(Q36296501)

13 August 2017

Cardiac Involvement in Glycogen Storage Disease Type IV: Two Cases and the Two Ends of a Spectrum (English)

1 reference

13 August 2017

glycogen storage disease

1 reference

Tolga Aksu

1

1 reference

13 August 2017

Ayse Colak

series ordinal

2

1 reference

13 August 2017

Omac Tufekcioglu

series ordinal

3

1 reference

13 August 2017

26 September 2012

1 reference

13 August 2017

Case Reports in Medicine

1 reference

13 August 2017

2012

1 reference

13 August 2017

764286

1 reference

Creative Commons Attribution 3.0 Unported

13 August 2017

start time

1 January 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

cites work

Liver transplantation in children with glycogen storage disease: controversies and evaluation of the risk/benefit of this procedure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463931

Familial cirrhosis of the liver with storage of abnormal glycogen

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463931

The variable presentations of glycogen storage disease type IV: a review of clinical, enzymatic and molecular studies

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463931

Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease).

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463931

Liver transplantation for glycogen storage disease types I, III, and IV

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463931

Chimerism after liver transplantation for type IV glycogen storage disease and type 1 Gaucher's disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463931

Lack of an alpha-1,4-glucan: alpha-1,4-glucan 6-glycosyl transferase in a case of type IV glycogenosis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463931

[Glycogenosis type IV as a seldom cause of cardiomyopathy - report about a successful heart transplantation]

30 September 2017

1 reference

Crossref

https://api.crossref.org/works/10.1155%2F2012%2F764286

A new variant of type IV glycogenosis with primary cardiac manifestation and complete branching enzyme deficiency. In vivo detection by heart muscle biopsy

21 January 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Severe cardiopathy in branching enzyme deficiency

1 reference

12 December 2020

Identifiers

DOI

10.1155/2012/764286

1 reference

release_rffnfex7gjatzorb3a6kbw3t6y

13 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/rffnfex7gjatzorb3a6kbw3t6y

24 November 2022

mapped directly with Wikidata item

1 reference

13 August 2017

PubMed publication ID

23056054

1 reference