Works matching IS 00778923 AND DT 2010 AND VI 1202 AND IP 1
Results: 39
Treatment options for thalassemia patients with osteoporosis.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 237, doi. 10.1111/j.1749-6632.2010.05542.x
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Progress in hematopoietic stem cell transplantation as allogeneic cellular gene therapy in thalassemia.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 149, doi. 10.1111/j.1749-6632.2010.05543.x
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Pathogenesis and management of iron toxicity in thalassemia.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 1, doi. 10.1111/j.1749-6632.2010.05544.x
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Predicting pituitary iron and endocrine dysfunction.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 123, doi. 10.1111/j.1749-6632.2010.05545.x
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Thalassemia as a global health problem: recent progress toward its control in the developing countries.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 17, doi. 10.1111/j.1749-6632.2010.05546.x
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Humanized mouse models of Cooley's anemia: correct fetal-to-adult hemoglobin switching, disease onset, and disease pathology.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 45, doi. 10.1111/j.1749-6632.2010.05547.x
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Redefining thalassemia as a hypercoagulable state.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 231, doi. 10.1111/j.1749-6632.2010.05548.x
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Ninth Cooley's Anemia Symposium: summary and perspective.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 248, doi. 10.1111/j.1749-6632.2010.05549.x
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The natural history of thalassemia intermedia.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 214, doi. 10.1111/j.1749-6632.2010.05550.x
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Cardiovascular MRI in thalassemia major.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 173, doi. 10.1111/j.1749-6632.2010.05571.x
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Complexity of alpha thalassemia: growing health problem with new approaches to screening, diagnosis, and therapy.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 180, doi. 10.1111/j.1749-6632.2010.05572.x
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Monitoring the efficiency of iron chelation therapy: the potential of nontransferrin-bound iron.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 94, doi. 10.1111/j.1749-6632.2010.05573.x
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Transcriptional silencing of fetal hemoglobin by BCL11A.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 64, doi. 10.1111/j.1749-6632.2010.05574.x
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Ferritin iron minerals are chelator targets, antioxidants, and coated, dietary iron.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 197, doi. 10.1111/j.1749-6632.2010.05575.x
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Hematopoietic stem cell mobilization strategies for gene therapy of beta thalassemia and sickle cell disease.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 59, doi. 10.1111/j.1749-6632.2010.05576.x
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The role of antioxidants and iron chelators in the treatment of oxidative stress in thalassemia.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 10, doi. 10.1111/j.1749-6632.2010.05577.x
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Nutritional deficiencies in patients with thalassemia.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 188, doi. 10.1111/j.1749-6632.2010.05578.x
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Emerging insights in the management of hemoglobin E beta thalassemia.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 155, doi. 10.1111/j.1749-6632.2010.05579.x
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Pulmonary hypertension in thalassemia.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 205, doi. 10.1111/j.1749-6632.2010.05580.x
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The challenge of obtaining therapeutic levels of genetically modified hematopoietic stem cells in β-thalassemia patients.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 69, doi. 10.1111/j.1749-6632.2010.05581.x
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Deferasirox—current knowledge and future challenges.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 87, doi. 10.1111/j.1749-6632.2010.05582.x
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Fertility potential in thalassemia major women: current findings and future diagnostic tools.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 226, doi. 10.1111/j.1749-6632.2010.05583.x
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Therapy for β-globinopathies: a brief review and determinants for successful and safe correction.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 36, doi. 10.1111/j.1749-6632.2010.05584.x
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Hepcidin in β-thalassemia.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 31, doi. 10.1111/j.1749-6632.2010.05585.x
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Deferiprone.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 75, doi. 10.1111/j.1749-6632.2010.05586.x
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Magnetic resonance assessment of iron overload by separate measurement of tissue ferritin and hemosiderin iron.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 115, doi. 10.1111/j.1749-6632.2010.05587.x
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Better survival and less cardiac morbidity in female patients with thalassemia major: a review of the literature.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 129, doi. 10.1111/j.1749-6632.2010.05588.x
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Critical appraisal of growth retardation and pubertal disturbances in thalassemia.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 100, doi. 10.1111/j.1749-6632.2010.05589.x
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The role of reduced intensity preparative regimens in patients with thalassemia given hematopoietic transplantation.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 141, doi. 10.1111/j.1749-6632.2010.05590.x
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Combined iron chelation therapy.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 79, doi. 10.1111/j.1749-6632.2010.05591.x
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Clinical trials in thalassemia: insights from the patient community.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. xi, doi. 10.1111/j.1749-6632.2010.05592.x
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Fetal globin gene inducers: novel agents and new potential.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 158, doi. 10.1111/j.1749-6632.2010.05593.x
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A preclinical approach for gene therapy of β-thalassemia.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 134, doi. 10.1111/j.1749-6632.2010.05594.x
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Hepcidin and Hfe in iron overload in β-thalassemia.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 221, doi. 10.1111/j.1749-6632.2010.05595.x
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Iron metabolism and ineffective erythropoiesis in β-thalassemia mouse models.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 24, doi. 10.1111/j.1749-6632.2010.05596.x
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Strategy for a multicenter phase I clinical trial to evaluate globin gene transfer in β-thalassemia.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 52, doi. 10.1111/j.1749-6632.2010.05597.x
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Health care transition in thalassemia: pediatric to adult-oriented care.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 244, doi. 10.1111/j.1749-6632.2010.05598.x
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Detection of the cardiovascular complications of thalassemia by echocardiography.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 165, doi. 10.1111/j.1749-6632.2010.05643.x
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Preface to Cooley's Anemia: Ninth Symposium.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. ix, doi. 10.1111/j.1749-6632.2010.05672.x
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