Works matching IS 00778923 AND DT 1989 AND VI 565 AND IP 1
Results: 87
Geography and the Clinical Picture of Sickle Cell Disease.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 109, doi. 10.1111/j.1749-6632.1989.tb24157.x
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Pain Management in Sickle Cell Disease.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 189, doi. 10.1111/j.1749-6632.1989.tb24166.x
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Protein C Levels in Sickle Cell Diseases<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 430, doi. 10.1111/j.1749-6632.1989.tb24213.x
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Bone Scintigraphy in Patients with Sickle Cell Disease and Osteomyelitis.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 452, doi. 10.1111/j.1749-6632.1989.tb24222.x
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Effect of Sickle Cell Shape on Filterability.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 463, doi. 10.1111/j.1749-6632.1989.tb24226.x
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Molecular Genetic Approach to Newborn Screening for Sickle Cell Disease.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 434, doi. 10.1111/j.1749-6632.1989.tb24215.x
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Modification of the Intraerythrocytic Hemoglobin S Affinity for Oxygen by a Zinc Chelator<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 360, doi. 10.1111/j.1749-6632.1989.tb24187.x
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Volume Regulation of Sickle Cells.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 371, doi. 10.1111/j.1749-6632.1989.tb24192.x
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Influence of Amidation of Glu 43(β) on the Polymerization of Deoxy Hemoglobin S<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 416, doi. 10.1111/j.1749-6632.1989.tb24208.x
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2,6-Di(isobutyrylamino)hexanoic Acid as a Potential Therapeutic Agent for the Treament of Sickle Cell Disease.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 353, doi. 10.1111/j.1749-6632.1989.tb24184.x
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Nature of Cardiac Findings in Sickle Cell Anemia.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 393, doi. 10.1111/j.1749-6632.1989.tb24200.x
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Regulatory Regions Flanking the Human Fetal γ-Globin Genes.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 13, doi. 10.1111/j.1749-6632.1989.tb24145.x
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Observation of Intracellular Sickle Cell Hemoglobin Polymers with a Differential Polarization Microscope<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 438, doi. 10.1111/j.1749-6632.1989.tb24217.x
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Electron Microscopic Quantitation of Hemoglobin S Polymer in SS Red Blood Cells and Rheological Correlation.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 409, doi. 10.1111/j.1749-6632.1989.tb24206.x
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Experience with an Animal Model for Sickle Cell Vasoocclusion.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 379, doi. 10.1111/j.1749-6632.1989.tb24195.x
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A Profile of Sickle Cell Disease in Nigeria.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 126, doi. 10.1111/j.1749-6632.1989.tb24159.x
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Polymerization of Partially Liganded Hemoglobin S<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 356, doi. 10.1111/j.1749-6632.1989.tb24185.x
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Erythrocyte Membrane Protein Kinase C in Sickle Cell Disease.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 449, doi. 10.1111/j.1749-6632.1989.tb24221.x
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Membrane Modifiers in Sickle Cell Disease.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 247, doi. 10.1111/j.1749-6632.1989.tb24173.x
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The Natural History of Sickle Cell Disease<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 104, doi. 10.1111/j.1749-6632.1989.tb24156.x
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Intracellular Polymerization.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 75, doi. 10.1111/j.1749-6632.1989.tb24152.x
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The Possible Role of Genetic Modifiers in the Clinical Severity of Sickle Cell Syndromes<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 207, doi. 10.1111/j.1749-6632.1989.tb24167.x
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Current Perspectives on the Kinetics of Hemoglobin S Gelation.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 53, doi. 10.1111/j.1749-6632.1989.tb24150.x
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Lipid Alterations and Cellular Properties of Sickle Red Cells<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 86, doi. 10.1111/j.1749-6632.1989.tb24154.x
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Modulation of the Yield Stress of Sickle and Normal Blood by Fibrinogen<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 440, doi. 10.1111/j.1749-6632.1989.tb24218.x
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The Flow of Sickle Red Cells through Microvascular Bifurcations<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 422, doi. 10.1111/j.1749-6632.1989.tb24210.x
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Inhibition of Deoxygenation-Induce Cation Fluxes in Sickle Cells by Stilbene Disulfonates.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 404, doi. 10.1111/j.1749-6632.1989.tb24204.x
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Hemorheologic Parameters in Children with Homozygous Sickle Cell Anemia Receiving Chronic Red Cell Transfusions for Large Cerebral Vessel Vasculopathy.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 455, doi. 10.1111/j.1749-6632.1989.tb24223.x
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Delayed Growth and Sexual Maturation in Sickle Cell Disease.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 137, doi. 10.1111/j.1749-6632.1989.tb24160.x
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α-thalassemia among Pediatric Hemoglobin S Homozygotes.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 381, doi. 10.1111/j.1749-6632.1989.tb24196.x
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Rheological Properties of SickleErythrocytes in the Steady State Predict the Frequency and Severity of the Sickle Cell Painful Crisis.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 363, doi. 10.1111/j.1749-6632.1989.tb24188.x
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Preface.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. xiii, doi. 10.1111/j.1749-6632.1989.tb24143.x
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Genetic Determinant for Increased Fetal Hemoglobin Linked to the Benin Haplotype in Some Sickle Cell Anemia Patients<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 385, doi. 10.1111/j.1749-6632.1989.tb24198.x
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Erythrocytic and Vascular Factors Influencing the Microcirculatory Behavior of Blood in Sickle Cell Anemia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 316, doi. 10.1111/j.1749-6632.1989.tb24179.x
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Rheological Action of Oxpentifylline and Structurally Related Xanthine Derivatives on Sickle Cells.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 466, doi. 10.1111/j.1749-6632.1989.tb24227.x
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Alpha Thalassemia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 213, doi. 10.1111/j.1749-6632.1989.tb24169.x
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Rheological and Adherence Properties of Sickle Cells<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 327, doi. 10.1111/j.1749-6632.1989.tb24180.x
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Blood Center Initiatives and Role in Sickle Cell Disease.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 367, doi. 10.1111/j.1749-6632.1989.tb24190.x
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The Impact of a Child with Sickle Cell Disease on Family Dynamics.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 161, doi. 10.1111/j.1749-6632.1989.tb24163.x
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Hemodynamic Studies in Sickle Cell Disease.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 338, doi. 10.1111/j.1749-6632.1989.tb24181.x
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Nonreductive Modification of Proteins by Glyceraldehyde<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 349, doi. 10.1111/j.1749-6632.1989.tb24183.x
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Independent Origin of a β<sup>S</sup>-Globin Gene in a Caucasian with Sickle Cell Anemia.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 389, doi. 10.1111/j.1749-6632.1989.tb24199.x
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Adjustment and Coping in Adolescents with Sickle Cell Disease.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 172, doi. 10.1111/j.1749-6632.1989.tb24164.x
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The Emerging Complexity of Genetic Control of Persistent Fetal Hemoglobin Biosynthesis in Adults.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 23, doi. 10.1111/j.1749-6632.1989.tb24146.x
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Kinetic Models and the Pathophysiology of Sickle Cell Disease<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 63, doi. 10.1111/j.1749-6632.1989.tb24151.x
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Saudi Arabian Sickle Cell Anemia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 143, doi. 10.1111/j.1749-6632.1989.tb24161.x
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Rare Blood for Patients with Sickle Cell Anemia.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 432, doi. 10.1111/j.1749-6632.1989.tb24214.x
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Known and Potential Sources for Epistatic Effects in Sickle Cell Anemia.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 228, doi. 10.1111/j.1749-6632.1989.tb24171.x
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Covalent Chemical Modifiers of Sickle Cell Hemoglobin<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 239, doi. 10.1111/j.1749-6632.1989.tb24172.x
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The Rheology of Sickle Cell Hemoglobin<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1989, v. 565, n. 1, p. 279, doi. 10.1111/j.1749-6632.1989.tb24175.x
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