Add to ORKGPrimary hyperoxaluria type 1 (PH1) usually presents with recurrent urolithiasis, nephrocalcinosis and progressive renal failure at a relatively young age. This report describes a patient who, due to the late onset of end-stage renal disease, had been diagnosed with PH1 only after failure of his second kidney graft. Retrospectively, his vascular problems, skeletal abnormalities and cardiac arrhythmias fit the picture of severe systemic oxalosis. Possible therapeutic options are discussed
Optimal transplantation strategies are uncertain in primary hyperoxaluria (PH) due to potential for ...
A case is reported of a patient with renal failure and developing systemic and renal oxalosis due to...
Primary hyperoxaluria type 1 (PH1) is an autosomal recessive disease caused by the functional defect...
The primary hyperoxalurias (PHs) are rare disorders of glyoxylate metabolism in which specific hepat...
Primary hyperoxaluria is a genetic disorder in glyoxylate metabolism that leads to systemic overprod...
Primary hyperoxaluria type-1 (PH1) is a rare inherited autosomal recessive disorder in which a defic...
Primary hyperoxaluria type-1 (PH1) is a rare inherited autosomal recessive disorder in which a defic...
Abstract Background Primary hyperoxaluria (PH) is a rare inherited autosomal recessive disease cause...
A 37-year-old patient underwent two successive renal transplantations 7 months apart. He remained di...
Primary hyperoxaluria type I (PH1) is a rare hereditary metabolic disorder, due to the deficiency of...
Primary hyperoxaluria type 1 (PH1) is a rare inherited metabolic disorder in which deficiency of the...
Primary hyperoxalurias (PH) are inborn errors in the metabolism of glyoxylate and oxalate. PH type 1...
Primary hyperoxaluria type 1 (PH1) is the most common form of primary hyperoxalurias. It results in ...
Hyperoxaluria is an important and underrecognized cause for allograft dysfunction and loss after tra...
Primary hyperoxaluria (PH) is a rare genetic disorder characterized by overproduction of oxalate due...
Optimal transplantation strategies are uncertain in primary hyperoxaluria (PH) due to potential for ...
A case is reported of a patient with renal failure and developing systemic and renal oxalosis due to...
Primary hyperoxaluria type 1 (PH1) is an autosomal recessive disease caused by the functional defect...
The primary hyperoxalurias (PHs) are rare disorders of glyoxylate metabolism in which specific hepat...
Primary hyperoxaluria is a genetic disorder in glyoxylate metabolism that leads to systemic overprod...
Primary hyperoxaluria type-1 (PH1) is a rare inherited autosomal recessive disorder in which a defic...
Primary hyperoxaluria type-1 (PH1) is a rare inherited autosomal recessive disorder in which a defic...
Abstract Background Primary hyperoxaluria (PH) is a rare inherited autosomal recessive disease cause...
A 37-year-old patient underwent two successive renal transplantations 7 months apart. He remained di...
Primary hyperoxaluria type I (PH1) is a rare hereditary metabolic disorder, due to the deficiency of...
Primary hyperoxaluria type 1 (PH1) is a rare inherited metabolic disorder in which deficiency of the...
Primary hyperoxalurias (PH) are inborn errors in the metabolism of glyoxylate and oxalate. PH type 1...
Primary hyperoxaluria type 1 (PH1) is the most common form of primary hyperoxalurias. It results in ...
Hyperoxaluria is an important and underrecognized cause for allograft dysfunction and loss after tra...
Primary hyperoxaluria (PH) is a rare genetic disorder characterized by overproduction of oxalate due...
Optimal transplantation strategies are uncertain in primary hyperoxaluria (PH) due to potential for ...
A case is reported of a patient with renal failure and developing systemic and renal oxalosis due to...
Primary hyperoxaluria type 1 (PH1) is an autosomal recessive disease caused by the functional defect...