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Maria Domenica Cappellini

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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Italy

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Physiology

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Blood Transfusion

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Publications

TOP 3
Taher Ali; Hershko Chaim; Cappellini Maria Domenica
Iron overload in thalassaemia intermedia: reassessment of iron chelation strategies.
Tripodi Armando; Cappellini Maria Domenica; Chantarangkul Veena; Padovan Lidia; Fasulo Maria Rosaria; Marcon Alessia; Mannucci Pier Mannuccio
Hypercoagulability in splenectomized thalassemic patients detected by whole-blood thromboelastometry, but not by thrombin generation in platelet-poor plasma.
Duca Lorena; Delbini Paola; Nava Isabella; Vaja Valentina; Fiorelli Gemino; Cappellini Maria Domenica
Mutation analysis of hepcidin and ferroportin genes in Italian prospective blood donors with iron overload.

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All Publications

2009: Taher Ali; Hershko Chaim; Cappellini Maria Domenica
Iron overload in thalassaemia intermedia: reassessment of iron chelation strategies.
British journal of haematology 2009;147(5):634-40.
2009: Tripodi Armando; Cappellini Maria Domenica; Chantarangkul Veena; Padovan Lidia; Fasulo Maria Rosaria; Marcon Alessia; Mannucci Pier Mannuccio
Hypercoagulability in splenectomized thalassemic patients detected by whole-blood thromboelastometry, but not by thrombin generation in platelet-poor plasma.
Haematologica 2009;94(11):1520-7.
2009: Duca Lorena; Delbini Paola; Nava Isabella; Vaja Valentina; Fiorelli Gemino; Cappellini Maria Domenica
Mutation analysis of hepcidin and ferroportin genes in Italian prospective blood donors with iron overload.
American journal of hematology 2009;84(9):592-3.
2009: Refaldi Chiara; Gensini Francesca; Cappellini Maria Domenica
Novel human pathological mutations. Gene symbol: HBA1. Disease: haemoglobin variant.
Human genetics 2009;126(2):343.
2009: Refaldi Chiara; Zanella Alberto; Cappellini Maria Domenica
Novel human pathological mutations. Gene symbol: HBB. Disease: haemoglobin variant.
Human genetics 2009;126(2):343.
2009: Refaldi Chiara; Cesaretti Claudia; Fasulo Maria Rosaria; Cappellini Maria Domenica
Novel human pathological mutations. Gene symbol: HBB. Disease: haemoglobin variant.
Human genetics 2009;126(2):343.
2009: Ausenda Sabrina; Di Pierro E; Brancaleoni V; Tavazzi D; Cappellini M D
Novel human pathological mutations. Gene symbol: CPOX. Disease: Coproporphyria.
Human genetics 2009;126(2):342.
2009: Refaldi Chiara; Fasulo Maria Rosaria; Cesaretti Claudia; Cappellini Maria Domenica
Novel human pathological mutations. Gene symbol: HBA2. Disease: Thalassemia alpha.
Human genetics 2009;126(2):342.
2009: Di Pierro Elena; Brancaleoni V; Stanzial F; Benedicenti F; Castellan C; Cappellini M D
Novel human pathological mutations. Gene symbol: HMBS. Disease: Porphyria, acute intermittent.
Human genetics 2009;126(2):339.
2009: Di Pierro Elena; Brancaleoni Valentina; Besana Valeria; Cappellini Maria Domenica
Multiplex ligation-dependent probe amplification: a novel approach for genetic diagnosis of Porphyria.
Journal of human genetics 2009;54(8):479-87.
2009: Ventura Paolo; Cappellini Maria Domenica; Rocchi Emilio
The acute porphyrias: a diagnostic and therapeutic challenge in internal and emergency medicine.
Internal and emergency medicine 2009;4(4):297-308.
2009: Baldini Marina; Colasanti Alessandro; Orsatti Alessandra; Airaghi Lorena; Mauri Massimo C; Cappellini Maria Domenica
Neuropsychological functions and metabolic aspects in subclinical hypothyroidism: the effects of l-thyroxine.
Progress in neuro-psychopharmacology & biological psychiatry 2009;33(5):854-9.
2009: Di Pierro Elena; Besana V; Brancaleoni V; Fasulo M R; Cesaretti C; Cappellini M D
Novel human pathological mutations. Gene symbol: HMBS. Disease: porphyria, acute intermittent.
Human genetics 2009;125(3):347.
2009: Besana Valeria; Di Pierro E; Brancaleoni V; Sabrina A; Fiocchi M; Cappellini M D
Novel human pathological mutations. Gene symbol: HMBS. Disease: porphyria, acute intermittent.
Human genetics 2009;125(3):344.
2009: Ausenda Sabrina; Moriondo V; Marchini S; Besana V; Di Pierro E; Brancaleoni V; Ventura P; Rocchi E; Cappellini M D
Novel human pathological mutations. Gene symbol: PPOX. Disease: porphyria, variegate.
Human genetics 2009;125(3):344.
2009: Pattoneri Paolo; Sozzi Fabiola; Pelà Giovanna; Montanari Enrico; Moruzzi Paolo; Borghetti Alberico; Cappellini Maria Domenica
Assessment of mitoxantrone-induced cardiotoxicity in patients with multiple sclerosis: a tissue Doppler echocardiographic analysis.
Echocardiography (Mount Kisco, N.Y.) 2009;26(4):397-402.
2009: Negrini Simone; Zoppoli Gabriele; Setti Maurizio; Cappellini Maria Domenica; Indiveri Francesco
Paralytic ileus and liver failure--an unusual presentation of advanced erythropoietic protoporphyria.
Digestive diseases and sciences 2009;54(2):411-5.
2009: Piga Antonio; Longo Filomena; Duca Lorena; Roggero Simona; Vinciguerra Tiziana; Calabrese Roberto; Hershko Chaim; Cappellini Maria Domenica
High nontransferrin bound iron levels and heart disease in thalassemia major.
American journal of hematology 2009;84(1):29-33.
2009: Taher Ali; Cappellini Maria Domenica
Update on the use of deferasirox in the management of iron overload.
Therapeutics and clinical risk management 2009;5():857-68.
2009: Di Pierro E; Ventura P; Brancaleoni V; Moriondo V; Marchini S; Tavazzi D; Nascimbeni F; Ferrari M C; Rocchi E; Cappellini M D
Clinical, biochemical and genetic characteristics of Variegate Porphyria in Italy.
Cellular and molecular biology (Noisy-le-Grand, France) 2009;55(2):79-88.
2009: Cappellini Maria Domenica; Pattoneri Paolo
Oral iron chelators.
Annual review of medicine 2009;60():25-38.
2009: Li Chumei; Di Pierro Elena; Brancaleoni Valentina; Cappellini Maria Domenica; Steensma David P
A novel large deletion and three polymorphisms in the FECH gene associated with erythropoietic protoporphyria.
Clinical chemistry and laboratory medicine : CCLM / FESCC 2009;47(1):44-6.
2008: Cappellini Maria Domenica
Long-term efficacy and safety of deferasirox.
Blood reviews 2008;22 Suppl 2():S35-41.
2008: Cappellini Maria Domenica
Management of iron overload. Introduction.
Blood reviews 2008;22 Suppl 2():S13.
2008: Messina Giuseppina; Colombo Elisa; Cassinerio Elena; Ferri Francesca; Curti Rita; Altamura Carlo; Cappellini Maria Domenica
Psychosocial aspects and psychiatric disorders in young adult with thalassemia major.
Internal and emergency medicine 2008;3(4):339-43.
2008: Meo A; Cassinerio E; Castelli R; Bignamini D; Perego L; Cappellini M D
Effect of hydroxyurea on extramedullary haematopoiesis in thalassaemia intermedia: case reports and literature review.
International journal of laboratory hematology 2008;30(5):425-31.
2008: Delbini Paola; Duca Lorena; Nava Isabella; Meo Anna; Cappellini Maria Domenica
Gene symbol: HAMP. Disease: Haemochromatosis, juvenile.
Human genetics 2008;124(3):313.
2008: Delbini Paola; Duca Lorena; Nava Isabella; Tavazzi Dario; Cappellini Maria Domenica
Gene symbol: G6PD. Disease: Glucose-6-phosphate dehydrogenase deficiency.
Human genetics 2008;124(3):312-3.
2008: Brancaleoni Valentina; Di Pierro E; Besana V; Ausenda S; Cappellini M D
Gene symbol: FECH. Disease: Porphyria, erythropoietic.
Human genetics 2008;124(3):296.
2008: Brancaleoni Valentina; Di Pierro E; Besana V; Ausenda S; Cappellini M D
Gene symbol: FECH. Disease: Porphyria, erythropoietic.
Human genetics 2008;124(3):296.
2008: Taher Ali; El Rassi Fuad; Isma'eel Hussain; Koussa Suzane; Inati Adlette; Cappellini Maria Domenica
Correlation of liver iron concentration determined by R2 magnetic resonance imaging with serum ferritin in patients with thalassemia intermedia.
Haematologica 2008;93(10):1584-6.
2008: Nassar Anwar H; Naja Mohammed; Cesaretti Claudia; Eprassi Bruno; Cappellini Maria Domenica; Taher Ali
Pregnancy outcome in patients with beta-thalassemia intermedia at two tertiary care centers, in Beirut and Milan.
Haematologica 2008;93(10):1586-7.
2008: Cappellini M D; Taher A
Long-term experience with deferasirox (ICL670), a once-daily oral iron chelator, in the treatment of transfusional iron overload.
Expert opinion on pharmacotherapy 2008;9(13):2391-402.
2008: Baldini Marina; Airaghi Lorena; Orsatti Alessandra; Tedeschi Alberto; Ceraldi Tiziana; Sina Clara; Cappellini Maria Domenica
Unusual association of a pituitary adenoma and a neurological emergency: case report and diagnostic steps.
Internal and emergency medicine 2008;3(3):297-300.
2008: Di Rocco Maja; Giona Fiorina; Carubbi Francesca; Linari Silvia; Minichilli Fabrizio; Brady Roscoe O; Mariani Giuliano; Cappellini Maria Domenica
A new severity score index for phenotypic classification and evaluation of responses to treatment in type I Gaucher disease.
Haematologica 2008;93(8):1211-8.
2008: Libani Ilaria V; Guy Ella C; Melchiori Luca; Schiro Raffaella; Ramos Pedro; Breda Laura; Scholzen Thomas; Chadburn Amy; Liu YiFang; Kernbach Margrit; Baron-Lühr Bettina; Porotto Matteo; de Sousa Maria; Rachmilewitz Eliezer A; Hood John D; Cappellini M Domenica; Giardina Patricia J; Grady Robert W; Gerdes Johannes; Rivella Stefano
Decreased differentiation of erythroid cells exacerbates ineffective erythropoiesis in beta-thalassemia.
Blood 2008;112(3):875-85.
2008: Scacchi Massimo; Danesi Leila; Cattaneo Agnese; Valassi Elena; Pecori Giraldi Francesca; Argento Crocetta; D'Angelo Emanuela; Mirra Nadia; Carnelli Vittorio; Zanaboni Laura; Tampieri Benedetta; Cappellini Maria Domenica; Cavagnini Francesco
Bone demineralization in adult thalassaemic patients: contribution of GH and IGF-I at different skeletal sites.
Clinical endocrinology 2008;69(2):202-7.
2008: El Rassi Fuad; Cappellini Maria Domenica; Inati Adlette; Taher Ali
Beta-thalassemia intermedia: an overview.
Pediatric annals 2008;37(5):322-8.
2008: Tavazzi Dario; Taher Ali; Cappellini Maria Domenica
Red blood cell enzyme disorders: an overview.
Pediatric annals 2008;37(5):303-10.
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: Taher Ali; Mehio Ghassan; Isma'eel Hussain; Cappellini Maria Domenica
Stroke in thalassemia: a dilemma.
American journal of hematology 2008;83(4):343.
2008: Ronzoni Luisa; Bonara Paola; Rusconi Daniela; Frugoni Cecilia; Libani Ilaria; Cappellini Maria Domenica
Erythroid differentiation and maturation from peripheral CD34+ cells in liquid culture: cellular and molecular characterization.
Blood cells, molecules & diseases 2008;40(2):148-55.
2008: Di Pierro Elena; Brancaleoni Valentina; Besana Valeria; Ausenda Sabrina; Drury Stella; Cappellini Maria Domenica
A 10376 bp deletion of FECH gene responsible for erythropoietic protoporphyria.
Blood cells, molecules & diseases 2008;40(2):233-6.
2008: Ausenda Sabrina; Di Pierro E; Besana V; Brancaleoni V; Cappellini M D
Gene symbol: PPOX. Disease: Porphyria, variegate.
Human genetics 2008;123(1):109.
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: Cappellini M D; Fiorelli G
Glucose-6-phosphate dehydrogenase deficiency.
Lancet 2008;371(9606):64-74.
2008: Porter John B; Taher Ali T; Cappellini Maria D; Vichinsky Elliott P
Ethical issues and risk/benefit assessment of iron chelation therapy: advances with deferiprone/deferoxamine combinations and concerns about the safety, efficacy and costs of deferasirox [Kontoghiorghes GJ, Hemoglobin 2008; 32(1-2):1-15.].
Hemoglobin 2008;32(6):601-7.
2008: Pattoneri Paolo; Sozzi Fabiola B; Catellani Elisabetta; Piazza Antonella; Iotti Roberto; Michelini Massimo; Goldoni Matteo; Borghetti Alberico; Cappellini Maria Domenica; Manicardi Valeria
Myocardial involvement during the early course of type 2 diabetes mellitus: usefulness of myocardial performance index.
Cardiovascular ultrasound 2008;6():27.
2007: Brancaleoni Valentina; Di Pierro E; Besana V; Ausenda S; Cappellini M D
Novel human pathological mutations. Gene symbol: UROD. Disease: porphyria, cutaneous.
Human genetics 2007;122(5):554-5.
2007: Brancaleoni Valentina; Di Pierro E; Besana V; Ausenda S; Cappellini M D
Novel human pathological mutations. Gene symbol: UROD. Disease: porphyria, cutaneous.
Human genetics 2007;122(5):554.
2007: Di Pierro E; Besana V; Brancaleoni V; Ausenda S; Lonati P; Cappellini M D
Novel human pathological mutations. Gene symbol: HMBS. Disease: porphyria, acute intermittent.
Human genetics 2007;122(3-4):417.
2007: Ausenda S; Di Pierro E; Brancaleoni V; Besana V; Cappellini M D
Novel human pathological mutations. Gene symbol: PPOX. Disease: porphyria, variegate.
Human genetics 2007;122(3-4):417.
2007: Brancaleoni Valentina; Dipierro E; Ausenda S; Besana V; Cappellini M D
Novel human pathological mutations. Gene symbol: UROD. Disease: porphyria, cutaneous.
Human genetics 2007;122(3-4):415.
2007: Scacchi Massimo; Danesi Leila; Cattaneo Agnese; Valassi Elena; Pecori Giraldi Francesca; Argento Crocetta; D'Angelo Emanuela; Mirra Nadia; Carnelli Vittorio; Zanaboni Laura; Cappellini Maria Domenica; Cavagnini Francesco
Growth hormone deficiency (GHD) in adult thalassaemic patients.
Clinical endocrinology 2007;67(5):790-5.
2007: De Franceschi Lucia; Ronzoni Luisa; Cappellini Maria Domenica; Cimmino Flora; Siciliano Angela; Alper Seth L; Servedio Veronica; Pozzobon Christian; Iolascon Achille
K-CL co-transport plays an important role in normal and beta thalassemic erythropoiesis.
Haematologica 2007;92(10):1319-26.
2007: Castelli R; Cassinerio E; Cappellini M D; Porro F; Graziadei G; Fabris F
Heparin induced thrombocytopenia: pathogenetic, clinical, diagnostic and therapeutic aspects.
Cardiovascular & hematological disorders drug targets 2007;7(3):153-62.
2007: Hughes Derralynn; Cappellini Maria Domenica; Berger Marc; Van Droogenbroeck Jan; de Fost Maaike; Janic Dragana; Marinakis Theodore; Rosenbaum Hanna; Villarubia Jesús; Zhukovskaya Elena; Hollak Carla
Recommendations for the management of the haematological and onco-haematological aspects of Gaucher disease.
British journal of haematology 2007;138(6):676-86.
2007: Bailey Lakiea; Kuroyanagi Yuichi; Franco-Penteado Carla F; Conran Nicola; Costa Fernando F; Ausenda Sabrina; Cappellini Maria D; Ikuta Tohru
Expression of the gamma-globin gene is sustained by the cAMP-dependent pathway in beta-thalassaemia.
British journal of haematology 2007;138(3):382-95.
2007: Cappellini Maria Domenica
Exjade(R) (deferasirox, ICL670) in the treatment of chronic iron overload associated with blood transfusion.
Therapeutics and clinical risk management 2007;3(2):291-9.
2007: Brancaleoni V; Di Pierro E; Besana V; Ausenda S; Drury S; Cappellini M D
Novel human pathological mutations. Gene symbol: FECH. Disease: porphyria, erythropoietic.
Human genetics 2007;121(5):646.
2007: Cappellini Maria Domenica; Bejaoui Mohamed; Agaoglu Leyla; Porter John; Coates Thomas; Jeng Michael; Lai Maria Eliana; Mangiagli Antonio; Strauss Gabriele; Girot Robert; Watman Nora; Ferster Alina; Loggetto Sandra; Abish Sharon; Cario Holger; Zoumbos Nicolaos; Vichinsky Elliott; Opitz Herbert; Ressayre-Djaffer Catherine; Abetz Linda; Rofail Diana; Baladi Jean-Francois
Prospective evaluation of patient-reported outcomes during treatment with deferasirox or deferoxamine for iron overload in patients with beta-thalassemia.
Clinical therapeutics 2007;29(5):909-17.
2007: Besana V; Di Pierro E; Brancaleoni V; Ausenda S; Cappellini M D
Gene symbol: HMBS.
Human genetics 2007;121(2):299.
2007: Refaldi C; Mocellin M C; Cappellini M D
Gene symbol: HBB.
Human genetics 2007;121(2):298.
2007: Brancaleoni Valentina; Di Pierro E; Ausenda S; Besana V; Cappellini M D
Gene symbol: UROD.
Human genetics 2007;121(2):296-7.
2007: Ausenda Sabrina; Di Pierro E; Besana V; Brancaleoni V; Cappellini M D
Gene symbol: CPOX.
Human genetics 2007;121(2):296.
2007: Refaldi Chiara; Cappellini Maria Domenica
Gene symbol: HBD.
Human genetics 2007;121(2):293.
2007: Stratta Piero; Barbè Maria C; Cappellini Maria D
A woman with black urine.
British journal of haematology 2007;137(1):1.
2007: Di Pierro E; Brancaleoni V; Moriondo V; Besana V; Cappellini M D
Co-existence of two functional mutations on the same allele of the human ferrochelatase gene in erythropoietic protoporphyria.
Clinical genetics 2007;71(1):84-8.
2007: Tringali Cristina; Anastasia Luigi; Papini Nadia; Bianchi Anna; Ronzoni Luisa; Cappellini Maria Domenica; Monti Eugenio; Tettamanti Guido; Venerando Bruno
Modification of sialidase levels and sialoglycoconjugate pattern during erythroid and erytroleukemic cell differentiation.
Glycoconjugate journal 2007;24(1):67-79.
2007: Fabio Giovanna; Minonzio Francesca; Delbini Paola; Bianchi Annamaria; Cappellini Maria Domenica
Reversal of cardiac complications by deferiprone and deferoxamine combination therapy in a patient affected by a severe type of juvenile hemochromatosis (JH).
Blood 2007;109(1):362-4.
2007: Cappellini Maria Domenica
Coagulation in the pathophysiology of hemolytic anemias.
Hematology / the Education Program of the American Society of Hematology. American Society of Hematology. Education Program 2007;():74-8.
2006: Taher Ali; Isma'eel Hussain; Mehio Ghassan; Bignamini Daniela; Kattamis Antonis; Rachmilewitz Eliezer A; Cappellini Maria Domenica
Prevalence of thromboembolic events among 8,860 patients with thalassaemia major and intermedia in the Mediterranean area and Iran.
Thrombosis and haemostasis 2006;96(4):488-91.
2006: Karimi Mehran; Yarmohammadi Hooman; Cappellini Maria Domenica
Analysis of intelligence quotient in patients with homozygous beta-thalassemia.
Saudi medical journal 2006;27(7):982-5.
2006: Di Pierro Elena; Besana Valeria; Moriondo Valeria; Brancaleoni Valentina; Tavazzi Dario; Casalgrandi Giovanna; Ventura Paolo; Rocchi Emilio; Cappellini Maria Domenica
A large deletion on chromosome 11 in acute intermittent porphyria.
Blood cells, molecules & diseases 2006;37(1):50-4.
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: Taher Ali; Isma'eel Hussain; Cappellini Maria D
Thalassemia intermedia: revisited.
Blood cells, molecules & diseases 2006;37(1):12-20.
2006: Kuroyanagi Yuichi; Kaneko Yuji; Muta Kenjiro; Park Buem-Seek; Moi Paolo; Ausenda Sabrina; Cappellini Maria D; Ikuta Tohru
cAMP differentially regulates gamma-globin gene expression in erythroleukemic cells and primary erythroblasts through c-Myb expression.
Biochemical and biophysical research communications 2006;344(3):1038-47.
2006: Castelli Roberto; Cassinerio Elena; Iurlo Alessandra; Zanella Alberto; Gianelli Umberto; Cappellini Maria Domenica
Unusual severe development of common B lymphoblastic leukemia in Gaucher disease type I.
American journal of hematology 2006;81(5):383-4.
2006: Borgna-Pignatti Caterina; Cappellini Maria Domenica; De Stefano Piero; Del Vecchio Giovanni Carlo; Forni Gian Luca; Gamberini Maria Rita; Ghilardi Roberta; Piga Antonio; Romeo Maria Antonietta; Zhao Huaqing; Cnaan Avital
Cardiac morbidity and mortality in deferoxamine- or deferiprone-treated patients with thalassemia major.
Blood 2006;107(9):3733-7.
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: Di Pierro E; Besana V; Ausenda S; Brancaleoni V; Cappellini M D
Gene symbol: HMBS. Disease: porphyria, acute intermittent.
Human genetics 2006;119(3):360.
2006: Di Pierro E; Besana V; Brancaleoni V; Moriondo V; Cappellini M D
Gene symbol: HMBS. Disease: porphyria, acute intermittent.
Human genetics 2006;119(3):359.
2006: Di Pierro E; Besana V; Moriondo V; Brancaleoni V; Cappellini M D
Gene symbol: HMBS. Disease: porphyria, acute intermittent.
Human genetics 2006;119(3):364.
2006: Di Pierro E; Brancaleoni V; Moriondo V; Besana V; Cappellini M D
Gene symbol: FECH. Disease: Porphyria, erythropoietic. Accession #Hg0501.
Human genetics 2006;118(6):776.
2006: Duca Lorena; Da Ponte Alessandro; Cozzi Mariarita; Carbone Annalisa; Pomati Mauro; Nava Isabella; Cappellini Maria Domenica; Fiorelli Gemino
Changes in erythropoiesis, iron metabolism and oxidative stress after half-marathon.
Internal and emergency medicine 2006;1(1):30-4.
2006: Piatti G; Allegra L; Fasano V; Gambardella C; Bisaccia M; Cappellini M D
Lung function in beta-thalassemia patients: a longitudinal study.
Acta haematologica 2006;116(1):25-9.
2005: Agostoni Piergiuseppe; Cerino Mario; Palermo Pietro; Magini Alessandra; Bianchi Michele; Bussotti Maurizio; Fiorelli Gemino; Cappellini Maria D
Exercise capacity in patients with beta-thalassaemia intermedia.
British journal of haematology 2005;131(2):278-81.
2005: Cappellini M D
Iron-chelating therapy with the new oral agent ICL670 (Exjade).
Best practice & research. Clinical haematology 2005;18(2):289-98.
2005: Di Pierro E; Besana B; Cappellini M D
Gene symbol: HMBS. Disease: Porphyria, acute intermittent.
Human genetics 2005;116(6):543.
2005: Di Pierro E; Brancaleoni V; Cappellini M D
Gene symbol: HMBS. Disease: Porphyria, acute intermittent.
Human genetics 2005;116(6):537.
2005: Di Pierro E; Moriondo V; Cappellini M D
Gene symbol: HMBS. Disease: Porphyria, acute intermittent.
Human genetics 2005;116(6):535.
2005: Di Pierro Elena; Cappellini Maria Domenica; Mazzucchelli Renata; Moriondo Valeria; Mologni Daniela; Zanone Poma Barbara; Riva Agostino
A point mutation affecting an SP1 binding site in the promoter of the ferrochelatase gene impairs gene transcription and causes erythropoietic protoporphyria.
Experimental hematology 2005;33(5):584-91.
2005: Cappellini M D
Overcoming the challenge of patient compliance with iron chelation therapy.
Seminars in hematology 2005;42(2 Suppl 1):S19-21.
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: Cappellini M D; Grespi E; Cassinerio E; Bignamini D; Fiorelli G
Coagulation and splenectomy: an overview.
Annals of the New York Academy of Sciences 2005;1054():317-24.
2005: Borgna-Pignatti C; Cappellini M D; De Stefano P; Del Vecchio G C; Forni G L; Gamberini M R; Ghilardi R; Origa R; Piga A; Romeo M A; Zhao H; Cnaan A
Survival and complications in thalassemia.
Annals of the New York Academy of Sciences 2005;1054():40-7.
2004: Castelli Roberto; Graziadei Giovanna; Karimi Mehran; Cappellini Maria Domenica
Intrathoracic masses due to extramedullary hematopoiesis.
The American journal of the medical sciences 2004;328(5):299-303.
2004: Borgna-Pignatti Caterina; Rugolotto Simone; De Stefano Piero; Zhao Huaqing; Cappellini Maria Domenica; Del Vecchio Giovanni Carlo; Romeo Maria Antonietta; Forni Gian Luca; Gamberini Maria Rita; Ghilardi Roberta; Piga Antonio; Cnaan Avital
Survival and complications in patients with thalassemia major treated with transfusion and deferoxamine.
Haematologica 2004;89(10):1187-93.
2004: Prati Daniele; Maggioni Marco; Milani Silvano; Cerino Mario; Cianciulli Paolo; Coggi Guido; Forni Gian Luca; Magnano Carmelo; Meo Anna; Gramignoli Roberto; Rebulla Paolo; Fiorelli Gemino; Cappellini Maria Domenica;
Clinical and histological characterization of liver disease in patients with transfusion-dependent beta-thalassemia. A multicenter study of 117 cases.
Haematologica 2004;89(10):1179-86.
2004: Patti E; Di Pierro E; Cappellini M D
Gene symbol: PPOX. Disease: variegate porphyria.
Human genetics 2004;115(2):172.
2004: Di Pierro E; Patti E; Cappellini M D
Gene symbol: HMBS. Disease: porphyria, acute intermittent.
Human genetics 2004;115(2):172.
2004: Patti E; Di Pierro E; Cappellini M D
Gne symbol: PPOX. Disease: variegate porphyria.
Human genetics 2004;115(2):170.
2004: Di Pierro E; Moriondo V; Cappellini M D
Gene Symbol: FECH. Disease: Porphyria, erythropoietic.
Human genetics 2004;114(6):609.
2004: Di Pierro E; Moriondo V; Cappellini M D
Gene Symbol: FECH. Disease: Porphyria, erythropoietic.
Human genetics 2004;114(6):608.
2004: Di Pierro E; Roselli E A; Cappellini M D
Gene symbol: HBMS. Disease: Porphyria, acute intermittent.
Human genetics 2004;114(6):607.
2004: Castelli R; Tempesta A; Bianchi A; Porro T; Ivaldi G; Cappellini M D
Unreliable estimation of HbA due to the presence of Camperdown haemoglobin [beta 104 (G6) Arg --> Ser].
Diabetic medicine : a journal of the British Diabetic Association 2004;21(4):377-9.
2004: Martinez di Montemuros F; Tavazzi D; Patti E; Cappellini M D
Human gene mutations. Gene symbol: UROD. Disease: Porphyria, cutanea tarda.
Human genetics 2004;114(2):221.
2004: Di Pierro E; Moriondo V; Cappellini M D
Human gene mutations. Gene symbol: FECH. Disease: Porphyria, erythropoietic.
Human genetics 2004;114(2):221.
2004: Borgna-Pignatti Caterina; Vergine Gianluca; Lombardo Turi; Cappellini Maria Domenica; Cianciulli Paolo; Maggio Aurelio; Renda Disma; Lai Maria Eliana; Mandas Antonella; Forni Gianluca; Piga Antonio; Bisconte Maria Grazia
Hepatocellular carcinoma in the thalassaemia syndromes.
British journal of haematology 2004;124(1):114-7.
2004: Rocchi E; Ventura P; Ronzoni A; Rosa M C; Gozzi C; Marri L; Casalgrandi G; Cappellini M D
Pro-oxidant and antioxidant factors in acute intermittent porphyria: family studies.
Journal of inherited metabolic disease 2004;27(2):251-66.
2003: Martinez di Montemuros F; Tavazzi D; Patti E; Cappellini M D
Gene symbol: UROD. Disease: Porphyria, cutanea tarda.
Human genetics 2003;113(4):368.
2003: Dongiovanni P; Valenti L; Fracanzani A L; Cappellini M D; Fargion S; Taioli E
TNFalpha promoter polymorphisms in Italian patients with porphyria cutanea tarda.
Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2003;35(8):596-7.
2003: Karimi Mehran; Martinez di Montemuros Franco; Danielli Maria Gabriella; Farjadian Shirin; Afrasiabi Abdolreza; Fiorelli Gemino; Cappellini Maria Domenica
Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Fars province of Iran.
Haematologica 2003;88(3):346-7.
2002: Martinez di Montemuros F; Di Pierro E; Patti E; Tavazzi D; Danielli M G; Biolcati G; Rocchi E; Cappellini M D
Molecular characterization of porphyrias in Italy: a diagnostic flow-chart.
Cellular and molecular biology (Noisy-le-Grand, France) 2002;48(8):867-76.
2002: Littera Roberto; La Nasa Giorgio; Derchi Giorgio; Cappellini Maria D; Chang Christy Y P; Contu Licinio
Long-term treatment with sildenafil in a thalassemic patient with pulmonary hypertension.
Blood 2002;100(4):1516-7.
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: Karimi Mehran; Yarmohammadi Hooman; Farjadian Shirin; Zeinali Sirus; Moghaddam Zahra; Cappellini Maria D; Giordano Piero C
Beta-thalassemia intermedia from southern Iran: IVS-II-1 (G-->A) is the prevalent thalassemia intermedia allele.
Hemoglobin 2002;26(2):147-54.
2002: Cighetti Giuliana; Duca L; Bortone L; Sala S; Nava I; Fiorelli G; Cappellini M D
Oxidative status and malondialdehyde in beta-thalassaemia patients.
European journal of clinical investigation 2002;32 Suppl 1():55-60.
2002: Fiorelli Gemino; De Feo T M; Duca L; Tavazzi D; Nava I; Fargion S; Cappellini M D
Red blood cell antioxidant and iron status in alcoholic and nonalcoholic cirrhosis.
European journal of clinical investigation 2002;32 Suppl 1():21-7.
2002: Tavazzi Dario; Martinez di Montemuros Franco; Fargion Silvia; Fracanzani Anna Ludovica; Fiorelli Gemino; Cappellini Maria Domenica
Levels of uroporphyrinogen decarboxylase (URO-D) in erythrocytes of Italian porphyria cutanea tarda patients.
Cellular and molecular biology (Noisy-le-Grand, France) 2002;48(1):27-32.
2002: Cappellini Maria Domenica; Martinez di Montemuros Franco; Di Pierro Elena; Fiorelli Gemino
Hematologically important mutations: acute intermittent porphyria.
Blood cells, molecules & diseases 2002;28(1):5-12.
2001: Martinez di Montemuros F; Di Pierro E; Biolcati G; Rocchi E; Bissolotti E; Tavazzi D; Fiorelli G; Cappellini M D
Acute intermittent porphyria: heterogeneity of mutations in the hydroxymethylbilane synthase gene in Italy.
Blood cells, molecules & diseases 2001;27(6):961-70.
2001: De Feo T M; Fargion S; Duca L; Cesana B M; Boncinelli L; Lozza P; Cappellini M D; Fiorelli G
Non-transferrin-bound iron in alcohol abusers.
Alcoholism, clinical and experimental research 2001;25(10):1494-9.
2001: Castellani M; Cappellini M D; Cappelletti M; Fedriga E; Reschini E; Cerino M; Gerundini P
Tc-99m sulphur colloid scintigraphy in the assessment of residual splenic tissue after splenectomy.
Clinical radiology 2001;56(7):596-8.
2001: Cappellini M D; Martinez di Montemuros F; Tavazzi D; Fargion S; Pizzuti A; Comino A; Cainelli T; Fiorelli G
Seven novel point mutations in the uroporphyrinogen decarboxylase (UROD) gene in patients with familial porphyria cutanea tarda (f-PCT).
Human mutation 2001;17(4):350.
2001: Ikuta T; Ausenda S; Cappellini M D
Mechanism for fetal globin gene expression: role of the soluble guanylate cyclase-cGMP-dependent protein kinase pathway.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(4):1847-52.
2001: Tavazzi D; Duca L; Graziadei G; Comino A; Fiorelli G; Cappellini M D
Membrane-bound iron contributes to oxidative damage of beta-thalassaemia intermedia erythrocytes.
British journal of haematology 2001;112(1):48-50.
2001: Sampietro M; Tavazzi D; Martinez di Montemuros F; Cerino M; Zatelli S; Lunghi G; Orlandi A; Fargion S; Fiorelli G; Cappellini M D
TT virus infection in adult beta-thalassemia major patients.
Haematologica 2001;86(1):39-43.
2000: Perrotta S; Cappellini M D; Bertoldo F; Servedio V; Iolascon G; D'Agruma L; Gasparini P; Siciliani M C; Iolascon A
Osteoporosis in beta-thalassaemia major patients: analysis of the genetic background.
British journal of haematology 2000;111(2):461-6.
2000: Fargion S; Valenti L; Fracanzani A L; Sampietro M; Cappellini M D; Scaccabarozzi A; Soligo D; Mariani C; Fiorelli G
Hereditary hemochromatosis in a patient with congenital dyserythropoietic anemia.
Blood 2000;96(10):3653-5.
2000: Ambrosetti U; Dondè E; Piatti G; Cappellini M D
Audiological evaluation in adult beta-thalassemia major patients under regular chelation treatment.
Pharmacological research : the official journal of the Italian Pharmacological Society 2000;42(5):485-7.
2000: Ciceri L; Amato M; Cappellini M D; Fiorelli G
A case of pulmonary thromboembolism in thalassemia intermedia: are these patients at risk for thrombotic events?
Annali italiani di medicina interna : organo ufficiale della Società italiana di medicina interna 2000;15(3):218-20.
2000: Martinez di Montemuros F; Di Pierro E; Fargion S; Biolcati G; Griso D; Macrì A; Fiorelli G; Cappellini M D
Molecular analysis of the hydroxymethylbilane synthase (HMBS) gene in Italian patients with acute intermittent porphyria: report of four novel mutations.
Human mutation 2000;15(5):480.
2000: Fiorelli G; Martinez di Montemuros F; Cappellini M D
Chronic non-spherocytic haemolytic disorders associated with glucose-6-phosphate dehydrogenase variants.
Baillière's best practice & research. Clinical haematology 2000;13(1):39-55.
2000: Cortelezzi A; Cattaneo C; Cristiani S; Duca L; Sarina B; Deliliers G L; Fiorelli G; Cappellini M D
Non-transferrin-bound iron in myelodysplastic syndromes: a marker of ineffective erythropoiesis?
The hematology journal : the official journal of the European Haematology Association / EHA 2000;1(3):153-8.
1999: Gillis S; Cappellini M D; Goldfarb A; Ciceri L; Fiorelli G; Rachmilewitz E A
Pulmonary thromboembolism in thalassemia intermedia patients.
Haematologica 1999;84(10):959-60.
1999: Piatti G; Allegra L; Ambrosetti U; Cappellini M D; Turati F; Fiorelli G
Beta-thalassemia and pulmonary function.
Haematologica 1999;84(9):804-8.
1999: Derchi G; Fonti A; Forni G L; Galliera E O; Cappellini M D; Turati F; Policlinico O M
Pulmonary hypertension in patients with thalassemia major.
American heart journal 1999;138(2 Pt 1):384.
1999: Cappellini M D; Martinez di Montemuros F; Sampietro M; Tavazzi D; Fiorelli G
The interaction between Gilbert's syndrome and G6PD deficiency influences bilirubin levels.
British journal of haematology 1999;104(4):928-9.
1999: Cappellini M D; Tavazzi D; Duca L; Graziadei G; Mannu F; Turrini F; Arese P; Fiorelli G
Metabolic indicators of oxidative stress correlate with haemichrome attachment to membrane, band 3 aggregation and erythrophagocytosis in beta-thalassaemia intermedia.
British journal of haematology 1999;104(3):504-12.
1999: De Feo T M; Fargion S; Duca L; Mattioli M; Cappellini M D; Sampietro M; Cesana B M; Fiorelli G
Carbohydrate-deficient transferrin, a sensitive marker of chronic alcohol abuse, is highly influenced by body iron.
Hepatology (Baltimore, Md.) 1999;29(3):658-63.
1998: Cappellini M D; Fargion S R; Sampietro M; Graziadei G; Fiorelli G
Nontransfusional iron overload in thalassemia intermedia: role of the hemochromatosis allele.
Blood 1998;92(11):4479-80.
1998: Tavazzi D; Comino A; Turrini F; Fiorelli G; Cappellini M D
Indices of membrane alterations in beta-thalassemic erythrocytes.
Hemoglobin 1998;22(5-6):483-92.
1998: Bulbarelli A; Valentini A; DeSilvestris M; Cappellini M D; Borgese N
An erythroid-specific transcript generates the soluble form of NADH-cytochrome b5 reductase in humans.
Blood 1998;92(1):310-9.
1998: Borgna-Pignatti C; Rugolotto S; De Stefano P; Piga A; Di Gregorio F; Gamberini M R; Sabato V; Melevendi C; Cappellini M D; Verlato G
Survival and disease complications in thalassemia major.
Annals of the New York Academy of Sciences 1998;850():227-31.
1998: Cappellini M D; Graziadei G; Ciceri L; Comino A; Bianchi P; Pomati M; Fiorelli G
Butyrate trials.
Annals of the New York Academy of Sciences 1998;850():110-9.
1998: De Franceschi L; Cappellini M D; Graziadei G; Manzato F; Olivieri O; Corrocher R; Fiorelli G; Beuzard Y; Brugnara C
The effect of dietary magnesium supplementation on the cellular abnormalities of erythrocytes in patients with beta thalassemia intermedia.
Haematologica 1998;83(2):118-25.
1998: Sampietro M; Piperno A; Lupica L; Arosio C; Vergani A; Corbetta N; Malosio I; Mattioli M; Fracanzani A L; Cappellini M D; Fiorelli G; Fargion S
High prevalence of the His63Asp HFE mutation in Italian patients with porphyria cutanea tarda.
Hepatology (Baltimore, Md.) 1998;27(1):181-4.
1998: Danesi L; Cherubini R; Ciceri L; Graziadei G; Cappellini M D; Cavagnini F; Ortolani S
Evaluation of spine and hip bone density by DXA and QCT in thalassemic patients.
Journal of pediatric endocrinology & metabolism : JPEM 1998;11 Suppl 3():961-2.
1997: Sampietro M; Lupica L; Perrero L; Comino A; Martinez di Montemuros F; Cappellini M D; Fiorelli G
The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous beta-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency.
British journal of haematology 1997;99(2):437-9.
1997: Martinez di Montemuros F; Dotti C; Tavazzi D; Fiorelli G; Cappellini M D
Molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) variants in Italy.
Haematologica 1997;82(4):440-5.
1997: Sampietro M; Corbetta N; Cerino M; Fabiani P; Ticozzi A; Orlandi A; Lunghi G; Fargion S; Fiorelli G; Cappellini M D
Prevalence and clinical significance of hepatitis G virus infection in adult beta-thalassaemia major patients.
British journal of haematology 1997;97(4):904-7.
1996: Camaschella C; Gonella S; Calabrese R; Vischia F; Roetto A; Graziadei G; Mazza U; Cappellini M D
Serum erythropoietin and circulating transferrin receptor in thalassemia intermedia patients with heterogeneous genotypes.
Haematologica 1996;81(5):397-403.
1996: Fargion S; Fracanzani A L; Romano R; Cappellini M D; Faré M; Mattioli M; Piperno A; Ronchi G; Fiorelli G
Genetic hemochromatosis in Italian patients with porphyria cutanea tarda: possible explanation for iron overload.
Journal of hepatology 1996;24(5):564-9.
1996: Cappellini M D; Martinez di Montemuros F; De Bellis G; Debernardi S; Dotti C; Fiorelli G
Multiple G6PD mutations are associated with a clinical and biochemical phenotype similar to that of G6PD Mediterranean.
Blood 1996;87(9):3953-8.
1996: Fargion S; Sergi C; Bissoli F; Fracanzani A L; Suigo E; Carazzone A; Roberto C; Cappellini M D; Fiorelli G
Lack of association between porphyria cutanea tarda and alpha 1-antitrypsin deficiency.
European journal of gastroenterology & hepatology 1996;8(4):387-91.
1995: Mannu F; Arese P; Cappellini M D; Fiorelli G; Cappadoro M; Giribaldi G; Turrini F
Role of hemichrome binding to erythrocyte membrane in the generation of band-3 alterations in beta-thalassemia intermedia erythrocytes.
Blood 1995;86(5):2014-20.
1995: Zanella A; Rossi F; Cesana C; Foresti A; Nador F; Binda A S; Lunghi G; Cappellini M D; Furione M; Sirchia G
Transfusion-transmitted human parvovirus B19 infection in a thalassemic patient.
Transfusion 1995;35(9):769-72.
1995: Cappellini M D; Martinez di Montemuros F; Dotti C; Tavazzi D; Fiorelli G
Molecular characterisation of the glucose-6-phosphate dehydrogenase (G6PD) Ferrara II variant.
Human genetics 1995;95(4):440-2.
1995: Camaschella C; Mazza U; Roetto A; Gottardi E; Parziale A; Travi M; Fattore S; Bacchiega D; Fiorelli G; Cappellini M D
Genetic interactions in thalassemia intermedia: analysis of beta-mutations, alpha-genotype, gamma-promoters, and beta-LCR hypersensitive sites 2 and 4 in Italian patients.
American journal of hematology 1995;48(2):82-7.
1995: Camaschella C; Cappellini M D
Thalassemia intermedia.
Haematologica 1995;80(1):58-68.
1994: Cappellini M D; Martinez di Montemuros F; Fiorelli G
Different origin of nt 1246 glucose-6-phosphate dehydrogenase mutation.
Blood 1994;84(10):3592.
1994: Martinez di Montemuros F; Cappellini M D; Dotti C; Tavazzi D; De Bellis G; Debernardi S; Fiorelli G
Molecular characterisation of an Italian G6PD variant responsible for chronic non-spherocytic haemolytic anaemia.
Clinical genetics 1994;46(5):357-9.
1994: Cappellini M D; Sampietro M; Toniolo D; Carandina G; Pittalis S; Martinez di Montemuros F; Tavazzi D; Fiorelli G
Biochemical and molecular characterization of a new sporadic glucose-6-phosphate dehydrogenase variant described in Italy: G6PD Modena.
British journal of haematology 1994;87(1):209-11.
1994: Cappellini M D; Sampietro M; Toniolo D; Carandina G; Martinez di Montemuros F; Tavazzi D; Fiorelli G
G6PD Ferrara I has the same two mutations as G6PD A(-) but a distinct biochemical phenotype.
Human genetics 1994;93(2):139-42.
1993: Cappellini M D; Tavazzi D; Martinez di Montemuros F; Sampietro M; Gaviraghi A; Carandini D; Fiorelli G
Alternative splicing of human G6PD messenger RNA in K562 cells but not in cultured erythroblasts.
European journal of clinical investigation 1993;23(3):188-91.
1992: Fargion S; Piperno A; Cappellini M D; Sampietro M; Fracanzani A L; Romano R; Caldarelli R; Marcelli R; Vecchi L; Fiorelli G
Hepatitis C virus and porphyria cutanea tarda: evidence of a strong association.
Hepatology (Baltimore, Md.) 1992;16(6):1322-6.
1992: Moss D; Fargion S; Fracanzani A L; Levi S; Cappellini M D; Arosio P; Powell L W; Halliday J W
Functional roles of the ferritin receptors of human liver, hepatoma, lymphoid and erythroid cells.
Journal of inorganic biochemistry 1992;47(3-4):219-27.
1992: Fargion S; Cappellini M D; Fracanzani A L; De Feo T M; Levi S; Arosio P; Fiorelli G
Binding and suppressive activity of human recombinant ferritins on erythroid cells.
American journal of hematology 1992;39(4):264-8.
1992: Brunati C; Cappellini M D; De Feo T; Stefanoni I; Civati G; Ballerini L; Fiorelli G; Minetti L
Circulating burst-forming-unit erythroid and the responsiveness to recombinant human erythropoietin in patients on regular hemodialytic treatment.
Nephron 1992;62(2):150-4.
1992: Brunati C; Cappellini M D; De Feo T; Guastoni C; Ballerini L; Busnach G; Civati G; Fiorelli G; Minetti L
Uremic inhibitors of erythropoiesis: a study during treatment with recombinant human erythropoietin.
American journal of nephrology 1992;12(1-2):9-13.
1991: Fargion S; Piperno A; Fracanzani A L; Cappellini M D; Romano R; Fiorelli G
Iron in the pathogenesis of hepatocellular carcinoma.
The Italian journal of gastroenterology 1991;23(9):584-8.
1991: De Feo T M; Cappellini M D; Fiorelli G
Effect of estrogens and progesterone on human peripheral erythroid burst-forming unit (BFU-E) growth.
American journal of hematology 1991;38(2):81-5.
1991: Cappellini M D; Villa S; Gaviraghi A; Martinez di Montemuros F; Tavazzi D; Panzeri D; Fiorelli G
Behaviour of glucose-6-phosphate dehydrogenase during erythroid maturation.
Advances in experimental medicine and biology 1991;307():37-43.
1991: Fargion S; Fracanzani A L; Cislaghi V; Levi S; Cappellini M D; Fiorelli G
Characteristics of the membrane receptor for human H-ferritin.
Current studies in hematology and blood transfusion 1991;(58):164-70.
1990: Fiorelli G; Meloni T; Palomba V; Manoussakis C; Villa S; Cappellini M D
Gene frequency of glucose-6-phosphate dehydrogenase (G6PD) polymorphic variants in Sardinia.
Gene geography : a computerized bulletin on human gene frequencies 1990;4(3):139-42.
1990: Fiorelli G; Fargion S; Piperno A; Battafarano N; Cappellini M D
Iron metabolism in thalassemia intermedia.
Haematologica 1990;75 Suppl 5():89-95.
1989: Fiorelli G; Manoussakis C; Sampietro M; Pittalis S; Guglielmino C R; Cappellini M D
Different polymorphic variants of glucose-6-phosphate dehydrogenase (G6PD) in Italy.
Annals of human genetics 1989;53(Pt 3):229-36.
1987: Sampietro M; Camerino G; Romano M; Cappellini M D; Fiorelli G; Brambati B; Guerneri S; Ferrari M; Travi M; Krachmalnicoff A
Combined use of DNA probes in first-trimester prenatal diagnosis of hemophilia A.
Thrombosis and haemostasis 1987;58(4):988-92.
1987: Fiorelli G; Sampietro M; Romano M; Albano M; Cappellini M D
Clinical features of thalassemia intermedia in Italy.
Birth defects original article series 1987;23(5A):287-95.
1987: Sampietro M; Cappellini M D; Fiorelli G; Wainscoat J S; Thein S L; Weatherall D J
Genotypes of thalassemia major and intermedia in Italy.
Birth defects original article series 1987;23(5A):117-23.
1986: Fargion S; Cappellini M D; Piperno A; Panajotopoulos N; Ronchi G; Fiorelli G
Association of hereditary spherocytosis and idiopathic hemochromatosis. A synergistic effect in determining iron overload.
American journal of clinical pathology 1986;86(5):645-9.

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