136 related articles for article (PubMed ID: 8459532)
1. [Adenine phosphoribosyltransferase deficiency].
Kamatani N
Nihon Rinsho; 1993 Jan; 51 Suppl():1087-95. PubMed ID: 8459532
[No Abstract] [Full Text] [Related]
2. Complete deficiency of adenine phosphoribosyltransferase. Report of a family.
Van Acker KJ; Simmonds HA; Potter C; Cameron JS
N Engl J Med; 1977 Jul; 297(3):127-32. PubMed ID: 865583
[TBL] [Abstract][Full Text] [Related]
3. [2,8-Dihydroxyadenine lithiasis].
Yagisawa T; Toma H
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):467-9. PubMed ID: 9590103
[No Abstract] [Full Text] [Related]
4. Search for the mechanisms of high incidence of APRT deficiency among Japanese.
Kamatani N; Yamanaka H; Hakoda M; Terai C; Kashiwazaki S
Adv Exp Med Biol; 1994; 370():327-30. PubMed ID: 7660920
[No Abstract] [Full Text] [Related]
5. 2,8-Dihydroxyadeninuria--or when is a uric acid stone not a uric acid stone?
Simmonds HA
Clin Nephrol; 1979 Nov; 12(5):195-7. PubMed ID: 389507
[No Abstract] [Full Text] [Related]
6. Complete adenine phosphoribosyltransferase (APRT) deficiency in two siblings: report of a new case.
Cartier P; Hamet M; Vincens A; Perignon JL
Adv Exp Med Biol; 1980; 122A():343-8. PubMed ID: 7424655
[No Abstract] [Full Text] [Related]
7. The origin of APRT*J. The most common disease-related mutation of APRT gene among Japanese goes back to a prehistoric era.
Kamatani N; Terai C; Kim SY; Chen CL; Yamanaka H; Hakoda M; Totokawa S; Kashiwazaki S
Adv Exp Med Biol; 1998; 431():135-9. PubMed ID: 9598046
[No Abstract] [Full Text] [Related]
8. 2,8-Dihydroxyadenine urolithiasis: report of an adult case in the United States.
Manyak MJ; Frensilli FJ; Miller HC
J Urol; 1987 Feb; 137(2):312-4. PubMed ID: 3806829
[TBL] [Abstract][Full Text] [Related]
9. Distribution of patients with 2,8-dihydroxyadenine urolithiasis and adenine phosphoribosyltransferase deficiency in Japan.
Kamatani N; Sonoda T; Nishioka K
J Urol; 1988 Dec; 140(6):1470-2. PubMed ID: 3193517
[TBL] [Abstract][Full Text] [Related]
10. [Adenine phosphoribosyltransferase (APRT) deficiency].
Taniguchi A
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):464-6. PubMed ID: 9590102
[No Abstract] [Full Text] [Related]
11. Long-term evolution of type 1 adenine phosphoribosyltransferase (APRT) deficiency.
Van Acker KJ; Simmonds HA
Adv Exp Med Biol; 1991; 309B():91-4. PubMed ID: 1781413
[No Abstract] [Full Text] [Related]
12. [Phosphoribosyltransferase (APRT) deficiency--molecular and clinical aspects of dihydroxyadeninuria].
Safranow K
Postepy Hig Med Dosw; 1998; 52(1):89-104. PubMed ID: 9608233
[TBL] [Abstract][Full Text] [Related]
13. Corneal dystrophy and total adenine phosphoribosyltransferase (APRT) deficiency.
Neetens A; Van Acker KJ; Marien N
Bull Soc Belge Ophtalmol; 1986; 213():93-7. PubMed ID: 3487363
[No Abstract] [Full Text] [Related]
14. 2,8-Dihydroxyadenine urolithiasis due to partial deficit in adenine phosphoribosyltransferase: a case report.
Katsuoka Y; Miyakita H; Shiramizu M; Iwagaki H; Ikeda T
Hinyokika Kiyo; 1992 May; 38(5):573-7. PubMed ID: 1609669
[TBL] [Abstract][Full Text] [Related]
15. Purine excretion in complete adenine phosphoribosyltransferase deficiency: effect of diet and allopurinol therapy.
Simmonds HA; Van Acker KJ; Cameron JS; McBurney A
Adv Exp Med Biol; 1977; 76B():304-11. PubMed ID: 857624
[TBL] [Abstract][Full Text] [Related]
16. Common altered characteristics of mutant enzymes from patients with Japanese type APRT deficiencies.
Kamatani N; Yamanaka H; Nobori T; Nishioka K; Fujimori S; Akaoka I; Mikanagi K
Adv Exp Med Biol; 1986; 195 Pt A():39-46. PubMed ID: 3487919
[No Abstract] [Full Text] [Related]
17. 2,8-dihydroxyadeninuria: are there no cases in Scandinavia?
Arnadottir M; Laxdal T; Halldorsdottir B
Scand J Urol Nephrol; 2005; 39(1):82-6. PubMed ID: 15764278
[TBL] [Abstract][Full Text] [Related]
18. [Hereditary deficiency in adenine phosphoribosyltransferase: a metabolic cause of urinary lithiasis in children (author's transl)].
Cartier P; Hamet M; Perignon JL
Nouv Presse Med; 1980 Jun; 9(25):1767-70. PubMed ID: 6892958
[TBL] [Abstract][Full Text] [Related]
19. [Uric acid stones in children. Identification and therapy of a newly detected defect of adenine-phosphoribosyltransferase (author's transl)].
Simmonds HA
MMW Munch Med Wochenschr; 1979 Dec; 121(49):1654-6. PubMed ID: 118367
[TBL] [Abstract][Full Text] [Related]
20. Adenine phosphoribosyltransferase deficiency: a case diagnosed by GC-MS identification of 2,8-dihydroxyadenine in urinary crystals.
Christensen E; Brandt NJ; Laxdal T
J Inherit Metab Dis; 1987; 10(2):187-94. PubMed ID: 3116337
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
