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English
Aspartylglucosaminuria: unique biochemical and ultrastructural characteristics
scientific article published on 01 July 1976
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
939543
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:939543%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 September 2019
title
Aspartylglucosaminuria: unique biochemical and ultrastructural characteristics
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
939543
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:939543%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 September 2019
main subject
aspartylglucosaminuria
1 reference
based on heuristic
inferred from title
author name string
J. N. Isenberg
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
939543
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A939543
retrieved
8 August 2022
H. L. Sharp
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
939543
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A939543
retrieved
8 August 2022
language of work or name
English
1 reference
stated in
National Center for Biotechnology Information
PubMed publication ID
939543
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=939543
retrieved
8 August 2022
publication date
1 July 1976
1 reference
stated in
Europe PubMed Central
PubMed publication ID
939543
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:939543%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 September 2019
published in
Human Pathology
1 reference
stated in
Europe PubMed Central
PubMed publication ID
939543
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:939543%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 September 2019
volume
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
939543
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:939543%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 September 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
939543
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:939543%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 September 2019
page(s)
469-481
1 reference
stated in
Europe PubMed Central
PubMed publication ID
939543
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:939543%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 September 2019
cites work
Aspartylglycosaminuria. An inborn error of metabolism associated with mental defect.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2876%2980061-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glycoproteins: their biochemistry, biology and role in human disease (first of two parts).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2876%2980061-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glycoproteins: their biochemistry, biology and role in human disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2876%2980061-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Biochemical and fine structural studies on brain and liver biopsies in aspartylglucosaminuria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2876%2980061-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Aspartylglucosaminuria II: biochemical studies on brain, liver, kidney and spleen
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2876%2980061-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Aspartylglucosaminuria I: fine structural studies on liver, kidney and brain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2876%2980061-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Aspartylglucosaminuria: psychomotor retardation masquerading as a mucopolysaccharidosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2876%2980061-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Thin-layer chromatographic demonstration of aspartylglycosylamine and a novel acidic carbohydrate in human tissues
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2876%2980061-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cholestyramine therapy in patients with a paucity of intrahepatic bile ducts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2876%2980061-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Generalized accumulation of neutral glycosphingolipids with GM2 ganglioside accumulation in the brain. Sandhoff's disease (variant of Tay-Sachs disease).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2876%2980061-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cardiac involvement in Sandhoff's disease. Inborn error of glycosphingolipid metabolism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2876%2980061-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mannosidosis: A clinical and histopathologic study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2876%2980061-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The genetic mucolipidoses. Diagnosis and differential diagnosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2876%2980061-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
I-cell disease: a clinical picture.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2876%2980061-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical, biochemical and ultrastructural studies of an atypical form of mucopolysaccharidosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2876%2980061-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Enzymatic cleavage of 2-acetamido-1-(beta'-L-aspartamido)-1,2-dideoxy-beta-D-glucose by human plasma and seminal fluid. Failure to detect the heterozygous state for aspartylglycosaminuria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2876%2980061-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Aspartylglucosaminuria: Deficiency of aspartylglucosaminidase in cultured fibroblasts of patients and their heterozygous parents
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2876%2980061-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Studies on serum and urinary glycopeptides and glycosaminoglycans in aspartylglucosaminuria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2876%2980061-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glycoasparagine metabolites in patients with aspartylglycosaminuria: comparison between english and finnish patients with special reference to storage materials
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2876%2980061-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0046-8177(76)80061-5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
939543
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:939543%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 September 2019
PubMed publication ID
939543
1 reference
stated in
Europe PubMed Central
PubMed publication ID
939543
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:939543%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 September 2019
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