(Q38623776)

English

Adrenoleukodystrophy and other peroxisomal disorders that affect the nervous system, including new observations on L-pipecolic acid oxidase in primates

scientific article published on January 1989

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

4 September 2017

1 reference

Europe PubMed Central

Adrenoleukodystrophy and other peroxisomal disorders that affect the nervous system, including new observations on L-pipecolic acid oxidase in primates (English)

1 reference

Europe PubMed Central

PubMed publication ID

4 September 2017

author name string

Moser HW

1

1 reference

Europe PubMed Central

PubMed publication ID

4 September 2017

Mihalik SJ

2

1 reference

Europe PubMed Central

PubMed publication ID

4 September 2017

Watkins PA

3

1 reference

Europe PubMed Central

PubMed publication ID

4 September 2017

publication date

1 January 1989

1 reference

Europe PubMed Central

PubMed publication ID

4 September 2017

Brain and Development

1 reference

Europe PubMed Central

PubMed publication ID

4 September 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

4 September 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

4 September 2017

80-90

1 reference

Europe PubMed Central

PubMed publication ID

4 September 2017

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Pseudo-Zellweger syndrome: deficiencies in several peroxisomal oxidative activities

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Peroxisomal disorders: a newly recognised group of genetic diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

New approaches in peroxisomal disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Phenotypic and genotypic variability of generalized peroxisomal disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Studies on microperoxisomes. V. Are microperoxisomes ubiquitous in mammalian cells?

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Microperoxisomes in the central nervous system of the postnatal rat

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Peroxisomal organization in normal and cerebrohepatorenal (Zellweger) syndrome fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Metabolic pathways in peroxisomes and glyoxysomes

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Peroxisomes (microbodies and related particles)

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Individual peroxisomal beta-oxidation enzymes

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Oxidation of oxalate and polyamines by rat peroxisomes

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Glycerolipid biosynthesis in peroxisomes via the acyl dihydroxyacetone phosphate pathway

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Conversion of 3 alpha, 7 alpha, 12 alpha-trihydroxy-5 beta-cholestanoic acid into cholic acid by rat liver peroxisomes

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Defects of Bile Acid Synthesis in Zellweger's Syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Biogenesis of peroxisomes

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

The cerebrohepatorenal syndrome of Zellweger, morphologic and metabolic aspects

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Primary hyperparathyroidism associated with pancytosis

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Biochemical abnormalities in rhizomelic chondrodysplasia punctata

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Adrenoleukodystrophy: survey of 303 cases: biochemistry, diagnosis, and therapy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Enzymological diagnosis of primary hyperoxaluria type 1 by measurement of hepatic alanine: glyoxylate aminotransferase activity

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Lignoceroyl-CoASH ligase: enzyme defect in fatty acid beta-oxidation system in X-linked childhood adrenoleukodystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

X-linked adrenoleukodystrophy: defective peroxisomal oxidation of very long chain fatty acids but not of very long chain fatty acyl-CoA esters

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Characterization of rat brain microsomal acyl-coenzyme A ligases: different enzymes for the synthesis of palmitoyl-coenzyme A and lignoceroyl-coenzyme A.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Linkage of adrenoleukodystrophy to a polymorphic DNA probe

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular genetics of human color vision: the genes encoding blue, green, and red pigments

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular genetics of inherited variation in human color vision

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Adrenoleukodystrophy: increased plasma content of saturated very long chain fatty acids

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Adrenoleukodystrophy: Elevated C26 fatty acid in cultured skin fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Adrenoleukodystrophy. A clinical and pathological study of 17 cases

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Adrenomyeloneuropathy: A probable variant of adrenoleukodystrophy I. Clinical and endocrinologic aspects

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Membrane microviscosity is increased in the erythrocytes of patients with adrenoleukodystrophy and adrenomyeloneuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Effects of long-chain, saturated fatty acids on membrane microviscosity and adrenocorticotropin responsiveness of human adrenocortical cells in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Specificities of human and rat brain enzymes of cholesterol ester metabolism toward very long chain fatty acids: implication for biochemical pathogenesis of adrenoleukodystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Brain tissue immunoglobulins in adrenoleukodystrophy: A comparison with multiple sclerosis and systemic lupus erythematosus

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Adrenoleukodystrophy. Failure of immunosuppression to prevent neurological progression

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Childhood adrenoleukodystrophy. Failure of intensive immunosuppression to arrest neurologic progression

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Adrenoleukodystrophy: dietary oleic acid lowers hexacosanoate levels

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

A new dietary therapy for adrenoleukodystrophy: biochemical and preliminary clinical results in 36 patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Bone marrow transplant in adrenoleukodystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Presence of the peroxisomal 22-kDa integral membrane protein in the liver of a person lacking recognizable peroxisomes (Zellweger syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Peroxisomal integral membrane proteins in livers of patients with Zellweger syndrome, infantile Refsum's disease and X-linked adrenoleukodystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Peroxisomal membrane ghosts in Zellweger syndrome--aberrant organelle assembly

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

The cerebrohepatorenal (Zellweger) syndrome: an improved method for the biochemical diagnosis and its potential value for prenatal detection

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Lysine metabolism in rabbits

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Prenatal diagnosis of rhizomelic chondrodysplasia punctata

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Prenatal diagnosis of Zellweger cerebrohepatorenal syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

The cerebro-hepato-renal (Zellweger) syndrome: prenatal detection based on impaired biosynthesis of plasmalogens

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

A prenatal test for the cerebro-hepato-renal (Zellweger) syndrome by demonstration of the absence of catalase-containing particles (peroxisomes) in cultured amniotic fluid cells

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Peroxisomal bifunctional enzyme deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2889%2980074-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0387-7604(89)80074-9

1 reference

Europe PubMed Central

PubMed publication ID

4 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 September 2017

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