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

Biophysical changes of red cells with thalassemia-like abnormal hemoglobin.

The Southeast Asian journal of tropical medicine and public health - 1 Jan 1992

Bunyaratvej A, Fucharoen S, Tatsumi N

Abstract excerpt

Hemoglobin (Hb) E and Hb Constant Spring (CS) are known to have thalassemia-like effects. Investigation on the red cell physical changes in these two abnormalities has been done to clarify the diversity of red cell changes between thalassemia and thalassemia-like abnormal hemoglobin (Hb E represents beta-thalassemia and Hb CS represents alpha-thalassemia). Eleven cases with homozygous Hb CS (CS/CS), 7 homozygous...

Read the complete abstract on PubMed

Topics

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

Share to alpha-Thalassemia
Share to beta-Thalassemia
Share to Biophysical Phenomena

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Biophysics

Share to Genotype

Share to Hemoglobinopathies

Share to Hemoglobins, Abnormal

Share to Thailand

Source

Identifiers

PMID: 1299000

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Biophysical changes of red cells with thalassemia-like abnormal hemoglobin.PMID 1299000Read ↗

The Unusual Pathobiology of Hemoglobin Constant Spring Red Blood CellsSemantic proximity Read ↗

Mild Hb Constant Spring-Hb H disease with beta zero-thalassemia trait.Semantic proximity Read ↗

Changing patterns of thalassemia worldwide.Semantic proximity Read ↗

[Analysis of the phenotype-genotype relationship of Hb Constant Spring].Semantic proximity Read ↗

[The haematological phenotype and genotype analysis on 14 co-inheritance of hemoglobin Constant Spring and β-thalassemia].Semantic proximity Read ↗

Pathobiology of thalassemic erythrocytesSemantic proximity Read ↗

Hematological Characteristics of Hb Constant Spring (HBA2: c.427T>C) Carriers in Mainland China.Semantic proximity Read ↗

Number and maturation of reticulocytes in various genotypes of thalassaemia as assessed by flow cytometry.Semantic proximity Read ↗

[Homozygous hemoglobin constant spring in Guangxi province].Semantic proximity Read ↗

Thalassemia intermedia associated with the Hb Constant Spring EE Bart's disease in pregnancy: a molecular and hematological analysis.Semantic proximity Read ↗

Fetal Anemia and Hydrops Fetalis Associated with Homozygous Hb Constant Spring (HBA2: c.427T > C).Semantic proximity Read ↗

Red Blood Cell Stiffness Driving Patient Symptoms: A Study of Red Blood Cell Population Rigidity in Sickle Cell Patient Genotype SC Relation to Overlooked Clinical SymptomsSemantic proximity Read ↗

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