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Glucose-6-phosphate dehydrogenase deficiency

The Lancet (British edition), 2008-01, Vol.371 (9606), p.64-74

2008

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Laboratory diagnosis of thalassemia

International journal of laboratory hematology, 2016-05, Vol.38 (S1), p.32-40

2016

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Iron overload and toxicity: the hidden risk of multiple blood transfusions

Vox sanguinis, 2009-10, Vol.97 (3), p.185-197

2009

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Cardiopulmonary testing in adult patients with β-thalassemia major in comparison to healthy subjects

Annals of hematology, 2022-11, Vol.101 (11), p.2445-2452

2022

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Iron deficiency anaemia revisited

Journal of internal medicine, 2020-02, Vol.287 (2), p.153-170

2020

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Survival and Complications in Thalassemia

Annals of the New York Academy of Sciences, 2005-11, Vol.1054 (1), p.40-47

2005

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Management of non-neuronopathic Gaucher disease with special reference to pregnancy, splenectomy, bisphosphonate therapy, use of biomarkers and bone disease monitoring

Journal of inherited metabolic disease, 2008-06, Vol.31 (3), p.319-336

2008

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Clostridium difficile infection epidemiology and management: Comparison of results of a prospective study with a retrospective one in a reference teaching and research hospital in Northern Italy

American journal of infection control, 2016-11, Vol.44 (11), p.1214-1218

2016

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Venous thromboembolism and hypercoagulability in splenectomized patients with thalassaemia intermedia

British journal of haematology, 2000-11, Vol.111 (2), p.467-473

2000

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X-chromosomal inactivation directly influences the phenotypic manifestation of X-linked protoporphyria

Clinical genetics, 2016-01, Vol.89 (1), p.20-26

2016

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Spine Bone Texture Assessed by Trabecular Bone Score (TBS) to Evaluate Bone Health in Thalassemia Major

Calcified tissue international, 2014-12, Vol.95 (6), p.540-546

2014

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Beta-Thalassaemia Intermedia : Evaluation of Endocrine and Bone Complications

BioMed research international, 2014-01, Vol.2014 (2014), p.1-5

2014

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Coagulation and Splenectomy: An Overview

Annals of the New York Academy of Sciences, 2005-01, Vol.1054 (1), p.317-324

2005

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Pregnancy in patients with thalassemia major: a cohort study and conclusions for an adequate care management approach

Annals of hematology, 2017-06, Vol.96 (6), p.1015-1021

2017

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Overcoming the challenge of patient compliance with iron chelation therapy

Seminars in hematology, 2005-04, Vol.42 (2), p.S19-S21

Cappellini, M.D.

2005

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Long-term experience with deferasirox (ICL670), a once-daily oral iron chelator, in the treatment of transfusional iron overload

Expert opinion on pharmacotherapy, 2008-09, Vol.9 (13), p.2391-2402

2008

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Ribavirin suppresses erythroid differentiation and proliferation in chronic hepatitis C patients

Journal of viral hepatitis, 2014-06, Vol.21 (6), p.416-423

2014

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Resveratrol accelerates erythroid maturation by activation of FoxO3 and ameliorates anemia in beta-thalassemic mice

Haematologica (Roma), 2014-02, Vol.99 (2), p.267-275

2014

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Splenectomy and thrombosis: the case of thalassemia intermedia

Journal of thrombosis and haemostasis, 2010-10, Vol.8 (10), p.2152-2158

2010

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High prevalence of the His63Asp HFE mutation in italian patients with porphyria cutanea tarda

Hepatology (Baltimore, Md.), 1998-01, Vol.27 (1), p.181-184

1998

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Oxidative status and malondialdehyde in β-thalassaemia patients

European journal of clinical investigation, 2002-03, Vol.32 (s1), p.55-60

2002

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Combination of deferasirox and deferoxamine in clinical practice: An alternative scheme of chelation in thalassemia major patients

Blood cells, molecules, & diseases, 2014-09, Vol.53 (3), p.164-167

2014

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Skeletal involvement in type 1 Gaucher disease: Not just bone mineral density

Blood cells, molecules, & diseases, 2018-02, Vol.68, p.148-152

2018

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Co-existence of two functional mutations on the same allele of the human ferrochelatase gene in erythropoietic protoporphyria

Clinical genetics, 2007-01, Vol.71 (1), p.84-88

2007

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Progression of liver fibrosis can be controlled by adequate chelation in transfusion-dependent thalassemia (TDT)

Annals of hematology, 2017-11, Vol.96 (11), p.1931-1936

2017

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Glucose-6-phosphate dehydrogenase deficiency

Laboratory diagnosis of thalassemia

Iron overload and toxicity: the hidden risk of multiple blood transfusions

Cardiopulmonary testing in adult patients with β-thalassemia major in comparison to healthy subjects

Iron deficiency anaemia revisited

Survival and Complications in Thalassemia

Management of non-neuronopathic Gaucher disease with special reference to pregnancy, splenectomy, bisphosphonate therapy, use of biomarkers and bone disease monitoring

Clostridium difficile infection epidemiology and management: Comparison of results of a prospective study with a retrospective one in a reference teaching and research hospital in Northern Italy

Venous thromboembolism and hypercoagulability in splenectomized patients with thalassaemia intermedia

X-chromosomal inactivation directly influences the phenotypic manifestation of X-linked protoporphyria

Spine Bone Texture Assessed by Trabecular Bone Score (TBS) to Evaluate Bone Health in Thalassemia Major

Beta-Thalassaemia Intermedia : Evaluation of Endocrine and Bone Complications

Coagulation and Splenectomy: An Overview

Pregnancy in patients with thalassemia major: a cohort study and conclusions for an adequate care management approach

Overcoming the challenge of patient compliance with iron chelation therapy

Long-term experience with deferasirox (ICL670), a once-daily oral iron chelator, in the treatment of transfusional iron overload

Ribavirin suppresses erythroid differentiation and proliferation in chronic hepatitis C patients

Resveratrol accelerates erythroid maturation by activation of FoxO3 and ameliorates anemia in beta-thalassemic mice

Splenectomy and thrombosis: the case of thalassemia intermedia

High prevalence of the His63Asp HFE mutation in italian patients with porphyria cutanea tarda

Oxidative status and malondialdehyde in β-thalassaemia patients

Combination of deferasirox and deferoxamine in clinical practice: An alternative scheme of chelation in thalassemia major patients

Skeletal involvement in type 1 Gaucher disease: Not just bone mineral density

Co-existence of two functional mutations on the same allele of the human ferrochelatase gene in erythropoietic protoporphyria

Progression of liver fibrosis can be controlled by adequate chelation in transfusion-dependent thalassemia (TDT)

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