Serum ferritin level changes in children with sickle cell disease on chronic blood transfusion are nonlinear and are associated with iron load and liver injury.
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Blood transfusion for preventing primary and secondary stroke in people with sickle cell diseaseTowards a unifying, systems biology understanding of large-scale cellular death and destruction caused by poorly liganded iron: Parkinson's, Huntington's, Alzheimer's, prions, bactericides, chemical toxicology and others as examplesSerum ferritin: Past, present and futureIron overload in sickle cell disease.Liver Iron Content (LIC) in Adults with Sickle Cell Disease (SCD): Correlation with Serum Ferritin and Liver Enzymes Concentrations in Trasfusion Dependent (TD-SCD) and Non-Transfusion Dependent (NT-SCD) Patients.Trends in blood transfusion among hospitalized children with sickle cell disease.Discontinuing prophylactic transfusions increases the risk of silent brain infarction in children with sickle cell disease: data from STOP II.Transcranial Doppler ultrasonography and prophylactic transfusion program is effective in preventing overt stroke in children with sickle cell disease.Quantification of liver iron with MRI: state of the art and remaining challenges.Management of transfusional iron overload - differential properties and efficacy of iron chelating agents.Real-life experience with liver iron concentration R2 MRI measurement in patients with hemoglobinopathies: baseline data from LICNET.Blood transfusion for preventing primary and secondary stroke in people with sickle cell disease.Partial manual exchange reduces iron accumulation during chronic red cell transfusions for sickle cell disease.Profound morphological changes in the erythrocytes and fibrin networks of patients with hemochromatosis or with hyperferritinemia, and their normalization by iron chelators and other agents.Transfusional Iron Overload in a Cohort of Children with Sickle Cell Disease: Impact of Magnetic Resonance Imaging, Transfusion Method, and Chelation.A Young Adult with Unintended Acute Intravenous Iron Intoxication Treated with Oral Chelation: The Use of Liver Ferriscan for Diagnosing and Monitoring Tissue Iron Load.Iron in sickle-cell disease: what have we learned over the years?Indications and complications of transfusions in sickle cell disease.Utility of labile plasma iron and transferrin saturation in addition to serum ferritin as iron overload markers in different underlying anemias before and after deferasirox treatment.Clinical monitoring and management of complications related to chelation therapy in patients with β-thalassemia.Deferiprone for the treatment of transfusional iron overload in thalassemia.Comparison of automated erythrocytapheresis versus manual exchange transfusion to treat cerebral macrovasculopathy in sickle cell anemia.Acute and chronic hepatobiliary manifestations of sickle cell disease: A review.Hepatic Iron Quantification on 3 Tesla (3 T) Magnetic Resonance (MR): Technical Challenges and Solutions.A pilot study of manual chronic partial exchange transfusion in children with sickle disease.Long-term results using hydroxyurea/phlebotomy for reducing secondary stroke risk in children with sickle cell anemia and iron overload.Iron overload in non-transfusion-dependent thalassemia: association with genotype and clinical risk factors.Retrospective epidemiological study of Latin American patients with transfusional hemosiderosis: the first Latin American epidemiological study in iron overload--the RELATH study.Iron overload in children undergoing cancer treatments.Ferritin trends do not predict changes in total body iron in patients with transfusional iron overload.Assessing the Non-tumorous Liver: Implications for Patient Management and Surgical Therapy.Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload.Assessing cardiac and liver iron overload in chronically transfused patients with sickle cell disease.Noninvasive measurement of liver iron concentration at MRI in children with acute leukemia: initial results.Interim assessment of liver damage in patients with sickle cell disease using new non-invasive techniques.Serum ferritin is an important inflammatory disease marker, as it is mainly a leakage product from damaged cells
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Serum ferritin level changes in children with sickle cell disease on chronic blood transfusion are nonlinear and are associated with iron load and liver injury.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 31 August 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Serum ferritin level changes i ...... th iron load and liver injury.
@en
Serum ferritin level changes i ...... th iron load and liver injury.
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type
label
Serum ferritin level changes i ...... th iron load and liver injury.
@en
Serum ferritin level changes i ...... th iron load and liver injury.
@nl
prefLabel
Serum ferritin level changes i ...... th iron load and liver injury.
@en
Serum ferritin level changes i ...... th iron load and liver injury.
@nl
P2093
P2860
P50
P1433
P1476
Serum ferritin level changes i ...... th iron load and liver injury.
@en
P2093
Abdullah Kutlar
Beatrice Gee
Carole Paley
Gerald M Woods
James F Casella
Janet L Kwiatkowski
Julio C Barredo
Kathleen M McKie
Margaret T Lee
Melanie Kirby-Allen
P2860
P304
P356
10.1182/BLOOD-2009-02-203323
P407
P577
2009-08-31T00:00:00Z