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Oral chelators deferasirox and deferiprone for transfusional iron overload in thalassemia major: new data, new questions

Blood, 2006-05, Vol.107 (9), p.3436-3441

Neufeld, Ellis J.

2006

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Novel therapeutics and future directions for refractory immune thrombocytopenia

British journal of haematology, 2023-10, Vol.203 (1), p.65-78

2023

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Erythrocyte pyruvate kinase deficiency: 2015 status report

American journal of hematology, 2015-09, Vol.90 (9), p.825-830

2015

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Platelet function tests, independent of platelet count, are associated with bleeding severity in ITP

Blood, 2015-08, Vol.126 (7), p.873-879

2015

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Liver MRI is more precise than liver biopsy for assessing total body iron balance: a comparison of MRI relaxometry with simulated liver biopsy results

Magnetic resonance imaging, 2015-07, Vol.33 (6), p.761-767

2015

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Prevalence and management of iron overload in pyruvate kinase deficiency: report from the Pyruvate Kinase Deficiency Natural History Study

Haematologica (Roma), 2019-02, Vol.104 (2), p.e51

2019

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Transfusion complications in thalassemia patients: a report from the Centers for Disease Control and Prevention (CME)

Transfusion (Philadelphia, Pa.), 2014-04, Vol.54 (4), p.972-981

2014

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The cost-effectiveness of gene therapy for severe hemophilia B: a microsimulation study from the United States perspective

Blood, 2021-11, Vol.138 (18), p.1677-1690

2021

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An update on the US adult thalassaemia population: a report from the CDC thalassaemia treatment centres

British journal of haematology, 2022-01, Vol.196 (2), p.380-389

2022

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Simoctocog alfa (Nuwiq®) in previously untreated patients with severe haemophilia A-Final efficacy and safety results from the NuProtect study

European journal of haematology, 2023-10, Vol.111 (4), p.544-552

2023

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The frequency and management of asparaginase‐related thrombosis in paediatric and adult patients with acute lymphoblastic leukaemia treated on Dana‐Farber Cancer Institute consortium protocols

British journal of haematology, 2011-02, Vol.152 (4), p.452-459

2011

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Pediatric Heparin-Induced Thrombocytopenia: Prevalence, Thrombotic Risk, and Application of the 4Ts Scoring System

The Journal of pediatrics, 2015-01, Vol.166 (1), p.144-150.e1

2015

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Prevalence of the metabolic syndrome in American adolescents: Findings from the Third National Health and nutrition examination survey

Circulation (New York, N.Y.), 2004-10, Vol.110 (16), p.2494-2497

2004

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Update on iron chelators in thalassemia

Hematology, 2010, Vol.2010 (1), p.451-455

Neufeld, Ellis J

2010

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Regional variation and cost implications of prescribed extended half‐life factor concentrates among U.S. Haemophilia Treatment Centres for patients with moderate and severe haemophilia

Haemophilia : the official journal of the World Federation of Hemophilia, 2019-07, Vol.25 (4), p.668-675

2019

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Complications of β-thalassemia major in North America

Blood, 2004-07, Vol.104 (1), p.34-39

2004

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Rituximab for treatment of inhibitors in haemophilia A. A Phase II study

Thrombosis and haemostasis, 2014-09, Vol.112 (3), p.445

2014

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Risk of Post-Procedural Bleeding in Children on Intravenous Fish Oil

The American journal of surgery, 2017-10, Vol.214 (4), p.733-737

2017

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Safety update on the use of recombinant activated factor VII in approved indications

Blood reviews, 2015-06, Vol.29, p.S34-S41

2015

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Bleeding risks are higher in children versus adults given prophylactic platelet transfusions for treatment-induced hypoproliferative thrombocytopenia

Blood, 2012-07, Vol.120 (4), p.748-760

2012

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Systematic molecular genetic analysis of congenital sideroblastic anemia: Evidence for genetic heterogeneity and identification of novel mutations

Pediatric blood & cancer, 2010-02, Vol.54 (2), p.273-278

2010

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Comorbidities and complications in adults with pyruvate kinase deficiency

European journal of haematology, 2021-04, Vol.106 (4), p.484-492

2021

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Relationship among chelator adherence, change in chelators, and quality of life in Thalassemia

Quality of life research, 2014-10, Vol.23 (8), p.2277-2288

2014

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Phase 3 randomised trial of eltrombopag versus standard first-line pharmacological management for newly diagnosed immune thrombocytopaenia (ITP) in children: study protocol

BMJ open, 2021-08, Vol.11 (8), p.e044885

2021

Volltextzugriff (PDF)

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Oral chelators deferasirox and deferiprone for transfusional iron overload in thalassemia major: new data, new questions

Novel therapeutics and future directions for refractory immune thrombocytopenia

Erythrocyte pyruvate kinase deficiency: 2015 status report

Platelet function tests, independent of platelet count, are associated with bleeding severity in ITP

Liver MRI is more precise than liver biopsy for assessing total body iron balance: a comparison of MRI relaxometry with simulated liver biopsy results

Prevalence and management of iron overload in pyruvate kinase deficiency: report from the Pyruvate Kinase Deficiency Natural History Study

Transfusion complications in thalassemia patients: a report from the Centers for Disease Control and Prevention (CME)

The cost-effectiveness of gene therapy for severe hemophilia B: a microsimulation study from the United States perspective

An update on the US adult thalassaemia population: a report from the CDC thalassaemia treatment centres

Simoctocog alfa (Nuwiq®) in previously untreated patients with severe haemophilia A-Final efficacy and safety results from the NuProtect study

The frequency and management of asparaginase‐related thrombosis in paediatric and adult patients with acute lymphoblastic leukaemia treated on Dana‐Farber Cancer Institute consortium protocols

Pediatric Heparin-Induced Thrombocytopenia: Prevalence, Thrombotic Risk, and Application of the 4Ts Scoring System

Prevalence of the metabolic syndrome in American adolescents: Findings from the Third National Health and nutrition examination survey

Update on iron chelators in thalassemia

Simoctocog Alfa (Nuwiq) in Previously Untreated Patients with Severe Haemophilia A: Final Results of the NuProtect Study

Regional variation and cost implications of prescribed extended half‐life factor concentrates among U.S. Haemophilia Treatment Centres for patients with moderate and severe haemophilia

Complications of β-thalassemia major in North America

Rituximab for treatment of inhibitors in haemophilia A. A Phase II study

Risk of Post-Procedural Bleeding in Children on Intravenous Fish Oil

Safety update on the use of recombinant activated factor VII in approved indications

Bleeding risks are higher in children versus adults given prophylactic platelet transfusions for treatment-induced hypoproliferative thrombocytopenia

Systematic molecular genetic analysis of congenital sideroblastic anemia: Evidence for genetic heterogeneity and identification of novel mutations

Comorbidities and complications in adults with pyruvate kinase deficiency

Relationship among chelator adherence, change in chelators, and quality of life in Thalassemia

Phase 3 randomised trial of eltrombopag versus standard first-line pharmacological management for newly diagnosed immune thrombocytopaenia (ITP) in children: study protocol

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