SATTA, STEFANIA
SATTA, STEFANIA
DIPARTIMENTO DI SCIENZE MEDICHE E SANITA' PUBBLICA
Vascular Abnormalities and Neurofibromatosis Type 1: A Paediatric Case Series
2024-01-01 Currao, P.; Balzarini, M.; Pruna, D.; Marica, M.; Soddu, C.; Marras, M.; Pavanello, M.; Satta, S.; Savasta, S.
Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation
2017-01-01 Satta, Stefania; Paglietti, MARIA ELISABETTA; Sollaino, Maria Carla; Barella, Susanna; Moi, Paolo; Desogus, Maria Franca; Demartis, FRANCA ROSA; Manunza, Laura; Origa, Raffaella
A validated cellular biobank for β-thalassemia
2016-01-01 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
The problem of borderline hemoglobin A2 levels in the Screening for β-thalassemia carriers in Sardinia.
2016-01-01 Paglietti, MARIA ELISABETTA; Satta, Stefania; Sollaino, Mc; Barella, S; Ventrella, A; Desogus, Mf; Demartis, FRANCA ROSA; Manunza, Laura; Origa, Raffaella
A genetic score for the prediction of beta-thalassemia severity
2015-01-01 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.
IFNL3 polymorphisms and HCV infection in patients with beta thalassemia
2015-01-01 Origa, Raffaella; Marceddu, Giuseppe; Danjou, Fabrice; Perseu, Luciana; Satta, Stefania; Demartis, FRANCA ROSA; Piga, Antonio; Longo, Filomena; Lai, MARIA ELIANA; Vacquer, Stefania; Galanello, Renzo
HPFH from Klf1 haploinsufficiency combined to transcriptional heterozygous b-thalassemia
2014-01-01 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
2012-01-01 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.
2012-01-01 Satta, Stefania; Perseu, L; Maccioni, L; Giagu, N; Galanello, R.
Genetic modifiers of β-thalassemia and clinical severity as assessed by age at first transfusion
2012-01-01 Danjou, Fabrice; Anni, Franco; Perseu, L; Satta, Stefania; Dessi', C; Lai, MARIA ELIANA; Fortina, P; Devoto, M; Galanello, Renzo
GENOME-WIDE ASSOCIATION STUDY FOR HB F DETERMINANTS IN SARDINIAN PATIENTS WITH Β THALASSEMIA
2012-01-01 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”
2011-01-01 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
2011-01-01 Satta, Stefania; Perseu, L; Moi, Paolo; Asunis, I; Cabriolu, Annalisa; Maccioni, L; Demartis, Fr; Manunza, Laura; Cao, A; Galanello, R.
HPFH From Klf1 Haploinsufficiency Combined to Transcriptional Heterozygous β-Thalassemia
2011-01-01 Moi, Paolo; Marini, Giuseppina M.; Isadora, Asunis; Loredana, Porcu; Cabriolu, Annalisa; Satta, Stefania; Luciana, Perseu; Liliana, Maccioni; Antonio, Cao; Renzo, Galanello
KLF1 gene mutations cause borderline HbA(2).
2011-01-01 Perseu, L; Satta, Stefania; Moi, Paolo; Demartis, Fr; Manunza, Laura; Sollaino, Mc; Barella, S; Cao, A; Galanello, R.
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach
2011-01-01 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.
Red cell pyruvate kinase deficiency in Southern Sardinia.
2010-01-01 Perseu, L.; Giagu, N.; Satta, Stefania; Sollaino, M. C.; Congiu, R.; Galanello, R.
“Genetic modifiers of fetal hemoglobin expression”
2010-01-01 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.
2009-01-01 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.
2009-01-01 Galanello, R; Sanna, S; Perseu, L; Sollaino, Mc; Satta, Stefania; Lai, Me; Barella, S; Uda, M; Usala, G; Abecasis, Gr; Cao, A.
| Titolo | Data di pubblicazione | Autore(i) | Rivista | Editore |
|---|---|---|---|---|
| Vascular Abnormalities and Neurofibromatosis Type 1: A Paediatric Case Series | 1-gen-2024 | Currao, P.; Balzarini, M.; Pruna, D.; Marica, M.; Soddu, C.; Marras, M.; Pavanello, M.; Satta, S.; Savasta, S. | JOURNAL OF CHILD NEUROLOGY | - |
| 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. | BLOOD | - |
| 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. | - | - |