author-photo

Paola Pistidda

University of Sassari

12

Papers

78

Citations

Citation Trend

Filter By

Papers (10) Sort By

Journal Conference Others

Maximal γ‐globin expression in the compound heterozygous state for –175 Gγ HPFH and β°39 nonsense thalassaemia: a case study

2009 European Journal of Haematology
Show All
- Source
- Cite
- Save
Citations (5)
Haematological phenotypes in a family with triplicated α-globin gene, β∘39 and δ+27 thalassaemia mutations

2008 Clinical and Laboratory Haematology
Show All
- Source
- Cite
- Save
Citations (3)
A 12‐year preventive program for β‐thalassemia in Northern Sardinia

2008 Clinical Genetics
Show All
- Source
- Cite
- Save
Citations (9)
The homozygous state of Hb J Sardegna.

2002 Hematology Journal
Show All
- Source
- Cite
- Save
Citations (3)
Hb Tigraye [β79(EF3)Asp→His] in a Caucasian family from Sardinia

2001 Hemoglobin
Show All
- Source
- Cite
- Save
Citations (1)
Fetal hemoglobin expression in compound heterozygotes for −117 (G→A) Aγ HPFH and β039 nonsense thalassemia

1995 American Journal of Hematology
Show All
- Source
- Cite
- Save
Citations (12)
Low doses of rHuEPO administered to adult patients with thalassemia intermedia

1994 Annals of Hematology
Show All
- Source
- Cite
- Save
Citations (2)
A novel mediterranean δβ-thalassemia determinant containing the Δ+27 and β°39 point mutations in cis

1994 American Journal of Hematology
Show All
- Source
- Cite
- Save
Citations (14)
Mild β+(−87)‐thalassemia CACCC box mutation is associated with elevated fetal hemoglobin expression in cis

1994 American Journal of Hematology
Show All
- Source
- Cite
- Save
Citations (12)
Current views of thalassemia intermedia

1992 Recenti progressi in medicina
Show All
- Source
- Cite
- Save
Citations (0)