(Q69870952)

English

The infantile form of sialidosis type II associated with congenital adrenal hyperplasia: possible linkage between HLA and the neuraminidase deficiency gene

scientific article published on 01 January 1985

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3874816%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

The infantile form of sialidosis type II associated with congenital adrenal hyperplasia: possible linkage between HLA and the neuraminidase deficiency gene (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3874816%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

congenital adrenal hyperplasia

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

sialidosis type 2

1 reference

based on heuristic

inferred from title

author name string

T Oohira

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3874816%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

N Nagata

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3874816%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

I Akaboshi

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3874816%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

I Matsuda

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3874816%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

S Naito

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3874816%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

publication date

1 January 1985

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3874816%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3874816%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

70

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3874816%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3874816%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

341-343

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3874816%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

https://scigraph.springernature.com/pub.10.1007/bf00295374

0 references

Sialidosis type 2 (acid neuraminidase deficiency): clinical and biochemical features of a further case.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3874816

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fluorometric assay of neuraminidase with a sodium (4-methylumbelliferyl-alpha-D-N-acetylneuraminate) substrate

1 reference

https://pubmed.ncbi.nlm.nih.gov/3874816

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis of I-cell disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/3874816

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sialidosis: a review of human neuraminidase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/3874816

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency).

1 reference

https://pubmed.ncbi.nlm.nih.gov/3874816

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzymatic assay of serum sialic acid

1 reference

https://pubmed.ncbi.nlm.nih.gov/3874816

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene for neuraminidase activity on mouse chromosome 17 near h-2: pleiotropic effects on multiple hydrolases

1 reference

https://pubmed.ncbi.nlm.nih.gov/3874816

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of mononuclear cells and granulocytes from human blood. Isolation of monuclear cells by one centrifugation, and of granulocytes by combining centrifugation and sedimentation at 1 g

1 reference

https://pubmed.ncbi.nlm.nih.gov/3874816

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q69870952&oldid=2123489647"