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Susanna Barella

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Maria Elisabetta Paglietti; Maria Carla Sollaino; Susanna Barella; Maria Franca Desogus; Daniela Loi; Renzo Galanello
First detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in an Italian child.
Antonella Fais; Lucia Perseu; Maria Carla Sollaino; Susanna Barella; Benedetta Era; Marcella Corda
A new β chain hemoglobin variant with increased oxygen affinity: Hb Santa Giusta Sardegna [β93(F9)Cys→Trp; HBB c.282T>G].
Luciana Perseu; Stefania Satta; Maria Carla Sollaino; Laura Manunza; Paolo Moi; Susanna Barella; Antonio Cao; Franca Rosa Demartis; Renzo Galanello
KLF1 gene mutations cause borderline HbA(2).

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All Publications

2012: Maria Elisabetta Paglietti; Maria Carla Sollaino; Susanna Barella; Maria Franca Desogus; Daniela Loi; Renzo Galanello
First detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in an Italian child.
Hemoglobin 2012;36(3):299-304.
2012: Antonella Fais; Lucia Perseu; Maria Carla Sollaino; Susanna Barella; Benedetta Era; Marcella Corda
A new β chain hemoglobin variant with increased oxygen affinity: Hb Santa Giusta Sardegna [β93(F9)Cys→Trp; HBB c.282T>G].
Hemoglobin 2012;36(2):151-6.
2011: Luciana Perseu; Stefania Satta; Maria Carla Sollaino; Laura Manunza; Paolo Moi; Susanna Barella; Antonio Cao; Franca Rosa Demartis; Renzo Galanello
KLF1 gene mutations cause borderline HbA(2).
Blood 2011;118(16):4454-8.
2009: Renzo Galanello; Serena Sanna; Luciana Perseu; Maria Carla Sollaino; Stefania Satta; Maria Eliana Lai; Susanna Barella; Manuela Uda; Gianluca Usala; Goncalo R Abecasis; Antonio Cao
Amelioration of Sardinian beta0 thalassemia by genetic modifiers.
Blood 2009;114(18):3935-7.
2008: Maria Antonietta Melis; Milena Cau; Rita Congiu; Gabriella Sole; Susanna Barella; Antonio Cao; Mark Westerman; Mario Cazzola; Renzo Galanello
A mutation in the TMPRSS6 gene, encoding a transmembrane serine protease that suppresses hepcidin production, in familial iron deficiency anemia refractory to oral iron.
Haematologica 2008;93(10):1473-9.
2008: Raffaella Origa; Susanna Barella; Giovanni Maria Argiolas; Patrizio Bina; Annalisa Agus; Renzo Galanello
No evidence of cardiac iron in 20 never- or minimally-transfused patients with thalassemia intermedia.
Haematologica 2008;93(7):1095-6.
2007: Raffaella Origa; M C Sollaino; Nicolina Giagu; Susanna Barella; S Campus; C Mandas; Patrizio Bina; Luciana Perseu; Renzo Galanello
Clinical and molecular analysis of haemoglobin H disease in Sardinia: haematological, obstetric and cardiac aspects in patients with different genotypes.
British journal of haematology 2007;136(2):326-32.
2004: Renzo Galanello; Luciana Perseu; Chiara Perra; Liliana Maccioni; Susanna Barella; Maurizio Longinotti; Antonio Cao; Mario Cazzola
Somatic deletion of the normal beta-globin gene leading to thalassaemia intermedia in heterozygous beta-thalassaemic patients.
British journal of haematology 2004;127(5):604-6.
2004: Renzo Galanello; Luciana Perseu; Susanna Barella; Stefania Satta; Antonella Fais; Benedetta Era; Maria G Corda
Hb Belfast [beta15(A12)Trp-->Arg]: definition of the clinical and hematological phenotype.
Hemoglobin 2004;28(3):217-22.
2002: Maria G Corda; Antonella Fais; Luciana Perseu; Loretta Cipollina; Susanna Barella; Renzo Galanello
Identification and functional characterization of a new hemoglobin variant in Sardinia: Hb Muravera [beta47 GAT->GTT, (CD6) Asp->Val].
Haematologica 2002;87(10):1111-2.
2002: Renzo Galanello; Susanna Barella; Stefania Satta; Liliana Maccioni; Carlo Pintor; Antonio Cao
Homozygosity for nondeletion delta-beta(0) thalassemia resulting in a silent clinical phenotype.
Blood 2002;100(5):1913-4.
2002: Maria Antonietta Melis; Milena Cau; Federica Deidda; Susanna Barella; Antonio Cao; Renzo Galanello
H63D mutation in the HFE gene increases iron overload in beta-thalassemia carriers.
Haematologica 2002;87(3):242-5.
2001: Renzo Galanello; Silvia Piras; Susanna Barella; Giovanbattista Leoni; MD Cipollina; Luciana Perseu; Antonio Cao
Cholelithiasis and Gilbert's syndrome in homozygous beta-thalassaemia.
British journal of haematology 2001;115(4):926-8.
1999: Renzo Galanello; MD Cipollina; G Carboni; Luciana Perseu; Susanna Barella; A Corrias; Antonio Cao
Hyperbilirubinemia, glucose-6-phosphate-dehydrogenase deficiency and Gilbert's syndrome.
European journal of pediatrics 1999;158(11):914-6.
1999: Mario Cazzola; Yves Beguin; Gaetano Bergamaschi; R Guarnone; Paola Cerani; Susanna Barella; Antonio Cao; Renzo Galanello
Soluble transferrin receptor as a potential determinant of iron loading in congenital anaemias due to ineffective erythropoiesis.
British journal of haematology 1999;106(3):752-5.
1998: Renzo Galanello; Carla Sollaino; E Paglietti; Susanna Barella; Chiara Perra; I Doneddu; M G Pirroni; Liliana Maccioni; Antonio Cao
Alpha-thalassemia carrier identification by DNA analysis in the screening for thalassemia.
American journal of hematology 1998;59(4):273-8.
1998: Andrea Mosca; Renata Paleari; Carla Sollaino; Susanna Barella; Renzo Galanello
Limits to the use of the glucose 6-phosphate dehydrogenase/6-phosphogluconate dehydrogenase index for the detection of glucose 6-phosphate dehydrogenase deficiency.
Clinical chemistry and laboratory medicine : CCLM / FESCC 1998;36(9):737-8.
1998: E Paglietti; Susanna Barella; Stefania Satta; Chiara Perra; Antonio Cao; Renzo Galanello
Hb Sassari [alpha 126(H9)Asp-->His] results from a GAC-->CAC mutation in the alpha 1-globin gene.
Hemoglobin 1998;22(1):65-7.
1997: Renzo Galanello; Luciana Perseu; Maria Antonietta Melis; L Cipollina; Susanna Barella; Nicolina Giagu; M P Turco; O Maccioni; Antonio Cao
Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndrome.
British journal of haematology 1997;99(2):433-6.
1997: Renzo Galanello; Renata Paleari; Luciana Perseu; Susanna Barella; Liliana Maccioni; Antonio Cao; G Mulas; E Cocco; Andrea Mosca
Hb Puttelange [beta 140(H19)Ala-->Val] in an Italian man with polycythemia.
Hemoglobin 1997;21(1):17-26.
1996: Andrea Mosca; Renata Paleari; E Rosti; M Luzzana; Susanna Barella; Carla Sollaino; Renzo Galanello
Simultaneous automated determination of glucose 6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase activities in whole blood.
European journal of clinical chemistry and clinical biochemistry : journal of the Forum of European Clinical Chemistry Societies 1996;34(5):431-8.
1995: Mario Cazzola; Piero De Stefano; Luisa Ponchio; Franco Locatelli; Yves Beguin; C Dessi; Susanna Barella; Antonio Cao; Renzo Galanello
Relationship between transfusion regimen and suppression of erythropoiesis in beta-thalassaemia major.
British journal of haematology 1995;89(3):473-8.
1995: Renzo Galanello; Susanna Barella; D Gasperini; Luciana Perseu; E Paglietti; Carla Sollaino; L Paderi; M G Pirroni; Liliana Maccioni; Andrea Mosca
Evaluation of an automatic HPLC analyser for thalassemia and haemoglobin variants screening.
The Journal of automatic chemistry 1995;17(2):73-6.
1994: Renzo Galanello; D Gasperini; Luciana Perseu; Susanna Barella; A Ideo; Antonio Cao
Hb A2-Sant' Antioco [alpha 2 delta (2)93(F9)Cys-->Gly]: a new delta chain variant identified by sequencing of amplified DNA.
Hemoglobin 1994;18(6):437-9.
1994: Renzo Galanello; Susanna Barella; A Ideo; D Gasperini; C Rosatelli; L Paderi; E Paglietti; Carla Sollaino; Luciana Perseu; D Loi
Genotype of subjects with borderline hemoglobin A2 levels: implication for beta-thalassemia carrier screening.
American journal of hematology 1994;46(2):79-81.
1994: Renzo Galanello; Susanna Barella; M P Turco; Nicolina Giagu; Antonio Cao; F Dore; Nicola Liberato; R Guarnone; Giovanni Barosi
Serum erythropoietin and erythropoiesis in high- and low-fetal hemoglobin beta-thalassemia intermedia patients.
Blood 1994;83(2):561-5.
1993: D Gasperini; Antonio Cao; L Paderi; Susanna Barella; E Paglietti; Luciana Perseu; D Loi; Renzo Galanello
Normal individuals with high Hb A2 levels.
British journal of haematology 1993;84(1):166-8.
1992: Renzo Galanello; B Aru; C Dessì; M Addis; E Paglietti; Maria Antonietta Melis; S Cocco; P Massa; Nicolina Giagu; Susanna Barella
HbH disease in Sardinia: molecular, hematological and clinical aspects.
Acta haematologica 1992;88(1):1-6.
1990: Renzo Galanello; M P Turco; Susanna Barella; Nicolina Giagu; C Dessì; G Cornacchia; Antonio Cao
Iron stores and iron deficiency anemia in children heterozygous for beta-thalassemia.
Haematologica 1990;75(4):319-22.
1989: Renzo Galanello; Susanna Barella; Liliana Maccioni; E Paglietti; Maria Antonietta Melis; Maria Cristina Rosatelli; F Argiolu; Antonio Cao
Erythropoiesis following bone marrow transplantation from donors heterozygous for beta-thalassaemia.
British journal of haematology 1989;72(4):561-6.