SCOPUS 정보 검색 플랫폼

Volumn 23, Issue 7, 2000, Pages 662-668

Influence of dose and age on the response of the allopurinol test for ornithine carbamoyltransferase deficiency in control infants

(6) Riudor, E a Arranz, J A a Rodes M b Rubio, V c Sentis M a Burlina, A B d

a UNIVERSITAT AUTÒNOMA DE BARCELONA (Spain)

b Institut de Bioquimica Clinica Barcelona (Spain)

c INSTITUTO DE BIOMEDICINA DE VALENCIA (Spain)

d UNIVERSITY OF PADOVA (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ALLOPURINOL; ORNITHINE CARBAMOYLTRANSFERASE; OROTIC ACID; OROTIDINE;

AGE; ARTICLE; CLINICAL ARTICLE; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; DIAGNOSTIC TEST; DOSE RESPONSE; ENZYME DEFICIENCY; HUMAN; INFANT; INFANT DISEASE; URINARY EXCRETION;

ADOLESCENT; ADULT; AGE FACTORS; ALLOPURINOL; CHILD; CHILD, PRESCHOOL; DOSE-RESPONSE RELATIONSHIP, DRUG; FEMALE; HUMANS; INFANT; MALE; ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY DISEASE; OROTIC ACID; URIDINE;

EID: 0033737406 PISSN: 01418955 EISSN: None Source Type: Journal
DOI: 10.1023/A:1005610325170 Document Type: Article

Times cited : (5)

References (10)

1
- 0032779266
- Optimization of allopurinol challenge: Sample purification, protein intake control and the use of orotidine response as a discriminative variable improve performance of the test for diagnosing ornithine carbamoyltransferase deficiency
- (1999) Clin Chem , vol.45 , Issue.7 , pp. 995-1001
- Arranz, J.A.¹ Riudor, E.² Rodes, M.³

2
- 0032953027
- The allopurinol load test lacks specificity for primary urea cycle defects but may indicate unrecognized mitochondrial disease
- (1999) J Inherit Metab Dis , vol.22 , pp. 174-184
- Bonham, J.R.¹ Guthrie, P.² Downing, M.³

3
- 0001034416
- Urea cycle enzymes
- Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease, 7th edn. New York: McGraw-Hill
- (1995) , pp. 1187-1232
- Brusilow, S.W.¹ Horwich, A.L.²

4
- 0026666061
- Allopurinol challenge test in children
- (1992) J Inherit Metab Dis , vol.15 , pp. 707-712
- Burlina, A.B.¹ Ferrari, V.² Dionisi-Vici, C.³ Bordugo, A.⁴ Zachello, F.⁵ Tuchman, M.⁶

5
- 0025293198
- Allopurinol-induced orotidinuria. A test for mutations at the ornithine carbamoyltransferase locus in women
- (1990) N Engl J Med , vol.322 , pp. 1641-1645
- Hauser, E.R.¹ Finkelstein, J.E.² Valle, D.³ Brusilow, S.W.⁴

6
- 0018823799
- Pyrimidine nucleotide biosynthesis in animals: Genes, enzymes and regulation of UMP biosynthesis
- (1980) Annu Rev Biochem , vol.49 , pp. 253-279
- Jones, M.E.¹

7
- 0033506343
- Neonatal onset ornithine transcarbamylase deficiency: A retrospective analysis
- (1999) J Pediatr , vol.134 , pp. 268-272
- Maestri, N.E.¹ Clissold, D.² Brusilow, S.W.³

8
- 0014670722
- Control of pyrimidine biosynthesis in mammalian tissues. Partial purification and characterization of glutamine-utilizing carbamoyl-phosphate synthetase of mouse spleen and tissue distribution
- (1969) J Biol Chem , vol.244 , pp. 5403-5413
- Tatibana, M.¹ Ito, K.²

9
- 0025131042
- Episodic hyperammonemia in adult siblings with hyperornithinemia, hyperammonemia and homocitrullinuria syndrome
- (1990) Arch Neurol , vol.47 , pp. 1134-1137
- Tuchman, M.¹ Knopman, D.S.² Shih, V.E.³

10
- 0030039992
- Relative frequency of mutations causing ornithine transcarbamylase deficiency in 78 families
- (1996) Hum Genet , vol.27 , pp. 274-276
- Tuchman, M.¹ Plante, R.J.² Garcia-Perez, M.A.³ Rubio, V.⁴

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