(Q68989169)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2435984%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

title

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

1 reference

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29 September 2019

author name string

M E Beard

1

1 reference

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29 September 2019

A B Moser

2

1 reference

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29 September 2019

V Sapirstein

3

1 reference

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29 September 2019

E Holtzman

4

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29 September 2019

publication date

1 January 1986

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Journal of Inherited Metabolic Disease

29 September 2019

published in

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29 September 2019

volume

9

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29 September 2019

page(s)

321-334

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29 September 2019

issue

4

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https://scigraph.springernature.com/pub.10.1007/bf01800481

29 September 2019

exact match

0 references

cites work

Adrenoleukodystrophy: impaired oxidation of very long chain fatty acids in white blood cells, cultured skin fibroblasts, and amniocytes

1 reference

12 December 2020

Refsum's disease: nature of the enzyme defect

1 reference

12 December 2020

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

Infantile Refsum's disease: biochemical findings suggesting multiple peroxisomal dysfunction.

1 reference

12 December 2020

Peroxisomal defects in neonatal-onset and X-linked adrenoleukodystrophies

1 reference

12 December 2020

Refsum's disease: characterization of the enzyme defect in cell culture

1 reference

12 December 2020

Hyperpipecolic acidemia: Clinical and biochemical observations in two male siblings

1 reference

12 December 2020

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

1 reference

12 December 2020

Visualization of peroxisomes (microbodies) and mitochondria with diaminobenzidine

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Glycerolipid biosynthesis in peroxisomes via the acyl dihydroxyacetone phosphate pathway

1 reference

12 December 2020

Cerebro-hepato-renal (Zellweger) syndrome, adrenoleukodystrophy, and Refsum's disease: plasma changes and skin fibroblast phytanic acid oxidase

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

Degradation of cholesterol to propionic acid by rat liver peroxisomes

1 reference

12 December 2020

Rhizomelic chondrodysplasia punctata: another peroxisomal disorder.

1 reference

12 December 2020

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

1 reference

12 December 2020

Disturbances in bile acid metabolism of infants with the Zellweger (cerebro-hepato-renal) syndrome

1 reference

12 December 2020

Peroxisomes (microbodies) in cell pathology.

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

Peroxisomes in fibroblasts from skin of Refsum's disease patients

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

Refsum's disease: defective oxidation of phytanic acid in tissue cultures derived from homozygotes and heterozygotes.

1 reference

12 December 2020

The use of lead citrate at high pH as an electron-opaque stain in electron microscopy

1 reference

12 December 2020

Cell junctions in amphibian skin

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

The peroxisomal disorders

1 reference

12 December 2020

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

1 reference

12 December 2020

Studies on the alpha oxidation of phytanic acid by rat liver mitochondria

1 reference

12 December 2020

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

1 reference

12 December 2020

Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome).

1 reference

12 December 2020

Plasma and skin fibroblast C26 fatty acids in infantile Refsum's disease

1 reference

12 December 2020

A fatty acyl-CoA oxidizing system in rat liver peroxisomes; enhancement by clofibrate, a hypolipidemic drug

1 reference

12 December 2020

Adrenoleukodystrophy: impaired oxidation of long chain fatty acids in cultured skin fibroblasts an adrenal cortex

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01800481

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2435984%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

1 reference