selected publications
- Anemia and iron overload as prognostic markers of outcomes in β-thalassemia. Expert review of hematology. 2024 Review GET IT
- Iron chelation therapy for children with transfusion-dependent β-thalassemia: How young is too young?. Pediatric blood & cancer. 2024 Review GET IT
- Exagamglogene Autotemcel for Transfusion-Dependent β-Thalassemia. The New England journal of medicine. 2024 Academic Article GET IT
- Rates of severe neutropenia and infection risk in patients treated with deferiprone: 28 years of data. Blood advances. 2024 Academic Article GET IT
- Αlpha-thalassemia: A practical overview. Blood reviews. 2024 Review GET IT
- When should gene therapy be considered for transfusion-dependent β-thalassemia patients?. Hematology. American Society of Hematology. Education Program. 2023 Academic Article GET IT
- Luspatercept for transfusion-dependent β-thalassemia: time to get real. Therapeutic advances in hematology. 2023 Editorial Article GET IT
- Profile of Luspatercept in the Treatment of Anemia in Adults with Non-Transfusion-Dependent β-Thalassemia (NTDT): Design, Development and Potential Place in Therapy. Drug design, development and therapy. 2023 Review GET IT
- Management of luspatercept therapy in patients with transfusion-dependent β-thalassaemia. British journal of haematology. 2023 Review GET IT
- Clinical Classification, Screening, and Diagnosis in Beta-Thalassemia and Hemoglobin E/Beta-Thalassemia. Hematology/oncology clinics of North America. 2023 Review GET IT
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Thalassaemia-A global view.
British journal of haematology.
2023
Review
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Times cited: 1 - Untreated Anemia in Nontransfusion-dependent β-thalassemia: Time to Sound the Alarm. HemaSphere. 2022 Editorial Article GET IT
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Health-related quality of life and fatigue in children and adults with pyruvate kinase deficiency.
Blood advances.
2022
Academic Article
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Times cited: 13 -
The safety and acceptability of twice-daily deferiprone for transfusional iron overload: A multicentre, open-label, phase 2 study.
British journal of haematology.
2021
Letter
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Times cited: 8 -
Optimal strategies for carrier screening and prenatal diagnosis of α- and β-thalassemia.
Hematology. American Society of Hematology. Education Program.
2021
Review
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Times cited: 8 -
Pyruvate kinase deficiency in children.
Pediatric blood & cancer.
2021
Academic Article
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Times cited: 2 -
Comorbidities and complications in adults with pyruvate kinase deficiency.
European journal of haematology.
2021
Academic Article
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Times cited: 20 -
CRISPR-Cas9 Gene Editing for Sickle Cell Disease and β-Thalassemia.
The New England journal of medicine.
2020
Academic Article
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Times cited: 421 - An assessment of the continuing medical education needs of US physicians in the management of patients with beta thalassemia. Annals of hematology. 2020 Academic Article GET IT
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Extracellular Vesicle and Particle Biomarkers Define Multiple Human Cancers.
Cell.
2020
Academic Article
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Times cited: 769 -
Characterization of the severe phenotype of pyruvate kinase deficiency.
American journal of hematology.
2020
Letter
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Times cited: 7 -
Systematic Literature Review of the Burden of Disease and Treatment for Transfusion-dependent β-Thalassemia.
Clinical therapeutics.
2019
Academic Article
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Times cited: 10 -
Bone Marrow Failure in Children: Approach to Diagnosis and Treatment.
Indian journal of pediatrics.
2019
Review
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Times cited: 2 -
Safety and Efficacy of Mitapivat in Pyruvate Kinase Deficiency.
The New England journal of medicine.
2019
Academic Article
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Times cited: 36 - Stem cell transplantation in sickle-cell disease. The Lancet. Haematology. 2019 Comment GET IT
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Bleeding Scales Applicable to Critically Ill Children: A Systematic Review.
Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies.
2019
Academic Article
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Times cited: 3 -
Strategies for managing transfusional iron overload: conventional treatments and novel strategies.
Current opinion in hematology.
2019
Review
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Times cited: 1 -
Clinical and economic burden of regularly transfused adult patients with β-thalassemia in the United States: A retrospective cohort study using payer claims.
American journal of hematology.
2019
Letter
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Times cited: 3 -
Measurement of the liver iron concentration in transfusional iron overload by MRI R2* and by high-transition-temperature superconducting magnetic susceptometry.
Clinical imaging.
2019
Academic Article
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Times cited: 10 -
Rapid automated liver quantitative susceptibility mapping.
Journal of magnetic resonance imaging : JMRI.
2019
Academic Article
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Times cited: 27 -
Prevalence and management of iron overload in pyruvate kinase deficiency: report from the Pyruvate Kinase Deficiency Natural History Study.
Haematologica.
2018
Letter
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Times cited: 47 -
Association of Perioperative Red Blood Cell Transfusions With Venous Thromboembolism in a North American Registry.
JAMA surgery.
2018
Academic Article
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Times cited: 143 -
Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study.
Blood.
2018
Academic Article
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Times cited: 52 -
Pediatric Gastroenterologists' Approach to Venous Thromboembolism Prophylaxis in Pediatric Inflammatory Bowel Disease.
Journal of pediatric gastroenterology and nutrition.
2018
Academic Article
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Times cited: 18 -
Prolonged red cell storage before transfusion increases extravascular hemolysis.
The Journal of clinical investigation.
2016
Academic Article
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Times cited: 159 -
Red blood cell transfusion is associated with increased hemolysis and an acute phase response in a subset of critically ill children.
American journal of hematology.
2015
Academic Article
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Times cited: 38 -
Hematopoietic stem cell transplantation in sickle cell disease: patient selection and special considerations.
Journal of blood medicine.
2015
Review
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Times cited: 47 -
Iron chelation: an update.
Current opinion in hematology.
2014
Review
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Times cited: 47 -
Red blood cell transfusions for thalassemia: results of a survey assessing current practice and proposal of evidence-based guidelines.
Transfusion.
2014
Review
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Times cited: 23 -
Regulatory B-cell compartment in transfused alloimmunized and non-alloimmunized patients with sickle cell disease.
American journal of hematology.
2013
Academic Article
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Times cited: 49 -
Sickle cell disease: time for a closer look at treatment options?.
British journal of haematology.
2013
Review
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Times cited: 38 -
MR characterization of hepatic storage iron in transfusional iron overload.
Journal of magnetic resonance imaging : JMRI.
2013
Academic Article
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Times cited: 18 -
Measurement and correction of stimulated echo contamination in T2-based iron quantification.
Magnetic resonance imaging.
2012
Academic Article
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Times cited: 6 -
Managing incidentally diagnosed isolated factor VII deficiency perioperatively: a brief expert consensus report.
Expert review of hematology.
2012
Academic Article
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Times cited: 6 -
Transfusion of human volunteers with older, stored red blood cells produces extravascular hemolysis and circulating non-transferrin-bound iron.
Blood.
2011
Academic Article
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Times cited: 247 -
Fetal hemoglobin levels in African American and Hispanic children with sickle cell disease at baseline and in response to hydroxyurea.
Journal of pediatric hematology/oncology.
2011
Academic Article
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Times cited: 6 -
The use of recombinant tissue-type plasminogen activator in a newborn with an intracardiac thrombus developed during extracorporeal membrane oxygenation.
2011
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Times cited: 17 -
Immune regulation in chronically transfused allo-antibody responder and nonresponder patients with sickle cell disease and β-thalassemia major.
American journal of hematology.
2011
Academic Article
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Times cited: 62 -
Rapid monitoring of iron-chelating therapy in thalassemia major by a new cardiovascular MR measure: the reduced transverse relaxation rate.
NMR in biomedicine.
2010
Academic Article
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Times cited: 6 -
Magnetic resonance assessment of iron overload by separate measurement of tissue ferritin and hemosiderin iron.
Annals of the New York Academy of Sciences.
2010
Academic Article
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Times cited: 24 -
Separate MRI quantification of dispersed (ferritin-like) and aggregated (hemosiderin-like) storage iron.
Magnetic resonance in medicine.
2010
Academic Article
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Times cited: 44 -
Transfusion of red blood cells after prolonged storage produces harmful effects that are mediated by iron and inflammation.
Blood.
2010
Academic Article
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Times cited: 399 -
Breathhold multiecho fast spin-echo pulse sequence for accurate R2 measurement in the heart and liver.
Magnetic resonance in medicine.
2009
Academic Article
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Times cited: 48 -
Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference.
British journal of haematology.
2008
Conference Paper
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Times cited: 367 - Magnetic measurement of liver iron stores: Engineering aspects of a new scanning susceptometer based on high-temperature superconductivity. IEEE Transactions on Magnetics. 2007 Article GET IT
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Methods for noninvasive measurement of tissue iron in Cooley's anemia.
Annals of the New York Academy of Sciences.
2005
Academic Article
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Times cited: 12 -
Prenatal diagnosis of factor X deficiency using a combination of direct mutation detection and linkage analysis with an intragenic single nucleotide polymorphism.
2003
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Times cited: 7 -
SQUID biosusceptometry in the measurement of hepatic iron.
Pediatric radiology.
2003
Review
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Times cited: 30 -
Pneumocystis carinii pneumonia in patients with Diamond-Blackfan anemia receiving high-dose corticosteroids.
2002
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Times cited: 8 -
Heart transplant in a factor VIII-deficient patient with a high-titre inhibitor: perioperative management using high-dose continuous infusion factor VIII and recombinant factor VIIa.
2001
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Times cited: 34 -
Noninvasive methods for quantitative assessment of transfusional iron overload in sickle cell disease.
Seminars in hematology.
2001
Review
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Times cited: 57 -
CT imaging of splenic sequestration in sickle cell disease.
Pediatric radiology.
2000
Academic Article
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Times cited: 10 -
Genetic disorders affecting proteins of iron metabolism: clinical implications.
Annual review of medicine.
2000
Review
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Times cited: 53 -
Serum transferrin receptor as a marker of erythropoiesis suppression in patients on chronic transfusion.
American journal of hematology.
1999
Academic Article
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Times cited: 21 -
Pulmonary embolism developing in patients with sickle cell disease on hypertransfusion and IV deferoxamine chelation therapy.
1997
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Times cited: 5 - Iron overload in reticuloendothelial systems of pediatric oncology patients who have undergone transfusions: MR observations. AJR. American journal of roentgenology. 1997 Academic Article GET IT
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Deferoxamine-induced platyspondyly in hypertransfused thalassemic patients.
1995
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Times cited: 14 -
Haplotypes of the human beta-like globin gene cluster: analyzing the 3' Hpa I polymorphic site by long distance PCR.
American journal of hematology.
1995
Academic Article
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Times cited: 2 -
MR marrow signs of iron overload in transfusion-dependent patients with sickle cell disease.
Pediatric radiology.
1995
Academic Article
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Times cited: 19 -
MRI marrow observations in thalassemia: the effects of the primary disease, transfusional therapy, and chelation.
Pediatric radiology.
1995
Academic Article
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Times cited: 28