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Luciana Perseu

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Fabrice Danjou; Carlo Dessì; Marcella Devoto; Paolo Fortina; Maria Eliana Lai; Luciana Perseu; Stefania Satta; Franco Anni; Renzo Galanello
Genetic modifiers of β-thalassemia and clinical severity as assessed by age at first transfusion.
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).
Luciana Perseu; N Giagu; Stefania Satta; M C Sollaino; R Congiu; Renzo Galanello
Red cell pyruvate kinase deficiency in Southern Sardinia.

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All Publications

2012: Fabrice Danjou; Carlo Dessì; Marcella Devoto; Paolo Fortina; Maria Eliana Lai; Luciana Perseu; Stefania Satta; Franco Anni; Renzo Galanello
Genetic modifiers of β-thalassemia and clinical severity as assessed by age at first transfusion.
Haematologica 2012;97(7):989-93.
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.
2010: Luciana Perseu; N Giagu; Stefania Satta; M C Sollaino; R Congiu; Renzo Galanello
Red cell pyruvate kinase deficiency in Southern Sardinia.
Blood cells, molecules & diseases 2010;45(4):280-3.
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.
2009: Maria Carla Sollaino; Maria Elisabetta Paglietti; Luciana Perseu; Nicolina Giagu; Daniela Loi; Renzo Galanello
Association of α globin gene quadruplication and heterozygous β thalassemia in patients with thalassemia intermedia.
Haematologica 2009;94(10):1445-8.
2009: serena Sanna; Fabio Busonero; Andrea Maschio; Patrick F McArdle; Gianluca Usala; Mariano Dei; Sandra Lai; Antonella Mulas; Maria Grazia Piras; Luciana Perseu; Marco Masala; Mara Marongiu; Laura Crisponi; Silvia Naitza; Renzo Galanello; Goncalo Abecasis; Alan R Shuldiner; David Schlessinger; Antonio Cao; Manuela Uda
Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia.
Human molecular genetics 2009;18(14):2711-8.
2008: Manuela Uda; Renzo Galanello; serena Sanna; Guillaume Lettre; Vijay G Sankaran; Weimin Chen; Gianluca Usala; Fabio Busonero; Andrea Maschio; Giuseppe Albai; Maria Grazia Piras; Natascia Sestu; Sandra Lai; Mariano Dei; Antonella Mulas; Laura Crisponi; Silvia Naitza; Isadora Asunis; Manila Deiana; Ramaiah Nagaraja; Luciana Perseu; Stefania Satta; MD Cipollina; Carla Sollaino; Paolo Moi; Joel N Hirschhorn; Stuart H Orkin; Goncalo Abecasis; David Schlessinger; Antonio Cao
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.
Proceedings of the National Academy of Sciences of the United States of America 2008;105(5):1620-5.
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.
2005: Renzo Galanello; Luciana Perseu; F Anni
Molecular basis of congenital and acquired deafness.
La Pediatria medica e chirurgica : Medical and surgical pediatrics 2005;27(5):53-5.
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.
2003: Caterina Borgna-Pignatti; Francesca Rigon; Luciano Merlo; Roksana Chakrok; Rocco Micciolo; Luciana Perseu; Renzo Galanello
Thalassemia minor, the Gilbert mutation, and the risk of gallstones.
Haematologica 2003;88(10):1106-9.
2003: Shaheen N Khan; Farrukh Hasan; Carla Sollaino; Luciana Perseu; Sheikh Amer Riazuddin
Molecular characterization of alpha-thalassemia in Pakistan.
Hemoglobin 2003;27(3):161-6.
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.
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.
1998: D Gasperini; Luciana Perseu; Maria Antonietta Melis; Liliana Maccioni; M C Sollaino; E Paglietti; Antonio Cao; Renzo Galanello
Heterozygous beta-thalassemia with thalassemia intermedia phenotype.
American journal of hematology 1998;57(1):43-7.
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.
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: D Gasperini; Luciana Perseu; P Cossu; R Podda; Antonio Cao; Renzo Galanello
A novel delta O-thalassemia mutation: TGG-->TAG (TRP-->STOP) at codon 37.
Human mutation 1994;3(1):71-2.
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.
1993: Renzo Galanello; meloni alessandra; D Gasperini; L Saba; Antonio Cao; Maria Cristina Rosatelli; Luciana Perseu
The repeated sequence (AT)x(T)y upstream to the beta-globin gene is a simple polymorphism.
Blood 1993;81(7):1974-5.
1991: Antonello Podda; Renzo Galanello; Liliana Maccioni; Maria Antonietta Melis; C Rosatelli; Luciana Perseu; Antonio Cao
Hemoglobin Cagliari (beta 60 [E4] Val----Glu): a novel unstable thalassemic hemoglobinopathy.
Blood 1991;77(2):371-5.
1990: Renzo Galanello; Maria Antonietta Melis; Antonello Podda; M Monne; Luciana Perseu; Georgios Loudianos; Antonio Cao; Mario Pirastu; A Piga
Deletion delta-thalassemia: the 7.2 kb deletion of Corfu delta beta-thalassemia in a non-beta-thalassemia chromosome.
Blood 1990;75(8):1747-9.
1989: Luciana Perseu; M S Ristaldi; SP Dibenedetto; R Testa; Gino Schilirò; Mario Pirastu; Antonio Cao
The effect of the beta thalassemia mutation on the clinical severity of the sickle beta thalassemia syndrome.
Haematologica 1989;74(4):341-5.
1987: L Oggiano; Mario Pirastu; Paolo Moi; M Longinotti; Luciana Perseu; Antonio Cao
Molecular characterization of a normal Hb A2 beta-thalassaemia determinant in a Sardinian family.
British journal of haematology 1987;67(2):225-9.
1984: Renzo Galanello; Liliana Maccioni; R Ruggeri; Luciana Perseu; Antonio Cao
Alpha thalassaemia in Sardinian newborns.
British journal of haematology 1984;58(2):361-8.