Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Glycogen storage disease type Ib without hypoglycemia.

Molecular genetics and metabolism - 1 Mar 2007

Kovacevic Alexander, Ehrlich Roland, Mayatepek Ertan, Wendel Udo, Schwahn Bernd

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Antiporters
Share to Blood Glucose
Share to Child, Preschool
Share to Glycogen Storage Disease Type I

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hepatomegaly

Share to Monosaccharide Transport Proteins

Share to Mutation, Missense

Share to Phenotype

Source

Identifiers

PMID: 17174133
DOI: 10.1016/j.ymgme.2006.11.002

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Glycogen storage disease type Ib without hypoglycemia.PMID 17174133Read ↗

[Glycogen storage disease type Ib].Semantic proximity Read ↗

[Glycogen storage disease type Ia, Ic and Id].Semantic proximity Read ↗

[Hepatic glycogen storage diseases: Symptoms, management and associated mutations].Semantic proximity Read ↗

Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcome.Semantic proximity Read ↗

Clinical Analysis and Long-term Treatment Monitoring of 3 Patients with Glycogen Storage Disease Type IbSemantic proximity Read ↗

Glycogen storage disease type I: diagnosis and phenotype/genotype correlationSemantic proximity Read ↗

A patient with common glycogen storage disease type Ib mutations without neutropenia or neutrophil dysfunction.Semantic proximity Read ↗

Neonatal glycogen storage disease Ia.Semantic proximity Read ↗

Clinical analysis and long-term treatment monitoring of 3 patients with glycogen storage disease type Ib.Semantic proximity Read ↗

Glycogen storage disease type Ib without neutropenia.Semantic proximity Read ↗

Glycogen storage diseases. Phenotypic, genetic, and biochemical characteristics, and therapy.Semantic proximity Read ↗

A Rare Case of Glycogen Storage Disease Type IIIa with a Novel Homozygous AGL Splice Variant in a Two-Year-Old Female born out of Consanguineous MarriageSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.