(Q28338863)

English

Accumulation of pristanic acid (2, 6, 10, 14 tetramethylpentadecanoic acid) in the plasma of patients with generalised peroxisomal dysfunction

scientific article (publication date: February 1988)

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scholarly article

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Accumulation of pristanic acid (2, 6, 10, 14 tetramethylpentadecanoic acid) in the plasma of patients with generalised peroxisomal dysfunction (English)

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author name string

A Poulos

1

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P Sharp

2

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A J Fellenberg

3

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D W Johnson

4

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language of work or name

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publication date

February 1988

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European Journal of Pediatrics

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147

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143-7

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2

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The occurrence of polyenoic fatty acids with greater than 22 carbon atoms in mammalian spermatozoa

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

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Refsum's disease, adrenoleucodystrophy, and the Zellweger syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

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Hepatic peroxisomes are deficient in infantile refsum disease: a cytochemical study of 4 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

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Pristanic acid (2,6,10,14-tetramethylpentadecanoic acid) and phytanic acid (3,7,11,15-tetramethylhexadecanoic acid) content of human and animal tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

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Peroxisomal defects in neonatal-onset and X-linked adrenoleukodystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

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Heterogeneity of Chondrodysplasia punctata

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

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Disorders related to the metabolism of phytanic acid

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Refsum's disease: characterization of the enzyme defect in cell culture

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

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Occurrence of novel branched-chain fatty acids in Refsum's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

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Cerebro-hepato-renal syndrome of Zellweger. A report of eight cases with comments upon the incidence, the liver lesion, and a fault in pipecolic acid metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Accumulation and defective beta-oxidation of very long chain fatty acids in Zellweger's syndrome, adrenoleukodystrophy and Refsum's disease variants

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

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Deficiency of acyl-CoA: dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

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The cerebro-hepato-renal (Zellweger) syndrome: lamellar lipid profiles in adrenocortical, hepatic mesenchymal, astrocyte cells and increased levels of very long chain fatty acids and phytanic acid in the plasma.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The chemistry and biochemistry of phytanic, pristanic and related acids

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Treatment of infantile phytanic acid storage disease: clinical, biochemical and ultrastructural findings in two children treated for 2 years

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adrenoleukodystrophy: survey of 303 cases: biochemistry, diagnosis, and therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A comparative study of stearic and lignoceric acid oxidation by human skin fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rhizomelic chondrodysplasia punctata: another peroxisomal disorder.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

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Adrenomyeloneuropathy--clinical and biochemical diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phytanic acid oxidase activity in cultured skin fibroblasts. Diagnostic usefulness and limitations

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomes in fibroblasts from skin of Refsum's disease patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cerebrohepatorenal (Zellweger) syndrome. Increased levels and impaired degradation of very-long-chain fatty acids and their use in prenatal diagnosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Beta-oxidation of very-long-chain fatty acids and their coenzyme A derivatives by human skin fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Minor constituents of human milk. IV. Analysis of the branched chain fatty acids

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomal disorders: a newly recognised group of genetic diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile Refsum disease: deficiency of catalase-containing particles (peroxisomes), alkyldihydroxyacetone phosphate synthase and peroxisomal beta-oxidation enzyme proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The isolation and identification of 2,6,10,14-tetramethylpentadecanoic acid from butterfat

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of a homologous series of C26-C38 polyenoic fatty acids in the brain of patients without peroxisomes (Zellweger's syndrome).

1 reference

https://pubmed.ncbi.nlm.nih.gov/2452737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00442211

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Springer Nature article ID

10.1007/bf00442211

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