Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q36307328)
Watch
English
Peroxisomal diseases.
scientific article
In more languages
default for all languages
No label defined
No description defined
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1627308
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1627308%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
review article
1 reference
stated in
Europe PubMed Central
title
Peroxisomal diseases
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1627308
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1627308%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
author
J Kalervo Hiltunen
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1627308
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1627308%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
author name string
P M Palosaari
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1627308
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1627308%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
J M Kilponen
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1627308
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1627308%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
language of work or name
English
0 references
publication date
1 June 1992
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1627308
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1627308%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
published in
Annals of Medicine
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1627308
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1627308%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
volume
24
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1627308
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1627308%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1627308
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1627308%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
page(s)
163-166
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1627308
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1627308%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 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/10.3109%2F07853899209147814
retrieved
21 January 2018
Low-density particles (W-particles) containing catalase in Zellweger syndrome and normal fibroblasts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.3109%2F07853899209147814
retrieved
21 January 2018
Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzyme
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.3109%2F07853899209147814
retrieved
21 January 2018
Peroxisomal bifunctional enzyme deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.3109%2F07853899209147814
retrieved
21 January 2018
Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.3109%2F07853899209147814
retrieved
21 January 2018
An enzyme trafficking defect in two patients with primary hyperoxaluria type 1: peroxisomal alanine/glyoxylate aminotransferase rerouted to mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.3109%2F07853899209147814
retrieved
21 January 2018
Identification of mutations associated with peroxisome-to-mitochondrion mistargeting of alanine/glyoxylate aminotransferase in primary hyperoxaluria type 1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.3109%2F07853899209147814
retrieved
21 January 2018
Neonatal adrenoleukodystrophy: new cases, biochemical studies, and differentiation from Zellweger and related peroxisomal polydystrophy syndromes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.3109%2F07853899209147814
retrieved
21 January 2018
Infantile Refsum's disease: biochemical findings suggesting multiple peroxisomal dysfunction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.3109%2F07853899209147814
retrieved
21 January 2018
Identifiers
DOI
10.3109/07853899209147814
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1627308
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1627308%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
PubMed publication ID
1627308
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1627308
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1627308%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit