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

Acquired α-thalassemia in association with myelodysplastic syndrome and other hematologic malignancies

10 Sept 2004

Abstract excerpt

Abnormalities of hemoglobin synthesis are usually inherited but may also arise as a secondary manifestation of another disease, most commonly hematologic neoplasia. Acquired hemoglobin disorders can be seen in any population and are not restricted to areas of the world with high incidences of inherited hemoglobinopathies. In fact, the acquired hemoglobinopathies may be more readily recognized where inherited...

Read the complete abstract on PubMed

Topics

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

Share to Acute Myeloid Leukemia Research
Share to Epigenetics and DNA Methylation
Share to Hemoglobinopathies and Related Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 15358626
DOI: 10.1182/blood-2004-07-2792

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Acquired α-thalassemia in association with myelodysplastic syndrome and other hematologic malignanciesPMID 15358626Read ↗

Deletion of the alpha-globin gene cluster as a cause of acquired alpha-thalassemia in myelodysplastic syndrome.Semantic proximity Read ↗

[Acquired alpha-thalassemia in an 86-year-old patient with myelodysplastic syndrome].Semantic proximity Read ↗

α-Thalassemia, mental retardation, and myelodysplastic syndrome.Semantic proximity Read ↗

A new ATRX mutation in a patient with acquired α-thalassemia myelodysplastic syndrome.Semantic proximity Read ↗

Acquired somatic ATRX mutations in myelodysplastic syndrome associated with alpha thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations.Semantic proximity Read ↗

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the alpha-thalassemia myelodysplasia syndrome (ATMDS).Semantic proximity Read ↗

Clonal hematopoiesis and acquired genetic abnormalities of the red cell: An historical review.Semantic proximity Read ↗

[Somatic Mutations of Acquired Aplastic Anemia].Semantic proximity Read ↗

[Clinical and genetic background of familial myelodysplasia and acute myeloid leukemia].Semantic proximity Read ↗

Mutations in the chromatin-associated protein ATRX.Semantic proximity Read ↗

Molecular pathogenesis of acquired aplastic anemiaSemantic proximity Read ↗

The role of X-inactivation in the gender bias of patients with acquired alpha-thalassaemia and myelodysplastic syndrome (ATMDS).Semantic proximity Read ↗

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