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

Hematological characterization of compound heterozygous hemoglobin Hope/E patients with and without alpha-thalassemia-1 SEA type deletion.

Clinical laboratory - 1 Jan 2013

Pornprasert Sakorn

Abstract excerpt

BACKGROUND: There is no report of hematological data in patients with co-inheritance of compound heterozygous hemoglobin (Hb) Hope/E and alpha-thalassemia-1 Southeast Asian (SEA) type deletion. METHODS: Hematological parameters were studied in 3 Thai patients with compound heterozygous Hb Hope/E and 1 of them had alpha-thalassemia-1 SEA type deletion. Red cell counts, hemoglobin, hematocrit, and red cell indices...

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 Hematologic Tests
Share to Hemoglobin E

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hemoglobins, Abnormal

Share to Heterozygote

Share to Mutation

Share to Polymerase Chain Reaction

Share to Sequence Deletion

Source

Identifiers

PMID: 24273946

Genes

SEA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hematological characterization of compound heterozygous hemoglobin Hope/E patients with and without alpha-thalassemia-1 SEA type deletion.PMID 24273946Read ↗

α-Thalassemia Intermedia Results from Interactions of Unstable Hb Prato [α31(B12)Arg→Ser (HBA1 or HBA2 c.96G>T or C)] with the α-Thalassemia-1 [- -SEA (Southeast Asian)] Deletion in Thailand.Semantic proximity Read ↗

Compound Heterozygous Hemoglobin Minneapolis-Laos and Codon 41/42 (-TTCT) in a Thai Female Adult: A Case Report and Literature Review.Semantic proximity Read ↗

Genetic heterogeneity of hemoglobin AEBart's disease: a large cohort data from a single referral center in northeast Thailand.Semantic proximity Read ↗

Molecular Characterization of Hb H and AEBart’s Diseases in Thai Children: Phramongkutklao Hospital Experiences.Semantic proximity Read ↗

Molecular epidemiology and hematological profiles of hemoglobin variants in southern Thailand.Semantic proximity Read ↗

Compound heterozygosity for hemoglobin variant Hb-Broomhill and the Southeast Asian α-thalassemia deletion does not worsen outcome: a case report of two unrelated patients.Semantic proximity Read ↗

Comparison of capillary electrophoregram among heterozygous Hb Hope, Hb Hope/α-thalassemia-1 SEA type deletion and Hb Hope/β(0)-thalassemia.Semantic proximity Read ↗

Curative Stem Cell Transplantation for Severe Hb H Disease Manifesting From Early Infancy: Phenotypic and Genotypic Analyses.Semantic proximity Read ↗

Hb Athens-Georgia (beta 40(C6) Arg > Lys, HBB:c.122G > A) with a single α-globin gene (Hb H disease) in a Thai family: molecular, hematological, and diagnostic aspects.Semantic proximity Read ↗

Hematological and Molecular Characterization of a Novel Hb A2 Variant with Homozygous α-Thalassemia-2 in a Southern Thai Individual.Semantic proximity Read ↗

A large cohort of hemoglobin variants in Thailand: molecular epidemiological study and diagnostic consideration.Semantic proximity Read ↗

Clinical phenotypes and molecular diagnosis in a hitherto interaction of Hb E/beta thalassemia syndrome (beta(E)/beta(-31), (A -->G)).Semantic proximity Read ↗

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