(Q36930280)

17 August 2017

1 reference

title

Liver pathology and immunocytochemistry in congenital peroxisomal diseases: a review (English)

1 reference

https://api.crossref.org/works/10.1007/BF01800464

17 August 2017

0 references

1 reference

21 November 2022

author name string

F. Roels

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1779645

21 November 2022

M. Espeel

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1779645

21 November 2022

D. De Craemer

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1779645

21 November 2022

language of work or name

1 reference

1 January 1991

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full work available at URL

17 August 2017

http://link.springer.com/content/pdf/10.1007/BF01800464

1 reference

https://api.crossref.org/works/10.1007/BF01800464

Journal of Inherited Metabolic Disease

21 November 2022

published in

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17 August 2017

14

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17 August 2017

6

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17 August 2017

853-875

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https://scigraph.springernature.com/pub.10.1007/bf01800464

17 August 2017

0 references

cites work

Peroxisomes in fibroblasts from skin of Refsum's disease patients

1 reference

https://api.crossref.org/works/10.1007%2FBF01800464

Peroxisomal and mitochondrial proliferation and increased alanine: glyoxylate aminotransferase activity in human liver after chlorpromazine-induced cholestasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01800464

Histochemical characteristics of the striated inclusions of adrenoleukodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01800464

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01800464

Peroxisomes (Microbodies) in Human Liver: Cytochemical and Quantitative Studies of 85 Biopsies 12.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01800464

Adreno-leukodystrophy (sex-linked Schilder disease). Ultrastructural demonstration of specific cytoplasmic inclusions in the central nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01800464

Adrenoleukodystrophy. A clinical and pathological study of 17 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF01800464

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

21 January 2018

1 reference

12 December 2020

Light microscopic visualization of peroxisomes and plasmalogens in first trimester chorionic villi

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12 December 2020

Phytol and peroxisome proliferation

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12 December 2020

Zellweger-like syndrome with detectable hepatic peroxisomes: a variant form of peroxisomal disorder

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12 December 2020

Ultrastructure of the Liver in the Cerebrohepatorenal Syndrome of Zellweger

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12 December 2020

Heredopathia atactica polyneuritiformis (Refsum's disease)

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12 December 2020

Nonspecific lipid transfer protein (sterol carrier protein-2) defective in patients with deficient peroxisomes

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12 December 2020

The inhibition by valproic acid of the mitochondrial oxidation of monocarboxylic and omega-hydroxymonocarboxylic acids: possible implications for the metabolism of gamma-aminobutyric acid

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12 December 2020

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

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12 December 2020

Peroxisomal defects in neonatal-onset and X-linked adrenoleukodystrophies

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12 December 2020

Morphology and distribution of cytoplasmic inclusions in adrenoleukodystrophy

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12 December 2020

The synthesis and turnover of rat liver peroxisomes. 3. The size distribution of peroxisomes and the incorporation of new catalase

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12 December 2020

Infantile Refsum disease: an inherited peroxisomal disorder. Comparison with Zellweger syndrome and neonatal adrenoleukodystrophy.

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12 December 2020

Peroxisomal bifunctional enzyme deficiency

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12 December 2020

Central nervous system malformations and white matter changes in pseudo-neonatal adrenoleukodystrophy.

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12 December 2020

Rhizomelic chondrodysplasia punctata: Biochemical studies of peroxisomes isolated from cultured skin fibroblasts

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12 December 2020

Heterogeneity of catalase staining in human hepatocellular peroxisomes

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12 December 2020

The peroxisomes of human hepatocytes

1 reference

12 December 2020

Hepatic peroxisomes are deficient in infantile refsum disease: a cytochemical study of 4 cases

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12 December 2020

Increased sensitivity of cerebrohepatorenal syndrome fibroblasts to antimycin A

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12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Adrenoleukodystrophy in a mother and son.

1 reference

12 December 2020

Peroxisomes (Microbodies) in Human Liver: Cytochemical and Quantitative Studies of 85 Biopsies

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12 December 2020

Dysmorphic syndrome with phytanic acid oxidase deficiency, abnormal very long chain fatty acids, and pipecolic acidemia: studies in four children

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12 December 2020

Pathologic alterations in the brain and liver in hyperpipecolic acidemia.

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12 December 2020

Ultrastructure of liver in inherited disorders of fat oxidation

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12 December 2020

Biosynthesis and maturation of peroxisomal beta-oxidation enzymes in fibroblasts in relation to the Zellweger syndrome and infantile Refsum disease

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12 December 2020

Peroxisomes and peroxisomal functions in hyperpipecolic acidaemia

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12 December 2020

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

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12 December 2020

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

1 reference

12 December 2020

Cerebro-hepato-renal syndrome of Zellweger. A report of eight cases with comments upon the incidence, the liver lesion, and a fault in pipecolic acid metabolism

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12 December 2020

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

1 reference

12 December 2020

Light and electron microscopic liver changes in the cerebro-hepato-renal syndrome of Zellweger (Peroxisome deficiency) (author's transl)

1 reference

12 December 2020

Studies of malformation syndromes of man XIB: the cerebro-hepato-renal syndrome of zellweger: Comparative pathology

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

Peroxisomal integral membrane proteins in control and Zellweger fibroblasts

1 reference

12 December 2020

New phenotypic variant of adrenoleukodystrophy. Pathologic, ultrastructural, and biochemical study in two brothers

1 reference

12 December 2020

Mitochondrial Ultrastructure in Reye's Syndrome (Encephalopathy and Fatty Degeneration of the Viscera)

1 reference

12 December 2020

Presence of peroxisomal membrane proteins in liver and fibroblasts from patients with the Zellweger syndrome and related disorders: evidence for the existence of peroxisomal ghosts

1 reference

12 December 2020

Mechanisms of Adaption of Hepatocytes to a Chronical Hypothyroidism (A Cytophotometrical and Morphometrical Study)

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12 December 2020

Primary hyperoxaluria type I: ultrastructural observations in liver biopsies

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12 December 2020

Different types of peroxisomes in human duodenal epithelium

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12 December 2020

Adreno-leukodystrophy (adreno-testiculo-leukomyelo-neuropathic-complex).

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomes

1 reference

12 December 2020

Hyperpipecolatemia: A new metabolic disorder associated with neuropathy and hepatomegaly: A case study

1 reference

12 December 2020

Treatment of infantile phytanic acid storage disease: clinical, biochemical and ultrastructural findings in two children treated for 2 years

1 reference

12 December 2020

Peroxisomal proliferation in heart and liver of mice receiving chlorpromazine, ethyl 2(5(4-chlorophenyl)pentyl) oxiran-2-carboxylic acid or high fat diet: a biochemical and morphometrical comparative study

1 reference

12 December 2020

Phenotypic heterogeneity in cultured skin fibroblasts from patients with disorders of peroxisome biogenesis belonging to the same complementation group

1 reference

12 December 2020

A case of Refsum's disease: clinical, pathological, ultrastructural and biochemical study.

1 reference

12 December 2020

Pathology of hepatic peroxisomes and mitochondria in patients with peroxisomal disorders

1 reference

12 December 2020

Time course of peroxisome biogenesis during adaptation to mild hyperthyroidism in rat liver: a morphometric/stereologic study by electron microscopy

1 reference

12 December 2020

Phytanic acid alpha-oxidation and complementation analysis of classical Refsum and peroxisomal disorders

1 reference

12 December 2020

Altered acyl-CoA metabolism in riboflavin deficiency

1 reference

12 December 2020

Molecular analysis of peroxisomal beta-oxidation enzymes in infants with Zellweger syndrome and Zellweger-like syndrome: further heterogeneity of the peroxisomal disorder

1 reference

12 December 2020

Effects of marine oil diet on peroxisomes and mitochondria of rat liver. A combined biochemical and morphometric study

1 reference

12 December 2020

Neonatal seizures and retardation in a girl with biochemical features of X-linked adrenoleukodystrophy: a possible new peroxisomal disease entity

1 reference

12 December 2020

Mitochondrial myopathy of cerebro-hepato-renal (Zellweger) syndrome.

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

Mitochondrial oxidation of phytanic acid in human and monkey liver: Implication that Refsum's disease is not a peroxisomal disorder

1 reference

12 December 2020

Peroxisomal functions in classical Refsum's disease: comparison with the infantile form of Refsum's disease

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Normal peroxisomal function and absent skeletal manifestations in Conradi-Hünermann syndrome

1 reference

12 December 2020

Post-mortem visualization of peroxisomes in rat and in human liver

1 reference

12 December 2020

Biosynthesis of peroxisomal beta-oxidation enzymes in infants with Zellweger syndrome

1 reference

12 December 2020

Immunocytochemical localization of peroxisomal enzymes in human liver biopsies

1 reference

12 December 2020

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

1 reference

12 December 2020

Liver in the cerebro-hepato-renal syndrome: defective bile acid synthesis and abnormal mitochondria

1 reference

12 December 2020

Polarizing inclusions in some organs of children with congenital peroxisomal diseases (Zellweger's, Refsum's, chondrodysplasia punctata (rhizomelic form), X-linked adrenoleukodystrophy)

1 reference

12 December 2020

Hyperpipecolic acidemia: Clinical and biochemical observations in two male siblings

1 reference

12 December 2020

Rhizomelic chondrodysplasia punctata: clinical, pathologic, and biochemical findings in two patients

1 reference

12 December 2020

Pseudo-Zellweger syndrome: deficiencies in several peroxisomal oxidative activities.

1 reference

12 December 2020

Neonatal-onset adrenoleukodystrophy in a girl

1 reference

12 December 2020

Peroxisomes in infantile phytanic acid storage disease: a cytochemical study of skin fibroblasts

1 reference

12 December 2020

Peroxisomal disorders in neurology

1 reference

12 December 2020

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

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

Integral membrane polypeptides of rat liver peroxisomes: topology and response to different metabolic states

1 reference

12 December 2020

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

The involvement of carnitine intermediates in peroxisomal fatty acid oxidation: a study with 2-bromofatty acids

1 reference

12 December 2020

Pathology of the liver in Reye's syndrome

1 reference

12 December 2020

Alterations of hepatocellular peroxisomes in viral hepatitis in the mouse

https://api.crossref.org/works/10.1007/BF01800464

15

1 reference

21 November 2022

Identifiers

DOI

10.1007/BF01800464

1 reference

17 August 2017

1 reference