Works matching IS 00778923 AND DT 1980 AND VI 344 AND IP 1
Results: 42
NEW CLINICAL AND BIOCHEMICAL FINDINGS FROM 235 PATIENTS WITH HEMOGLOBIN LEPORE.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 364, doi. 10.1111/j.1749-6632.1980.tb33675.x
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CHELATION THERAPY, TRANSFUSION REQUIREMENT, AND IRON BALANCE IN YOUNG THALASSEMIC PATIENTS*.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 409, doi. 10.1111/j.1749-6632.1980.tb33680.x
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CURRENT CONCEPTS IN THE OVERALL MANAGEMENT OF THALASSEMIA.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 375, doi. 10.1111/j.1749-6632.1980.tb33676.x
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LONGITUDINAL STUDY OF CARDIAC FUNCTION IN THALASSEMIA MAJOR *.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 397, doi. 10.1111/j.1749-6632.1980.tb33678.x
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THE CLINICAL AND MOLECULAR HETEROGENEITY OF THE THALASSEMIA SYNDROMES *.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 83, doi. 10.1111/j.1749-6632.1980.tb33652.x
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PRENATAL DIAGNOSIS OF HEMOGLOBINOPATHIES: THE NEW ENGLAND APPROACH*.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 151, doi. 10.1111/j.1749-6632.1980.tb33658.x
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THE STRUCTURAL ANALYSIS OF THE HUMAN EPSILON-GLOBIN GENE AND ITS PRODUCT.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 76, doi. 10.1111/j.1749-6632.1980.tb33651.x
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CLOSING REMARKS.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 444, doi. 10.1111/j.1749-6632.1980.tb33684.x
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THALASSEMIA IN THAILAND *.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 352, doi. 10.1111/j.1749-6632.1980.tb33674.x
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PROTEOLYSIS IN THALASSEMIA: STUDIES WITH PROTEASE INHIBITORS*.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 323, doi. 10.1111/j.1749-6632.1980.tb33672.x
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IN VITRO GLOBIN CHAIN SYNTHESIS AFTER BLOOD TRANSFUSION IN SICILIAN HOMOZYGOUS β THALASSEMIA*.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 305, doi. 10.1111/j.1749-6632.1980.tb33670.x
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MOLECULAR MECHANISMS IN α THALASSEMIA: RACIAL DIFFERENCES IN α-GLOBIN GENE ORGANIZATION *.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 31, doi. 10.1111/j.1749-6632.1980.tb33646.x
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THE RATIO OF Gγ AND Aγ CHAINS OF THE HEMOGLOBIN F SYNTHESIZED BY BFU-E-DERIVED COLONIES FROM BLOOD OF SUBJECTS WITH β+ THALASSEMIA AND RELATED HEMOGLOBINOPATHIES *.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 253, doi. 10.1111/j.1749-6632.1980.tb33666.x
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CELLULAR REGULATION OF FETAL HEMOGLOBIN PRODUCTION *.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 206, doi. 10.1111/j.1749-6632.1980.tb33662.x
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GLOBIN SYNTHESIS IN SEVERE AND INTERMEDIATE HOMOZYGOUS β THALASSEMIA IN ISRAEL *.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 132, doi. 10.1111/j.1749-6632.1980.tb33656.x
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PRENATAL DIAGNOSIS OF β THALASSEMIA: EXPERIENCE WITH 133 CASES AND THE EFFECT OF FETAL BLOOD SAMPLING ON CHILD DEVELOPMENT *.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 165, doi. 10.1111/j.1749-6632.1980.tb33659.x
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THE STATUS OF NEW IRON CHELATORS*.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 425, doi. 10.1111/j.1749-6632.1980.tb33682.x
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THE CLINICAL SIGNIFICANCE OF MAGNESIUM DEPLETION IN THALASSEMIA*.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 436, doi. 10.1111/j.1749-6632.1980.tb33683.x
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GENERAL DISCUSSION:CLINICAL MANAGEMENT.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 418, doi. 10.1111/j.1749-6632.1980.tb33681.x
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EVALUATION OF CARDIAC FUNCTION IN PATIENTS WITH THALASSEMIA MAJOR.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 384, doi. 10.1111/j.1749-6632.1980.tb33677.x
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CHANGES IN GENE ORGANIZATION IN THE THALASSEMIAS.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 41, doi. 10.1111/j.1749-6632.1980.tb33647.x
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ANALYSIS OF β-GLOBIN GENES IN β^ THALASSEMIA*.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 12, doi. 10.1111/j.1749-6632.1980.tb33645.x
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β-GLOBIN MESSENGER RNA IN FERRARA β THALASSEMIA*.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 120, doi. 10.1111/j.1749-6632.1980.tb33655.x
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NONSENSE MUTATION AS A CAUSE OF β THALASSEMIA *.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 113, doi. 10.1111/j.1749-6632.1980.tb33654.x
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OPENING REMARKS.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. ix, doi. 10.1111/j.1749-6632.1980.tb33643.x
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SUSCEPTIBILITY OF THALASSEMIC RED BLOOD CELLS TO PHAGOCYTOSIS BY HUMAN MACROPHAGES IN VITRO.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 314, doi. 10.1111/j.1749-6632.1980.tb33671.x
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HEMOGLOBIN F IN β THALASSEMIA AND RELATED CONDITIONS *.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 240, doi. 10.1111/j.1749-6632.1980.tb33665.x
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EXPRESSION OF EMBRYONIC HEMOGLOBIN GENES IN α-THALASSEMIC AND IN ß-DUPLICATION MICE *.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 280, doi. 10.1111/j.1749-6632.1980.tb33668.x
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FISH AS MODELS FOR HEMOSIDEROSIS *.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 336, doi. 10.1111/j.1749-6632.1980.tb33673.x
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REGULATION OF GLOBIN GENE EXPRESSION AT THE MOLECULAR LEVEL.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 262, doi. 10.1111/j.1749-6632.1980.tb33667.x
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EMBRYONIC HEMOGLOBIN SYNTHESIS IN HUMAN ERYTHROLEUKEMIA CELLS *.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 233, doi. 10.1111/j.1749-6632.1980.tb33664.x
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α THALASSEMIA AND THE EXPRESSION OF HEMOGLOBIN G-PHILADELPHIA *.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 62, doi. 10.1111/j.1749-6632.1980.tb33649.x
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THE STRUCTURE OF THE HUMAN γ-GLOBIN GENE LOCUS AND ITS RELATION TO THE δ/β-GLOBIN GENE LOCUS.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 73, doi. 10.1111/j.1749-6632.1980.tb33650.x
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PATHOPHYSIOLOGY OF THALASSEMIA.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 284, doi. 10.1111/j.1749-6632.1980.tb33669.x
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HETEROGENEITY OF MESSENGER RNA DEFECTS IN THE THALASSEMIA SYNDROMES.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 101, doi. 10.1111/j.1749-6632.1980.tb33653.x
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PRENATAL DIAGNOSIS OF HEMOGLOBINOPATHIES *.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 141, doi. 10.1111/j.1749-6632.1980.tb33657.x
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DISCUSSION PAPER PRENATAL DIAGNOSIS OF THALASSEMIA MAJOR IN GREECE: EVALUATION OF THE FIRST LARGE SERIES OF ATTEMPTS *.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 181, doi. 10.1111/j.1749-6632.1980.tb33660.x
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F-CELL REGULATION.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 219, doi. 10.1111/j.1749-6632.1980.tb33663.x
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SPECIFIC ABNORMALITIES OF GLOBIN GENE ORGANIZATION IN THE THALASSEMIA SYNDROMES *.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 48, doi. 10.1111/j.1749-6632.1980.tb33648.x
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OVERVIEW: MECHANISMS OF THE REGULATION OF HEMOGLOBIN SYNTHESIS AT THE CELLULAR LEVEL.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 189, doi. 10.1111/j.1749-6632.1980.tb33661.x
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DETECTION OF GENE DEFECTS IN THE THALASSEMIAS AND RELATED DISORDERS*.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 1, doi. 10.1111/j.1749-6632.1980.tb33644.x
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DECREASING IRON STORES DURING INTENSIVE CHELATION THERAPY *.
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- Annals of the New York Academy of Sciences, 1980, v. 344, n. 1, p. 405, doi. 10.1111/j.1749-6632.1980.tb33679.x
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