Abnormal profiles of polyunsaturated fatty acids in the brain, liver, kidney and retina of patients with peroxisomal disorders (Q45156613)

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scientific article published in June 1992

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

Language	Label	Description	Also known as
English	Abnormal profiles of polyunsaturated fatty acids in the brain, liver, kidney and retina of patients with peroxisomal disorders	scientific article published in June 1992	Abnormal profiles of polyunsaturated fatty acids in the brain, liver, kidney and retina of patients with peroxisomal disorders

Statements

scholarly article

1 reference

Europe PubMed Central

10 December 2017

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

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Europe PubMed Central

10 December 2017

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author name string

M Martinez

1

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Europe PubMed Central

10 December 2017

Manuela Martinez

1

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language of work or name

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publication date

1 June 1992

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Europe PubMed Central

10 December 2017

June 1992

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number of pages

12

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based on heuristic

inferred from page(s)

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Europe PubMed Central

10 December 2017

583

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Europe PubMed Central

10 December 2017

1-2

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Europe PubMed Central

10 December 2017

171-182

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Europe PubMed Central

10 December 2017

Ultrastructural and cytochemical demonstration of peroxisomes in cultured fibroblasts from patients with peroxisomal deficiency disorders

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https://api.crossref.org/works/10.1016%2FS0006-8993%2810%2980021-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2810%2980021-6

7 January 2021

A comparison of pyrrolidide and picolinyl ester derivatives for the identification of fatty acids in natural samples by gas chromatography-mass spectrometry

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2810%2980021-6

7 January 2021

Deficiency of enzymes catalyzing the biosynthesis of glycerol-ether lipids in Zellweger syndrome. A new category of metabolic disease involving the absence of peroxisomes.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2810%2980021-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2810%2980021-6

7 January 2021

The Zellweger syndrome: deficient conversion of docosahexaenoic acid (22:6(n-3)) to eicosapentaenoic acid (20:5(n-3)) and normal delta 4-desaturase activity in cultured skin fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2810%2980021-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2810%2980021-6

7 January 2021

Primary hyperparathyroidism associated with pancytosis

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2810%2980021-6

7 January 2021

GLC Identification Techniques for Long-Chain Unsaturated Fatty Acids

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2810%2980021-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2810%2980021-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2810%2980021-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2810%2980021-6

7 January 2021

Retroconversion and delta 4 desaturation of docosatetraenoate (22:4(n-6)) and docosapentaenoate (22:5(n-3)) by human cells in culture

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2810%2980021-6

7 January 2021

Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2810%2980021-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2810%2980021-6

7 January 2021

Direct demonstration that the deficient oxidation of very long chain fatty acids in X-linked adrenoleukodystrophy is due to an impaired ability of peroxisomes to activate very long chain fatty acids

1 reference

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7 January 2021

Peroxisomal bifunctional enzyme deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2810%2980021-6

7 January 2021

Identifiers

10.1016/S0006-8993(10)80021-6

0 references

1 reference

Europe PubMed Central

10 December 2017

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