The cherry red spot-myoclonus syndrome: a newly recognized inherited lysosomal storage disease due to acid neuraminidase deficiency (Q67366247)

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scientific article published on 01 July 1978

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Language	Label	Description	Also known as
English	The cherry red spot-myoclonus syndrome: a newly recognized inherited lysosomal storage disease due to acid neuraminidase deficiency	scientific article published on 01 July 1978

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

679523

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:679523%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 September 2019

title

The cherry red spot-myoclonus syndrome: a newly recognized inherited lysosomal storage disease due to acid neuraminidase deficiency (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

679523

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:679523%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 September 2019

main subject

lysosomal storage disease

1 reference

based on heuristic

inferred from title

sialidosis type 2

1 reference

based on heuristic

inferred from title

author name string

J. S. O'Brien

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

679523

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A679523

retrieved

20 July 2022

language of work or name

English

1 reference

stated in

National Center for Biotechnology Information

PubMed publication ID

679523

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=679523

retrieved

20 July 2022

publication date

1 July 1978

1 reference

stated in

Europe PubMed Central

PubMed publication ID

679523

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:679523%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 September 2019

published in

Clinical Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

679523

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:679523%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 September 2019

volume

14

1 reference

stated in

Europe PubMed Central

PubMed publication ID

679523

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:679523%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 September 2019

issue

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

679523

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:679523%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 September 2019

page(s)

55-60

1 reference

stated in

Europe PubMed Central

PubMed publication ID

679523

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:679523%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 September 2019

Identifiers

DOI

10.1111/J.1399-0004.1978.TB02061.X

1 reference

stated in

Europe PubMed Central

PubMed publication ID

679523

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:679523%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 September 2019

PubMed publication ID

679523

1 reference

stated in

Europe PubMed Central

PubMed publication ID

679523

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:679523%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 September 2019

 

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