(Q46367988)

21 December 2017

title

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

1 reference

21 December 2017

author name string

Suzuki Y

1

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21 December 2017

Shimozawa N

2

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21 December 2017

Orii T

3

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21 December 2017

Igarashi N

4

1 reference

21 December 2017

Kono N

5

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21 December 2017

Matsui A

6

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21 December 2017

Inoue Y

7

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21 December 2017

Yokota S

8

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21 December 2017

Hashimoto T

9

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21 December 2017

language of work or name

English

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publication date

1 November 1988

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21 December 2017

The Journal of Pediatrics

published in

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21 December 2017

volume

113

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21 December 2017

issue

5

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21 December 2017

page(s)

841-845

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21 December 2017

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

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980011-8

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%2888%2980011-8

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%2888%2980011-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980011-8

Peroxisomal disorders: a newly recognised group of genetic diseases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980011-8

Light microscopic immunocytochemical demonstration of peroxisomal enzymes in epon sections

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980011-8

Abnormality of long-chain fatty acids in erythrocyte membrane sphingomyelin from patients with adrenoleukodystrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980011-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980011-8

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980011-8

Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980011-8

10.1016/S0022-3476(88)80011-8

7 January 2021

Identifiers

DOI

1 reference

21 December 2017

1 reference

21 December 2017