Works matching IS 00778923 AND DT 2005 AND VI 1054 AND IP 1
Results: 69
Nutrition: Role in Health and Therapy.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 522, doi. 10.1196/annals.1345.080
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Genotypes and Phenotypes of Thalassemia: A Discussion.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 518, doi. 10.1196/annals.1345.079
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Management of the "Difficult" Iron-Overloaded Patient.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 516, doi. 10.1196/annals.1345.078
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Diagnosis and Management of Alpha Thalassemia Disorders.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 514, doi. 10.1196/annals.1345.077
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Workshop Summaries: The Splenectomy Controversy.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 511, doi. 10.1196/annals.1345.076
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Prenatal Diagnosis of Hemoglobinopathies in Ontario, Canada.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 507, doi. 10.1196/annals.1345.052
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Utility of Holter Electrocardiogram in Iron-Overloaded Hemoglobinopathies.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 476, doi. 10.1196/annals.1345.064
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Separation of Normoblasts from Whole Blood by Ultracentrifugation on Arabino-Galactane Discontinuous Gradients A Tool for Prenatal Diagnosis.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 504, doi. 10.1196/annals.1345.073
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Therapeutic Approaches to Pulmonary Hypertension in: Hemoglobinopathies Efficacy and Safety of Sildenafil in the Treatment of Severe Pulmonary Hypertension in Patients with Hemoglobinopathy.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 471, doi. 10.1196/annals.1345.070
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Preclinical and Clinical Development of Deferitrin, a Novel, Orally Available Iron Chelator.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 492, doi. 10.1196/annals.1345.071
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A Simple Model to Assess and Improve Adherence to Iron Chelation Therapy with Deferoxamine in Patients with Thalassemia.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 486, doi. 10.1196/annals.1345.065
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Hemolysis-Associated Pulmonary Hypertension in Thalassemia.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 481, doi. 10.1196/annals.1345.058
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Outcomes of Preimplantation Genetic Diagnosis Therapy in Treatment of β-Thalassemia A Retrospective Analysis.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 500, doi. 10.1196/annals.1345.060
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Allosensitization in Patients Receiving Multiple Blood Transfusions.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 495, doi. 10.1196/annals.1345.072
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Does Heterozygous β-Thalassemia Confer a Protection against Coronary Artery Disease?
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 467, doi. 10.1196/annals.1345.068
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Low Bone Mineral Density in Adolescents with β-Thalassemia.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 462, doi. 10.1196/annals.1345.063
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Quality of Life in Patients with Thalassemia Intermedia Compared to Thalassemia Major.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 457, doi. 10.1196/annals.1345.059
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Osteoporosis in β-Thalassemia: Clinical and Genetic Aspects.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 451, doi. 10.1196/annals.1345.051
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Longitudinal Study of Survival and Causes of Death in Patients with Thalassemia Major in Greece.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 445, doi. 10.1196/annals.1345.067
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Measuring Chromosome Breaks in Patients with Thalassemia.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 439, doi. 10.1196/annals.1345.050
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Genetic Analysis of Candidate Modifier Polymorphisms in Hb E-β<sup>0</sup>-Thalassemia Patients.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 433, doi. 10.1196/annals.1345.066
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Non-Transferrin-Bound Iron during Blood Transfusion Cycles in β-Thalassemia Major.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 429, doi. 10.1196/annals.1345.074
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Murine and Math Models for the Level of Stable Mixed Chimerism to Cure β-Thalassemia by Nonmyeloablative Bone Marrow Transplantation.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 423, doi. 10.1196/annals.1345.061
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Exploring the Role of Hepcidin, an Antimicrobial and Iron Regulatory Peptide, in Increased Iron Absorption in β-Thalassemia.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 417, doi. 10.1196/annals.1345.069
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Rescued Mice with Hb E Transgene-Developed Red Cell Changes Similar to Human β-Thalassemia/HbE Disease.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 407, doi. 10.1196/annals.1345.049
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Eighth Cooley's Anemia Symposium: Summation and Perspective.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 396, doi. 10.1196/annals.1345.048
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Physiology and Pathophysiology of Iron Cardiomyopathy in Thalassemia.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 386, doi. 10.1196/annals.1345.047
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Measurement and Mapping of Liver Iron Concentrations Using Magnetic Resonance Imaging.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 379, doi. 10.1196/annals.1345.046
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T2* Magnetic Resonance and Myocardial Iron in Thalassemia.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 373, doi. 10.1196/annals.1345.045
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Methods for Noninvasive Measurement of Tissue Iron in Cooley's Anemia.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 358, doi. 10.1196/annals.1345.044
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Monitoring Long-Term Efficacy of Iron Chelation Treatment with Biomagnetic Liver Susceptometry.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 350, doi. 10.1196/annals.1345.043
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Transfusion Safety: Where Are We Today?
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 325, doi. 10.1196/annals.1345.040
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Coagulation and Splenectomy: An Overview.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 317, doi. 10.1196/annals.1345.039
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A Phase I/II Clinical Trial of β-Globin Gene Therapy for β-Thalassemia.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 308, doi. 10.1196/annals.1345.007
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Fertility and Pregnancy in Thalassemia Major.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 300, doi. 10.1196/annals.1345.062
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Treatment of Hepatitis C Virus Infection in Thalassemia.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 290, doi. 10.1196/annals.1345.038
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Thalassemia and Learning: Neurocognitive Functioning in Children.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 283, doi. 10.1196/annals.1345.036
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Quality of Life in Thalassemia.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 273, doi. 10.1196/annals.1345.035
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Caring for Adults with Thalassemia in a Pediatric World.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 266, doi. 10.1196/annals.1345.034
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Induction of Fetal Globin in β-Thalassemia: Cellular Obstacles and Molecular Progress.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 257, doi. 10.1196/annals.1345.033
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Single and Combination Drug Therapy for Fetal Hemoglobin Augmentation in Hemoglobin E-β<sup>o</sup>-Thalassemia: Considerations for Treatment.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 250, doi. 10.1196/annals.1345.031
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Successful Correction of the Human Cooley's Anemia β-Thalassemia Major Phenotype Using a Lentiviral Vector Flanked by the Chicken Hypersensitive Site 4 Chromatin Insulator.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 238, doi. 10.1196/annals.1345.030
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Pharmacological Induction of Fetal Hemoglobin: Why Haven't We Been More Successful in Thalassemia?
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 228, doi. 10.1196/annals.1345.029
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Preimplantation Genetics: Improving Access to Stem Cell Therapy.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 223, doi. 10.1196/annals.1345.028
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Stem Cell Transplantation with S-59 Photochemically Treated T-Cell Add-Backs to Establish Allochimerism in Murine Thalassemia.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 214, doi. 10.1196/annals.1345.026
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Sibling Donor Cord Blood Transplantation for Thalassemia Major: Experience of the Sibling Donor Cord Blood Program.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 206, doi. 10.1196/annals.1345.025
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Bone Marrow Transplantation in Adults with Thalassemia: Treatment and Long-Term Follow-Up.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 196, doi. 10.1196/annals.1345.024
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Unrelated Bone Marrow Transplantation for β-Thalassemia Patients: The Experience of the Italian Bone Marrow Transplant Group.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 186, doi. 10.1196/annals.1345.023
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Evaluation of ICL670, a Once-Daily Oral Iron Chelator in a Phase III Clinical Trial of β-Thalassemia Patients with Transfusional Iron Overload.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 183, doi. 10.1196/annals.1345.021
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Combined Therapy with Deferoxamine and Deferiprone.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 175, doi. 10.1196/annals.1345.020
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- Article