Oxalosis

 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1952-2017
0102019522016

Papers overview

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2002
2002
BACKGROUND Primary hyperoxaluria is a rare autosomal recessive metabolic disease that often progresses to end-stage renal disease… (More)
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1996
1996
Oxalosis, or calcium oxalate deposition in the tissues, may develop in patients with inherited disorders of oxalate metabolism or… (More)
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1991
1991
We describe the clinical, radiographic and histological features of skeletal involvement in four patients with end-stage renal… (More)
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1990
1990
This paper reports the results of 98 first kidney transplantations in patients with oxalosis as the primary renal disease as… (More)
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1984
1984
Eleven patients, aged 6 months to 47 years, with renal failure due to primary oxalosis, received renal allografts and were… (More)
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1983
1983
A female infant had progressive atypical pigmentary retinopathy with type 1 hereditary oxalosis. At the age of 3 months she had a… (More)
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1983
1983
Immune triggered granulocyte (PMN)-endothelial interactions have been implicated in the pathogenesis of vascular diseases. While… (More)
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1982
1982
We describe 3 infants with nephrocalcinosis and terminal renal failure. In all 3 there was widespread oxalate deposition… (More)
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1981
1981
Primary hyperoxaluria is a rare metabolic disease characterized by exaggerated production of oxalic acid. Clinically the disease… (More)
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1980
1980
Bone biopsy specimens from four patients with hyperoxaluria who underwent hemodialysis were studied. Calcium oxalate crystals are… (More)
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