Pregnancy complications are frequent in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

This publication has 17 references indexed in Scilit:

• Long-chain 3-hydroxyacyl–coenzyme A dehydrogenase deficiency with the G1528C mutation: Clinical presentation of thirteen patients
  The Journal of Pediatrics, 1997
• The Genes for the α and β Subunits of the Mitochondrial Trifunctional Protein Are Both Located in the Same Region of Human Chromosome 2p23
  Genomics, 1996
• Maternal Acute Fatty Liver of Pregnancy Associated with Fetal Trifunctional Protein Deficiency: Molecular Characterization of a Novel Maternal Mutant Allele
  Pediatric Research, 1996
• Common missense mutation G1528C in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Characterization and expression of the mutant protein, mutation analysis on genomic DNA and chromosomal localization of the mitochondrial trifunctional protein alpha subunit gene.
  Journal of Clinical Investigation, 1996
• The clinical spectrum of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
  Pediatric Neurology, 1996
• Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency: high frequency of the G1528C mutation with no apparent correlation with the clinical phenotype
  Journal of Inherited Metabolic Disease, 1995
• Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of the major disease-causing mutation in the α-subunit of the mitochondrial trifunctional protein
  Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1994
• Pregnancy and fetal long-chain 3-hydroxyacyl coenzyme A dehydrogenase deficiency
  The Lancet, 1993
• Human liver long-chain 3-hydroxyacyl-coenzyme a dehydrogenase is a multifunctional membrane-bound beta-oxidation enzyme of mitochondria
  Biochemical and Biophysical Research Communications, 1992
• Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
  The Journal of Pediatrics, 1991