(Q49113700)

18 February 2018

title

Cytoplasmic catalase and ghostlike peroxisomes in the liver from a child with atypical chondrodysplasia punctata. (English)

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18 February 2018

author name string

Espeel M

1

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18 February 2018

Heikoop JC

2

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18 February 2018

Smeitink JA

3

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18 February 2018

Beemer FA

4

1 reference

18 February 2018

De Craemer D

5

1 reference

18 February 2018

Van den Berg M

6

1 reference

18 February 2018

Hashimoto T

7

1 reference

18 February 2018

Wanders RJ

8

1 reference

18 February 2018

Schutgens RB

9

1 reference

18 February 2018

Poll-The BT

10

1 reference

18 February 2018

publication date

1 November 1993

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18 February 2018

Ultrastructural Pathology

published in

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18 February 2018

volume

17

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18 February 2018

issue

6

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18 February 2018

page(s)

623-636

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18 February 2018

Very large peroxisomes in distinct peroxisomal disorders (rhizomelic chondrodysplasia punctata and acyl-CoA oxidase deficiency): novel data.

cites work

1 reference

https://api.crossref.org/works/10.3109%2F01913129309027798

Aberrant subcellular localization of peroxisomal 3-ketoacyl-CoA thiolase in the Zellweger syndrome and rhizomelic chondrodysplasia punctata.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913129309027798

Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzyme

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913129309027798

Peroxisomes of normal morphology but deficient in 3-oxoacyl-CoA thiolase in Rhizomelic Chondrodysplasia Punctata fibroblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913129309027798

Congenital rubella syndrome associated with calcific epiphyseal stippling and peroxisomal dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913129309027798

A new type of chondrodysplasia punctata associated with peroxisomal dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913129309027798

Hepatic peroxisomes in adrenoleukodystrophy and related syndromes: cytochemical and morphometric data

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913129309027798

Immunocytochemical detection of peroxisomal β-oxidation enzymes in cryostat and paraffin sections of human post mortem liver

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913129309027798

Alanine glyoxylate aminotransferase and the urinary excretion of oxalate and glycollate in hyperoxaluria type I and the Zellweger syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913129309027798

Hepatocellular peroxisomes in human alcoholic and drug-induced hepatitis: a quantitative study

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913129309027798

Immunocytochemical localization of human hepatic alanine: glyoxylate aminotransferase in control subjects and patients with primary hyperoxaluria type 1

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913129309027798

Chondrodysplasia punctata--rhizomelic form. Pathologic and radiologic studies of three infants

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913129309027798

Chondrodysplasia punctata-23 cases of a mild and relatively common variety

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913129309027798

Genetic and biochemical heterogeneity in patients with the rhizomelic form of chondrodysplasia punctata ? a complementation study

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913129309027798

Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913129309027798

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913129309027798

Peroxisomal disorders in neurology

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913129309027798

Ataxia and peripheral neuropathy: a benign variant of peroxisome dysgenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913129309027798

Liver pathology and immunocytochemistry in congenital peroxisomal diseases: a review

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913129309027798

Biochemical abnormalities in rhizomelic chondrodysplasia punctata

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01913129309027798

10.3109/01913129309027798

21 January 2018

Identifiers

DOI

1 reference

18 February 2018

1 reference

18 February 2018