Sfoglia per Rivista HAEMATOLOGICA
B-GLOBIN HAPLOTYPE AND XMNI POLYMORPHISM AT POSITION GY-158 AND HBF PRODUCTION IN FANCONI'S ANEMIA
1992-01-01 Rosatelli, MARIA CRISTINA; Altay, C; Oner, R; Leoni, Gb; Moi, B; Atzori, G; Cao, A.
Back to life -living, treating, managing myelofibrosis: the burden of illness for patients and their families.
2014-01-01 Mg, Marini; A., Cappuccio; E., Abruzzese; A., Carella; M., Lunghi; I., Loiacono; G., Palumbo; M., Bonifacio; D., Cilloni; A., Iurlo; A., Andriani1; G., Benevolo; C., Minoia; D., Turri; Em, Elli; Ap, Falcone; B., Anaclerico; A., Traficante; N., Di Renzo; M., Tiribelli; E., Calistri; R., Zambello; C., Spinosa; A., Ricco; F., Palandri; L., Raucci; B., Martino; M., Annunziata; M., D’Alosio; Am, Liberati; Caocci, Giovanni; M., Maffioli; M., Breccia; N., Pugliese; S., Betti; G., Giglio; L., Reale
Beta-thalassemia: from genotype to phenotype
2011-01-01 Danjou, Fabrice; Anni, Franco; Galanello, Renzo
Bone marrow transplantation from unrelated donors in class 3 adult thalassemic patients
2005-01-01 LA NASA, Giorgio; Argiolu, F; Giardini, C; Locatelli, F; Caocci, Giovanni; Ledda, A; Piras, E; Vacca, A; Contu, L.
C-->T MUTATION AT -158 G GAMMA HPFH ASSOCIATED WITH 4 BP DELETION (-225-222) IN THE PROMOTER REGION OF THE A GAMMA GENE IN HOMOZYGOUS BETA0 39 NONSENSE THALASSEMIA
1999-01-01 ATAULFO GONZALEZ, F; Ropero, P; Sanchez, J; Rosatelli, MARIA CRISTINA; Galanello, R; Villegas, A.
Un caso di deficit congenito di triosofosfato-isomerasi (TPI) : studio ematologico, biochimico, immunologico e genetico
1985-01-01 Contu, L; LA NASA, Giorgio; Frigerio, R; Olla, N; Sole, G; Carcassi, Carlo; Pitzus, F.
Clinical management of acute and chronic pain in patients with sickle cell disease
2019-01-01 Finco, G.; Sardo, S.
Communication bias during the decision making process for unrelated bone marrow transplantation in adult thalassemia patients
2007-01-01 Caocci, Giovanni; Pisu, S; Ledda, A; Arras, M; Vacca, A; Piras, E; Floris, R; Littera, R; Pizzati, A; Oppi, S; Orofino, Mg; Argiolu, E; LA NASA, Giorgio
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.
CONDITIONING SYSTEM BASED ON THE USE OF TREOSULFAN FOR ALLOGENEIC TRANSPLANT OF HEMATOPOIETIC STEM CELLS IN PATIENTS WITH THALASSEMIA MAJOR
2008-01-01 Bernardo, Me; Zecca, M; Piras, E; Vacca, A; Giorgiani, G; Cugno, C; Caocci, Giovanni; Comoli, P; Mastronuzzi, A; LA NASA, Giorgio; Locatelli, F.
The Coup-TFII orphan nuclear receptor is an activator of the γ-globin gene
2021-01-01 Fugazza, Cristina; Barbarani, Gloria; Elangovan, Sudharshan; Marini, Maria Giuseppina; Giolitto, Serena; Font-Monclus, Isaura; Marongiu, Maria Franca; Manunza, Laura; Strouboulis, John; Cantù, Claudio; Gasparri, Fabio; Barabino, Silvia M L; Nakamura, Yukio; Ottolenghi, Sergio; Moi, Paolo; Ronchi, Antonella Ellena
Cross-cultural development of an eortc questionnaire for assessing quality of life in chronic myeloid leukemia patients: the eortc qlq-cml24.
2013-01-01 F., Efficace; G., Rosti; M., Breccia; S., Saussele; G., Abel; Caocci, Giovanni; F., Guilhot; A., Naeem; F., Cottone; S., Oerlemans; F., Castagnetti; F., Bombaci; G., Sharf; L., Noens; S., Pallua; F., Mandelli; M., Baccarani
Decision making in high risk adult thalassemia patients undergoing unrelated bone marrow transplantation: Quality of life, motivation and communication factors, ethical issues
2005-01-01 Caocci, Giovanni; Pisu, S; Argiolu, F; Giardini, C; Locatelli, F; Vacca, A; Orofino, Mg; Piras, E; Addari, Mc; Ledda, A; LA NASA, Giorgio
DEFERASIROX-DEFEROXAMINE COMBINATION THERAPY REDUCES CARDIAC IRON WITH RAPID LIVER IRON REMOVAL AFTER 24 MONTHS IN PATIENTS WITH SEVERE TRANSFUSIONAL IRON OVERLOAD (HYPERION)
2014-01-01 Ayidinok, Y; Kattamis, A; Cappellini, Md; Beshlawy, Ae; Origa, Raffaella; Elalfy, M; Kilinc, Y; Perrotta, S; Karakas Z., ); Viprakasit, V; Musallam, K; Constantinovici, N; Shen, J; Porter, Jb
DIAGNOSI PRENATALE DI EMOGLOBINOPATIE EREDITARIE. (REVIEW)
1989-01-01 Cao, A; Pirastu, M; Rosatelli, MARIA CRISTINA
Differences in the erythropoiesis-hepcidin-iron store axis between hemoglobin H disease and β-thalassemia intermedia
2015-01-01 Origa, Raffaella; Cazzola, M; Mereu, E; Danjou, Fabrice; Barella, S; Giagu, N; Galanello, R; Swinkels, D. W.
Donor-recipient status for HLA class I ligands and not the KIR genotype, is predictive of unrelated hsct outcome in beta-thalassemia patients
2007-01-01 LA NASA, Giorgio; Littera, R.; Ledda, A.; Piras, E.; Vacca, A.; Caocci, Giovanni; Pizzati, A.; Arras, M.; Floris, R.; Giardini, C.; Locatelli, F.; Carcassi, Carlo
Donor-recipient status for HLA class I ligands and not the KIR genotype, is predictive of unrelated hsct outcome in beta-thalassemia patients
2007-01-01 LA NASA, Giorgio; Littera, R; Ledda, A; Piras, E; Vacca, A; Caocci, Giovanni; Pizzati, A; Arras, M; Floris, R; Giardini, C; Locatelli, F; Carcassi, Carlo
Le emocromatosi
1981-01-01 Carcassi, U.; Mela, Quirico
Ethical concerns surrounding the conception of an HLA compatible child for medical purposes
2012-01-01 Pisu, S; Demuru, F; Caocci, Giovanni; LA NASA, Giorgio
| Titolo | Data di pubblicazione | Autore(i) | Rivista | Editore |
|---|---|---|---|---|
| B-GLOBIN HAPLOTYPE AND XMNI POLYMORPHISM AT POSITION GY-158 AND HBF PRODUCTION IN FANCONI'S ANEMIA | 1-gen-1992 | Rosatelli, MARIA CRISTINA; Altay, C; Oner, R; Leoni, Gb; Moi, B; Atzori, G; Cao, A. | HAEMATOLOGICA | - |
| Back to life -living, treating, managing myelofibrosis: the burden of illness for patients and their families. | 1-gen-2014 | Mg, Marini; A., Cappuccio; E., Abruzzese; A., Carella; M., Lunghi; I., Loiacono; G., Palumbo; M., Bonifacio; D., Cilloni; A., Iurlo; A., Andriani1; G., Benevolo; C., Minoia; D., Turri; Em, Elli; Ap, Falcone; B., Anaclerico; A., Traficante; N., Di Renzo; M., Tiribelli; E., Calistri; R., Zambello; C., Spinosa; A., Ricco; F., Palandri; L., Raucci; B., Martino; M., Annunziata; M., D’Alosio; Am, Liberati; Caocci, Giovanni; M., Maffioli; M., Breccia; N., Pugliese; S., Betti; G., Giglio; L., Reale | HAEMATOLOGICA | - |
| Beta-thalassemia: from genotype to phenotype | 1-gen-2011 | Danjou, Fabrice; Anni, Franco; Galanello, Renzo | HAEMATOLOGICA | - |
| Bone marrow transplantation from unrelated donors in class 3 adult thalassemic patients | 1-gen-2005 | LA NASA, Giorgio; Argiolu, F; Giardini, C; Locatelli, F; Caocci, Giovanni; Ledda, A; Piras, E; Vacca, A; Contu, L. | HAEMATOLOGICA | - |
| C-->T MUTATION AT -158 G GAMMA HPFH ASSOCIATED WITH 4 BP DELETION (-225-222) IN THE PROMOTER REGION OF THE A GAMMA GENE IN HOMOZYGOUS BETA0 39 NONSENSE THALASSEMIA | 1-gen-1999 | ATAULFO GONZALEZ, F; Ropero, P; Sanchez, J; Rosatelli, MARIA CRISTINA; Galanello, R; Villegas, A. | HAEMATOLOGICA | - |
| Un caso di deficit congenito di triosofosfato-isomerasi (TPI) : studio ematologico, biochimico, immunologico e genetico | 1-gen-1985 | Contu, L; LA NASA, Giorgio; Frigerio, R; Olla, N; Sole, G; Carcassi, Carlo; Pitzus, F. | HAEMATOLOGICA | - |
| Clinical management of acute and chronic pain in patients with sickle cell disease | 1-gen-2019 | Finco, G.; Sardo, S. | HAEMATOLOGICA | - |
| Communication bias during the decision making process for unrelated bone marrow transplantation in adult thalassemia patients | 1-gen-2007 | Caocci, Giovanni; Pisu, S; Ledda, A; Arras, M; Vacca, A; Piras, E; Floris, R; Littera, R; Pizzati, A; Oppi, S; Orofino, Mg; Argiolu, E; LA NASA, Giorgio | HAEMATOLOGICA | - |
| 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 | - |
| CONDITIONING SYSTEM BASED ON THE USE OF TREOSULFAN FOR ALLOGENEIC TRANSPLANT OF HEMATOPOIETIC STEM CELLS IN PATIENTS WITH THALASSEMIA MAJOR | 1-gen-2008 | Bernardo, Me; Zecca, M; Piras, E; Vacca, A; Giorgiani, G; Cugno, C; Caocci, Giovanni; Comoli, P; Mastronuzzi, A; LA NASA, Giorgio; Locatelli, F. | HAEMATOLOGICA | - |
| The Coup-TFII orphan nuclear receptor is an activator of the γ-globin gene | 1-gen-2021 | Fugazza, Cristina; Barbarani, Gloria; Elangovan, Sudharshan; Marini, Maria Giuseppina; Giolitto, Serena; Font-Monclus, Isaura; Marongiu, Maria Franca; Manunza, Laura; Strouboulis, John; Cantù, Claudio; Gasparri, Fabio; Barabino, Silvia M L; Nakamura, Yukio; Ottolenghi, Sergio; Moi, Paolo; Ronchi, Antonella Ellena | HAEMATOLOGICA | - |
| Cross-cultural development of an eortc questionnaire for assessing quality of life in chronic myeloid leukemia patients: the eortc qlq-cml24. | 1-gen-2013 | F., Efficace; G., Rosti; M., Breccia; S., Saussele; G., Abel; Caocci, Giovanni; F., Guilhot; A., Naeem; F., Cottone; S., Oerlemans; F., Castagnetti; F., Bombaci; G., Sharf; L., Noens; S., Pallua; F., Mandelli; M., Baccarani | HAEMATOLOGICA | - |
| Decision making in high risk adult thalassemia patients undergoing unrelated bone marrow transplantation: Quality of life, motivation and communication factors, ethical issues | 1-gen-2005 | Caocci, Giovanni; Pisu, S; Argiolu, F; Giardini, C; Locatelli, F; Vacca, A; Orofino, Mg; Piras, E; Addari, Mc; Ledda, A; LA NASA, Giorgio | HAEMATOLOGICA | - |
| DEFERASIROX-DEFEROXAMINE COMBINATION THERAPY REDUCES CARDIAC IRON WITH RAPID LIVER IRON REMOVAL AFTER 24 MONTHS IN PATIENTS WITH SEVERE TRANSFUSIONAL IRON OVERLOAD (HYPERION) | 1-gen-2014 | Ayidinok, Y; Kattamis, A; Cappellini, Md; Beshlawy, Ae; Origa, Raffaella; Elalfy, M; Kilinc, Y; Perrotta, S; Karakas Z., ); Viprakasit, V; Musallam, K; Constantinovici, N; Shen, J; Porter, Jb | HAEMATOLOGICA | - |
| DIAGNOSI PRENATALE DI EMOGLOBINOPATIE EREDITARIE. (REVIEW) | 1-gen-1989 | Cao, A; Pirastu, M; Rosatelli, MARIA CRISTINA | HAEMATOLOGICA | - |
| Differences in the erythropoiesis-hepcidin-iron store axis between hemoglobin H disease and β-thalassemia intermedia | 1-gen-2015 | Origa, Raffaella; Cazzola, M; Mereu, E; Danjou, Fabrice; Barella, S; Giagu, N; Galanello, R; Swinkels, D. W. | HAEMATOLOGICA | - |
| Donor-recipient status for HLA class I ligands and not the KIR genotype, is predictive of unrelated hsct outcome in beta-thalassemia patients | 1-gen-2007 | LA NASA, Giorgio; Littera, R.; Ledda, A.; Piras, E.; Vacca, A.; Caocci, Giovanni; Pizzati, A.; Arras, M.; Floris, R.; Giardini, C.; Locatelli, F.; Carcassi, Carlo | HAEMATOLOGICA | - |
| Donor-recipient status for HLA class I ligands and not the KIR genotype, is predictive of unrelated hsct outcome in beta-thalassemia patients | 1-gen-2007 | LA NASA, Giorgio; Littera, R; Ledda, A; Piras, E; Vacca, A; Caocci, Giovanni; Pizzati, A; Arras, M; Floris, R; Giardini, C; Locatelli, F; Carcassi, Carlo | HAEMATOLOGICA | - |
| Le emocromatosi | 1-gen-1981 | Carcassi, U.; Mela, Quirico | HAEMATOLOGICA | - |
| Ethical concerns surrounding the conception of an HLA compatible child for medical purposes | 1-gen-2012 | Pisu, S; Demuru, F; Caocci, Giovanni; LA NASA, Giorgio | HAEMATOLOGICA | - |
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