Results 191 to 200 of about 13,488 (222)
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[Adenine phosphoribosyltransferase(APRT) deficiency].

Nihon rinsho. Japanese journal of clinical medicine, 1997
Adenine phosphoribosyltransferase(APRT) deficiency is an autosomal recessive disorder and the homozygotes develop 2,8-dihydroxyadenine(DHA) urolithiasis and, in severe cases, renal failure. The prevalence is higher among the Japanese than other ethnic groups. So far 120 cases have been reported among the Japanese. The disease is classified into 2 types;
openaire   +1 more source

Adenine phosphoribosyltransferase

1996
Dietmar Schomburg, Dörte Stephan
openaire   +1 more source

Adenine Phosphoribosyltransferase Deficiency

2009
Hubert Scharnagl   +199 more
openaire   +1 more source

Adenine phosphoribosyltransferase (APRT) deficiency

2020
William L. Nyhan   +3 more
openaire   +1 more source

Adenine phosphoribosyltransferase.

Methods in enzymology, 1978
W J, Arnold, W N, Kelley
openaire   +1 more source

Nicotinamide Phosphoribosyltransferase in Malignancy: A Review

Genes and Cancer, 2013
Rodney E Shackelford   +2 more
exaly  

Adenine phosphoribosyltransferase deficiency in man

The American Journal of Medicine, 1973
Irving H. Fox   +2 more
openaire   +1 more source

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