Sfoglia per Autore
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.
Analysis of candidate SNPs for high Hb F in beta thalassemia intermedia patients
2008-01-01 Anni, Franco; L., Perseu; Satta, Stefania; M., Bowser; P., Fortina; M., Devoto; S., Surrey; R., Galanello
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia
2008-01-01 Uda, M; Galanello, R; Sanna, S; Lettre, G; Sankaran, Vg; Chen, W; Usala, G; Busonero, Fabio; Maschio, A; Albai, G; Piras, Mg; Sestu, N; Lai, S; Dei, M; Mulas, A; Crisponi, Laura; Naitza, S; Asunis, I; Deiana, M; Nagaraja, R; Perseu, L; Satta, Stefania; Cipollina, Md; Sollaino, C; Moi, Paolo; Hirschhorn, Jn; Orkin, Sh; Abecasis, Gr; Schlessinger, D; Cao, A.
Glutathione S-transferase gene polymorphism and cardiac iron overload in thalassaemia major
2008-01-01 Origa, Raffaella; Satta, Stefania; Matta, G; Galanello, R.
Studio del gene AHSP nelle β-Talassemie
2007-12-14
Polymorphism of S-transferase glutathione gene and a major thalassaemia cardiac iron
2007-01-01 Origa, Raffaella; Satta, Stefania; Cipollina, Md; Perseu, L; Galanello, Renzo
Glutathione S-transferase se gene polymorphism and heart iron overload in Thalassemia major
2007-01-01 Origa, Raffaella; Satta, Stefania; Cipollina, Md; Perseu, L; Agus, A; Galanello, Renzo
I difetti emoglobinici e la loro valutazione di laboratorio
2007-01-01 Galanello, R.; Cipollina, M. D.; Demartis, F. R.; Sollaino, M. C.; Satta, Stefania; Loi, D.; Perseu, L.; Anni, Franco
“Neonatal Anemia”
2006-01-01 Galanello, R.; Satta, Stefania; Cipollina, Md
Alfa-thalassemia in Sardinia
2006-01-01 D., Loi; M. C., Sollaino; Anni, Franco; R., Congiu; Satta, Stefania; R., Galanello
Hb Belfast [β15(A12)Trp→Arg]: Definition of the clinical and hematological phenotype
2004-01-01 R., Galanello; L., Perseu; S., Barella; Satta, Stefania; Fais, Antonella; Era, Benedetta; M., Corda
Hemoglobin Belfast (beta15, Trp→Arg) definition of the clinical and hematological phenotype
2003-01-01 Puddu, B; Fais, Antonella; Perseu, L; Barella, S; Satta, Stefania; Galanello, R.
Hemoglobin Belfast (beta15,Trp→Arg) definition of the clinical and hematological phenotype
2003-01-01 Galanello, R; Perseu, L; Barella, S; Satta, Stefania; Fais, Antonella; Era, Benedetta; Corda, M.
“Homozygosity for non deletion δβ° thalassemia resulting in a silent clinical phenotype”
2002-01-01 Galanello, R; Barella, S; Satta, Stefania; Maccioni, L; Pintor, C. AND CAO A.
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.
5. Galanello R., Satta S., Pirroni M.G., Travi M. and Maccioni L. “Globin chain synthesis analysis by high performance liquid chromatography in the screening of thalassemia syndromes”. European Concerted Action-Evaluation of fetal Hemoglobin Activating Therapies. Hemoglobin vol.22 (5&6): 501-508, 1998
1998-01-01 Satta, Stefania
“Meccanismi molecolari delle sindromi talassemiche e induttori della sintesi di catene γ” Riv. Ital. Pediatr. Vol.24: 84-86, 1998
1998-01-01 Galanello, R; Barella, S; Giagu, L; Perseu, L; Sollaino, C; Satta, Stefania; Origa, R. AND CAO A.
Chronic ethanol intoxication enhances [3H]CCPA binding and does not reduce A1 adenosine receptor function in rat cerebellum
1996-01-01 Concas, Alessandra; Mascia, Mp; Cuccheddu, T; Floris, S; Mostallino, Mc; Perra, C; Satta, Stefania; Biggio, G.
| Titolo | Data di pubblicazione | Autore(i) | Rivista | Editore |
|---|---|---|---|---|
| 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. | - | - |
| Analysis of candidate SNPs for high Hb F in beta thalassemia intermedia patients | 1-gen-2008 | Anni, Franco; L., Perseu; Satta, Stefania; M., Bowser; P., Fortina; M., Devoto; S., Surrey; R., Galanello | - | - |
| Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia | 1-gen-2008 | Uda, M; Galanello, R; Sanna, S; Lettre, G; Sankaran, Vg; Chen, W; Usala, G; Busonero, Fabio; Maschio, A; Albai, G; Piras, Mg; Sestu, N; Lai, S; Dei, M; Mulas, A; Crisponi, Laura; Naitza, S; Asunis, I; Deiana, M; Nagaraja, R; Perseu, L; Satta, Stefania; Cipollina, Md; Sollaino, C; Moi, Paolo; Hirschhorn, Jn; Orkin, Sh; Abecasis, Gr; Schlessinger, D; Cao, A. | PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA | - |
| Glutathione S-transferase gene polymorphism and cardiac iron overload in thalassaemia major | 1-gen-2008 | Origa, Raffaella; Satta, Stefania; Matta, G; Galanello, R. | BRITISH JOURNAL OF HAEMATOLOGY | - |
| Studio del gene AHSP nelle β-Talassemie | 14-dic-2007 | - | - | Università degli Studi di Cagliari |
| Polymorphism of S-transferase glutathione gene and a major thalassaemia cardiac iron | 1-gen-2007 | Origa, Raffaella; Satta, Stefania; Cipollina, Md; Perseu, L; Galanello, Renzo | HAEMATOLOGICA | - |
| Glutathione S-transferase se gene polymorphism and heart iron overload in Thalassemia major | 1-gen-2007 | Origa, Raffaella; Satta, Stefania; Cipollina, Md; Perseu, L; Agus, A; Galanello, Renzo | BLOOD | - |
| I difetti emoglobinici e la loro valutazione di laboratorio | 1-gen-2007 | Galanello, R.; Cipollina, M. D.; Demartis, F. R.; Sollaino, M. C.; Satta, Stefania; Loi, D.; Perseu, L.; Anni, Franco | LA RIVISTA ITALIANA DELLA MEDICINA DI LABORATORIO | - |
| “Neonatal Anemia” | 1-gen-2006 | Galanello, R.; Satta, Stefania; Cipollina, Md | - | - |
| Alfa-thalassemia in Sardinia | 1-gen-2006 | D., Loi; M. C., Sollaino; Anni, Franco; R., Congiu; Satta, Stefania; R., Galanello | - | - |
| Hb Belfast [β15(A12)Trp→Arg]: Definition of the clinical and hematological phenotype | 1-gen-2004 | R., Galanello; L., Perseu; S., Barella; Satta, Stefania; Fais, Antonella; Era, Benedetta; M., Corda | HEMOGLOBIN | - |
| Hemoglobin Belfast (beta15, Trp→Arg) definition of the clinical and hematological phenotype | 1-gen-2003 | Puddu, B; Fais, Antonella; Perseu, L; Barella, S; Satta, Stefania; Galanello, R. | - | - |
| Hemoglobin Belfast (beta15,Trp→Arg) definition of the clinical and hematological phenotype | 1-gen-2003 | Galanello, R; Perseu, L; Barella, S; Satta, Stefania; Fais, Antonella; Era, Benedetta; Corda, M. | ITALIAN JOURNAL OF BIOCHEMISTRY | - |
| “Homozygosity for non deletion δβ° thalassemia resulting in a silent clinical phenotype” | 1-gen-2002 | Galanello, R; Barella, S; Satta, Stefania; Maccioni, L; Pintor, C. AND CAO A. | BLOOD | - |
| 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 | - |
| 5. Galanello R., Satta S., Pirroni M.G., Travi M. and Maccioni L. “Globin chain synthesis analysis by high performance liquid chromatography in the screening of thalassemia syndromes”. European Concerted Action-Evaluation of fetal Hemoglobin Activating Therapies. Hemoglobin vol.22 (5&6): 501-508, 1998 | 1-gen-1998 | Satta, Stefania | HEMOGLOBIN | - |
| “Meccanismi molecolari delle sindromi talassemiche e induttori della sintesi di catene γ” Riv. Ital. Pediatr. Vol.24: 84-86, 1998 | 1-gen-1998 | Galanello, R; Barella, S; Giagu, L; Perseu, L; Sollaino, C; Satta, Stefania; Origa, R. AND CAO A. | RIVISTA ITALIANA DI PEDIATRIA | - |
| Chronic ethanol intoxication enhances [3H]CCPA binding and does not reduce A1 adenosine receptor function in rat cerebellum | 1-gen-1996 | Concas, Alessandra; Mascia, Mp; Cuccheddu, T; Floris, S; Mostallino, Mc; Perra, C; Satta, Stefania; Biggio, G. | PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR | - |
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