ALPHA GLOBIN GENE ANALYSIS IN A SARDINIAN FAMILY WITH INTERACTING ALPHA AND BETA THALASSAEMA GENESMELIS MA; GALANELLO R; CAO A et al.1983; BRITISH JOURNAL OF HAEMATOLOGY; ISSN 0007-1048; GBR; DA. 1983; VOL. 53; NO 4; PP. 667-671; BIBL. 12 REF.Article

QUANTITATION OF HBA2 WITH DE-52 MICROCHROMATOGRAPHY IN WHOLE BLOOD AS SCREENING TEST FOR BETA -THALASSEMIA HETEROZYGOTES.GALANELLO R; MELIS MA; MURONI P et al.1977; ACTA HAEMATOL.; SUISSE; DA. 1977; VOL. 57; NO 1; PP. 32-36; BIBL. 8 REF.Article

Genotype-phenotype correlations in β-thalassemiasCAO, A; GALANELLO, R; ROSATELLI, M. C et al.Blood reviews. 1994, Vol 8, Num 1, pp 1-12, issn 0268-960XArticle

SERUM FERRITIN LEVELS IN HEMOGLOBIN H DISEASEGALANELLO R; NELIS MA; PAGLIETTI E et al.1983; ACTA HAEMATOLOGICA; ISSN 0001-5792; CHE; DA. 1983; VOL. 69; NO 1; PP. 56-58; BIBL. 7 REF.Article

INTERACTION OF ALPHA - AND DELTA BETA ^O-THALASSAEMIA: HAEMATOLOGICAL FEATURES AND GLOBIN CHAIN SYNTHESIS ANALYSISGALANELLO R; FU BETTA M; MELIS MA et al.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 1; PP. 40-42; BIBL. 18 REF.Article

INTERACTION BETWEEN THE GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY AND THALASSAEMIA GENES AT PHENOTYPE LEVELSANNA G; FRAU F; MELIS MA et al.1980; BRIT. J. HAEMATOL.; GBR; DA. 1980; VOL. 44; NO 4; PP. 555-561; BIBL. 16 REF.Article

HAEMATOLOGICAL CHARACTERISTICS OF THE BETA ⁰ THALASSAEMIA TRAIT IN SARDINIAN CHILDRENGALANELLO R; DE VIRGILIIS S; ADDIS M et al.1980; J. CLIN. PATHOL.; ISSN 0021-9746; GBR; DA. 1980; VOL. 33; NO 10; PP. 946-948; BIBL. 12 REF.Article

Thallassemias in sardinia : molecular pathology, phenotype-genotype correlation, and preventionCAO, A; ROSATELLI, C; PIRASTU, M et al.The American journal of pediatric hematology/oncology. 1991, Vol 13, Num 2, pp 179-188, issn 0192-8562Article

Mechanism of Hb F stimulation by S-stage compounds: in vitro studies with bone marrow cells exposed to 5-azacytidine, Ara-C, or hydroxyureaGALANELLO, R; STAMATOYANNOPOULOS, G; PAPAYANNOPOULOU, T et al.The Journal of clinical investigation. 1988, Vol 81, Num 4, pp 1209-1216, issn 0021-9738Article

Stimulation of F-cell production in patients with sicklecell anemia treated with cytarabine or hydroxyureaVEITH, R; GALANELLO, R; PAPAYANNOPOULOU, T et al.The New England journal of medicine. 1985, Vol 313, Num 25, pp 1571-1575, issn 0028-4793Article

α-Thalassemia carrier identification by DNA analysis in the screening for thalassemiaGALANELLO, R; SOLLAINO, C; PAGLIETTI, E et al.American journal of hematology. 1998, Vol 59, Num 4, pp 273-278, issn 0361-8609Article

Variability of the immunoglobulin heavy chain constant region locus : a population studyBRUSCO, A; CARIOTA, U; BOTTARO, A et al.Human genetics. 1995, Vol 95, Num 3, pp 319-326, issn 0340-6717Article

Serum erythropoietin and erythropoiesis in high- and low-fetal hemoglobin β-thalassemia intermedia patientsGALANELLO, R; BARELLA, S; TURCO, M. P et al.Blood. 1994, Vol 83, Num 2, pp 561-565, issn 0006-4971Article

Prenatal diagnosis of inherited hemoglobinopathiesCAO, A; ROSATELLI, C; GALANELLO, R et al.Indian journal of pediatrics. 1989, Vol 56, Num 6, pp 707-717, issn 0019-5456, 11 p.Article

A genetic combination of silent β-thalassaemia, high Hb A₂ β-thalassaemia, and single α globin gene deletion causing mild thalassaemia intermadiaGALANELLO, R; MACCIONI, L; ROSATELLI, M. C et al.Journal of medical genetics. 1984, Vol 21, Num 2, pp 153-156, issn 0022-2593Article

The role of haemoglobin A₂ testing in the diagnosis of thalassaemias and related haemoglobinopathiesMOSCA, A; PALEARI, R; IVALDI, G et al.Journal of clinical pathology. 2009, Vol 62, Num 1, pp 13-17, issn 0021-9746, 5 p.Article

Clinical and molecular analysis of haemoglobin H disease in Sardinia : haematological, obstetric and cardiac aspects in patients with different genotypesORIGA, R; SOLLAINO, M. C; GIAGU, N et al.British journal of haematology. 2007, Vol 136, Num 2, pp 326-332, issn 0007-1048, 7 p.Article

Posttranslational deamidation of proteins : The case of hemoglobin J Sardegna [α50(CD8)His→Asn→Asp]PALEARI, R; PAGLIETTI, E; MOSCA, A et al.Clinical chemistry (Baltimore, Md.). 1999, Vol 45, Num 1, pp 21-28, issn 0009-9147Article

A promoter mutation, C → T at position : 92, leading to silent β-thalassaemiaROSATELLI, M. C; FAA, V; MELONI, A et al.British journal of haematology. 1995, Vol 90, Num 2, pp 483-485, issn 0007-1048Article

Y418C : a novel mutation in exon 9 of the glucocerebrosidase gene of a patient with Gaucher disease creates a new Bgl I siteRENU TUTEJA; NARENDRA TUTEJA; LILLIU, F et al.Human genetics. 1994, Vol 94, Num 3, pp 314-315, issn 0340-6717Article

HbH disease in sardinia : molecular, hematological and clinica aspectsGALANELLO, R; ARU, B; TURCO, M. P et al.Acta haematologica. 1992, Vol 88, Num 1, pp 1-6, issn 0001-5792Article

Molecular pathology of haemoglobin H disease in SardiniansPAGLIETTI, E; GALANELLO, R; MOI, P et al.British journal of haematology. 1986, Vol 63, Num 3, pp 485-496, issn 0007-1048Article

Multiple mutations produce δβ⁰ thalassemia in sardiniaPIRASTU, M; YUET WAI KAN; GALANELLO, R et al.Science (Washington, D.C.). 1984, Vol 223, Num 4639, pp 929-930, issn 0036-8075Article

δ⁺-Thalassemia in SardiniaPIRASTU, M; GALANELLO, R; MELIS, M. A et al.Blood. 1983, Vol 62, Num 2, pp 341-345, issn 0006-4971Article

A randomized, placebo-controlled, double-blind trial of the effect of combined therapy with deferoxamine and deferiprone on myocardial iron in thalassemia major using cardiovascular magnetic resonanceTANNER, M. A; GALANELLO, R; PENNELL, D. J et al.Circulation (New York, N.Y.). 2007, Vol 115, Num 14, pp 1876-1884, issn 0009-7322, 9 p.Article