Isovaleric acidaemia in a premature infant

Diagnosis and treatment

R. Heimler, H. Hennes, S. Khayata, P. Sasidharan, Reuben Matalon

Research output: Contribution to journalArticle

Original languageEnglish (US)
Pages (from-to)313-314
Number of pages2
JournalJournal of Inherited Metabolic Disease
Volume11
Issue number3
DOIs
StatePublished - Sep 1988
Externally publishedYes

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Infant, Premature, Diseases
Isovaleryl-CoA Dehydrogenase
Pentanoic Acids
Valerates
Premature Infants
Oxidoreductases
Newborn Infant
Amino Acids
Therapeutics
Oxidoreductases Acting on CH-CH Group Donors
Isovaleric acidemia

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics
  • Endocrinology

Cite this

Isovaleric acidaemia in a premature infant : Diagnosis and treatment. / Heimler, R.; Hennes, H.; Khayata, S.; Sasidharan, P.; Matalon, Reuben.

In: Journal of Inherited Metabolic Disease, Vol. 11, No. 3, 09.1988, p. 313-314.

Research output: Contribution to journalArticle

Heimler, R. ; Hennes, H. ; Khayata, S. ; Sasidharan, P. ; Matalon, Reuben. / Isovaleric acidaemia in a premature infant : Diagnosis and treatment. In: Journal of Inherited Metabolic Disease. 1988 ; Vol. 11, No. 3. pp. 313-314.
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