SATTA, STEFANIA

SATTA, STEFANIA  

DIPARTIMENTO DI SCIENZE MEDICHE E SANITA' PUBBLICA  

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Titolo Data di pubblicazione Autore(i) Rivista Editore
Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation 1-gen-2017 Satta, Stefania; Paglietti, MARIA ELISABETTA; Sollaino, Maria Carla; Barella, Susanna; Moi, Paolo; Desogus, Maria Franca; Demartis, FRANCA ROSA; Manunza, Laura; Origa, Raffaella BLOOD CELLS, MOLECULES, & DISEASES -
A validated cellular biobank for β-thalassemia 1-gen-2016 Cosenza, Lucia Carmela; Breda, Laura; Breveglieri, Giulia; Zuccato, Cristina; Finotti, Alessia; Lampronti, Ilaria; Borgatti, Monica; Chiavilli, Francesco; Gamberini, Maria Rita; Satta, Stefania; Manunza, Laura; De Martis, Franca Rosa; Moi, Paolo; Rivella, Stefano; Gambari, Roberto; Bianchi, Nicoletta JOURNAL OF TRANSLATIONAL MEDICINE -
The problem of borderline hemoglobin A2 levels in the Screening for β-thalassemia carriers in Sardinia. 1-gen-2016 Paglietti, MARIA ELISABETTA; Satta, Stefania; Sollaino, Mc; Barella, S; Ventrella, A; Desogus, Mf; Demartis, FRANCA ROSA; Manunza, Laura; Origa, Raffaella ACTA HAEMATOLOGICA -
A genetic score for the prediction of beta-thalassemia severity 1-gen-2015 Danjou, Fabrice; Francavilla, M; Anni, Franco; Satta, Stefania; Demartis, Fr; Perseu, L; Manca, Matteo; Sollaino, Mc; Manunza, Laura; Mereu, E; Marceddu, G; Pissard, S; Joly, P; Thuret, I; Origa, Raffaella; Borg, J; Forni, Gl; Piga, A; Lai, Me; Badens, C; Moi, Paolo; Galanello, R. HAEMATOLOGICA -
IFNL3 polymorphisms and HCV infection in patients with beta thalassemia 1-gen-2015 Origa, Raffaella; Marceddu, Giuseppe; Danjou, Fabrice; Perseu, Luciana; Satta, Stefania; Demartis, FRANCA ROSA; Piga, Antonio; Longo, Filomena; Lai, MARIA ELIANA; Vacquer, Stefania; Galanello, Renzo ANNALS OF HEPATOLOGY -
HPFH from Klf1 haploinsufficiency combined to transcriptional heterozygous b-thalassemia 1-gen-2014 Marini M., G; Asunis, I; Mingoia, Maura; Desogus, Alessia; Porcu, L; Satta, Stefania; Perseu, L; Manunza, L; Cabriolu, A; Moi, Paolo - -
Application of next generation sequencing to identify causative variants at the BCL11A locus 1-gen-2012 Danjou, Fabrice; Usala, L; Perseu, L; Sidore, C; Busonero, F; Berutti, R; Reinier, F; Angius, A.; Maschio, A; Jones, C; Anni, Franco; Satta, Stefania; Demartis, F; Ramaiah, N; Abecasis, G; Schlessinger, D; Galanello, R; Cucca, F; Sanna, S; Uda, M. - -
Delayed fetal hemoglobin switching in subjects with KLF1 gene mutation. 1-gen-2012 Satta, Stefania; Perseu, L; Maccioni, L; Giagu, N; Galanello, R. BLOOD CELLS, MOLECULES, & DISEASES -
Genetic modifiers of β-thalassemia and clinical severity as assessed by age at first transfusion 1-gen-2012 Danjou, Fabrice; Anni, Franco; Perseu, L; Satta, Stefania; Dessi', C; Lai, MARIA ELIANA; Fortina, P; Devoto, M; Galanello, Renzo HAEMATOLOGICA -
GENOME-WIDE ASSOCIATION STUDY FOR HB F DETERMINANTS IN SARDINIAN PATIENTS WITH Β THALASSEMIA 1-gen-2012 P., Fortina; Anni, Franco; Danjou, Fabrice; L., Perseu; Satta, Stefania; M., Devoto; R., Galanello - -
. “Variazioni al locus IL28B in pazienti sardi con talassemia major HCV positivi” 1-gen-2011 Satta, Stefania; Marceddu, G.; Perseu, L.; Danjou, Fabrice; De Martis, F. R.; Balzarini, M.; Follesa, I.; Cau, Milena; Lai, E. e. Galanello R. - -
Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin 1-gen-2011 Satta, Stefania; Perseu, L; Moi, Paolo; Asunis, I; Cabriolu, Annalisa; Maccioni, L; Demartis, Fr; Manunza, Laura; Cao, A; Galanello, R. HAEMATOLOGICA -
HPFH From Klf1 Haploinsufficiency Combined to Transcriptional Heterozygous β-Thalassemia 1-gen-2011 Moi, Paolo; Marini, Giuseppina M.; Isadora, Asunis; Loredana, Porcu; Cabriolu, Annalisa; Satta, Stefania; Luciana, Perseu; Liliana, Maccioni; Antonio, Cao; Renzo, Galanello BLOOD -
KLF1 gene mutations cause borderline HbA(2). 1-gen-2011 Perseu, L; Satta, Stefania; Moi, Paolo; Demartis, Fr; Manunza, Laura; Sollaino, Mc; Barella, S; Cao, A; Galanello, R. BLOOD -
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach 1-gen-2011 Giardine, B; Borg, J; Higgs, Dr; Peterson, Kr; Philipsen, S; Maglott, D; Singleton, Bk; Anstee, Dj; Basak, An; Clark, B; Costa, Fc; Faustino, P; Fedosyuk, H; Felice, Ae; Francina, A; Galanello, R; Gallivan, Mv; Georgitsi, M; Gibbons, Rj; Giordano, Pc; Harteveld, Cl; Hoyer, Jd; Jarvis, M; Joly, P; Kanavakis, E; Kollia, P; Menzel, S; Miller, W; Moradkhani, K; Old, J; Papachatzopoulou, A; Papadakis, Mn; Papadopoulos, P; Pavlovic, S; Perseu, L; Radmilovic, M; Riemer, C; Satta, Stefania; Schrijver, I; Stojiljkovic, M; Thein, Sl; Traeger Synodinos, J; Tully, R; Wada, T; Waye, Js; Wiemann, C; Zukic, B; Chui, Dh; Wajcman, H; Hardison, Rc; Patrinos, G. P. NATURE GENETICS -
Red cell pyruvate kinase deficiency in Southern Sardinia. 1-gen-2010 Perseu, L.; Giagu, N.; Satta, Stefania; Sollaino, M. C.; Congiu, R.; Galanello, R. BLOOD CELLS, MOLECULES, & DISEASES -
“Genetic modifiers of fetal hemoglobin expression” 1-gen-2010 Danjou, Fabrice; Anni, F.; Satta, Stefania; Perseu, L.; Demartis, F. R.; Francavilla, M.; Marceddu, G.; Uda, M.; Sanna, S.; Cucca, F.; Fortina, P.; Devoto, M.; Galanello, R. - -
Amelioration of Sardinian beta-zero thalassemia by genetic modifiers. 1-gen-2009 Galanello, R; Sanna, S; Perseu, L; Sollaino, Mc; Satta, Stefania; Lai, Me; Barella, S; Uda, M; Usala, G; Abecasis, Gr; Cao, A. - -
Amelioration of Sardinian beta-zero thalassemia by genetic modifiers. 1-gen-2009 Galanello, R; Sanna, S; Perseu, L; Sollaino, Mc; Satta, Stefania; Lai, Me; Barella, S; Uda, M; Usala, G; Abecasis, Gr; Cao, A. BLOOD -
Delezione di regioni regolatorie dei geni alfa globinici, responsabili di una grave forma di emoglobina H 1-gen-2009 M. C., Sollaino; Paglietti, MARIA ELISABETTA; Anni, Franco; Satta, Stefania; D., Loi; R., Congiu; R., Podda; R., Galanello - -