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English
Hyperprolinemia without Renal Disease
scientific article published on 01 January 1967
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
5587686
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5587686%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
title
Hyperprolinemia without renal disease
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
5587686
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5587686%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
Hyperprolinemia without Renal Disease
(English)
1 reference
stated in
Crossref
DOI
10.1111/J.1651-2227.1967.TB05259.X
reference URL
https://api.crossref.org/works/10.1111/J.1651-2227.1967.TB05259.X
retrieved
6 June 2023
main subject
hyperprolinemia
1 reference
based on heuristic
inferred from title
kidney disease
1 reference
based on heuristic
inferred from title
author name string
S. Similä
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
5587686
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5587686
retrieved
6 June 2023
J. K. Visakorpi
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
5587686
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5587686
retrieved
6 June 2023
language of work or name
English
1 reference
stated in
National Center for Biotechnology Information
PubMed publication ID
5587686
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=5587686
retrieved
6 June 2023
publication date
1 January 1967
1 reference
stated in
Europe PubMed Central
PubMed publication ID
5587686
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5587686%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
full work available at URL
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1651-2227.1967.tb05259.x
1 reference
stated in
Crossref
DOI
10.1111/J.1651-2227.1967.TB05259.X
reference URL
https://api.crossref.org/works/10.1111/J.1651-2227.1967.TB05259.X
retrieved
6 June 2023
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.1967.tb05259.x/fullpdf
1 reference
stated in
Crossref
DOI
10.1111/J.1651-2227.1967.TB05259.X
reference URL
https://api.crossref.org/works/10.1111/J.1651-2227.1967.TB05259.X
retrieved
6 June 2023
published in
Acta Paediatrica Scandinavica
1 reference
stated in
Europe PubMed Central
PubMed publication ID
5587686
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5587686%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
page(s)
Suppl 177:122+
1 reference
stated in
Europe PubMed Central
PubMed publication ID
5587686
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5587686%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
cites work
FAMILIAL HYPERPROLINEMIA. REPORT OF A SECOND CASE, ASSOCIATED WITH CONGENITAL RENAL MALFORMATIONS, HEREDITARY HEMATURIA AND MILD MENTAL RETARDATION, WITH DEMONSTRATION OF AN ENZYME DEFECT.
series ordinal
1
1 reference
stated in
Crossref
DOI
10.1111/J.1651-2227.1967.TB05259.X
reference URL
https://api.crossref.org/works/10.1111/J.1651-2227.1967.TB05259.X
retrieved
6 June 2023
[The syndrome of hereditary nephropathy with inner ear deafness (Alport syndrome).]
series ordinal
2
1 reference
stated in
Crossref
DOI
10.1111/J.1651-2227.1967.TB05259.X
reference URL
https://api.crossref.org/works/10.1111/J.1651-2227.1967.TB05259.X
retrieved
6 June 2023
HYPERPROLINAEMIA AND HEREDITARY NEPHRITIS
series ordinal
3
1 reference
stated in
Crossref
DOI
10.1111/J.1651-2227.1967.TB05259.X
reference URL
https://api.crossref.org/works/10.1111/J.1651-2227.1967.TB05259.X
retrieved
6 June 2023
Familial Hyperprolinemia, Cerebral Dysfunction and Renal Anomalies Occurring in a Family with Hereditary Nephropathy and Deafness
series ordinal
4
1 reference
stated in
Crossref
DOI
10.1111/J.1651-2227.1967.TB05259.X
reference URL
https://api.crossref.org/works/10.1111/J.1651-2227.1967.TB05259.X
retrieved
6 June 2023
Identifiers
DOI
10.1111/J.1651-2227.1967.TB05259.X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
5587686
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5587686%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
PubMed publication ID
5587686
1 reference
stated in
Europe PubMed Central
PubMed publication ID
5587686
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5587686%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
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