Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency-Reference-Cited by-同舟云学术

Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

Published:1991-05 Issue:5 Volume:118 Page:744-746
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Vici Carlo Dionisi,Burlina Alberto B.,Bertini Enrico,Bachmann Claude,Mazziotta Mercedes R.M.,Zacchello F.,Sabetta Gaetano,Hale Daniel E.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference7 articles.

1. Abnormalities of fatty acid oxidation;Nyhan;N Engl J Med,1988

2. The role of urinary organic acids analysis in the detection and management of inherited metabolic diseases;Burlina;Italian Journal of Pediatrics,1986

3. The l-3-hydroxyacyl-CoA dehydrogenase deficiency;Hale,1990

4. Sudden infant death and long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency;Wanders;Lancet,1989

5. Hypoglycemia, hepatic dysfunction, muscle weakness, cardiomyopathy, free carnitine deficiency and long-chain acylcarnitine excess responsive to medium-chain triglyceride diet;Glasgow;Pediatr Res,1983

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