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Psychosocial Impacts on a Thalassemic Patient's Life.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 324, doi. 10.1111/j.1749-6632.1985.tb17202.x
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Attempts at Gene Therapy in β-Thalassemic Mice.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 445, doi. 10.1111/j.1749-6632.1985.tb17214.x
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Antenatal Diagnosis of Thalassemia: A Review<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 393, doi. 10.1111/j.1749-6632.1985.tb17209.x
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Prenatal Diagnosis of Thalassemia and Hb S Syndromes in Greece: An Evaluation of 1500 Cases<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 357, doi. 10.1111/j.1749-6632.1985.tb17206.x
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Thalassemic Children's Understanding of Illness: A Study of Cognitive and Emotional Factors.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 327, doi. 10.1111/j.1749-6632.1985.tb17203.x
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The Silent Carrier of β-Thalassemia.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 111, doi. 10.1111/j.1749-6632.1985.tb17180.x
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Progress toward Increasing Fetal Hemoglobin Production in Man: Experience with 5-Azacytidine and Hydroxyurea<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 218, doi. 10.1111/j.1749-6632.1985.tb17191.x
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Molecular Analysis of Deletion and Nondeletion Hereditary Persistence of Fetal Hemoglobin and Identification of a New Mutation Causing β-Thalassemia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 159, doi. 10.1111/j.1749-6632.1985.tb17185.x
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Clinical and Molecular Heterogeneity of δ, β-Thalassemia in Sicily<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 148, doi. 10.1111/j.1749-6632.1985.tb17184.x
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- Article
Hb F Production in Stressed Erythropoiesis: Observations and Kinetic Modelsa<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 188, doi. 10.1111/j.1749-6632.1985.tb17188.x
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A Model for Hemoglobin F Synthesis in Adult Life: Evidence for Regulation at the Level of Erythroblasts<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 225, doi. 10.1111/j.1749-6632.1985.tb17192.x
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- Article
The Interaction of Coexistent α-Thalassemia and Sickle Cell Anemia: A Model for the Clinical and Cellular Results of Diminished Polymerization?<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 37, doi. 10.1111/j.1749-6632.1985.tb17173.x
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- Article
Regulation of Fetal Hemoglobin Synthesis in the Hemoglobinopathies.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 177, doi. 10.1111/j.1749-6632.1985.tb17187.x
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- Article
New Research Approaches to Cooley's Anemia Therapy.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 455, doi. 10.1111/j.1749-6632.1985.tb17216.x
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Marrow Transplantation for Thalassemia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 417, doi. 10.1111/j.1749-6632.1985.tb17211.x
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Current Therapy and New Approaches to the Treatment of Thalassemia Major.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 248, doi. 10.1111/j.1749-6632.1985.tb17194.x
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Thalassemia in Southeast Asia: Determination of Different Degrees of Severity of Anemia in Thalassemia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 119, doi. 10.1111/j.1749-6632.1985.tb17181.x
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A Psychosocial Needs Assessment of Patients with Homozygous β-Thalassemia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 316, doi. 10.1111/j.1749-6632.1985.tb17201.x
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- Article
Abnormal Globin Gene Structure and Expression in β-Thalassemia.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 1, doi. 10.1111/j.1749-6632.1985.tb17169.x
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Toward Providing Parents the Option of Avoiding the Birth of the First Child with Cooley's Anemia: Response to Hemoglobinopathy Screening and Counseling During Pregnancy.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 408, doi. 10.1111/j.1749-6632.1985.tb17210.x
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Concluding Remarks.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 452, doi. 10.1111/j.1749-6632.1985.tb17215.x
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- Article
The Effect of Subcutaneous Deferoxamine on the Cardiac Profile of Thalassemia Major: A Five-Year Study.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 282, doi. 10.1111/j.1749-6632.1985.tb17198.x
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Defective Vitamin D Metabolism in Thalassemia Major.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 127, doi. 10.1111/j.1749-6632.1985.tb17182.x
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Combined Subcutaneous and High-Dose Intravenous Deferoxamine Therapy of Thalassemia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 293, doi. 10.1111/j.1749-6632.1985.tb17199.x
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The Ratio of the <sup>G</sup>γ and <sup>A</sup>γ Chains: Variations due to Anomalies at the Molecular Level.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 235, doi. 10.1111/j.1749-6632.1985.tb17193.x
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First Trimester Diagnosis of the Hemoglobin Disorders.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 349, doi. 10.1111/j.1749-6632.1985.tb17205.x
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Deletion Analysis of the Human γ-Globin IVS2: Sequence Requirements for RNA Splicing.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 10, doi. 10.1111/j.1749-6632.1985.tb17170.x
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A Second Look at the Distribution and Frequency of the Hemoglobinopathies.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 268, doi. 10.1111/j.1749-6632.1985.tb17196.x
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Pharmacological Manipulation of Fetal Hemoglobin Synthesis in Patients with Severe β-Thalassemia.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 198, doi. 10.1111/j.1749-6632.1985.tb17189.x
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Hematology of a Murine β-Thalassemia: A Longitudinal Study<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 432, doi. 10.1111/j.1749-6632.1985.tb17213.x
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Antenatal Diagnosis of Thalassemia Major in Sardinia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 380, doi. 10.1111/j.1749-6632.1985.tb17208.x
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Improved Oxygen Delivery to Tissues and Iron Chelator Transport through the Use of Lysed and Resealed Red Blood Cells: A New Perspective on Cooley's Anemia Therapy<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 304, doi. 10.1111/j.1749-6632.1985.tb17200.x
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Analysis of Globin Gene Inversion Reveals Similarities with Immunoglobulin Rearrangement.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 212, doi. 10.1111/j.1749-6632.1985.tb17190.x
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- Article
Prenatal Diagnosis of Hemoglobinopathies by DNA Analysis.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 337, doi. 10.1111/j.1749-6632.1985.tb17204.x
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Treatment of Iron Overload in Cooley's Anemia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 274, doi. 10.1111/j.1749-6632.1985.tb17197.x
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- Article
A Novel Deletion in the β-Globin Gene Complex.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 20, doi. 10.1111/j.1749-6632.1985.tb17171.x
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- Article
Current Strategies in the Management of Cooley's Anemia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 256, doi. 10.1111/j.1749-6632.1985.tb17195.x
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Observations on Oxygen Delivery, Methemoglobinemia, and Arterial Oxygenation in Patients with β-Thalassemia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 135, doi. 10.1111/j.1749-6632.1985.tb17183.x
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- Article
Multiple Molecular Bases for Thalassemia Intermedia in East Sicily<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 106, doi. 10.1111/j.1749-6632.1985.tb17179.x
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Metabolism of Structurally Abnormal mRNAs Resulting from β-Thalassemia Mutations<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 57, doi. 10.1111/j.1749-6632.1985.tb17175.x
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Molecular Pathology of α-Thalassemia.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 28, doi. 10.1111/j.1749-6632.1985.tb17172.x
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Genetic and Molecular Analysis of Mild Forms of Homozygous β-Thalassemia.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 68, doi. 10.1111/j.1749-6632.1985.tb17176.x
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- Article
Heterogeneity of δ, β-Thalassemia and Hereditary Persistence of Hb F in the Mediterranean Area<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 170, doi. 10.1111/j.1749-6632.1985.tb17186.x
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- Article
Marrow Transplantation for Thalassemia after Treatment with Busulfan and Cyclophosphamide<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 428, doi. 10.1111/j.1749-6632.1985.tb17212.x
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The Hemoglobin Content and Concentration of Single Fetal Erythrocytes Obtained by Placentocentesis from Mothers with Heterozygous β-Thalassemia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 376, doi. 10.1111/j.1749-6632.1985.tb17207.x
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Alterations in Membrane Protein and Phosphorylation Pattern in β-Thalassemic Red Blood Cells.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 81, doi. 10.1111/j.1749-6632.1985.tb17177.x
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Thalassemia in China.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 92, doi. 10.1111/j.1749-6632.1985.tb17178.x
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- Article
Molecular Rearrangements of the Human α-Globin Gene Cluster.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 45, doi. 10.1111/j.1749-6632.1985.tb17174.x
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- Article