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

Fatal Kernicterus in a Girl Deficient in Glucose-6-Phosphate Dehydrogenase: A Paradigm of Synergistic Heterozygosity

25 Mar 2009

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 Metabolism and Genetic Disorders
Share to Methemoglobinemia and Tumor Lysis Syndrome
Share to Neonatal Health and Biochemistry

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 19324225
DOI: 10.1016/j.jpeds.2008.10.049

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 · 10 closest

Fatal Kernicterus in a Girl Deficient in Glucose-6-Phosphate Dehydrogenase: A Paradigm of Synergistic HeterozygosityPMID 19324225Read ↗

Heterozygosity: an expanding role in proteomics.Semantic proximity Read ↗

Kernicterus in an adult who is heterozygous for Crigler-Najjar syndrome and homozygous for Gilbert-type genetic defectSemantic proximity Read ↗

Synergistic heterozygosity: disease resulting from multiple partial defects in one or more metabolic pathways.Semantic proximity Read ↗

Heterozygosity for a Mendelian disorder as a risk factor for complex disease.Semantic proximity Read ↗

Genetic and Epigenetic Factors Co-Influence the Severity of Phenotypic Presentations in Compound G6PD MutationsSemantic proximity Read ↗

Gaucher disease, a paradigm for single gene defects.Semantic proximity Read ↗

Profound neurological presentation resulting from homozygosity for a mild glutaryl-CoA dehydrogenase mutation with a minimal biochemical phenotype.Semantic proximity Read ↗

HB H disease with homozygosity for red cell G6PD deficiency in a Turkish female.Semantic proximity Read ↗

Concerns regarding transience and heterozygosity in neonatal hyperglycenemia.Semantic proximity Read ↗

Dominant versus recessive: molecular mechanisms in metabolic disease.Semantic proximity Read ↗

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