PAGLIETTI, MARIA ELISABETTA
PAGLIETTI, MARIA ELISABETTA
DIPARTIMENTO DI SCIENZE MEDICHE E SANITA' PUBBLICA
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
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
Investigating the Alpha 1Ncol mutation
2015-01-01 Desogus, Mf; Paglietti, MARIA ELISABETTA; Sollaino, Mc; Barella, S; Origa, Raffaella
Complexity of the alpha-globin genotypes identified with thalassemia screening in Sardinia
2014-01-01 Origa, Raffaella; Paglietti, MARIA ELISABETTA; Sollaino, Mc; Desogus, Mf; Barella, S; Loi, D; Galanello, R.
First detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in an Italian child.
2012-01-01 Paglietti, MARIA ELISABETTA; Sollaino, M; Loi, D; Barella, S; Desogus, M; Galanello, R.
Two atypical forms of HbH disease in Sardinia.
2011-01-01 Paglietti, MARIA ELISABETTA; Sollaino, Mc; Loi, D; Sarra, F; Zaccheddu, E; Galanello, R.
Homozygous deletion of the major alpha-globin regulatory element (MCS-R2) responsible for a severe case of hemoglobin H disease.
2010-01-01 Sollaino, Mc; Paglietti, MARIA ELISABETTA; Loi, D; Congiu, R; Podda, R; Galanello, R.
Association of α globin gene quadruplication and heterozygous β thalassemia in patients with thalassemia intermedia
2009-01-01 Sollaino, Mc; Paglietti, MARIA ELISABETTA; Perseu, L; Giagu, N; Loi, D; Galanello, R.
Delezione di regioni regolatorie dei geni alfa globinici, responsabili di una grave forma di emoglobina H
2009-01-01 M. C., Sollaino; Paglietti, MARIA ELISABETTA; Anni, Franco; Satta, Stefania; D., Loi; R., Congiu; R., Podda; R., Galanello
Osteoporosis in beta-thalassemia: Clinical and genetic aspects.
2005-01-01 Origa, Raffaella; Fiumana, E; Gamberini, Mr; Armari, S; Mottes, M; Sangalli, A; Paglietti, MARIA ELISABETTA; Galanello, R; Borgna Pignatti, C.
Posttranslational deamidation of proteins: the case of hemoglobin J Sardegna [a50 (CD8) HIS→ASN→ASP]
1999-01-01 Paleari, R; Paglietti, MARIA ELISABETTA; Mosca, A; Mortasino, M; Maccioni, L; Satta, Stefania; Cao, A. AND GALANELLO R.
“Diagnosi di α e β talassemia”
1998-01-01 Galanello, R; Paglietti, MARIA ELISABETTA; Barella, S; Perseu, L; Perra, C; Cipollina, L; Satta, Stefania; Pirroni, M. G. AND MACCIONI L.
“Hb Sassari [α126 (H9) ASP→HIS] result from a GAC→CAC mutation in the α1-globin gene”
1998-01-01 Paglietti, MARIA ELISABETTA; Barella, S; Satta, Stefania; Perra, C; Cao, A. AND GALANELLO R.
HbH disease in Sardinia: molecular, hematological and clinical aspects
1992-01-01 Galanello, R; Aru, B; Dessì, C; Addis, Maria; Paglietti, MARIA ELISABETTA; Melis, Ma; Cocco, S; Massa, P; Giagu, N; Barella, S.
Homozygous non-deletion alpha 2 globin gene mutation (initiation codon mutation): clinical and haematological phenotype
1991-01-01 Galanello, R; Monne, Mi; Paderi, L; Paglietti, MARIA ELISABETTA; Atzori, G; Addis, Maria; Limongelli, O; Macciotta, A; Cao, A.
ERYTHROPOIESIS FOLLOWING BONE MARROW TRANSPLANTATION FROM DONORS HETEROZYGOUS FOR B-THALASSEMIA
1989-01-01 Galanello, R; Barella, S; Maccioni, L; Paglietti, MARIA ELISABETTA; Melis, Ma; Rosatelli, MARIA CRISTINA; Argiolu, F; Cao, A.
Delineation of the molecular basis of delta- and normal HbA2 beta-thalassemia
1988-01-01 Moi, Paolo; Paglietti, MARIA ELISABETTA; Sanna, A; Brancati, C; Tagarelli, A; Galanello, R; Cao, A; Pirastu, M.
Molecular pathology of haemoglobin H disease in Sardinians
1986-01-01 Paglietti, MARIA ELISABETTA; Galanello, R; Moi, Paolo; Pirastu, M; Cao, A.
Phenotype-genotype correlation in haemoglobin H disease in childhood
1983-01-01 Galanello, R; Pirastu, M; Melis, Ma; Paglietti, MARIA ELISABETTA; Moi, Paolo; Cao, A.
Control of homozygous beta-thalassemia by carrier screening and antenatal diagnosis in Sardinia
1982-01-01 Cao, A; Furbetta, M; Galanello, R; Melis, Ma; Angius, A; Rosatelli, MARIA CRISTINA; Ruggeri, R; Addis, Maria; Tuveri, T; Falchi, ANGELA MARIA; Maccioni, L; Paglietti, MARIA ELISABETTA; Scalas, Mt
| 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 | - |
| 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 | - |
| Investigating the Alpha 1Ncol mutation | 1-gen-2015 | Desogus, Mf; Paglietti, MARIA ELISABETTA; Sollaino, Mc; Barella, S; Origa, Raffaella | ACTA HAEMATOLOGICA | - |
| Complexity of the alpha-globin genotypes identified with thalassemia screening in Sardinia | 1-gen-2014 | Origa, Raffaella; Paglietti, MARIA ELISABETTA; Sollaino, Mc; Desogus, Mf; Barella, S; Loi, D; Galanello, R. | BLOOD CELLS, MOLECULES, & DISEASES | - |
| First detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in an Italian child. | 1-gen-2012 | Paglietti, MARIA ELISABETTA; Sollaino, M; Loi, D; Barella, S; Desogus, M; Galanello, R. | HEMOGLOBIN | - |
| Two atypical forms of HbH disease in Sardinia. | 1-gen-2011 | Paglietti, MARIA ELISABETTA; Sollaino, Mc; Loi, D; Sarra, F; Zaccheddu, E; Galanello, R. | HAEMATOLOGICA | - |
| Homozygous deletion of the major alpha-globin regulatory element (MCS-R2) responsible for a severe case of hemoglobin H disease. | 1-gen-2010 | Sollaino, Mc; Paglietti, MARIA ELISABETTA; Loi, D; Congiu, R; Podda, R; Galanello, R. | BLOOD | - |
| Association of α globin gene quadruplication and heterozygous β thalassemia in patients with thalassemia intermedia | 1-gen-2009 | Sollaino, Mc; Paglietti, MARIA ELISABETTA; Perseu, L; Giagu, N; Loi, D; Galanello, R. | HAEMATOLOGICA | - |
| 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 | - | - |
| Osteoporosis in beta-thalassemia: Clinical and genetic aspects. | 1-gen-2005 | Origa, Raffaella; Fiumana, E; Gamberini, Mr; Armari, S; Mottes, M; Sangalli, A; Paglietti, MARIA ELISABETTA; Galanello, R; Borgna Pignatti, C. | ANNALS OF THE NEW YORK ACADEMY OF SCIENCES | - |
| Posttranslational deamidation of proteins: the case of hemoglobin J Sardegna [a50 (CD8) HIS→ASN→ASP] | 1-gen-1999 | Paleari, R; Paglietti, MARIA ELISABETTA; Mosca, A; Mortasino, M; Maccioni, L; Satta, Stefania; Cao, A. AND GALANELLO R. | CLINICAL CHEMISTRY | - |
| “Diagnosi di α e β talassemia” | 1-gen-1998 | Galanello, R; Paglietti, MARIA ELISABETTA; Barella, S; Perseu, L; Perra, C; Cipollina, L; Satta, Stefania; Pirroni, M. G. AND MACCIONI L. | RIVISTA ITALIANA DI PEDIATRIA | - |
| “Hb Sassari [α126 (H9) ASP→HIS] result from a GAC→CAC mutation in the α1-globin gene” | 1-gen-1998 | Paglietti, MARIA ELISABETTA; Barella, S; Satta, Stefania; Perra, C; Cao, A. AND GALANELLO R. | PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR | - |
| HbH disease in Sardinia: molecular, hematological and clinical aspects | 1-gen-1992 | Galanello, R; Aru, B; Dessì, C; Addis, Maria; Paglietti, MARIA ELISABETTA; Melis, Ma; Cocco, S; Massa, P; Giagu, N; Barella, S. | ACTA HAEMATOLOGICA | - |
| Homozygous non-deletion alpha 2 globin gene mutation (initiation codon mutation): clinical and haematological phenotype | 1-gen-1991 | Galanello, R; Monne, Mi; Paderi, L; Paglietti, MARIA ELISABETTA; Atzori, G; Addis, Maria; Limongelli, O; Macciotta, A; Cao, A. | BRITISH JOURNAL OF HAEMATOLOGY | - |
| ERYTHROPOIESIS FOLLOWING BONE MARROW TRANSPLANTATION FROM DONORS HETEROZYGOUS FOR B-THALASSEMIA | 1-gen-1989 | Galanello, R; Barella, S; Maccioni, L; Paglietti, MARIA ELISABETTA; Melis, Ma; Rosatelli, MARIA CRISTINA; Argiolu, F; Cao, A. | BRITISH JOURNAL OF HAEMATOLOGY | - |
| Delineation of the molecular basis of delta- and normal HbA2 beta-thalassemia | 1-gen-1988 | Moi, Paolo; Paglietti, MARIA ELISABETTA; Sanna, A; Brancati, C; Tagarelli, A; Galanello, R; Cao, A; Pirastu, M. | BLOOD | - |
| Molecular pathology of haemoglobin H disease in Sardinians | 1-gen-1986 | Paglietti, MARIA ELISABETTA; Galanello, R; Moi, Paolo; Pirastu, M; Cao, A. | BRITISH JOURNAL OF HAEMATOLOGY | - |
| Phenotype-genotype correlation in haemoglobin H disease in childhood | 1-gen-1983 | Galanello, R; Pirastu, M; Melis, Ma; Paglietti, MARIA ELISABETTA; Moi, Paolo; Cao, A. | JOURNAL OF MEDICAL GENETICS | - |
| Control of homozygous beta-thalassemia by carrier screening and antenatal diagnosis in Sardinia | 1-gen-1982 | Cao, A; Furbetta, M; Galanello, R; Melis, Ma; Angius, A; Rosatelli, MARIA CRISTINA; Ruggeri, R; Addis, Maria; Tuveri, T; Falchi, ANGELA MARIA; Maccioni, L; Paglietti, MARIA ELISABETTA; Scalas, Mt | BIRTH DEFECTS ORIGINAL ARTICLE SERIES | - |