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2. Co-inheritance of HBB:c.−106G > C, a rare single nucleotide variation at position −56 relative to transcription initiation site, with other known mutations in the globin clusters. Issue 6 (3rd July 2018)

3. Deferiprone versus deferoxamine in thalassemia intermedia: Results from a 5‐year long‐term Italian multicenter randomized clinical trial. Issue 7 (3rd May 2015)

4. HBB: c.316-125A>G and HBB: c.316-42delC: Phenotypic Evaluations of Two Rare Changes in the Second Intron of the HBB Gene. (2nd November 2017)

5. Longitudinal changes in LIC and other parameters in patients receiving different chelation regimens: Data from LICNET. (7th December 2017)

6. Phenotypic evaluations of HBB:c.93-23T>C, a nucleotide substitution in the IVS I nt 108 of β-globin gene. Issue 4 (9th August 2017)

7. Real‐life experience with liver iron concentration R2 MRI measurement in patients with hemoglobinopathies: baseline data from LICNET. (23rd February 2016)

8. Second-line administration of thrombopoietin receptor agonists in immune thrombocytopenia: Italian Delphi-based consensus recommendations. (October 2021)

9. The era of comparable life expectancy between thalassaemia major and intermedia: Is it time to revisit the major‐intermedia dichotomy?. (17th October 2016)