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Peroxisomal disorders
scientific article published on 01 December 1996
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8969011
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8969011%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
review article
1 reference
stated in
Europe PubMed Central
title
Peroxisomal disorders
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8969011
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8969011%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
author name string
H W Moser
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8969011
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8969011%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
publication date
1 December 1996
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8969011
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8969011%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
published in
Seminars in pediatric neurology
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8969011
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8969011%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
volume
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8969011
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8969011%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8969011
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8969011%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
page(s)
298-304
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8969011
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8969011%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
cites work
Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Microperoxisomes in the central nervous system of the postnatal rat
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Biogenesis of peroxisomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Protein import into peroxisomes and biogenesis of the organelle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of peroxisomal targeting signals located at the carboxy terminus of four peroxisomal proteins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A human gene responsible for Zellweger syndrome that affects peroxisome assembly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Adrenoleukodystrophy: increased plasma content of saturated very long chain fatty acids
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
ABC Transporters: From Microorganisms to Man
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutational analysis of patients with X-linked adrenoleukodystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a two base pair deletion in five unrelated families with adrenoleukodystrophy: a possible hot spot for mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked adrenoleukodystrophy (ALD): a novel mutation of the ALD gene in 6 members of a family presenting with 5 different phenotypes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Missense mutations are frequent in the gene for X-chromosomal adrenoleukodystrophy (ALD)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Adrenoleukodystrophy: phenotypic variability and implications for therapy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Individual peroxisomal beta-oxidation enzymes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Peroxisomal bifunctional enzyme deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Distinction between peroxisomal bifunctional enzyme and acyl-CoA oxidase deficiencies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorder
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human alkyldihydroxyacetonephosphate synthase deficiency: a new peroxisomal disorder
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Biochemical abnormalities in rhizomelic chondrodysplasia punctata
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heredopathia atactica polyneuritiformis phytanic-acid storage disease, Refsum's disease:" a biochemically well-defined disease with a specific dietary treatment.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Adrenoleukodystrophy. A clinical and pathological study of 17 cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multislice proton magnetic resonance spectroscopic imaging in X-linked adrenoleukodystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Adrenoleukodystrophy: correlating MR imaging with CT.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prenatal and perinatal diagnosis of peroxisomal disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dietary erucic acid therapy for X-linked adrenoleukodystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A two-year trial of oleic and erucic acids ("Lorenzo's oil") as treatment for adrenomyeloneuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Visual evoked potentials in adrenoleukodystrophy: a trial with glycerol trioleate and Lorenzo oil
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Komrower Lecture. Adrenoleukodystrophy: natural history, treatment and outcome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Reversal of early neurologic and neuroradiologic manifestations of X-linked adrenoleukodystrophy by bone marrow transplantation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuropsychological outcomes of several storage diseases with and without bone marrow transplantation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Docosahexaenoic acid--a new therapeutic approach to peroxisomal-disorder patients: experience with two cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Predominance of the adrenomyeloneuropathy phenotype of X-linked adrenoleukodystrophy in The Netherlands: a survey of 30 kindreds
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980033-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S1071-9091(96)80033-7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8969011
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8969011%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
PubMed publication ID
8969011
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8969011
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8969011%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
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