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

α-Thalassemia frequency and mutations in children with hypochromic microcytic anemias and relation with β-thalassemia, iron deficiency anemia.

Pediatric hematology and oncology - 1 Apr 2012

Gulen Huseyin, Hanimeli Ozlem, Karaca Ozlem, Taneli Fatma

Abstract excerpt

The majority of the anemias during childhood are hypochromic and microcytic. The aim of the present study was to determine the status of α-thalassemia mutations and its association with other etiologies, such as iron deficiency anemia (IDA) and β-thalassemia trait, that are frequently seen hypochromic microcytic anemias in children. Children with hypochromic microcytic anemias were included in the study. Serum...

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 Anemia, Hypochromic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Anemia, Iron-Deficiency

Share to beta-Thalassemia

Share to Diagnosis, Differential

Share to Incidence

Share to Infant

Share to Turkey

Source

Identifiers

PMID: 22475300
DOI: 10.3109/08880018.2012.661831

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

α-Thalassemia frequency and mutations in children with hypochromic microcytic anemias and relation with β-thalassemia, iron deficiency anemia.PMID 22475300Read ↗

Correlation of beta-thalassemia mutations with alpha-thalassemia: an experience of the southwestern region of Iran.Semantic proximity Read ↗

Microcytic hypochromic anemia patients with thalassemia: genotyping approach.Semantic proximity Read ↗

Thalassemia, a human blood disorderSemantic proximity Read ↗

Frequency of beta-thalassemia or beta-hemoglobinopathy carriers simultaneously affected with alpha-thalassemia in Iran.Semantic proximity Read ↗

Hematological Parameters in Individuals with Beta Thalassemia Trait in South Sumatra, IndonesiaSemantic proximity Read ↗

The thalassemia syndromes and pregnancy, molecular basis, clinical aspects, prenatal diagnosis.Semantic proximity Read ↗

Evaluation of Alpha-Thalassemia Mutations in Cases with Hypochromic Microcytic Anemia: The İstanbul Perspective.Semantic proximity Read ↗

Current status of beta-thalassemia and its treatment strategies.Semantic proximity Read ↗

Understanding the Intricacies of Iron Overload Associated With β-Thalassemia: A Comprehensive ReviewSemantic proximity Read ↗

Study of Clinical, Hematological and Molecular Characteristics of Patients of Thalassemia and Hemoglobinopathies in Tertiary Care Hospital.Semantic proximity Read ↗

First report of the spectrum of δ-globin gene mutations among women of reproductive age in Fujian area-Discrimination of δ-thalassemia, α-thalassemia, and Iron Deficiency Anemia.Semantic proximity Read ↗

[Significance of the combined detection of routine blood test, serum iron and hemoglobin electrophoresis in screening thalassemia in non- high incidence area].Semantic proximity Read ↗

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