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TitoloData di pubblicazioneAutore(i)RivistaEditore
HEMOGLOBIN H DISEASE IN SARDINIA: PHENOTYPIC AND GENETIC OBSERVATIONS1978Galanello, R; Melis, Ma; Furbetta, M; Angius, A; Rosatelli, MARIA CRISTINA; Cao, A.HEMOGLOBIN
THALASSEMIA TYPES AND THEIR INCIDENCE IN SARDINIA1978Cao, A; Galanello, R; Furbetta, M; Muroni, Pp; Garbato, L; Rosatelli, MARIA CRISTINA; Scalas, Mt;... Addis, Maria; Ruggeri, R; Maccioni, L; Melis, MaJOURNAL OF MEDICAL GENETICS
Hematological characteristic of sardinian alpha-thalassemia carriers detected in a population study1980Melis, Ma; Rosatelli, MARIA CRISTINA; Falchi, ANGELA MARIA; Angius, A; Furbetta, M; Galanello, R;... Cao, A.ACTA HAEMATOLOGICA
PRENATAL DIAGNOSIS OF B-THALASSEMIA BY FETAL RED CELL ENRICHMENT WITH NH4CL-NH4HCO3 DIFFERENTIAL LYSIS OF MATERNAL CELLS1980Furbetta, M; Angius, A; Ximenes, A; Tuveri, T; Rosatelli, MARIA CRISTINA; Scalas, Mt; Fais, R; Ca...o, A; Angioni, G; Caminiti, F.BRITISH JOURNAL OF HAEMATOLOGY
ALPHA-THALASSEMIA IN SARDINIAN INFANTS1980Galanello, R; Diana, G; Furbetta, M; Angius, A; Melis, Ma; Rosatelli, MARIA CRISTINA; Cao, A.JOURNAL OF MEDICAL GENETICS
B-THALASSEMIA TYPES IN SOUTHERN SARDINIA1981CAO A; FURBETTA M; XIMENES A; ANGIUS A; ROSATELLI M.C.; TUVERI T; SCALAS MT; FALCHI AM; MACCIONI ...L; MELIS MA; GALANELLO RJOURNAL OF MEDICAL GENETICS
INTERACTION OF ALPHA AND *B°-THALASSEMIA: HAEMATOLOGICAL FEATURES AND GLOBIN CHAIN SYNTHESIS ANALYSIS1981GALANELLO R; FURBETTA M; MELIS MA; ROSATELLI M.C.; CAO AJOURNAL OF MEDICAL GENETICS
DIFFICULTIES IN ANTENATAL DIAGNOSIS OF INHERITED HEMOGLOBINOPATHIES: GAMMA-CHAIN VARIANTS. (SHORT COMMUNICATION)1981FURBETTA M; ANGIUS A; XIMENES A; ROSATELLI M.C.; SCALAS MT; TUVERI T; FALCHI AM; CAO ABRITISH JOURNAL OF HAEMATOLOGY
Beta-Thalassemia types in southern Sardinia1981Cao, A; Furbetta, M; Ximenes, A; Angius, A; Rosatelli, MARIA CRISTINA; Tuveri, T; Scalas, Mt; Fal...chi, ANGELA MARIA; Maccioni, L; Melis, Ma; Galanello, R.JOURNAL OF MEDICAL GENETICS
Difficulties in antenatal diagnosis of inherited haemoglobinopathies: gamma-chain variants1981Furbetta, M; Angius, A; Ximenes, A; Rosatelli, MARIA CRISTINA; Scalas, Mt; Tuveri, T; Falchi, ANG...ELA MARIA; Cao, A.BRITISH JOURNAL OF HAEMATOLOGY
Prevention of homozygous beta-thalassemia by carrier screening and prenatal diagnosis in Sardinia1981CAO A; FURBETTA M; GALANELLO R; MELIS MA; ANGIUS A; XIMENES A; ROSATELLI C; RUGGERI R; ADDIS M; T...UVERI T; FALCHI A; PAGLIETTI E; SCALAS MT
Diagnosis of beta o thalassemia trait at birth1981Furbetta, M; Angius, A; Tuveri, T; Rosatelli, MARIA CRISTINA; Scalas, Mt; Ximenes, A; Falchi, ANG...ELA MARIA; Cao, A.HEMOGLOBIN
ALPHA THALASSEMIA IN TWO MEDITERRANEAN POPULATIONS1982Pirastu, M; Lee, Ky; Dozy, Am; Kan, Yw; Stamatoyannopoulos, G; Hadjiminas, Mg; Zachariades, Z; An...gius, A; Furbetta, M; Rosatelli, MARIA CRISTINA; Cao, A.BLOOD
Haematological and obstetric aspects of antenatal diagnosis of beta-thalassemia: experience with 200 cases1982Cao, A; Furbetta, M; Angius, A; Ximenes, A; Rosatelli, MARIA CRISTINA; Tuveri, T; Scalas, Mt; Fal...chi, ANGELA MARIA; Angioni, G; Caminiti, F.JOURNAL OF MEDICAL GENETICS
Control of homozygous beta-thalassemia by carrier screening and antenatal diagnosis in Sardinia1982Cao, A; Furbetta, M; Galanello, R; Melis, Ma; Angius, A; Rosatelli, MARIA CRISTINA; Ruggeri, R; A...ddis, Maria; Tuveri, T; Falchi, ANGELA MARIA; Maccioni, L; Paglietti, MARIA ELISABETTA; Scalas, MtBIRTH DEFECTS ORIGINAL ARTICLE SERIES
Molecular mechanism accounting for milder types of thalassemia major1983Furbetta, M; Tuveri, T; Rosatelli, MARIA CRISTINA; Angius, A; Falchi, ANGELA MARIA; Cossu, P; Mel...oni, A; Giagu, N; Cao, A.JOURNAL OF PEDIATRICS
A genetic combination of silent beta-thalassaemia, high Hb A2 beta-thalassaemia, and single alpha globin gene deletion causing mild thalassaemia intermedia.1984R., Galanello; L., Maccioni; Rosatelli, MARIA CRISTINA; P., Ibba; Nurchi, ANNA MARIA; A., CaoJOURNAL OF MEDICAL GENETICS
DEVELOPMENTAL PATTERN OF B-CHAIN PRODUCTION AT MIDTRIMESTER PREGNANCY IN SARDINIAN B-THALASSEMIA HETEROZYGOTES1984Rosatelli, MARIA CRISTINA; Falchi, ANGELA MARIA; Scalas, Mt; Tuveri, T; Cao, A.HEMOGLOBIN
A GENETIC COMBINATION OF SILENT B-THALASSEMIA, HIGH HB A2 B-THALASSEMIA, AND SINGLE ALPHA-GLOBIN GENE DELETION CAUSING MILD THALASSEMIA INTERMEDIA1984Galanello, R; Maccioni, L; Rosatelli, MARIA CRISTINA; Ibba, P; Nurchi, ANNA MARIA; Cao, A.JOURNAL OF MEDICAL GENETICS
Developmental pattern of beta-chain production at midtrimester pregnancy in sardinian beta zero-thalassemia heterozygotes1984Rosatelli, MARIA CRISTINA; Falchi, ANGELA MARIA; SCALAS M., T; Tuveri, T; Cao, A.HEMOGLOBIN
   
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