Sfoglia per Rivista
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
Beta Thalassemia mutations in Corsica
2000-01-01 L., Varesi; G., Vona; M., Memmi; Marongiu, MARIA FRANCA; AND M. S., Ristaldi
beta-thalassemia haplotypes in Romania in the context of genetic mixing in the Mediterranean area
2016-01-01 Cherry, L; Calo', CARLA MARIA; Talmaci, R; Perrin, P; Gavrila, L.
Delta globin gene structure and expression in K562 cell line
2003-01-01 Poddie, D; Marongiu, MARIA FRANCA; CIGLIUTI FERRARI, S. PORCU S. RISTALDI M. S.
DEVELOPMENTAL PATTERN OF B-CHAIN PRODUCTION AT MIDTRIMESTER PREGNANCY IN SARDINIAN B-THALASSEMIA HETEROZYGOTES
1984-01-01 Rosatelli, MARIA CRISTINA; Falchi, ANGELA MARIA; Scalas, Mt; Tuveri, T; Cao, A.
Developmental pattern of beta-chain production at midtrimester pregnancy in sardinian beta zero-thalassemia heterozygotes
1984-01-01 Rosatelli, MARIA CRISTINA; Falchi, ANGELA MARIA; SCALAS M., T; Tuveri, T; Cao, A.
Diagnosis of beta o thalassemia trait at birth
1981-01-01 Furbetta, M; Angius, A; Tuveri, T; Rosatelli, MARIA CRISTINA; Scalas, Mt; Ximenes, A; Falchi, ANGELA MARIA; Cao, A.
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.
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