Sfoglia per Rivista HEMOGLOBIN
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.
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
Hb Hinwil or *38 (C4) Thr*Asn: a new * chain variant detected in a Swiss family
1996-01-01 Frischknecht, H; Ventruto, Ml; Hess, D; Hunziker, P; Rosatelli, MARIA CRISTINA; Cao, A; Breitenstein, U; Fehr, J; Tuchschmid, P.
Hematological phenotype of the double heterozygous state for alpha and beta thalassemia
1984-01-01 Rosatelli, MARIA CRISTINA; Falchi, ANGELA MARIA; Scalas, Mt; Tuveri, T; Furbetta, M; Cao, A.
HEMOGLOBIN H DISEASE IN SARDINIA: PHENOTYPIC AND GENETIC OBSERVATIONS
1978-01-01 Galanello, R; Melis, Ma; Furbetta, M; Angius, A; Rosatelli, MARIA CRISTINA; Cao, A.
HOMOZYGOUS B° 39 MUTATION WITH THALASSEMIA INTERMEDIA IN NORTHERN SARDINIA: CLINICAL, HEMATOLOGICAL AND MOLECULAR ANALYSIS
1988-01-01 Oggiano, L; Dore, A; Pistidda, P; Guiso, L; Manca, L; Masala, B; Pirastu, M; Rosatelli, MARIA CRISTINA; Cao, A; Longinotti, M.
A new β chain hemoglobin variant with increased oxygen affinity: Hb Santa Giusta Sardegna [β93(F9)Cys→Trp; HBB c.282T>G]
2012-01-01 Fais, Antonella; Sollaino M., C; Barella, S; Perseu, L; Era, Benedetta; Corda, M.
NORMAL DELTA-GLOBIN GENE-SEQUENCES IN SARDINIAN NONDELETIONAL DELTA-BETA-THALASSEMIA
1992-01-01 Loudianos, G; Moi, Paolo; Lavinha, J; Galanello, R; Cao, A; Pirastu, M.
| Titolo | Data di pubblicazione | Autore(i) | Rivista | Editore |
|---|---|---|---|---|
| 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 | - |
| 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 | - |
| Hb Hinwil or *38 (C4) Thr*Asn: a new * chain variant detected in a Swiss family | 1-gen-1996 | Frischknecht, H; Ventruto, Ml; Hess, D; Hunziker, P; Rosatelli, MARIA CRISTINA; Cao, A; Breitenstein, U; Fehr, J; Tuchschmid, P. | HEMOGLOBIN | - |
| Hematological phenotype of the double heterozygous state for alpha and beta thalassemia | 1-gen-1984 | Rosatelli, MARIA CRISTINA; Falchi, ANGELA MARIA; Scalas, Mt; Tuveri, T; Furbetta, M; Cao, A. | HEMOGLOBIN | - |
| HEMOGLOBIN H DISEASE IN SARDINIA: PHENOTYPIC AND GENETIC OBSERVATIONS | 1-gen-1978 | Galanello, R; Melis, Ma; Furbetta, M; Angius, A; Rosatelli, MARIA CRISTINA; Cao, A. | HEMOGLOBIN | - |
| HOMOZYGOUS B° 39 MUTATION WITH THALASSEMIA INTERMEDIA IN NORTHERN SARDINIA: CLINICAL, HEMATOLOGICAL AND MOLECULAR ANALYSIS | 1-gen-1988 | Oggiano, L; Dore, A; Pistidda, P; Guiso, L; Manca, L; Masala, B; Pirastu, M; Rosatelli, MARIA CRISTINA; Cao, A; Longinotti, M. | HEMOGLOBIN | - |
| A new β chain hemoglobin variant with increased oxygen affinity: Hb Santa Giusta Sardegna [β93(F9)Cys→Trp; HBB c.282T>G] | 1-gen-2012 | Fais, Antonella; Sollaino M., C; Barella, S; Perseu, L; Era, Benedetta; Corda, M. | HEMOGLOBIN | - |
| NORMAL DELTA-GLOBIN GENE-SEQUENCES IN SARDINIAN NONDELETIONAL DELTA-BETA-THALASSEMIA | 1-gen-1992 | Loudianos, G; Moi, Paolo; Lavinha, J; Galanello, R; Cao, A; Pirastu, M. | HEMOGLOBIN | - |
Legenda icone
- file ad accesso aperto
- file disponibili sulla rete interna
- file disponibili agli utenti autorizzati
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile