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… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1956-2017
0204019562016

Papers overview

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2010
2010
Primary hyperoxaluria (PH) is an autosomal-recessive disorder of endogenous oxalate synthesis characterized by accumulation of… (More)
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2010
2010
Optimal transplantation strategies are uncertain in primary hyperoxaluria (PH) due to potential for recurrent oxalosis. Outcomes… (More)
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Highly Cited
2006
Highly Cited
2006
Primary hyperoxaluria is characterized by severe urolithiasis, nephrocalcinosis, and early renal failure. As treatment options… (More)
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2002
2002
BACKGROUND Hyperoxaluria may be idiopathic, secondary, or due to primary hyperoxaluria (PH). Hepatic alanine:glyoxylate… (More)
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2001
2001
BACKGROUND The primary hyperoxalurias are autosomal recessive disorders resulting from deficiency of hepatic alanine:glyoxylate… (More)
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2000
2000
Glyoxylate is an immediate precursor of oxalate, but in its metabolism the conversion into glycine catalyzed by serine:pyruvate… (More)
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1995
1995
Urinary citrate is a potent inhibitor of calcium oxalate (CaOx) crystallization, but oral citrate has rarely been used in… (More)
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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… (More)
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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… (More)
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1986
1986
Primary hyperoxaluria is a rare metabolic disorder characterized by excessive synthesis and urinary excretion of oxalate… (More)
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