(Q41308204)

29 September 2017

1 reference

title

Peroxisomal disorders: overview (English)

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29 September 2017

Moser HW

1

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29 September 2017

Moser AB

series ordinal

2

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29 September 2017

language of work or name

English

0 references

publication date

1 December 1996

1 reference

Annals of the New York Academy of Sciences

29 September 2017

number of pages

15

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based on heuristic

inferred from page(s)

published in

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29 September 2017

volume

804

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29 September 2017

page(s)

427-441

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Adreno-leukodystrophy. Similar ultrastructural changes in adrenal cortical and Schwann cells.

29 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Bronzekrankheit und sklerosierende Encephalomyelitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Differential protein import deficiencies in human peroxisome assembly disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

The cerebrohepatorenal syndrome of Zellweger, morphologic and metabolic aspects

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Zellweger syndrome: diagnostic assays, syndrome delineation, and potential therapy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

The mechanism of arrest of neuronal migration in the Zellweger malformation: An hypothesis based upon cytoarchitectonic analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Neonatal adrenoleukodystrophy: new cases, biochemical studies, and differentiation from Zellweger and related peroxisomal polydystrophy syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Adrenoleukodystrophy: phenotypic variability and implications for therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Distinction between peroxisomal bifunctional enzyme and acyl-CoA oxidase deficiencies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Prenatal and perinatal diagnosis of peroxisomal disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Genomic organization of the adrenoleukodystrophy gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Genetic complementation in heterokaryons of human fibroblasts defective in cobalamin metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Identification of peroxisomal targeting signals located at the carboxy terminus of four peroxisomal proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Recent advances in the understanding, diagnosis and treatment of primary hyperoxaluria type 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Identification of the inflammatory cells in the central nervous system of patients with adrenoleukodystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Neuronal migration abnormality in peroxisomal bifunctional enzyme defect.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Dietary erucic acid therapy for X-linked adrenoleukodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Komrower Lecture. Adrenoleukodystrophy: natural history, treatment and outcome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

A two-year trial of oleic and erucic acids ("Lorenzo's oil") as treatment for adrenomyeloneuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Severe deficiency of docosahexaenoic acid in peroxisomal disorders: a defect of delta 4 desaturation?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Docosahexaenoic acid--a new therapeutic approach to peroxisomal-disorder patients: experience with two cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Predominance of the adrenomyeloneuropathy phenotype of X-linked adrenoleukodystrophy in The Netherlands: a survey of 30 kindreds

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

Bile acid analyses in "pseudo-Zellweger" syndrome; clues to the defect in peroxisomal beta-oxidation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB18634.X

10.1111/J.1749-6632.1996.TB18634.X

21 January 2018

Identifiers

DOI

1 reference

29 September 2017

1 reference