(Q71587095)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8830177%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

title

Clinical and laboratory findings in four patients with the non-progressive hepatic form of type IV glycogen storage disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8830177%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

main subject

glycogen storage disease

1 reference

glycogen metabolic process

inferred from title

1 reference

A McConkie-Rosell

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8830177%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

C Wilson

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8830177%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

D A Piccoli

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8830177%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

J Boyle

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8830177%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

T DeClue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8830177%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

P Kishnani

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8830177%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

J J Shen

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8830177%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

A Boney

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8830177%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

B Brown

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8830177%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

Y T Chen

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8830177%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

publication date

1 January 1996

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8830177%20AND%20SRC:MED&resulttype=core&format=json

Journal of Inherited Metabolic Disease

19 October 2019

published in

1 reference

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19 October 2019

volume

19

1 reference

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19 October 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8830177%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

page(s)

51-58

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8830177%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf01799348

19 October 2019

exact match

0 references

cites work

Glycogenosis IV: A new cause of infantile hypotonia

1 reference

12 December 2020

Glycogen branching enzyme deficiency in adult polyglucosan body disease

1 reference

12 December 2020

Concomitant branching enzyme and phosphorylase deficiencies. An unusual glycogenosis with extensive neuronal polyglucosan storage

1 reference

12 December 2020

Studies of the residual glycogen branching enzyme activity present in human skin fibroblasts from patients with Type IV glycogen storage disease

1 reference

12 December 2020

Liver transplantation for type IV glycogen storage disease

1 reference

12 December 2020

A new variant of type IV glycogenosis: deficiency of branching enzyme activity without apparent progressive liver disease

1 reference

12 December 2020

Branching enzyme activity of cultured amniocytes and chorionic villi: prenatal testing for type IV glycogen storage disease

1 reference

12 December 2020

Glycogenosis type IV: liver transplant at 12 years

1 reference

12 December 2020

A mild juvenile variant of type IV glycogenosis

1 reference

12 December 2020

Juvenile hereditary polyglucosan body disease with complete branching enzyme deficiency (type IV glycogenosis)

1 reference

12 December 2020

A juvenile variant of glycogenosis IV (Andersen disease)

1 reference

12 December 2020

A congenital variant of glycogenosis type IV

1 reference

12 December 2020

Hereditary branching enzyme dysfunction in adult polyglucosan body disease: A possible metabolic cause in two patients

1 reference

12 December 2020

Isolation of human glycogen branching enzyme cDNAs by screening complementation in yeast

1 reference

12 December 2020

Glycogen storage disease type IV, amylopectinosis

1 reference

12 December 2020

Severe cardiopathy in branching enzyme deficiency

1 reference

12 December 2020

Neonatal hypotonia and cardiomyopathy secondary to type IV glycogenosis.

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01799348

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8830177%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

1 reference