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Article

Do alpha deletions influence hydroxyurea response in thalassemia intermedia?

Hematology (Amsterdam, Netherlands) - 1 Feb 2005

Panigrahi I, Dixit A, Arora S, Kabra M, Mahapatra M, Choudhry V P, Saxena R

Abstract excerpt

Thalassemia intermedia patients show variable phenotypes. Hydroxyurea (HU) may benefit some of the thalassemia intermedia cases (1), however, the parameters influencing the response to HU have not been reported. In this study, the molecular parameters, alpha-globin and beta-globin genotype and the Xmn I polymorphism, were correlated with the HU response. Twenty patients with thalassemia intermedia were given HU...

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

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Identifiers

PMID: 16019448
DOI: 10.1080/10245330400020439

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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.

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