Skip to search formSkip to main contentSkip to account menu

2,8-dihydroxyadenine

Known as: 6-amino-1H-purine-2,8(3H,7H)-dione, 6-amino-2,8-dihydroxypurine 
National Institutes of Health

Related topics

Related topics

4 relations
8-aminoxanthine8-oxoguanineanalogs & derivatives

Broader (1)

Adenine

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2000
2000
Démarche diagnostique devant une lithiase rénale
La demarche diagnostique chez un patient lithiasique comporte deux etapes : tout d’abord affirmer le diagnostic de lithiase… 
1996
1996
Adeninephosphoribosyltr ansferase-defici ent micedevelop 2,8-dihydroxyadenine nephrolithiasis (purine metabolism/gene targeting/mouse model/renal disease)
Adenine phosphoribosyltransferase (APRT) deficiency inhumansisanautosomal recessive syndrome characterized bytheurinary excretion… 
1993
1993
The Clinical Aspects of APRT Deficiency
Adenine phosphoribosyltransferase (APRT) deficiency was first detected and described by Kelley et al. in 1968. The patient… 
1989
1989
Re: Adenine phosphoribosyltransferase deficiency: 2,8-dihydroxyadenine urolithiasis in a 48-year-old woman.
1986
1986
2,8-Dihydroxyadenine lithiasis--epidemiology, pathogenesis and therapy.
2,8-dihydroxyadenine (2,8-DHA) is the insoluble purine responsible for a potentially lethal form of kidney stones, previously… 
1985
1985
[A case of right ureteral stone with complete deficiency of adenine phosphoribosyltransferase].
We report a case of a 34-year-old male, who had urinary tract calculus, caused by complete deficiency of adenine… 
Review
1984
Review
1984
Genetic mechanism(s) responsible for a deficiency of adenine phosphoribosyltransferase in man.
Adenine phosphoribosyltransferase (APRT) is a relatively non-abundant soluble enzyme which in man is coded for by a single… 
1981
1981
Urolithiasis due to 2,8-dihydroxyadenine in an adult.
CARTIER and Hamet1 described a patient with calculi formed by 2,8-dihydroxyadenine in 1974. Such calculi are positive for uric… 
1981
1981
Dihydroxyadenine urolithiasis in children with partial deficiency of adenine phosphoribosyltransferase.
Urolithiasis composed of 2,8-dihydroxyadenine is not only formed in a complete defect of adenine phosphoribosyltransferase, but… 
1977
1977
Adenine metabolism in man. 1. After intravenous and peroral administration.
The basal plasma concentration of adenine and its renal excretion was studied in two men. For its analysis partly new…