(Q24324034)

Enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase

1 reference

Alanine--glyoxylate and serine--pyruvate aminotransferase

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Catalase

1 reference

Journal of Inherited Metabolic Disease

author name string

M Espeel

series ordinal

1

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G Van Limbergen

series ordinal

2

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language of work or name

English

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publication date

1995

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published in

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volume

18 Suppl 1

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page(s)

135-54

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cites work

A new acrylic resin formulation: a useful tool for histological, ultrastructural, and immunocytochemical investigations

1 reference

12 December 2020

Cytoplasmic catalase and ghostlike peroxisomes in the liver from a child with atypical chondrodysplasia punctata

1 reference

12 December 2020

Bone dysplasia associated with phytanic acid accumulation and deficient plasmalogen synthesis: a peroxisomal entity amenable to plasmapheresis

1 reference

12 December 2020

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

1 reference

12 December 2020

Cytosolic compartmentalization of hepatic alanine:glyoxylate aminotransferase in patients with aberrant peroxisomal biogenesis and its effect on oxalate metabolism

1 reference

12 December 2020

Human liver pathology in peroxisomal diseases: a review including novel data

1 reference

12 December 2020

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

1 reference

12 December 2020

Enzymological and mutational analysis of a complex primary hyperoxaluria type 1 phenotype involving alanine:glyoxylate aminotransferase peroxisome-to-mitochondrion mistargeting and intraperoxisomal aggregation

1 reference

12 December 2020

A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy)

1 reference

12 December 2020

Practical guide for morphometry of human peroxisomes on electron micrographs

1 reference

12 December 2020

An enzyme trafficking defect in two patients with primary hyperoxaluria type 1: peroxisomal alanine/glyoxylate aminotransferase rerouted to mitochondria

1 reference

12 December 2020

Ultrastructure and immunocytochemistry of hepatic peroxisomes in rhizomelic chondrodysplasia punctata

1 reference

12 December 2020

Autometallography: tissue metals demonstrated by a silver enhancement kit.

1 reference

12 December 2020

Peroxisome mosaicism in the livers of peroxisomal deficiency patients

1 reference

12 December 2020

A new method of preparing gold probes for multiple-labeling cytochemistry

1 reference

12 December 2020

Immunocytochemical localization of peroxisomal beta-oxidation enzymes in human fetal liver

1 reference

12 December 2020

X-linked recessive chondrodysplasia punctata with XY translocation in a stillborn fetus

1 reference

12 December 2020

A new variant of Zellweger syndrome with normal peroxisomal functions in cultured fibroblasts

1 reference

12 December 2020

Immunocytochemical localization of peroxisomal enzymes in human liver biopsies

1 reference

12 December 2020

Detection of peroxisomes in human liver and kidney fixed with formalin and embedded in paraffin: The use of catalase and lipid β-oxidation enzymes as immunocytochemical markers

1 reference

12 December 2020

Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis

1 reference

12 December 2020

Immunolocalization of a 43 kDa peroxisomal membrane protein in the liver of patients with generalized peroxisomal disorders.

1 reference

12 December 2020

Liver and chorion cytochemistry

1 reference

12 December 2020

A new type of peroxisomal disorder with variable expression in liver and fibroblasts

1 reference

12 December 2020

Morphometry of peroxisomes and immunolocalization of peroxisomal proteins in the liver of patients with generalised peroxisomal disorders

1 reference

12 December 2020

Ultrastructural autometallography: a method for silver amplification of catalytic metals.

1 reference

12 December 2020

Immunoblot analysis of peroxisomal proteins in liver and fibroblasts from patients

1 reference

12 December 2020

Peroxisomal localization of the immunoreactive beta-oxidation enzymes in a neonate with a beta-oxidation defect. Pathological observations in liver, adrenal cortex and kidney.

1 reference

12 December 2020

Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorder

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF00711436

7 January 2021

inferred from DOI database lookup

Neonatal seizures and severe hypotonia in a male infant suffering from a defect in peroxisomal beta-oxidation

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF00711436

7 January 2021