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English
Hereditary spastic paraplegia with neurogenic bladder disturbances and syndactylia
scientific article published on 01 January 1980
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
6249060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6249060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
title
Hereditary spastic paraplegia with neurogenic bladder disturbances and syndactylia
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
6249060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6249060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
main subject
hereditary spastic paraplegia
1 reference
based on heuristic
inferred from title
neurogenic bladder
1 reference
based on heuristic
inferred from title
neurology
1 reference
stated in
Crossref
DOI
10.1111/J.1600-0404.1980.TB02993.X
reference URL
https://api.crossref.org/works/10.1111/J.1600-0404.1980.TB02993.X
retrieved
6 September 2023
author
Stein Opjordsmoen Ilner
series ordinal
1
object named as
S Opjordsmoen
1 reference
stated in
Europe PubMed Central
PubMed ID
6249060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6249060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
author name string
S. Opjordsmoen
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
6249060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6249060
retrieved
6 September 2023
R. Nyberg-Hansen
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
6249060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6249060
retrieved
6 September 2023
language of work or name
English
0 references
publication date
1 January 1980
1 reference
stated in
Europe PubMed Central
PubMed ID
6249060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6249060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
full work available at URL
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1600-0404.1980.tb02993.x
1 reference
stated in
Crossref
DOI
10.1111/J.1600-0404.1980.TB02993.X
reference URL
https://api.crossref.org/works/10.1111/J.1600-0404.1980.TB02993.X
retrieved
6 September 2023
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0404.1980.tb02993.x/fullpdf
1 reference
stated in
Crossref
DOI
10.1111/J.1600-0404.1980.TB02993.X
reference URL
https://api.crossref.org/works/10.1111/J.1600-0404.1980.TB02993.X
retrieved
6 September 2023
published in
Acta Neurologica Scandinavica
1 reference
stated in
Europe PubMed Central
PubMed ID
6249060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6249060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
volume
61
1 reference
stated in
Europe PubMed Central
PubMed ID
6249060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6249060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
6249060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6249060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
page(s)
35-41
1 reference
stated in
Europe PubMed Central
PubMed ID
6249060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6249060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
cites work
Sphincter involvement in hereditary spastic paraplegia
series ordinal
4
1 reference
stated in
Crossref
DOI
10.1111/J.1600-0404.1980.TB02993.X
reference URL
https://api.crossref.org/works/10.1111/J.1600-0404.1980.TB02993.X
retrieved
6 September 2023
Hereditary spastic paraplegia and hereditary ataxia: a family demonstrating a variety of phenotypic manifestations
series ordinal
7
1 reference
stated in
Crossref
DOI
10.1111/J.1600-0404.1980.TB02993.X
reference URL
https://api.crossref.org/works/10.1111/J.1600-0404.1980.TB02993.X
retrieved
6 September 2023
Homocarnosinosis. 2. A familial metabolic disorder associated with spastic paraplegia, progressive mental deficiency, and retinal pigmentation
series ordinal
14
1 reference
stated in
Crossref
DOI
10.1111/J.1600-0404.1980.TB02993.X
reference URL
https://api.crossref.org/works/10.1111/J.1600-0404.1980.TB02993.X
retrieved
6 September 2023
Hereditary spastic paraplegia in Western Norway.
series ordinal
15
1 reference
stated in
Crossref
DOI
10.1111/J.1600-0404.1980.TB02993.X
reference URL
https://api.crossref.org/works/10.1111/J.1600-0404.1980.TB02993.X
retrieved
6 September 2023
Identifiers
DOI
10.1111/J.1600-0404.1980.TB02993.X
1 reference
stated in
Europe PubMed Central
PubMed ID
6249060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6249060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
PubMed ID
6249060
1 reference
stated in
Europe PubMed Central
PubMed ID
6249060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6249060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
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