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i primary hyperoxaluria (18) 18
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Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia, ISSN 1319-2442, 07/2016, Volume 27, Issue 4, pp. 791 - 794
Journal Article
Nephrology Dialysis Transplantation, ISSN 0931-0509, 1995, Volume 10, Issue 8, pp. 3 - 7
Primary hyperoxaluria type 1 (PH1) always leads to oxalate accumulation throughout the body (oxalosis). Currently available epidemiological data only concern... 
Prevalence rate | Incidence rate | Epidemiology | Primary hyperoxaluria type 1 | Kidney transplantation | Liver transplantation | INCIDENCE RATE | KIDNEY TRANSPLANTATION | PRIMARY OXALOSIS | PREVALENCE RATE | LIVER TRANSPLANTATION | UROLOGY & NEPHROLOGY | KIDNEY | EPIDEMIOLOGY | PRIMARY HYPEROXALURIA TYPE 1 | TRANSPLANTATION
Journal Article
International journal of organ transplantation medicine, ISSN 2008-6482, 2011, Volume 2, Issue 3, pp. 126 - 132
Primary hyperoxaluria type-1 (PH1) is a rare inherited autosomal recessive disorder in which a deficiency of the hepatic enzyme alanine-glyoxylate... 
Primary hyperoxaluria | renal transplantation | liver transplantation | Case Report
Journal Article
Pediatric Nephrology, ISSN 0931-041X, 10/2013, 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 | GENOTYPE-PHENOTYPE CORRELATION | I PRIMARY HYPEROXALURIA | HUMAN APRT GENE | KNOCKOUT MOUSE MODEL | FAMILIAL HYPOMAGNESEMIA | PRIMARY HYPEROXALURIA TYPE-1 | URINARY OXALATE EXCRETION | RENAL CHLORIDE CHANNEL | UROLOGY & NEPHROLOGY | PEDIATRICS | DENTS-DISEASE | 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 | nephrocalcinosis | kidney failure | hereditary disorders | adenine phosphoribosyltransferase deficiency | cystinuria | primary hyperoxaluria | crystalline nephropathy | familial hypomagnesemia with hypercalciuria and nephrocalcinosis
Journal Article
Journal Article
Kidney International, ISSN 0085-2538, 01/2018, Volume 93, Issue 1, pp. 204 - 213
Journal Article
FEBS JOURNAL, ISSN 1742-464X, 11/2017, Volume 284, Issue 21, pp. 3739 - 3764
Journal Article
AMERICAN JOURNAL OF DERMATOPATHOLOGY, ISSN 0193-1091, 06/2018, Volume 40, Issue 6, pp. E78 - E78
Journal Article
Indian Pediatrics, ISSN 0019-6061, 02/2005, Volume 42, Issue 2, pp. 173 - 174
Journal Article