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

[Beta thalassemia major in Argentina].

Medicina - 1 Jan 2002

Torres Feliu Aurora, Bonduel Mariana, Sciuccati Gabriela, del Pozo Ana, Roldán Ariel, Ciaccio Marta, Orazi Virginia, Fano Virginia, Ozuna Blanca, Lejarraga Horacio, Muriel Sackmann Federico

Abstract excerpt

An analysis of beta thalassemia major patients seen at Hospital Juan P. Garrahan was carried out in order to determine the characteristics and outcome of the population. From August 1987 to July 2000, 45 patients were admitted (27 males-18 females). The most common beta globin gene defects were C-39 (30.7%); IVS-I nt 110 (20%); IVS-I nt 6 (13.3%); IVS-I nt 1(4%). alpha globin genes were normal in 42 patients, 1...

Read the complete abstract on PubMed

Topics

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

Share to Genetic Testing
Share to Hematopoietic Stem Cell Transplantation

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

Share to Infant

Share to Argentina

Share to beta-Thalassemia

Share to Child, Preschool

Share to Follow-Up Studies

Source

Identifiers

PMID: 12038033

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

[Beta thalassemia major in Argentina].PMID 12038033Read ↗

[Beta-thalassemias: molecular, epidemiological, diagnostical and clinical aspects].Semantic proximity Read ↗

Molecular characterization of beta-thalassemia genes in an Argentine population.Semantic proximity Read ↗

The thalassemia syndromes: molecular characterization in the Spanish population.Semantic proximity Read ↗

[Beta thalassemia in Germany: molecular genetics and clinical phenotype in immigrant and in the native population].Semantic proximity Read ↗

[Molecular genetics of the thalassemias in Argentina].Semantic proximity Read ↗

Evaluation of the Clinical and Laboratory Characteristics of Previously Followed-up Thalassemia Intermedia Patients to Provide Them Better Care in the Future.Semantic proximity Read ↗

Identification of beta thalassemia mutations in South Brazilians.Semantic proximity Read ↗

β-Thalassemia in childhood: Current state of health in a high-income country.Semantic proximity Read ↗

[Identification of 2 distinct genes of thalassemia beta in a Mexican family].Semantic proximity Read ↗

β -thalassemia intermedia in Northern Iraq: a single center experience.Semantic proximity Read ↗

[The molecular changes in thalassemias in Spain. A review of existing studies].Semantic proximity Read ↗

Prevalence of -alpha3.7-thalassemia in Argentina.Semantic proximity Read ↗

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