidemiology | Metabolism, Inborn Errors - epidemiology | Metabolism, Inborn Errors - therapy | Renal Tubular Transport, Inborn Errors - genetics | Hyperoxaluria, Primary - therapy | Dent Disease - diagnosis | Renal Tubular Transport, Inborn Errors - epidemiology | Adenine Phosphoribosyltransferase - deficiency | Hypercalciuria - genetics | Renal Tubular Transport, Inborn Errors - diagnosis | Hypercalciuria - therapy | Hypercalciuria - diagnosis | Renal Tubular Transport, Inborn Errors - therapy | Metabolism, Inborn Errors - genetics | Cystinuria - genetics | Urolithiasis - therapy | Kidney Calculi - diagnosis | Animals | Urolithiasis - epidemiology | Kidney Calculi - epidemiology | Urolithiasis - diagnosis | Causes of | Genetic aspects | Research | Chronic kidney failure | Kidney stones | Index Medicus | nephrocalcinosis | kidney failure | hereditary disorders | adenine phosphoribosyltransferase deficiency | cystinuria | primary hyperoxaluria | crystalline nephropathy | familial hypomagnesemia with hypercalciuria and nephrocalcinosis
Journal Article