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English
A clinical and genetic study of Hunter's syndrome. 2. Differences between the mild and severe forms.
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1048951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6818348%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
title
A clinical and genetic study of Hunter's syndrome. 2. Differences between the mild and severe forms
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1048951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6818348%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
author name string
I D Young
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1048951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6818348%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
P S Harper
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1048951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6818348%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
R G Newcombe
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
1048951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6818348%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
I M Archer
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMCID
1048951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6818348%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
language of work or name
English
0 references
publication date
1 December 1982
1 reference
stated in
Europe PubMed Central
PMCID
1048951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6818348%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1048951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6818348%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
volume
19
1 reference
stated in
Europe PubMed Central
PMCID
1048951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6818348%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
issue
6
1 reference
stated in
Europe PubMed Central
PMCID
1048951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6818348%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
page(s)
408-411
1 reference
stated in
Europe PubMed Central
PMCID
1048951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6818348%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
cites work
Multiple peripheral nerve entrapments. An unusual phenotypical variant of the Hunter syndrome (mucopolysaccharidosis II) in a family.
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=1048951
retrieved
21 June 2018
Ultrastructure of the rectal wall in Hunter's 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=1048951
retrieved
21 June 2018
Clinical definition of the Hurler-Hunter phenotypes. A review of 50 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=1048951
retrieved
21 June 2018
Peripheral Nerve Involvement in Hunter Syndrome (Mucopolysaccharidosis II)
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=1048951
retrieved
21 June 2018
Long-term complications in Hunter's 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=1048951
retrieved
21 June 2018
Myelopathy in mucopolysaccharidosis type II (Hunter 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=1048951
retrieved
30 October 2018
Clinical and probable genetic heterogeneity within mucopolysaccharidosis. II. Report of a family with a mild form
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6818348
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Carpal tunnel syndrome in pediatric mucopolysaccharidoses. Report of four cases
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6818348
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Psychosocial problems in Hunter's syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6818348
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.19.6.408
1 reference
stated in
Europe PubMed Central
PMCID
1048951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6818348%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
PMCID
1048951
1 reference
stated in
Europe PubMed Central
PMCID
1048951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6818348%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
PubMed ID
6818348
1 reference
stated in
Europe PubMed Central
PMCID
1048951
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6818348%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
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