2,8-Dihydroxyadenine Urolithiasis

Known as: UROLITHIASIS, DHA, 2,8-Dihydroxyadeninuria, DHA Crystalline Nephropathy 
 
National Institutes of Health

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Highly Cited
2012
Highly Cited
2012
By 2009, there were worrying signs from western Cambodia that parasitological responses to artesunate-containing treatment… (More)
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Highly Cited
2008
Highly Cited
2008
Epoxidation and hydroxylation of arachidonic acid (AA) are both catalyzed by cytochromes P450s (CYPs). The oxidized metabolites… (More)
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Review
2000
Review
2000
Docosahexaenoate (DHA) has been increasingly recognized as an important fatty acid for neural and visual development during the… (More)
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1996
1996
2,8-Dihydroxyadenine urolithiasis is an inherited disorder caused by adenine phosphoribosyltransferase deficiency. A fast, simple… (More)
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Review
1994
Review
1994
We treated two children with 2,8-dihydroxyadenine urolithiasis for over 7 years. The male prepositus was admitted to the hospital… (More)
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1992
1992
A 48-year-old man with a history of recurrent urolithiasis and chronic renal failure underwent a nephrectomy for a renal mass. At… (More)
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1988
1988
2,8-Dihydroxyadenine urolithiasis is caused by genetic deficiencies of adenine phosphoribosyl-transferase. This disease has… (More)
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Review
1988
Review
1988
We report a case of homozygous adenine phosphoribosyl transferase (APRT) deficiency associated with 2,8-dihydroxyadenine stones… (More)
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1982
1982
A four-year-old girl presented in renal failure due to dihydroxyadenine urolithiasis. Prior to this she had been fed a high… (More)
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