Gas chromatography/mass spectrometry analysis of very long chain fatty acids, docosahexaenoic acid, phytanic acid and plasmalogen for the screening of peroxisomal disorders

Author:

Takemoto Yasuhiko,Suzuki Yasuyuki,Horibe Ryoko,Shimozawa Nobuyuki,Wanders Ronald J.A.,Kondo Naomi

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference22 articles.

1. Peroxisomal fatty acid alpha- and beta-oxidation in humans: enzymology, peroxisomal metabolite transporters and peroxisomal diseases;Wanders;Biochem Soc Trans,2001

2. Fatty acid abnormality in adrenoleukodystrophy;Igarashi;J Neurochem,1976

3. A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (Pseudo-neonatal adrenoleukodystrophy);Poll-The;Am J Hum Genet,1988

4. D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder;Suzuki;Am J Hum Genet,1997

5. Pseudo-Zellweger syndrome: deficiencies in several peroxisomal oxidative activities;Goldfischer;J Pediatr,1986

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