(Q48605021)

13 February 2018

title

Hypertrophic obstructive cardiomyopathy in a neonate with the carbohydrate-deficient glycoprotein syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1293380

https://api.crossref.org/works/10.1007/BF01800221

10 September 2022

Hypertrophic obstructive cardiomyopathy in a neonate with the carbohydrate‐deficient glycoprotein syndrome (English)

1 reference

hypertrophic obstructive cardiomyopathy

27 November 2023

main subject

0 references

1 reference

https://api.crossref.org/works/10.1007/BF01800221

27 November 2023

author name string

P. T. Clayton

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1293380

10 September 2022

B. G. Winchester

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1293380

10 September 2022

G. Keir

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1293380

10 September 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1293380

10 September 2022

publication date

1 January 1992

1 reference

13 February 2018

full work available at URL

https://onlinelibrary.wiley.com/doi/pdf/10.1007/BF01800221

1 reference

https://api.crossref.org/works/10.1007/BF01800221

Journal of Inherited Metabolic Disease

27 November 2023

published in

1 reference

13 February 2018

volume

15

1 reference

13 February 2018

page(s)

857-861

1 reference

13 February 2018

issue

6

1 reference

13 February 2018

https://scigraph.springernature.com/pub.10.1007/bf01800221

exact match

0 references

cites work

Lipoprotein disorder, cirrhosis, and olivopontocerebellar degeneration in two siblings.

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01800221

Disialotransferrin developmental deficiency syndrome and olivopontocerebellar atrophy

21 January 2018

1 reference

12 December 2020

Familial olivopontocerebellar atrophy with neonatal onset: a recessively inherited syndrome with systemic and biochemical abnormalities.

1 reference

12 December 2020

The carbohydrate-deficient glycoprotein syndrome. A new inherited multisystemic disease with severe nervous system involvement

1 reference

12 December 2020

Olivopontocerebellar atrophy of neonatal onset and disialotransferrin developmental deficiency syndrome

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01800221

1 reference

13 February 2018

1 reference

13 February 2018