151 related articles for article (PubMed ID: 7661029)
1. Application of capillary zone electrophoresis for rapid screening of enzymatic defects in purine metabolism.
Salerno C; Crifò C
Adv Exp Med Biol; 1994; 370():811-4. PubMed ID: 7661029
[No Abstract] [Full Text] [Related]
2. Capillary electrophoresis for detection of inherited disorders of purine and pyrimidine metabolism.
Adam T; Friedecký D; Fairbanks LD; Sevcík J; Barták P
Clin Chem; 1999 Dec; 45(12):2086-93. PubMed ID: 10585670
[TBL] [Abstract][Full Text] [Related]
3. Microassay of adenylosuccinase by capillary electrophoresis.
Salerno C; Crifò C
Anal Biochem; 1995 Apr; 226(2):377-9. PubMed ID: 7793642
[No Abstract] [Full Text] [Related]
4. Anomalous response to intravenous fructose tolerance test in a case of deficit of adenylosuccinate lyase.
Salerno C; Crifò C; Capuozzo E; Giardini O
Adv Exp Med Biol; 1994; 370():371-4. PubMed ID: 7660931
[No Abstract] [Full Text] [Related]
5. Problems in diagnosis and treatment of adenine and hypoxanthine-guanine phosphoribosyltransferase deficiency.
Dillon MJ; Simmonds HA; Barratt TM; Fairbanks LD; Holland PC
Adv Exp Med Biol; 1984; 165 Pt A():1-6. PubMed ID: 6720360
[No Abstract] [Full Text] [Related]
6. Adenylosuccinase deficiency: clinical and biochemical findings in 5 Czech patients.
Sebesta I; Krijt J; Kmoch S; Hartmannová H; Wojda M; Zeman J
J Inherit Metab Dis; 1997 Jul; 20(3):343-4. PubMed ID: 9266351
[No Abstract] [Full Text] [Related]
7. An HPLC-based assay of adenylosuccinate lyase in erythrocytes.
Bierau J; Pooters IN; Visser D; Bakker JA
Nucleosides Nucleotides Nucleic Acids; 2011 Nov; 30(11):908-17. PubMed ID: 22060555
[TBL] [Abstract][Full Text] [Related]
8. Adenylosuccinate lyase deficiency in a Czech girl and two siblings.
Krijt J; Sebesta I; Svehlakova A; Zumrova A; Zeman J
Adv Exp Med Biol; 1994; 370():367-70. PubMed ID: 7660930
[No Abstract] [Full Text] [Related]
9. Adenylosuccinate lyase deficiency: an update.
Van den Berghe G; Van den Bergh F; Vincent MF; Jaeken J
Adv Exp Med Biol; 1994; 370():363-6. PubMed ID: 7660929
[No Abstract] [Full Text] [Related]
10. Screening for adenylosuccinate lyase deficiency using tandem mass spectrometry analysis of succinylpurines in neonatal dried blood spots.
Zikanova M; Krijt J; Skopova V; Krijt M; Baresova V; Kmoch S
Clin Biochem; 2015 Jan; 48(1-2):2-7. PubMed ID: 25445730
[TBL] [Abstract][Full Text] [Related]
11. Adenylosuccinate lyase deficiency: the first identified polish patient.
Jurkiewicz E; Mierzewska H; Kuśmierska K
Brain Dev; 2007 Oct; 29(9):600-2. PubMed ID: 17485188
[TBL] [Abstract][Full Text] [Related]
12. [Inborn errors of purine metabolism].
Ito T; Sumi S; Ueta A
Ryoikibetsu Shokogun Shirizu; 2000; (29 Pt 4):410-1. PubMed ID: 11031983
[No Abstract] [Full Text] [Related]
13. [Determination and significance of adenine in the urine and the serum of a patient with congenital adenine phosphoribosyltransferase deficiency].
Noro T; Kamikawa A; Samori T; Kawamura T; Igawa F; Seki K; Ueki K; Fujimaki M
Rinsho Byori; 1985 Jan; 33(1):89-94. PubMed ID: 3990012
[No Abstract] [Full Text] [Related]
14. 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]
15. [Adenine phosphoribosyltransferase (APRT) deficiency].
Taniguchi A
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):464-6. PubMed ID: 9590102
[No Abstract] [Full Text] [Related]
16. Adenylosuccinate lyase deficiency: study of physiopathologic mechanism(s).
Race V; Marie S; Kienlen-Campard P; Hermans E; Octave JN; Van den Berghe G; Vincent MF
Nucleosides Nucleotides Nucleic Acids; 2004 Oct; 23(8-9):1227-9. PubMed ID: 15571234
[TBL] [Abstract][Full Text] [Related]
17. Screening for inborn errors of purine synthesis.
Jaeken J; van den Berghe G
Lancet; 1989 Mar; 1(8636):500. PubMed ID: 2563871
[No Abstract] [Full Text] [Related]
18. Inborn errors of the purine nucleotide cycle: adenylosuccinase deficiency.
Van den Berghe G; Vincent MF; Jaeken J
J Inherit Metab Dis; 1997 Jun; 20(2):193-202. PubMed ID: 9211192
[TBL] [Abstract][Full Text] [Related]
19. [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]
20. Genetic basis of adenylosuccinase deficiency in an Italian patient.
Verginelli D; Luckow B; Salerno C; Gross M
Adv Exp Med Biol; 1998; 431():323-5. PubMed ID: 9598084
[No Abstract] [Full Text] [Related]
[Next] [New Search]
