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Primary Hyperoxaluria

Known as: Primary Oxaluria, Hyperoxaluria, Primary, Hyperoxaluria, Primary [Disease/Finding] 
A genetic disorder characterized by excretion of large amounts of OXALATES in urine; NEPHROLITHIASIS; NEPHROCALCINOSIS; early onset of RENAL FAILURE… Expand
National Institutes of Health

Papers overview

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Highly Cited
2015
Highly Cited
2015
Primary hyperoxaluria (PH) is a rare autosomal recessive disease characterized by oxalate accumulation in the kidneys and other… Expand
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Review
2012
Review
2012
  • B. Hoppe
  • Nature Reviews Nephrology
  • 2012
  • Corpus ID: 26055010
The autosomal recessive inherited primary hyperoxalurias types I, II and III are caused by defects in glyoxylate metabolism that… Expand
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Highly Cited
2011
Highly Cited
2011
BACKGROUND Primary hyperoxaluria (PH) is a rare genetic disease, in which high urinary oxalate (Uox) cause recurrent kidney… Expand
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Highly Cited
2010
Highly Cited
2010
Primary hyperoxaluria (PH) is an autosomal-recessive disorder of endogenous oxalate synthesis characterized by accumulation of… Expand
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Highly Cited
2010
Highly Cited
2010
Optimal transplantation strategies are uncertain in primary hyperoxaluria (PH) due to potential for recurrent oxalosis. Outcomes… Expand
Review
2009
Review
2009
The primary hyperoxalurias (PHs) are rare disorders of glyoxylate metabolism in which specific hepatic enzyme deficiencies result… Expand
Highly Cited
2006
Highly Cited
2006
Primary hyperoxaluria is characterized by severe urolithiasis, nephrocalcinosis, and early renal failure. As treatment options… Expand
Review
2006
Review
2006
Primary hyperoxaluria type 1, the most common form of primary hyperoxaluria, is an autosomal recessive disorder caused by a… Expand
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Highly Cited
1990
Highly Cited
1990
We have previously shown that in some patients with primary hyperoxaluria type 1 (PH1), disease is associated with mistargeting… Expand
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Highly Cited
1986
Highly Cited
1986
Activities of alanine:glyoxylate aminotransferase in the livers of two patients with primary hyperoxaluria type I were… Expand