Clinical and molecular analysis of haemoglobin H disease in Sardinia: haematological, obstetric and cardiac aspects in patients with different genotypes
Origa, R., Sollaino, M. C., Giagu, N., Barella, S., Campus, S., Mandas, C., Bina, P., Perseu, L., Galanello, R.
Published in British journal of haematology (01.01.2007)
Published in British journal of haematology (01.01.2007)
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Red cell pyruvate kinase deficiency in Southern Sardinia
Perseu, L., Giagu, N., Satta, S., Sollaino, M.C., Congiu, R., Galanello, R.
Published in Blood cells, molecules, & diseases (15.12.2010)
Published in Blood cells, molecules, & diseases (15.12.2010)
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Relationship between neonatal screening results by HPLC and the number of α-thalassaemia gene mutations; consequences for the cut-off value
Bouva, M J, Sollaino, C, Perseu, L, Galanello, R, Giordano, P C, Harteveld, C L, Cnossen, M H, Schielen, P C J I, Elvers, L H, Peters, M
Published in Journal of medical screening (01.01.2011)
Published in Journal of medical screening (01.01.2011)
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Cholelithiasis and Gilbert's syndrome in homozygous β‐thalassaemia
Galanello, R., Piras, S., Barella, S., Leoni, G. B., Cipollina, M. D., Perseu, L., Cao, A.
Published in British journal of haematology (01.12.2001)
Published in British journal of haematology (01.12.2001)
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Amelioration of Sardinian 0 thalassemia by genetic modifiers
Galanello, R., Sanna, S., Perseu, L., Sollaino, M. C., Satta, S., Lai, M. E., Barella, S., Uda, M., Usala, G., Abecasis, G. R., Cao, A.
Published in Blood (29.10.2009)
Published in Blood (29.10.2009)
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Phenotype-Genotype Correlation in β-Thalassemia
Galanello, R., Perseu, L., Satta, S., Demartis, F.R., Campus, S.
Published in Thalassemia reports (30.12.2011)
Published in Thalassemia reports (30.12.2011)
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Hyperbilirubinaemia in heterozygous β‐thalassaemia is related to co‐inherited Gilbert's syndrome
Galanello, R., Perseu, L., Melis, M. A., Cipollina, L., Barella, S., Giagu, N., Turco, M. P., Maccioni, O., Cao, A.
Published in British journal of haematology (01.11.1997)
Published in British journal of haematology (01.11.1997)
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Hyperbilirubinemia, glucose-6-phosphate-dehydrogenase deficiency and Gilbert's syndrome
GALANELLO, R, CIPOLLINA, M. D, CARBONI, G, PERSEU, L, BARELLA, S, CORRIAS, A, CAO, A
Published in European journal of pediatrics (01.11.1999)
Published in European journal of pediatrics (01.11.1999)
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Genotype of subjects with borderline hemoglobin A2 levels: implication for beta-thalassemia carrier screening
Galanello, R, Barella, S, Ideo, A, Gasperini, D, Rosatelli, C, Paderi, L, Paglietti, E, Sollaino, C, Perseu, L, Loi, D
Published in American journal of hematology (01.06.1994)
Published in American journal of hematology (01.06.1994)
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Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin
SATTA, Stefania, PERSEU, Lucia, MOI, Paolo, ASUNIS, Isadora, CABRIOLU, Annalisa, MACCIONI, Liliana, ROSA DEMARTIS, Franca, MANUNZA, Laura, CAO, Antonio, GALANELLO, Renzo
Published in Haematologica (Roma) (01.05.2011)
Published in Haematologica (Roma) (01.05.2011)
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A genetic score for the prediction of beta-thalassemia severity
Danjou, Fabrice, Francavilla, Marcella, Anni, Franco, Satta, Stefania, Demartis, Franca-Rosa, Perseu, Lucia, Manca, Matteo, Sollaino, Maria Carla, Manunza, Laura, Mereu, Elisabetta, Marceddu, Giuseppe, Pissard, Serge, Joly, Philippe, Thuret, Isabelle, Origa, Raffaella, Borg, Joseph, Forni, Gian Luca, Piga, Antonio, Lai, Maria Eliana, Badens, Catherine, Moi, Paolo, Galanello, Renzo
Published in Haematologica (Roma) (01.04.2015)
Published in Haematologica (Roma) (01.04.2015)
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Heterozygous β‐thalassemia with thalassemia intermedia phenotype
Gasperini, D., Perseu, L., Melis, M.A., Maccioni, L., Sollaino, M.C., Paglietti, E., Cao, A., Galanello, R.
Published in American journal of hematology (01.01.1998)
Published in American journal of hematology (01.01.1998)
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Normal individuals with high Hb A2 levels
Gasperini, D, Cao, A, Paderi, L, Barella, S, Paglietti, E, Perseu, L, Loi, D, Galanello, R
Published in British journal of haematology (01.05.1993)
Published in British journal of haematology (01.05.1993)
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Hemoglobin Cagliari (β 60 [E4] VAL → GLU): A Novel Unstable Thalassemic Hemoglobinopathy
Podda, A., Galanello, R., Maccioni, L., Melis, M.A., Rosatelli, C., Perseu, L., Cao, A.
Published in Blood (15.01.1991)
Published in Blood (15.01.1991)
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Genetic modifiers of -thalassemia and clinical severity as assessed by age at first transfusion
Danjou, F., Anni, F., Perseu, L., Satta, S., Dessi, C., Lai, M. E., Fortina, P., Devoto, M., Galanello, R.
Published in Haematologica (Roma) (01.07.2012)
Published in Haematologica (Roma) (01.07.2012)
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A novel delta O-thalassemia mutation: TGG-->TAG (TRP-->STOP) at codon 37
Gasperini, D, Perseu, L, Cossu, P, Podda, R, Cao, A, Galanello, R
Published in Human mutation (1994)
Published in Human mutation (1994)
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Hb Puttelange [beta 140(H19)Ala-->Val] in an Italian man with polycythemia
Galanello, R, Paleari, R, Perseu, L, Barella, S, Maccioni, L, Cao, A, Mulas, G, Cocco, E, Mosca, A
Published in Hemoglobin (01.01.1997)
Published in Hemoglobin (01.01.1997)
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Evaluation of an automatic HPLC analyser for thalassemia and haemoglobin variants screening
Galanello, R, Barella, S, Gasperini, D, Perseu, L, Paglietti, E, Sollaino, C, Paderi, L, Pirroni, M G, Maccioni, L, Mosca, A
Published in Journal of analytical methods in chemistry (1995)
Published in Journal of analytical methods in chemistry (1995)
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