(Q68991115)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2436918%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

title

Plasma bile acids in patients with peroxisomal dysfunction syndromes: analysis by capillary gas chromatography-mass spectrometry (English)

1 reference

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29 September 2019

author name string

P T Clayton

1

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29 September 2019

B D Lake

2

1 reference

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29 September 2019

N A Hall

3

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29 September 2019

D B Shortland

4

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29 September 2019

R A Carruthers

5

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29 September 2019

A M Lawson

6

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29 September 2019

publication date

1 March 1987

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European Journal of Pediatrics

29 September 2019

published in

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29 September 2019

volume

146

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29 September 2019

issue

2

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29 September 2019

page(s)

166-173

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https://scigraph.springernature.com/pub.10.1007/bf02343226

29 September 2019

exact match

0 references

cites work

Refsum's disease, adrenoleucodystrophy, and the Zellweger syndrome

1 reference

12 December 2020

Subcellular localization of acyl coenzyme A: dihydroxyacetone phosphate acyltransferase in rat liver peroxisomes (microbodies)

1 reference

12 December 2020

Heterogeneity of Chondrodysplasia punctata

1 reference

12 December 2020

Bile acid abnormalities and the diagnosis of cerebro-hepato-renal syndrome (Zellweger syndrome).

1 reference

12 December 2020

Identification of 3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestan-26-oic acid, an intermediate in cholic acid synthesis, in the plasma of patients with infantile Refsum's disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Long term survival of a patient with the cerebro-hepato-renal (Zellweger) syndrome.

1 reference

12 December 2020

Gas-liquid chromatography-mass spectrometry of trimethylsilyl ethers of bile alcohols

1 reference

12 December 2020

Rhizomelic chondrodysplasia punctata: another peroxisomal disorder.

1 reference

12 December 2020

Patterns of Refsum's disease. Phytanic acid oxidase deficiency

1 reference

12 December 2020

The bile acid composition of gastric contents from neonates with high intestinal obstruction

1 reference

12 December 2020

Infantile Refsum's disease (phytanic acid storage disease): a variant of Zellweger's syndrome?

1 reference

12 December 2020

A milder variant of Zellweger syndrome.

1 reference

12 December 2020

Structure of the side chain of the C29 dicarboxylic bile acid occurring in infants with coprostanic acidemia.

1 reference

12 December 2020

Formation of cholic acid from 3 alpha, 7 alpha, 12 alpha-trihydroxy-5 beta-cholestanoic acid by rat liver peroxisomes

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

C27 Bile Acids in Infants with Coprostanic Acidemia and Occurrence of a 3alpha,7alpha,12alpha-Trihydroxy-5beta-C29 Dicarboxylic Bile Acid as a Major Component in Their Serum

1 reference

12 December 2020

Ultrastructure of the Liver in the Cerebrohepatorenal Syndrome of Zellweger

1 reference

12 December 2020

Phenobarbital-induced alterations of bile acid metabolism in cases of intrahepatic cholestasis

1 reference

12 December 2020

Defective peroxisomal cleavage of the C27-steroid side chain in the cerebro-hepato-renal syndrome of Zellweger

1 reference

12 December 2020

A simplified gas-liquid chromatographic methods for the estimation of non-sulphated plasma bile acids

1 reference

12 December 2020

Absence of hepatic peroxisomes in a case of infantile Refsum's disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Serum bile acid analysis

1 reference

12 December 2020

Cytochemistry of human catalase. The demonstration of hepatic and renal peroxisomes by a high temperature procedure

1 reference

12 December 2020

The cerebrohepatorenal syndrome of Zellweger, morphologic and metabolic aspects

1 reference

12 December 2020

Defects of Bile Acid Synthesis in Zellweger's Syndrome

1 reference

12 December 2020

Peroxisomal disorders: a newly recognised group of genetic diseases

1 reference

12 December 2020

Phenacyl esters of fatty acids via crown ether catalysts for enhanced ultraviolet detection in liquid chromatography

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF02343226

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2436918%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

1 reference