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English
Child neurology: Zellweger syndrome
scientific article published on May 2013
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
3908348
retrieved
20 August 2017
case report
0 references
title
Child neurology: Zellweger syndrome
(English)
1 reference
stated in
Europe PubMed Central
PMCID
3908348
retrieved
20 August 2017
author name string
Paul R Lee
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
3908348
retrieved
20 August 2017
Gerald V Raymond
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
3908348
retrieved
20 August 2017
language of work or name
English
0 references
publication date
1 May 2013
1 reference
stated in
Europe PubMed Central
PMCID
3908348
retrieved
20 August 2017
published in
Neurology
1 reference
stated in
Europe PubMed Central
PMCID
3908348
retrieved
20 August 2017
volume
80
1 reference
stated in
Europe PubMed Central
PMCID
3908348
retrieved
20 August 2017
issue
20
1 reference
stated in
Europe PubMed Central
PMCID
3908348
retrieved
20 August 2017
page(s)
e207-10
1 reference
stated in
Europe PubMed Central
PMCID
3908348
retrieved
20 August 2017
cites work
A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3908348
retrieved
23 August 2017
Peroxisome biogenesis disorders
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3908348
retrieved
23 August 2017
Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3908348
retrieved
23 August 2017
A FAMILIAL SYNDROME OF MULTIPLE CONGENITAL DEFECTS
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3908348
retrieved
23 August 2017
Clinical recognition of patients affected by a peroxisomal disorder: a retrospective study in 40 patients
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3908348
retrieved
23 August 2017
Effect of dietary Lorenzo's oil and docosahexaenoic acid treatment for Zellweger syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3908348
retrieved
1 September 2018
Anesthesia for the child with Zellweger syndrome: a case report.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3908348
retrieved
1 September 2018
Recognition of Zellweger syndrome in infancy.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3908348
retrieved
1 September 2018
Clinical, biochemical and molecular characterization of peroxisomal diseases in Arabs
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3908348
retrieved
3 December 2018
Identifiers
DOI
10.1212/WNL.0B013E3182929F8E
1 reference
stated in
Europe PubMed Central
PMCID
3908348
retrieved
20 August 2017
PMCID
3908348
1 reference
stated in
Europe PubMed Central
PMCID
3908348
retrieved
20 August 2017
PubMed ID
23671347
1 reference
stated in
Europe PubMed Central
PMCID
3908348
retrieved
20 August 2017
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