(Q41806915)

English

Multiple peroxisomal enzymatic deficiency disorders. A comparative biochemical and morphologic study of Zellweger cerebrohepatorenal syndrome and neonatal adrenoleukodystrophy

scientific article published on December 1986

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

12 October 2017

Multiple peroxisomal enzymatic deficiency disorders. A comparative biochemical and morphologic study of Zellweger cerebrohepatorenal syndrome and neonatal adrenoleukodystrophy (English)

1 reference

Europe PubMed Central

12 October 2017

Neonatal adrenoleukodystrophy

1 reference

based on heuristic

inferred from title

author name string

J Vamecq

1

1 reference

Europe PubMed Central

12 October 2017

J P Draye

2

1 reference

Europe PubMed Central

12 October 2017

F Van Hoof

3

1 reference

Europe PubMed Central

12 October 2017

J P Misson

4

1 reference

Europe PubMed Central

12 October 2017

P Evrard

5

1 reference

Europe PubMed Central

12 October 2017

G Verellen

6

1 reference

Europe PubMed Central

12 October 2017

H J Eyssen

7

1 reference

Europe PubMed Central

12 October 2017

J Van Eldere

8

1 reference

Europe PubMed Central

12 October 2017

R B Schutgens

9

1 reference

Europe PubMed Central

12 October 2017

R J Wanders

10

1 reference

Europe PubMed Central

12 October 2017

language of work or name

0 references

publication date

1 December 1986

1 reference

Europe PubMed Central

12 October 2017

The American Journal of Pathology

1 reference

Europe PubMed Central

12 October 2017

125

1 reference

Europe PubMed Central

12 October 2017

3

1 reference

Europe PubMed Central

12 October 2017

524-535

1 reference

Europe PubMed Central

12 October 2017

A FAMILIAL SYNDROME OF MULTIPLE CONGENITAL DEFECTS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

Fenofibrate: animal toxicology in relation to side-effects in man (author's transl)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

Review of the hepatic response to hypolipidaemic drugs in rodents and assessment of its toxicological significance to man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

Biochemical studies in the liver and muscle of patients with Zellweger syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

Implication of a peroxisomal enzyme in the catabolism of glutaryl-CoA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

Peroxisomes (microbodies) in cell pathology.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

The cerebrohepatorenal syndrome of Zellweger, morphologic and metabolic aspects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

Mitochondrial myopathy with loosely coupled oxidative phosphorylation in a case of Zellweger syndrome. A cytochemical-ultrastructural study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

Cerebro-hepato-renal syndrome of Zellweger: an inherited disorder of neuronal migration.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

Peroxisomal abnormalities in metabolic diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

In vivo and vitro studies on formation of bile acids in patients with Zellweger syndrome. Evidence that peroxisomes are of importance in the normal biosynthesis of both cholic and chenodeoxycholic acid

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

The microsomal dicarboxylyl-CoA synthetase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

Mitochondrial and peroxisomal metabolism of glutaryl-CoA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

The cerebro-hepato-renal (Zellweger) syndrome. Impaired de novo biosynthesis of plasmalogens in cultured skin fibroblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

Biogenesis of peroxisomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

Induction of fatty acid beta-oxidation and peroxisome proliferation in the liver of rhesus monkeys by DL-040, a new hypolipidemic agent

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

Peroxisomal disorders: a newly recognised group of genetic diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

Pipecolic acid is oxidized by renal and hepatic peroxisomes. Implications for Zellweger's cerebro-hepato-renal syndrome (CHRS).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

Peroxisomal matrix enzymes in Zellweger syndrome: activity and subcellular localization in liver

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

Neonatal adrenoleukodystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

A metabolic disorder similar to Zellweger syndrome with hepatic acatalasia and absence of peroxisomes, altered content and redox state of cytochromes, and infantile cirrhosis with hemosiderosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

The mechanism of arrest of neuronal migration in the Zellweger malformation: An hypothesis based upon cytoarchitectonic analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

Peroxisomes: new aspects of cell physiology and biochemistry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

Adrenoleukodystrophy. Preliminary report of a connatal case. Light- and electron microscopical, immunohistochemical and biochemical findings

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

6 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

18 August 2018

Glycerolipid biosynthesis in peroxisomes via the acyl dihydroxyacetone phosphate pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

18 August 2018

Serum very long chain fatty acid pattern in Zellweger syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

18 August 2018

Deficiency of plasmalogens in the cerebro-hepato-renal (Zellweger) syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

18 August 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

18 August 2018

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

18 August 2018

Striated adrenocortical cells in cerebro-hepato-renal (Zellweger) syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

18 August 2018

Activity of peroxisomal enzymes and intracellular distribution of catalase in Zellweger syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

18 August 2018

Zellweger syndrome: biochemical and morphological studies on two patients treated with clofibrate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1888479

18 August 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomal defects in neonatal-onset and X-linked adrenoleukodystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The peroxisomal disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of peroxisomes in the biosynthesis of bile acids

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

https://pubmed.ncbi.nlm.nih.gov/2879480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A correlative study of the adrenal cortex in adreno-leukodystrophy--evidence for a fatal intoxication with very long chain saturated fatty acids

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Subcellular distribution of coenzyme A: evidence for a separate coenzyme A pool in peroxisomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial and peroxisomal beta-oxidation of fatty acids in rat liver

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Light and electron microscopy of liver in hyperlipoproteinemic patients under long-term gemfibrozil treatment

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperpipecolic acidemia. Occurrence in an infant with clinical findings of the cerebrohepatorenal (Zellweger) syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Degradation of cholesterol to propionic acid by rat liver peroxisomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relationship between morphological changes and lipid-lowering action of p-chlorphenoxyisobutyric acid (CPIB) on hepatic mitochondria and peroxisomes in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The determination of pipecolic acid: method and results of hospital survey

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

12 October 2017

1 reference

Europe PubMed Central

12 October 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q41806915&oldid=2158128497"