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Predicting the probability of Gaucher disease in subjects with splenomegaly and thrombocytopenia

Scientific reports, 2021-01, Vol.11 (1), p.2594-2594, Article 2594

2021

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Role of T1 mapping as a complementary tool to T2 for non-invasive cardiac iron overload assessment

PloS one, 2018-02, Vol.13 (2), p.e0192890-e0192890

2018

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Migalastat Treatment in a Kidney-Transplanted Patient with Fabry Disease and N215S Mutation: The First Case Report

Pharmaceuticals (Basel, Switzerland), 2021-12, Vol.14 (12), p.1304

2021

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Management of chronic patients during the COVID-19 pandemic: the experience of a referral center for rare hematological disorders in the hardest-hit region in Italy

Annals of hematology, 2021-08, Vol.100 (8), p.2129-2131

2021

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Oocyte quality in women with thalassaemia major: insights from IVF cycles

European journal of obstetrics & gynecology and reproductive biology: X, 2019-07, Vol.3, p.100048, Article 100048

2019

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The Spectrum of Ocular Alterations in Patients with β-Thalassemia Syndromes Suggests a Pathology Similar to Pseudoxanthoma Elasticum

Ophthalmology (Rochester, Minn.), 2014-03, Vol.121 (3), p.709-718

2014

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An update on iron chelation therapy

Blood transfusion = Trasfusione del sangue, 2012-10, Vol.10 (4), p.411-422

2012

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An Intriguing Case of Anaemia and Splenomegaly

European journal of case reports in internal medicine, 2014-10, Vol.1 (1)

2014

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Efficacy and safety of ruxolitinib in regularly transfused patients with thalassemia: results from a phase 2a study

Blood, 2018-01, Vol.131 (2), p.263-265

2018

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Effects on hearing after long-term use of iron chelators in beta-thalassemia: Over twenty years of longitudinal follow-up

Auris, nasus, larynx, 2024-04, Vol.51 (2), p.271-275

2024

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Acute liver injury after SARS-CoV-2 vaccination and luspatercept administration in a patient with β-thalassemia

Annals of hematology, 2024-03, Vol.103 (3), p.1025-1026

2024

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Muscular de‐conditioning and reduced cardiac inotropism due to iron deposition reduce exercise tolerance in beta thalassemia major

American journal of hematology, 2021-10, Vol.96 (10), p.E370-E373

2021

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Gaucher disease: A diagnostic challenge for internists

European journal of internal medicine, 2014-02, Vol.25 (2), p.117-124

2014

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Ferric Carboxymaltose for Long-Term Correction of Iron Deficiency Anemia in the Emergency Department

Blood, 2022-11, Vol.140 (Supplement 1), p.10771-10772

2022

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Evaluation of in Vitro Macrophage Characterization in Gaucher Type 1 (GD1) Patients

Blood, 2019-11, Vol.134 (Supplement_1), p.3592-3592

2019

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High-Risk Population Screening for Gaucher Disease: Final Results and Key Learnings from an Italian Multicenter Observational Study

Blood, 2020-11, Vol.136 (Supplement 1), p.17-18

2020

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Reproductive health issues in female patients with beta-thalassaemia major: a narrative literature review

Journal of obstetrics and gynaecology, 2020-10, Vol.40 (7), p.902-911

2020

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Iron Chelation and Ferritin below 500 Mcg/L in Transfusion Dependent Thalassemia: Beyond the Limits of Clinical Trials

Blood, 2019-11, Vol.134 (Supplement_1), p.3542-3542

2019

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Splenomegaly: Dare to think rare

American journal of hematology, 2022-09, Vol.97 (9), p.1259-1265

2022

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A holistic approach to iron chelation therapy in transfusion‐dependent thalassemia patients with serum ferritin below 500 μg/L

American journal of hematology, 2020-09, Vol.95 (9), p.E230-E232

2020

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Liver steatosis is highly prevalent and is associated with metabolic risk factors and liver fibrosis in adult patients with type 1 Gaucher disease

Liver international, 2020-12, Vol.40 (12), p.3061-3070

2020

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Hemoglobinopathies and Cancer: Preliminary Results of an Italian Multicenter Experience

Blood, 2021-11, Vol.138 (Supplement 1), p.946-946

2021

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Reply to “Hepatocellular carcinoma in thalassemia and other hemoglobinopathies”

Cancer, 2023-05, Vol.129 (10), p.1616-1617

2023

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Prevalence and predictors of liver fibrosis evaluated by vibration controlled transient elastography in type 1 Gaucher disease

Molecular genetics and metabolism, 2018-09, Vol.125 (1-2), p.64-72

2018

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Predicting the probability of Gaucher disease in subjects with splenomegaly and thrombocytopenia

Role of T1 mapping as a complementary tool to T2 for non-invasive cardiac iron overload assessment

Migalastat Treatment in a Kidney-Transplanted Patient with Fabry Disease and N215S Mutation: The First Case Report

Management of chronic patients during the COVID-19 pandemic: the experience of a referral center for rare hematological disorders in the hardest-hit region in Italy

Oocyte quality in women with thalassaemia major: insights from IVF cycles

The Spectrum of Ocular Alterations in Patients with β-Thalassemia Syndromes Suggests a Pathology Similar to Pseudoxanthoma Elasticum

An update on iron chelation therapy

An Intriguing Case of Anaemia and Splenomegaly

Efficacy and safety of ruxolitinib in regularly transfused patients with thalassemia: results from a phase 2a study

Effects on hearing after long-term use of iron chelators in beta-thalassemia: Over twenty years of longitudinal follow-up

Acute liver injury after SARS-CoV-2 vaccination and luspatercept administration in a patient with β-thalassemia

Muscular de‐conditioning and reduced cardiac inotropism due to iron deposition reduce exercise tolerance in beta thalassemia major

Gaucher disease: A diagnostic challenge for internists

Ferric Carboxymaltose for Long-Term Correction of Iron Deficiency Anemia in the Emergency Department

Evaluation of in Vitro Macrophage Characterization in Gaucher Type 1 (GD1) Patients

High-Risk Population Screening for Gaucher Disease: Final Results and Key Learnings from an Italian Multicenter Observational Study

Reproductive health issues in female patients with beta-thalassaemia major: a narrative literature review

Iron Chelation and Ferritin below 500 Mcg/L in Transfusion Dependent Thalassemia: Beyond the Limits of Clinical Trials

Splenomegaly: Dare to think rare

Incidence of cancer and related deaths in hemoglobinopathies: A follow‐up of 4631 patients between 1970 and 2021

A holistic approach to iron chelation therapy in transfusion‐dependent thalassemia patients with serum ferritin below 500 μg/L

Liver steatosis is highly prevalent and is associated with metabolic risk factors and liver fibrosis in adult patients with type 1 Gaucher disease

Hemoglobinopathies and Cancer: Preliminary Results of an Italian Multicenter Experience

Reply to “Hepatocellular carcinoma in thalassemia and other hemoglobinopathies”

Prevalence and predictors of liver fibrosis evaluated by vibration controlled transient elastography in type 1 Gaucher disease

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