Recurrent episodes of bizarre behavior in a boy with ornithine transcarbamylase deficiency: Diagnostic failure of protein loading and allopurinol challenge tests-Reference-Cited by-同舟云学术

Recurrent episodes of bizarre behavior in a boy with ornithine transcarbamylase deficiency: Diagnostic failure of protein loading and allopurinol challenge tests

Published:1994-08 Issue:2 Volume:125 Page:249-251
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Spada M.,Guardamagna O.,Rabier D.,van der Meer S.B.,Parvy P.,Bardet J.,Ponzone A.,Saudubray J.M.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference10 articles.

1. Late-onset ornithine transcarbamylase deficiency in male patients;Finkelstein;J PEDIATR,1990

2. Risk of serious illness in heterozygotes for ornithine transcarbamylase deficiency;Batshaw;J PEDIATR,1986

3. Carrier detection in ornithine transcarbamylase deficiency;Hokanson;J PEDIATR,1978

4. Carrier detection of urea cycle disorders;Ng;Pediatrics,1981

5. Allopurinol-induced orotidinuria. A test for mutations at the ornithine carbamoyltransferase locus in women;Hauser;N Engl J Med,1990

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