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Renzo Galanello

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Genetic Counseling

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Publications

TOP 3
Taher Ali; Cappellini Maria D; Vichinsky Elliott; Galanello Renzo; Piga Antonio; Lawniczek Tomasz; Clark Joan; Habr Dany; Porter John B
Efficacy and safety of deferasirox doses of >30 mg/kg per d in patients with transfusion-dependent anaemia and iron overload.
Sollaino Maria Carla; Paglietti Maria Elisabetta; Perseu Lucia; Giagu Nicolina; Loi Daniela; Galanello Renzo
Association of alpha globin gene quadruplication and heterozygous beta thalassemia in patients with thalassemia intermedia.
Galanello Renzo; Sanna Serena; Perseu Lucia; Sollaino Maria Carla; Satta Stefania; Lai Maria Eliana; Barella Susanna; Uda Manuela; Usala Gianluca; Abecasis Goncalo R; Cao Antonio
Amelioration of Sardinian beta0 thalassemia by genetic modifiers.

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All Publications

2009: Taher Ali; Cappellini Maria D; Vichinsky Elliott; Galanello Renzo; Piga Antonio; Lawniczek Tomasz; Clark Joan; Habr Dany; Porter John B
Efficacy and safety of deferasirox doses of >30 mg/kg per d in patients with transfusion-dependent anaemia and iron overload.
British journal of haematology 2009;147(5):752-9.
2009: Sollaino Maria Carla; Paglietti Maria Elisabetta; Perseu Lucia; Giagu Nicolina; Loi Daniela; Galanello Renzo
Association of alpha globin gene quadruplication and heterozygous beta thalassemia in patients with thalassemia intermedia.
Haematologica 2009;94(10):1445-8.
2009: Galanello Renzo; Sanna Serena; Perseu Lucia; Sollaino Maria Carla; Satta Stefania; Lai Maria Eliana; Barella Susanna; Uda Manuela; Usala Gianluca; Abecasis Goncalo R; Cao Antonio
Amelioration of Sardinian beta0 thalassemia by genetic modifiers.
Blood 2009;114(18):3935-7.
2009: Phylipsen Marion; Amato Antonio; Cappabianca Maria Pia; Traeger-Synodinos Jan; Kanavakis Emmanuel; Basak Nazli; Galanello Renzo; Tuveri Teresa; Ivaldi Giovanni; Harteveld Cornelis L; Giordano Piero C
Two new beta-thalassemia deletions compromising prenatal diagnosis in an Italian and a Turkish couple seeking prevention.
Haematologica 2009;94(9):1289-92.
2009: Macciò Antonio; Madeddu Clelia; Chessa Paola; Mantovani Giovanni; Galanello Renzo
Use of erythropoiesis stimulating agents for the treatment of anaemia and related fatigue in a pregnant woman with HbH disease.
British journal of haematology 2009;146(3):335-7.
2009: Sanna Serena; Busonero Fabio; Maschio Andrea; McArdle Patrick F; Usala Gianluca; Dei Mariano; Lai Sandra; Mulas Antonella; Piras Maria Grazia; Perseu Lucia; Masala Marco; Marongiu Mara; Crisponi Laura; Naitza Silvia; Galanello Renzo; Abecasis Gonçalo R; Shuldiner Alan R; Schlessinger David; Cao Antonio; Uda Manuela
Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia.
Human molecular genetics 2009;18(14):2711-8.
2009: Galanello R; Campus S
Deferiprone chelation therapy for thalassemia major.
Acta haematologica 2009;122(2-3):155-64.
2009: Lederer Carsten W; Basak A Nazli; Aydinok Yesim; Christou Soteroula; El-Beshlawy Amal; Eleftheriou Androulla; Fattoum Slaheddine; Felice Alex E; Fibach Eitan; Galanello Renzo; Gambari Roberto; Gavrila Lucian; Giordano Piero C; Grosveld Frank; Hassapopoulou Helen; Hladka Eva; Kanavakis Emmanuel; Locatelli Franco; Old John; Patrinos George P; Romeo Giovanni; Taher Ali; Traeger-Synodinos Joanne; Vassiliou Panayiotis; Villegas Ana; Voskaridou Ersi; Wajcman Henri; Zafeiropoulos Anastasios; Kleanthous Marina
An electronic infrastructure for research and treatment of the thalassemias and other hemoglobinopathies: the Euro-mediterranean ITHANET project.
Hemoglobin 2009;33(3):163-76.
2008: Melis Maria Antonietta; Cau Milena; Congiu Rita; Sole Gabriella; Barella Susanna; Cao Antonio; Westerman Mark; Cazzola Mario; Galanello Renzo
A mutation in the TMPRSS6 gene, encoding a transmembrane serine protease that suppresses hepcidin production, in familial iron deficiency anemia refractory to oral iron.
Haematologica 2008;93(10):1473-9.
2008: Mosca Andrea; Paleari Renata; Galanello Renzo; Sollaino Carla; Perseu Lucia; Demartis Franca Rosa; Passarello Cristina; Giambona Antonino; Maggio Aurelio;
New analytical tools and epidemiological data for the identification of HbA2 borderline subjects in the screening for beta-thalassemia.
Bioelectrochemistry (Amsterdam, Netherlands) 2008;73(2):137-40.
2008: Origa Raffaella; Barella Susanna; Argiolas Giovanni Maria; Bina Patrizio; Agus Annalisa; Galanello Renzo
No evidence of cardiac iron in 20 never- or minimally-transfused patients with thalassemia intermedia.
Haematologica 2008;93(7):1095-6.
2008: Wood John C; Origa Raffaella; Agus Annalisa; Matta Gildo; Coates Thomas D; Galanello Renzo
Onset of cardiac iron loading in pediatric patients with thalassemia major.
Haematologica 2008;93(6):917-20.
2008: Angelucci Emanuele; Barosi Giovanni; Camaschella Clara; Cappellini Maria Domenica; Cazzola Mario; Galanello Renzo; Marchetti Monia; Piga Antonio; Tura Sante
Italian Society of Hematology practice guidelines for the management of iron overload in thalassemia major and related disorders.
Haematologica 2008;93(5):741-52.
2008: Galanello Renzo; Piga Antonio; Cappellini Maria Domenica; Forni Gian Luca; Zappu Antonella; Origa Raffaella; Dutreix Catherine; Belleli Rossella; Ford John M; Rivière Gilles-Jacques; Balez Sébastien; Alberti Daniele; Séchaud Romain
Effect of food, type of food, and time of food intake on deferasirox bioavailability: recommendations for an optimal deferasirox administration regimen.
Journal of clinical pharmacology 2008;48(4):428-35.
2008: Uda Manuela; Galanello Renzo; Sanna Serena; Lettre Guillaume; Sankaran Vijay G; Chen Weimin; Usala Gianluca; Busonero Fabio; Maschio Andrea; Albai Giuseppe; Piras Maria Grazia; Sestu Natascia; Lai Sandra; Dei Mariano; Mulas Antonella; Crisponi Laura; Naitza Silvia; Asunis Isadora; Deiana Manila; Nagaraja Ramaiah; Perseu Lucia; Satta Stefania; Cipollina Maria Dolores; Sollaino Carla; Moi Paolo; Hirschhorn Joel N; Orkin Stuart H; Abecasis Gonçalo R; Schlessinger David; Cao Antonio
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.
Proceedings of the National Academy of Sciences of the United States of America 2008;105(5):1620-5.
2008: Porter John; Galanello Renzo; Saglio Giuseppe; Neufeld Ellis J; Vichinsky Elliott; Cappellini Maria Domenica; Olivieri Nancy; Piga Antonio; Cunningham Melody J; Soulières Denis; Gattermann Norbert; Tchernia Gilbert; Maertens Johan; Giardina Patricia; Kwiatkowski Janet; Quarta Giovanni; Jeng Michael; Forni Gian Luca; Stadler Michael; Cario Holger; Debusscher Louisette; Della Porta Matteo; Cazzola Mario; Greenberg Peter; Alimena Giuliana; Rabault Bertrand; Gathmann Insa; Ford John Malcolm; Alberti Daniele; Rose Christian
Relative response of patients with myelodysplastic syndromes and other transfusion-dependent anaemias to deferasirox (ICL670): a 1-yr prospective study.
European journal of haematology 2008;80(2):168-76.
2008: Cao A; Congiu R; Sollaino M C; Desogus M F; Demartis F R; Loi D; Cau M; Galanello R
Thalassaemia and glucose-6-phosphate dehydrogenase screening in 13- to 14-year-old students of the Sardinian population: preliminary findings.
Community genetics 2008;11(3):121-8.
2008: Tanner Mark A; Galanello Renzo; Dessi Carlo; Smith Gillian C; Westwood Mark A; Agus Annalisa; Pibiri Martina; Nair Sunil V; Walker J Malcolm; Pennell Dudley J
Combined chelation therapy in thalassemia major for the treatment of severe myocardial siderosis with left ventricular dysfunction.
Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance 2008;10(1):12.
2007: Paroni Rita; Ceriotti Ferruccio; Galanello Renzo; Battista Leoni Giovan; Panico Alessandra; Scurati Emanuele; Paleari Renata; Chemello Liliana; Quaino Vania; Scaldaferri Luca; Lapolla Annunziata; Mosca Andrea
Performance characteristics and clinical utility of an enzymatic method for the measurement of glycated albumin in plasma.
Clinical biochemistry 2007;40(18):1398-405.
2007: Mai Antonello; Jelicic Katija; Rotili Dante; Di Noia Antonella; Alfani Elena; Valente Sergio; Altucci Lucia; Nebbioso Angela; Massa Silvio; Galanello Renzo; Brosch Gerald; Migliaccio Anna Rita; Migliaccio Giovanni
Identification of two new synthetic histone deacetylase inhibitors that modulate globin gene expression in erythroid cells from healthy donors and patients with thalassemia.
Molecular pharmacology 2007;72(5):1111-23.
2007: Galanello Renzo
Deferiprone in the treatment of transfusion-dependent thalassemia: a review and perspective.
Therapeutics and clinical risk management 2007;3(5):795-805.
2007: Origa Raffaella; Galanello Renzo; Ganz Tomas; Giagu Nicolina; Maccioni Liliana; Faa Gavino; Nemeth Elizabeta
Liver iron concentrations and urinary hepcidin in beta-thalassemia.
Haematologica 2007;92(5):583-8.
2007: Tanner M A; Galanello R; Dessi C; Smith G C; Westwood M A; Agus A; Roughton M; Assomull R; Nair S V; Walker J M; Pennell D J
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 resonance.
Circulation 2007;115(14):1876-84.
2007: Porcu Maurizio; Landis Novella; Salis Stefano; Corda Marco; Orrù Pierpaolo; Serra Emanuela; Usai Barbara; Matta Gildo; Galanello Renzo
Effects of combined deferiprone and desferrioxamine iron chelating therapy in beta-thalassemia major end-stage heart failure: a case report.
European journal of heart failure : journal of the Working Group on Heart Failure of the European Society of Cardiology 2007;9(3):320-2.
2007: Sadelain Michel; Boulad Farid; Galanello Renzo; Giardina Patricia; Locatelli Franco; Maggio Aurelio; Rivella Stefano; Riviere Isabelle; Tisdale John
Therapeutic options for patients with severe beta-thalassemia: the need for globin gene therapy.
Human gene therapy 2007;18(1):1-9.
2007: Origa R; Sollaino M C; Giagu N; Barella S; Campus S; Mandas C; Bina P; Perseu L; Galanello R
Clinical and molecular analysis of haemoglobin H disease in Sardinia: haematological, obstetric and cardiac aspects in patients with different genotypes.
British journal of haematology 2007;136(2):326-32.
2006: Galanello Renzo; Piga Antonio; Forni Gian Luca; Bertrand Yves; Foschini Maria Loreta; Bordone Elena; Leoni Giovanbattista; Lavagetto Antonella; Zappu Antonietta; Longo Filomena; Maseruka Henry; Hewson Nicola; Sechaud Romain; Belleli Rossella; Alberti Daniele
Phase II clinical evaluation of deferasirox, a once-daily oral chelating agent, in pediatric patients with beta-thalassemia major.
Haematologica 2006;91(10):1343-51.
2006: Galanello Renzo; Kattamis Antonis; Piga Antonio; Fischer Roland; Leoni Giovanbattista; Ladis Vassilios; Voi Vincenzo; Lund Ulrich; Tricta Fernando
A prospective randomized controlled trial on the safety and efficacy of alternating deferoxamine and deferiprone in the treatment of iron overload in patients with thalassemia.
Haematologica 2006;91(9):1241-3.
2006: Piga Antonio; Galanello Renzo; Forni Gian Luca; Cappellini Maria Domenica; Origa Raffaella; Zappu Antonietta; Donato Guido; Bordone Elena; Lavagetto Antonella; Zanaboni Laura; Sechaud Romain; Hewson Nicola; Ford John M; Opitz Herbert; Alberti Daniele
Randomized phase II trial of deferasirox (Exjade, ICL670), a once-daily, orally-administered iron chelator, in comparison to deferoxamine in thalassemia patients with transfusional iron overload.
Haematologica 2006;91(7):873-80.
2006: Pennell Dudley J; Berdoukas Vasili; Karagiorga Markissia; Ladis Vasili; Piga Antonio; Aessopos Athanassios; Gotsis Efstathios D; Tanner Mark A; Smith Gill C; Westwood Mark A; Wonke Beatrix; Galanello Renzo
Randomized controlled trial of deferiprone or deferoxamine in beta-thalassemia major patients with asymptomatic myocardial siderosis.
Blood 2006;107(9):3738-44.
2006: Cappellini Maria Domenica; Cohen Alan; Piga Antonio; Bejaoui Mohamed; Perrotta Silverio; Agaoglu Leyla; Aydinok Yesim; Kattamis Antonis; Kilinc Yurdanur; Porter John; Capra Marcello; Galanello Renzo; Fattoum Slaheddine; Drelichman Guillermo; Magnano Carmelo; Verissimo Monica; Athanassiou-Metaxa Miranda; Giardina Patricia; Kourakli-Symeonidis Alexandra; Janka-Schaub Gritta; Coates Thomas; Vermylen Christiane; Olivieri Nancy; Thuret Isabelle; Opitz Herbert; Ressayre-Djaffer Catherine; Marks Peter; Alberti Daniele
A phase 3 study of deferasirox (ICL670), a once-daily oral iron chelator, in patients with beta-thalassemia.
Blood 2006;107(9):3455-62.
2006: Borgna-Pignatti Caterina; Ventola Mariela; Friedman David; Cohen Alan R; Origa Raffaella; Galanello Renzo; Lindeman Robert; Francis Sally; Reverberi Roberto; Volpato Stefano
Seasonal variation of pretransfusion hemoglobin levels in patients with thalassemia major.
Blood 2006;107(1):355-7.
2006: Tanner M A; Galanello R; Dessi C; Westwood M A; Smith G C; Nair S V; Anderson L J; Walker J M; Pennell D J
Myocardial iron loading in patients with thalassemia major on deferoxamine chelation.
Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance 2006;8(3):543-7.
2005: Origa Raffaella; Bina Patrizio; Agus Annalisa; Crobu Gabriella; Defraia Elisabetta; Dessì Carlo; Leoni GiovanBattista; Muroni Pier Paolo; Galanello Renzo
Combined therapy with deferiprone and desferrioxamine in thalassemia major.
Haematologica 2005;90(10):1309-14.
2005: Galanello R; Perseu L; Anni F
Molecular basis of congenital and acquired deafness.
La Pediatria medica e chirurgica : Medical and surgical pediatrics 2005;27(5):53-5.
2005: Derchi Giorgio; Forni Gian Luca; Formisano Francesco; Cappellini Maria Domenica; Galanello Renzo; D'Ascola Giandomenico; Bina Patrizio; Magnano Carmelo; Lamagna Martina
Efficacy and safety of sildenafil in the treatment of severe pulmonary hypertension in patients with hemoglobinopathies.
Haematologica 2005;90(4):452-8.
2005: Paleari Renata; Cannata Monica; Leto Filippo; Maggio Aurelio; Demartis Franca R; Desogus Maria F; Galanello Renzo; Mosca Andrea
Analytical evaluation of the Tosoh HLC-723 G7 automated HPLC analyzer for hemoglobin A2 and F determination.
Clinical biochemistry 2005;38(2):159-65.
2005: Origa R; Fiumana E; Gamberini M R; Armari S; Mottes M; Sangalli A; Paglietti E; Galanello R; Borgna-Pignatti C
Osteoporosis in beta-thalassemia: Clinical and genetic aspects.
Annals of the New York Academy of Sciences 2005;1054():451-6.
2005: Galanello Renzo
Evaluation of ICL670, a once-daily oral iron chelator in a phase III clinical trial of beta-thalassemia patients with transfusional iron overload.
Annals of the New York Academy of Sciences 2005;1054():183-5.
2004: Galanello Renzo; Perseu Lucia; Perra Chiara; Maccioni Liliana; Barella Susanna; Longinotti Maurizio; Cao Antonio; Cazzola Mario
Somatic deletion of the normal beta-globin gene leading to thalassaemia intermedia in heterozygous beta-thalassaemic patients.
British journal of haematology 2004;127(5):604-6.
2004: Galanello Renzo; Perseu Lucia; Barella Susanna; Satta Stefania; Fais Antonella; Era Benedetta; Corda Marcella
Hb Belfast [beta15(A12)Trp-->Arg]: definition of the clinical and hematological phenotype.
Hemoglobin 2004;28(3):217-22.
2004: Hershko Chaim; Cappellini Maria D; Galanello Renzo; Piga Antonio; Tognoni Gianni; Masera Giuseppe
Purging iron from the heart.
British journal of haematology 2004;125(5):545-51.
2004: Paleari Renata; Ceriotti Ferruccio; Azzario Franco; Maccioni Liliana; Galanello Renzo; Mosca Andrea
Experiences in the measurement of RBC-bound IgG as markers of cell age.
Bioelectrochemistry (Amsterdam, Netherlands) 2004;62(2):175-9.
2004: Cohen Alan R; Galanello Renzo; Pennell Dudley J; Cunningham Melody J; Vichinsky Elliott
Thalassemia.
Hematology / the Education Program of the American Society of Hematology. American Society of Hematology. Education Program 2004;():14-34.
2003: Borgna-Pignatti Caterina; Rigon Francesca; Merlo Luciano; Chakrok Roksana; Micciolo Rocco; Perseu Luciana; Galanello Renzo
Thalassemia minor, the Gilbert mutation, and the risk of gallstones.
Haematologica 2003;88(10):1106-9.
2003: Marshall R; Tricta F; Galanello R; Leoni G; Kirkland D; Minto S; Spino M
Chromosomal aberration frequencies in patients with thalassaemia major undergoing therapy with deferiprone and deferoxamine in a comparative crossover study.
Mutagenesis 2003;18(5):457-63.
2003: Cohen Alan R; Galanello Renzo; Piga Antonio; De Sanctis Vincenzo; Tricta Fernando
Safety and effectiveness of long-term therapy with the oral iron chelator deferiprone.
Blood 2003;102(5):1583-7.
2003: Galanello Renzo; Piga Antonio; Alberti Daniele; Rouan Marie-Claude; Bigler Hilde; Séchaud Romain
Safety, tolerability, and pharmacokinetics of ICL670, a new orally active iron-chelating agent in patients with transfusion-dependent iron overload due to beta-thalassemia.
Journal of clinical pharmacology 2003;43(6):565-72.
2003: Galanello Renzo
A thalassemic child becomes adult.
Reviews in clinical and experimental hematology 2003;7(1):4-21.
2002: Gemignani Federica; Perra Chiara; Landi Stefano; Canzian Federico; Kurg Ants; Tõnisson Neeme; Galanello Renzo; Cao Antonio; Metspalu Andres; Romeo Giovanni
Reliable detection of beta-thalassemia and G6PD mutations by a DNA microarray.
Clinical chemistry 2002;48(11):2051-4.
2002: Cao Antonio; Galanello Renzo
Effect of consanguinity on screening for thalassemia.
The New England journal of medicine 2002;347(15):1200-2.
2002: Corda Marcella; Fais Antonella; Perseu Luciana; Cipollina Loretta; Barella Susanna; Galanello Renzo
Identification and functional characterization of a new hemoglobin variant in Sardinia: Hb Muravera [beta47 GAT->GTT, (CD6) Asp->Val].
Haematologica 2002;87(10):1111-2.
2002: Galanello Renzo; Barella Susanna; Satta Stefania; Maccioni Liliana; Pintor Carlo; Cao Antonio
Homozygosity for nondeletion delta-beta(0) thalassemia resulting in a silent clinical phenotype.
Blood 2002;100(5):1913-4.
2002: Wanless Ian R; Sweeney George; Dhillon Amar P; Guido Maria; Piga Antonio; Galanello Renzo; Gamberini M Rita; Schwartz Elias; Cohen Alan R
Lack of progressive hepatic fibrosis during long-term therapy with deferiprone in subjects with transfusion-dependent beta-thalassemia.
Blood 2002;100(5):1566-9.
2002: Ceci Adriana; Baiardi Paola; Felisi Mariagrazia; Cappellini Maria Domenica; Carnelli Vittorio; De Sanctis Vincenzo; Galanello Renzo; Maggio Aurelio; Masera Giuseppe; Piga Antonio; Schettini Francesco; Stefàno Ippazio; Tricta Fernando
The safety and effectiveness of deferiprone in a large-scale, 3-year study in Italian patients.
British journal of haematology 2002;118(1):330-6.
2002: Cao Antonio; Rosatelli Maria Cristina; Monni Giovanni; Galanello Renzo
Screening for thalassemia: a model of success.
Obstetrics and gynecology clinics of North America 2002;29(2):305-28, vi-vii.
2002: Migliaccio Giovanni; Di Pietro Roberta; di Giacomo Viviana; Di Baldassarre Angela; Migliaccio Anna Rita; Maccioni Liliana; Galanello Renzo; Papayannopoulou Thalia
In vitro mass production of human erythroid cells from the blood of normal donors and of thalassemic patients.
Blood cells, molecules & diseases 2002;28(2):169-80.
2002: Melis Maria Antonietta; Cau Milena; Deidda Federica; Barella Susanna; Cao Antonio; Galanello Renzo
H63D mutation in the HFE gene increases iron overload in beta-thalassemia carriers.
Haematologica 2002;87(3):242-5.
2002: Melis Maria Antonietta; Cau Milena; Congiu Rita; Ruvoletto Livia; Cao Antonio; Galanello Renzo
Frequency of hemochromatosis C282Y and H63D mutations in Sardinia.
Genetic testing 2002;6(4):327-9.
2001: Galanello R; Piras S; Barella S; Leoni G B; Cipollina M D; Perseu L; Cao A
Cholelithiasis and Gilbert's syndrome in homozygous beta-thalassaemia.
British journal of haematology 2001;115(4):926-8.
2000: Mancosu M G; Galanello R; Ambu R; De Virgiliis S; Giagu N; Cao A; Faa G
[Histological picture of liver disease in thalassemia intermedia]
Pathologica 2000;92(4):241-8.
2000: Cohen A R; Galanello R; Piga A; Dipalma A; Vullo C; Tricta F
Safety profile of the oral iron chelator deferiprone: a multicentre study.
British journal of haematology 2000;108(2):305-12.
1999: Galanello R; Cipollina M D; Carboni G; Perseu L; Barella S; Corrias A; Cao A
Hyperbilirubinemia, glucose-6-phosphate-dehydrogenase deficiency and Gilbert's syndrome.
European journal of pediatrics 1999;158(11):914-6.
1999: Cazzola M; Beguin Y; Bergamaschi G; Guarnone R; Cerani P; Barella S; Cao A; Galanello R
Soluble transferrin receptor as a potential determinant of iron loading in congenital anaemias due to ineffective erythropoiesis.
British journal of haematology 1999;106(3):752-5.
1999: Galanello R; Cipollina M D; Dessì C; Giagu N; Lai E; Cao A
Co-inherited Gilbert's syndrome: a factor determining hyperbilirubinemia in homozygous beta-thalassemia.
Haematologica 1999;84(2):103-5.
1999: Paleari R; Paglietti E; Mosca A; Mortarino M; Maccioni L; Satta S; Cao A; Galanello R
Posttranslational deamidation of proteins: the case of hemoglobin J Sardegna [alpha50(CD8)His-->Asn-->Asp].
Clinical chemistry 1999;45(1):21-8.
1998: Galanello R; Sollaino C; Paglietti E; Barella S; Perra C; Doneddu I; Pirroni M G; Maccioni L; Cao A
Alpha-thalassemia carrier identification by DNA analysis in the screening for thalassemia.
American journal of hematology 1998;59(4):273-8.
1998: Galanello R; Satta S; Pirroni M G; Travi M; Maccioni L
Globin chain synthesis analysis by high performance liquid chromatography in the screening of thalassemia syndromes.
Hemoglobin 1998;22(5-6):501-8.
1998: Mosca A; Paleari R; Sollaino C; Barella S; Galanello R
Limits to the use of the glucose 6-phosphate dehydrogenase/6-phosphogluconate dehydrogenase index for the detection of glucose 6-phosphate dehydrogenase deficiency.
Clinical chemistry and laboratory medicine : CCLM / FESCC 1998;36(9):737-8.
1998: Galanello R; Cao A
Relationship between genotype and phenotype. Thalassemia intermedia.
Annals of the New York Academy of Sciences 1998;850():325-33.
1998: Cohen A; Galanello R; Piga A; Vullo C; Tricta F
A multi-center safety trial of the oral iron chelator deferiprone.
Annals of the New York Academy of Sciences 1998;850():223-6.
1998: Cao A; Galanello R; Rosatelli M C
Prenatal diagnosis and screening of the haemoglobinopathies.
Baillière's clinical haematology 1998;11(1):215-38.
1998: Paglietti E; Barella S; Satta S; Perra C; Cao A; Galanello R
Hb Sassari [alpha 126(H9)Asp-->His] results from a GAC-->CAC mutation in the alpha 1-globin gene.
Hemoglobin 1998;22(1):65-7.
1998: Gasperini D; Perseu L; Melis M A; Maccioni L; Sollaino M C; Paglietti E; Cao A; Galanello R
Heterozygous beta-thalassemia with thalassemia intermedia phenotype.
American journal of hematology 1998;57(1):43-7.
1998: Melis M A; Cau M; Muntoni F; Mateddu A; Galanello R; Boccone L; Deidda F; Loi D; Cao A
Elevation of serum creatine kinase as the only manifestation of an intragenic deletion of the dystrophin gene in three unrelated families.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 1998;2(5):255-61.
1998: Galanello R; Loi D; Sollaino C; Dessì S; Cao A; Melis M A
A new glucose 6 phosphate dehydrogenase variant G6PD Sinnai (34 G-->T). Mutations in brief no. 156. Online.
Human mutation 1998;12(1):72-3.
1997: Galanello R; Perseu L; Melis M A; Cipollina L; Barella S; Giagu N; Turco M P; Maccioni O; Cao A
Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndrome.
British journal of haematology 1997;99(2):433-6.
1997: Cao A; Saba L; Galanello R; Rosatelli M C
Molecular diagnosis and carrier screening for beta thalassemia.
JAMA : the journal of the American Medical Association 1997;278(15):1273-7.
1997: Galanello R; Paleari R; Perseu L; Barella S; Maccioni L; Cao A; Mulas G; Cocco E; Mosca A
Hb Puttelange [beta 140(H19)Ala-->Val] in an Italian man with polycythemia.
Hemoglobin 1997;21(1):17-26.
1996: Mosca A; Paleari R; Rosti E; Luzzana M; Barella S; Sollaino C; Galanello R
Simultaneous automated determination of glucose 6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase activities in whole blood.
European journal of clinical chemistry and clinical biochemistry : journal of the Forum of European Clinical Chemistry Societies 1996;34(5):431-8.
1996: Cao A; Galanello R; Rosatelli M C; Argiolu F; De Virgiliis S
Clinical experience of management of thalassemia: the Sardinian experience.
Seminars in hematology 1996;33(1):66-75.
1996: Cao A; Rosatelli M C; Galanello R
Control of beta-thalassaemia by carrier screening, genetic counselling and prenatal diagnosis: the Sardinian experience.
Ciba Foundation symposium 1996;197():137-51; discussion 151-5.
1995: Rosatelli M C; Faà V; Meloni A; Fiorenza F; Galanello R; Gasperini D; Amendola G; Cao A
A promoter mutation, C-->T at position -92, leading to silent beta-thalassaemia.
British journal of haematology 1995;90(2):483-5.
1995: Cazzola M; De Stefano P; Ponchio L; Locatelli F; Beguin Y; Dessi C; Barella S; Cao A; Galanello R
Relationship between transfusion regimen and suppression of erythropoiesis in beta-thalassaemia major.
British journal of haematology 1995;89(3):473-8.
1995: Galanello R; Barella S; Gasperini D; Perseu L; Paglietti E; Sollaino C; Paderi L; Pirroni M G; Maccioni L; Mosca A
Evaluation of an automatic HPLC analyser for thalassemia and haemoglobin variants screening.
The Journal of automatic chemistry 1995;17(2):73-6.
1994: Pardini S; Addis M; Dore F; Bonfigli S; Nieddu R M; Galanello R; Longinotti M; Pau M G
Interferon-alpha 2a therapy in CML: disappearance of BCR/ABL transcript in a case of long-lasting continuous cytogenetic conversion.
Haematologica 1994;79(6):540-1.
1994: Galanello R; Gasperini D; Perseu L; Barella S; Ideo A; Cao A
Hb A2-Sant' Antioco [alpha 2 delta (2)93(F9)Cys-->Gly]: a new delta chain variant identified by sequencing of amplified DNA.
Hemoglobin 1994;18(6):437-9.
1994: Galanello R; Barella S; Ideo A; Gasperini D; Rosatelli C; Paderi L; Paglietti E; Sollaino C; Perseu L; Loi D
Genotype of subjects with borderline hemoglobin A2 levels: implication for beta-thalassemia carrier screening.
American journal of hematology 1994;46(2):79-81.
1994: Cao A; Galanello R; Rosatelli M C
Genotype-phenotype correlations in beta-thalassemias.
Blood reviews 1994;8(1):1-12.
1994: Galanello R; Barella S; Turco M P; Giagu N; Cao A; Dore F; Liberato N L; Guarnone R; Barosi G
Serum erythropoietin and erythropoiesis in high- and low-fetal hemoglobin beta-thalassemia intermedia patients.
Blood 1994;83(2):561-5.
1994: Gasperini D; Perseu L; Cossu P; Podda R; Cao A; Galanello R
A novel delta O-thalassemia mutation: TGG-->TAG (TRP-->STOP) at codon 37.
Human mutation 1994;3(1):71-2.
1993: Gasperini D; Cao A; Paderi L; Barella S; Paglietti E; Perseu L; Loi D; Galanello R
Normal individuals with high Hb A2 levels.
British journal of haematology 1993;84(1):166-8.
1993: Galanello R; Meloni A; Gasperini D; Saba L; Cao A; Rosatelli M C; Perseu L
The repeated sequence (AT)x(T)y upstream to the beta-globin gene is a simple polymorphism.
Blood 1993;81(7):1974-5.
1992: Gasperini D; Galanello R; Melis M A; Iannelli S; Giordano P; Bernini L F; Cao A
Hemoglobin Sabine [beta 91 (F7) Leu-->Pro]: occurrence in a Sardinian individual with hemolytic anemia and inclusion bodies.
Haematologica 1992;77(5):381-3.
1992: Rosatelli C; Leoni G B; Tuveri T; Scalas M T; Mosca A; Galanello R; Gasperini D; Cao A
Heterozygous beta-thalassemia: relationship between the hematological phenotype and the type of beta-thalassemia mutation.
American journal of hematology 1992;39(1):1-4.
1992: Loudianos G; Moi P; Lavinha J; Galanello R; Cao A; Pirastu M
Normal delta-globin gene sequences in Sardinian nondeletional delta beta-thalassemia.
Hemoglobin 1992;16(6):503-9.
1992: Galanello R; Aru B; Dessì C; Addis M; Paglietti E; Melis M A; Cocco S; Massa P; Giagu N; Barella S
HbH disease in Sardinia: molecular, hematological and clinical aspects.
Acta haematologica 1992;88(1):1-6.
1991: Galanello R; Monne M I; Paderi L; Paglietti E; Atzori G; Addis M; Limongelli O; Macciotta A; Cao A
Homozygous non-deletion alpha 2 globin gene mutation (initiation codon mutation): clinical and haematological phenotype.
British journal of haematology 1991;79(1):117-9.
1991: Podda A; Galanello R; Maccioni L; Melis M A; Rosatelli C; Perseu L; Cao A
Hemoglobin Cagliari (beta 60 [E4] Val----Glu): a novel unstable thalassemic hemoglobinopathy.
Blood 1991;77(2):371-5.
1991: Mosca A; Paleari R; Modenese A; Rossini S; Parma R; Rocco C; Russo V; Caramenti G; Paderi M L; Galanello R
Clinical utility of fractionating erythrocytes into "Percoll" density gradients.
Advances in experimental medicine and biology 1991;307():227-38.
1990: Galanello R; Sanna M A; Maccioni L; Gasperini D; Melis M A; Rosatelli C; Monni G; Cao A
Fetal hydrops in Sardinia: implications for genetic counselling.
Clinical genetics 1990;38(5):327-31.
1990: Mosca A; Paderi M; Sanna A; Paleari R; Cao A; Galanello R
Preliminary experience with the differential pH technique for glucose-6-phosphate dehydrogenase (G6PD) measurement in whole blood: application to an area with high prevalence of thalassaemia and G6PD deficiency.
Haematologica 1990;75(4):397-9.
1990: Galanello R; Turco M P; Barella S; Giagu N; Dessì C; Cornacchia G; Cao A
Iron stores and iron deficiency anemia in children heterozygous for beta-thalassemia.
Haematologica 1990;75(4):319-22.
1990: Galanello R; Melis M A; Podda A; Monne M; Perseu L; Loudianos G; Cao A; Pirastu M; Piga A
Deletion delta-thalassemia: the 7.2 kb deletion of Corfu delta beta-thalassemia in a non-beta-thalassemia chromosome.
Blood 1990;75(8):1747-9.
1990: Cao A; Rosatelli M C; Leoni G B; Tuveri T; Scalas M T; Monni G; Olla G; Galanello R
Antenatal diagnosis of beta-thalassemia in Sardinia.
Annals of the New York Academy of Sciences 1990;612():215-25.
1989: Cao A; Rosatelli C; Galanello R; Ristaldi M S
Prenatal diagnosis of inherited hemoglobinopathies.
Indian journal of pediatrics 1989;56(6):707-17.
1989: Cao A; Rosatelli C; Galanello R; Monni G; Olla G; Cossu P; Ristaldi M S
The prevention of thalassemia in Sardinia.
Clinical genetics 1989;36(5):277-85.
1989: Galanello R; Barella S; Maccioni L; Paglietti E; Melis M A; Rosatelli M C; Argiolu F; Cao A
Erythropoiesis following bone marrow transplantation from donors heterozygous for beta-thalassaemia.
British journal of haematology 1989;72(4):561-6.
1989: Galanello R; Dessi E; Melis M A; Addis M; Sanna M A; Rosatelli C; Argiolu F; Giagu N; Turco M P; Cacace E
Molecular analysis of beta zero-thalassemia intermedia in Sardinia.
Blood 1989;74(2):823-7.
1989: Galanello R; Podda A; Melis M A; Monne M; Cao A
Interaction between deletion delta-thalassemia and beta zero-thalassemia (codon 39 nonsense mutation) in a Sardinian family.
Progress in clinical and biological research 1989;316B():113-21.
1988: Galanello R; Paglietti E; Melis M A; Crobu M G; Addis M; Moi P; Cao A
Interaction of heterozygous beta zero-thalassemia with single functional alpha-globin gene.
American journal of hematology 1988;29(2):63-6.
1988: Moi P; Paglietti E; Sanna A; Brancati C; Tagarelli A; Galanello R; Cao A; Pirastu M
Delineation of the molecular basis of delta- and normal HbA2 beta-thalassemia.
Blood 1988;72(2):530-3.
1988: Galanello R; Paglietti M E; Addis M; Melis M A; Tuveri T; Furbetta M; Cao A
Pitfalls in genetic counselling for beta-thalassemia: an individual with 4 different thalassemia mutations.
Clinical genetics 1988;33(3):151-5.
1986: Maccioni L; Galanello R; Ruggeri R; Puddu R; Rosatelli D; Marras A; Chiappe S; Macciotta A; Cao A
Alpha-thalassemia in premature newborns.
Pediatric research 1986;20(11):1077-81.
1986: Paglietti E; Galanello R; Moi P; Pirastu M; Cao A
Molecular pathology of haemoglobin H disease in Sardinians.
British journal of haematology 1986;63(3):485-96.
1985: Paglietti E; Galanello R; Addis M; Cao A
Genetic counseling and genetic heterogeneity in the thalassemias.
Clinical genetics 1985;28(1):1-7.
1985: Galanello R; Paglietti E; Giagu N; Melis M A; Scalas M T; Cao A
Hematological phenotype of carriers of deletion alpha-thalassemia according to the alpha-globin genotype.
Haematologica 1985;70(3):191-8.
1984: Galanello R; Maccioni L; Ruggeri R; Perseu L; Cao A
Alpha thalassaemia in Sardinian newborns.
British journal of haematology 1984;58(2):361-8.
1984: Cao A; Pintus L; Lecca U; Olla G; Cossu P; Rosatelli C; Galanello R
Control of homozygous beta-thalassemia by carrier screening and antenatal diagnosis in Sardinians.
Clinical genetics 1984;26(1):12-22.
1984: Galanello R; Maccioni L; Rosatelli M C; Ibba P; Nurchi A M; Cao A
A genetic combination of silent beta-thalassaemia, high Hb A2 beta-thalassaemia, and single alpha globin gene deletion causing mild thalassaemia intermedia.
Journal of medical genetics 1984;21(2):153-6.
1984: Galanello R; Melis M A; Maccioni L; Pirastu M; Cao A
Longitudinal study of a newborn with a combination of deletion and nondeletion alpha-thalassemia-2.
Pediatric research 1984;18(2):158-62.
1984: Maccioni L; Galanello R; Melis M A; Cao A
Hemoglobin constitution of double heterozygotes for alpha or beta-thalassemia and Hb J Sardegna.
Hemoglobin 1984;8(5):497-507.
1983: Galanello R; Pirastu M; Melis M A; Paglietti E; Moi P; Cao A
Phenotype-genotype correlation in haemoglobin H disease in childhood.
Journal of medical genetics 1983;20(6):425-9.
1983: Galanello R; Ruggeri R; Paglietti E; Addis M; Melis M A; Cao A
A family with segregating triplicated alpha globin loci and beta thalassemia.
Blood 1983;62(5):1035-40.
1983: Pirastu M; Galanello R; Melis M A; Brancati C; Tagarelli A; Cao A; Kan Y W
Delta +-thalassemia in Sardinia.
Blood 1983;62(2):341-5.
1983: Melis M A; Pirastu M; Galanello R; Furbetta M; Tuveri T; Cao A
Phenotypic effect of heterozygous alpha and beta 0-thalassemia interaction.
Blood 1983;62(1):226-9.
1983: Galanello R; Melis M A; Paglietti E; Cornacchia G; de Virgiliis S; Cao A
Serum ferritin levels in hemoglobin H disease.
Acta haematologica 1983;69(1):56-8.
1982: Cao A; Melis M A; Galanello R; Angius A; Furbetta M; Giordano P; Bernini L F
Delta beta (F)-thalassaemia in Sardinia.
Journal of medical genetics 1982;19(3):184-92.
1982: Cao A; Furbetta M; Galanello R; Melis M A; Angius A; Rosatelli C; Ruggeri R; Addis M; Tuveri T; Falchi A M; Maccioni L; Paglietti E; Scalas M T
Control of homozygous beta-thalassemia by carrier screening and antenatal diagnosis in Sardinia.
Birth defects original article series 1982;18(7):303-11.
1981: Cao A; Furbetta M; Galanello R; Melis M A; Angius A; Ximenes A; Rosatelli C; Ruggeri R; Addis M; Tuveri T; Falchi A M; Paglietti E; Scalas M T
Prevention of homozygous beta-thalassemia by carrier screening and prenatal diagnosis in Sardinia.
American journal of human genetics 1981;33(4):592-605.
1981: Galanello R; Melis M A; Ruggeri R; Cao A
Prospective study of red blood cell indices, hemoglobin A2, and hemoglobin F in infants heterozygous for Beta-thalassemia.
The Journal of pediatrics 1981;99(1):105-8.
1981: Cao A; Furbetta M; Ximenes A; Angius A; Rosatelli C; Tuveri T; Scalas M T; Falchi A M; Maccioni L; Melis M A; Galanello R
Beta-Thalassaemia types in southern Sardinia.
Journal of medical genetics 1981;18(3):196-9.
1981: Cao A; Galanello R; Melis M A; Ruggeri R; Addis M; Maccioni L; Paglietti E
[Our experience in screening and genetic counseling for beta-thalassemia]
Minerva medica 1981;72(10):623-8.
1981: Galanello R; Furbetta M; Melis M A; Rosatelli C; Cao A
Interaction of alpha- and delta beta o- thalassaemia: haematological features and globin chain synthesis analysis.
Journal of medical genetics 1981;18(1):40-2.
1981: Galanello R; Ruggeri R; Addis M; Paglietti E; Cao A
Hemoglobin A2 in iron deficient beta-thalassemia heterozygotes.
Hemoglobin 1981;5(6):613-8.
1981: Galanello R; Melis M A; Furbetta M; Angius A; Scalas M T; Paglietti E; Cao A
Globin chain synthesis analysis in obligate beta 0-thalassemia heterozygotes with isolated increase of hemoglobin A2 levels.
Nouvelle revue française d'hématologie 1981;23(4):193-5.
1981: Galanello R; Cossu P; Pirastu M; Cao A
Clinical presentation of thalassemia major due to homozygous beta (0)-thalassemia.
Nouvelle revue française d'hématologie 1981;23(2):101-6.
1981: De Virgiliis S; Cornacchia G; Sanna G; Argiolu F; Galanello R; Fiorelli G; Rais M; Cossu P; Bertolino F; Cao A
Chronic liver disease in transfusion-dependent thalassemia: liver iron quantitation and distribution.
Acta haematologica 1981;65(1):32-9.
1980: Galanello R; De Virgiliis S; Addis M; Paglietti E; Ruggeri R; Cao A
Haematological characteristics of the beta 0 thalassaemia trait in Sardinian children.
Journal of clinical pathology 1980;33(10):946-8.
1980: Galanello R; Diana G; Furbetta M; Angius A; Melis M A; Rosatelli C; Cao A
alpha-Thalassaemia in Sardinian infants.
Journal of medical genetics 1980;17(5):357-62.
1980: Melis M A; Rosatelli C; Falchi A M; Angius A; Furbetta M; Galanello R; Cao A
Hematological characteristics of sardinian alpha-thalassemia carriers detected in a population study.
Acta haematologica 1980;63(1):32-6.

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