(Q28372514)

12 December 2020

Neonatal adrenoleukodystrophy: clinical, pathologic, and biochemical delineation of a syndrome affecting both males and females

1 reference

12 December 2020

MRI evidence that docosahexaenoic acid ethyl ester improves myelination in generalized peroxisomal disorders.

1 reference

12 December 2020

Lignoceric acid is oxidized in the peroxisome: implications for the Zellweger cerebro-hepato-renal syndrome and adrenoleukodystrophy

1 reference

12 December 2020

Polyunsaturated fatty acid changes suggesting a new enzymatic defect in Zellweger syndrome

1 reference

12 December 2020

Cerebroside galactosidase of brain.

1 reference

12 December 2020

Evidence for the involvement of docosahexaenoic acid in cholinergic stimulated signal transduction at the synapse.

1 reference

12 December 2020

Blood polyunsaturated fatty acids in patients with peroxisomal disorders. A multicenter study

1 reference

12 December 2020

Cerebro-hepato-renal (Zellweger) syndrome and neonatal adrenoleukodystrophy: similarities in phenotype and accumulation of very long chain fatty acids.

1 reference

12 December 2020

Glycerolipid biosynthesis in peroxisomes via the acyl dihydroxyacetone phosphate pathway

1 reference

12 December 2020

Cerebro-hepato-renal (Zellweger) syndrome, adrenoleukodystrophy, and Refsum's disease: plasma changes and skin fibroblast phytanic acid oxidase

1 reference

12 December 2020

Lipids of the developing human retina: I. Total fatty acids, plasmalogens, and fatty acid composition of ethanolamine and choline phosphoglycerides.

1 reference

12 December 2020

Distribution and fatty acid composition of phosphoglycerides in normal human brain.

1 reference

12 December 2020

Peroxisomal disorders: genotype, phenotype, major neuropathologic lesions, and pathogenesis.

1 reference

12 December 2020

Specificity of galactosylceramidase activation by phosphatidylserine

1 reference

12 December 2020

Infantile phytanic acid storage disease, a possible variant of Refsum's disease: three cases, including ultrastructural studies of the liver

1 reference

12 December 2020

Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome

1 reference

12 December 2020

Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups

1 reference

12 December 2020

A FAMILIAL SYNDROME OF MULTIPLE CONGENITAL DEFECTS

1 reference

12 December 2020

Characterization of epoxides of polyunsaturated fatty acids by mass spectrometry via 3-pyridinylmethyl esters

1 reference

12 December 2020

Direct transesterification of all classes of lipids in a one-step reaction

1 reference

12 December 2020

Polyunsaturated fatty acids of photoreceptor membranes

1 reference

12 December 2020

The lipid composition of adult rat brain synaptosomal plasma membranes.

1 reference

12 December 2020

Defects of Bile Acid Synthesis in Zellweger's Syndrome

1 reference

12 December 2020

Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome).

1 reference

12 December 2020

Severe deficiency of docosahexaenoic acid in peroxisomal disorders: a defect of delta 4 desaturation?

1 reference

12 December 2020

Fatty acid composition of human brain phospholipids during normal development.

1 reference

12 December 2020

Abnormal profiles of polyunsaturated fatty acids in the brain, liver, kidney and retina of patients with peroxisomal disorders

1 reference

12 December 2020