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

Red blood cell phenotypes in the alpha + thalassaemias from early childhood to maturity.

British journal of haematology - 1 Nov 1996

Williams T N, Maitland K, Ganczakowski M, Peto T E, Clegg J B, Weatherall D J, Bowden D K

Abstract excerpt

The alpha+ thalassaemias are the most common single gene disorders of humans, yet little is known about their haematological characteristics in childhood. Blood samples have been collected randomly from more than 2000 individuals in village communities in Vanuatu in the South West Pacific and ana...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Aged
Share to Aged, 80 and over

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Child, Preschool

Share to Heterozygote

Share to Homozygote

Share to Phenotype

Source

Identifiers

PMID: 8904880
DOI: 10.1046/j.1365-2141.1996.d01-1906.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-8904880-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Red blood cell phenotypes in the alpha + thalassaemias from early childhood to maturity.PMID 8904880Read ↗

Thalassaemia in Vanuatu, south-west Pacific: frequency and haematological phenotypes of young children.Semantic proximity Read ↗

High incidence of malaria in alpha-thalassaemic children.Semantic proximity Read ↗

Co-inheritance of alpha+-thalassaemia and sickle trait results in specific effects on haematological parameters.Semantic proximity Read ↗

Increased Microerythrocyte Count in Homozygous α+-Thalassaemia Contributes to Protection against Severe Malarial AnaemiaSemantic proximity Read ↗

Alpha thalassaemia is associated with increased soluble transferrin receptor levels.Semantic proximity Read ↗

An investigation of the protective effect of alpha+-thalassaemia against severe Plasmodium falciparum amongst children in Kumasi, Ghana.Semantic proximity Read ↗

Haematological abnormalities in children with sickle cell disease and non-severe malaria infection in western Kenya.Semantic proximity Read ↗

Haematological Abnormalities in Children With Sickle Cell Disease and Non-severe Malaria Infection in Western KenyaSemantic proximity Read ↗

Reduced risk of uncomplicated malaria episodes in children with alpha+-thalassemia in northeastern Tanzania.Semantic proximity Read ↗

Phenotypic and genotypic expression of alpha thalassaemia in Ibadan, Nigeria.Semantic proximity Read ↗

An investigation of the protective effect of alpha+-thalassaemia against severe Plasmodium falciparum amongst children in Kumasi, GhanaSemantic proximity Read ↗

The contribution of alpha+-thalassaemia to anaemia in a Nigerian population exposed to intense malaria transmission.Semantic proximity Read ↗

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