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English
Argininosuccinic aciduria. A new form of mental deficiency due to metabolic causes
scientific article published on October 1959
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1869735
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13815969%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 December 2019
title
Argininosuccinic aciduria. A new form of mental deficiency due to metabolic causes
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1869735
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13815969%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 December 2019
author name string
DENT CE
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1869735
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13815969%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 December 2019
language of work or name
English
0 references
publication date
1 October 1959
1 reference
stated in
Europe PubMed Central
PMC publication ID
1869735
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13815969%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 December 2019
published in
Journal of the Royal Society of Medicine
1 reference
stated in
Europe PubMed Central
PMC publication ID
1869735
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13815969%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 December 2019
volume
52
1 reference
stated in
Europe PubMed Central
PMC publication ID
1869735
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13815969%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 December 2019
page(s)
885
1 reference
stated in
Europe PubMed Central
PMC publication ID
1869735
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13815969%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 December 2019
cites work
A disease, probably hereditary characterised by severe mental deficiency and a constant gross abnormality of aminoacid metabolism.
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=1869735
retrieved
18 August 2018
Identifiers
PMC publication ID
1869735
1 reference
stated in
Europe PubMed Central
PMC publication ID
1869735
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13815969%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 December 2019
PubMed publication ID
13815969
1 reference
stated in
Europe PubMed Central
PMC publication ID
1869735
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13815969%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 December 2019
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