Pseudo-Zellweger syndrome: deficiencies in several peroxisomal oxidative activities (Q48422324)

11 February 2018

title

Pseudo-Zellweger syndrome: deficiencies in several peroxisomal oxidative activities (English)

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11 February 2018

author name string

Goldfischer S

1

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11 February 2018

Collins J

2

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11 February 2018

Rapin I

3

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11 February 2018

Neumann P

4

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11 February 2018

Neglia W

5

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11 February 2018

Spiro AJ

6

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11 February 2018

Ishii T

7

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11 February 2018

Roels F

8

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11 February 2018

Vamecq J

9

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11 February 2018

Van Hoof F

10

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11 February 2018

language of work or name

English

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publication date

1 January 1986

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11 February 2018

The Journal of Pediatrics

published in

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11 February 2018

volume

108

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11 February 2018

issue

1

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11 February 2018

page(s)

25-32

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11 February 2018

The cerebrohepatorenal syndrome of Zellweger, morphologic and metabolic aspects

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

Glycerolipid biosynthesis in peroxisomes via the acyl dihydroxyacetone phosphate pathway

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

Cerebro-hepato-renal syndrome of Zellweger: clinical symptoms and relevant laboratory findings in 16 patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

Deficiency of enzymes catalyzing the biosynthesis of glycerol-ether lipids in Zellweger syndrome. A new category of metabolic disease involving the absence of peroxisomes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

Peroxisomal abnormalities in metabolic diseases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

Fatty-Acid Composition of Rat Brain Lipids Determined by Support-Coated Open-Tubular Gas Chromatography

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

Quantitative estimation of bile salts in serum

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

Histochemical characteristics of the striated inclusions of adrenoleukodystrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

Adrenoleukodystrophy. A clinical and pathological study of 17 cases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

Peroxisomal beta-oxidation of long fatty acids: effects of high fat diets

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

Defective peroxisomal cleavage of the C27-steroid side chain in the cerebro-hepato-renal syndrome of Zellweger

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

Peroxisomal defects in neonatal-onset and X-linked adrenoleukodystrophies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

Primary hyperparathyroidism associated with pancytosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

Neonatal-onset adrenoleukodystrophy in a girl

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

Refsum's disease, adrenoleucodystrophy, and the Zellweger syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

Disturbed adrenocortical function in cerebro-hepato-renal syndrome of Zellweger

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

The metabolism of D- and L-lysine in the intact rat, perfused liver and liver mitochondria.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

Peroxisomes in fibroblasts from skin of Refsum's disease patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2886%2980764-8

10.1016/S0022-3476(86)80764-8

7 January 2021

Identifiers

DOI

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11 February 2018

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11 February 2018