Rezultati

Paper Electrophoresis of Abnormal Hemoglobins and Its Clinical Applications od Arno G. Motulsky, Milton H. Paul, EMMETT L. DURRUM

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Malaria continues to select for sickle cell trait in Central Africa od Éric Elguero, Lucrèce M. Délicat-Loembet, Virginie Rougeron, Céline Arnathau, Benjamín Roche, Pierre Becquart, Jean‐Paul Gonzalez, Dieudonné Nkoghe, Lucas Sica, Eric M. Leroy, Patrick Durand, Francisco J. Ayala, Benjamin Ollomo, François Renaud, Franck Prugnolle

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Combinations of Hemoglobin G, Hemoglobin S and Thalassemia Occurring in One Family od Herbert C. Schwartz, Theodore H. Spaet, W. W. Zuelzer, James V. Neel, Arthur Robinson, Sarah Kaufman

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High fetal hemoglobin production in sickle cell anemia in the eastern province of Saudi Arabia is genetically determined od BA Miller, Mohammed Salameh, KK Mueen Ahmed, J. S. Wainscoat, Giovanna Antognetti, Stuart H. Orkin, D. J. Weatherall, DG Nathan

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Genetic Aspects of Sickle Cell Anemia and Microdrepanocytic Disease od E Silvestroni, I Bianco

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Sickle cell disease in tribal populations in India od Roshan Colah, Malay B. Mukherjee, Snehal L. Martin, Kanjaksha Ghosh

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A New Inherited Abnormality of Hemoglobin and Its Interaction with Sickle Cell Hemoglobin od Eugene Kaplan, Wolf W. Zuelzer, James V. Neel

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Student screening for inherited blood disorders in Bahrain od S. Al Arrayed, Nada Hafadh, Shreyans Amrutlal Amin, H. Al Mukhareq, Hassan Sanad

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Neonatal screening program for hemoglobinopathies in the city of São Carlos, state of São Paulo, Brazil: analysis of a series of cases od Camila de Azevedo Silva, Letícia Botigeli Baldim, Geiza César Nhoncanse, Isabeth da Fonseca Estevão, Débora Gusmão Melo

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Hemoglobin D Los Angeles in Two Caucasian Families: Hemoglobin SD Disease and Hemoglobin D Thalassemia od Rose G. Schneider, Satoshi Ueda, Jack B. Alperin, William C. Levin, Richard T. Jones, Bernadine Brimhall

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Sickle cell disease: Selected aspects of pathophysiology od Tamás Alexy, Suvimol Sangkatumvong, Philippe Connes, Eszter Pais, Julien Tripette, Jean Barthélemy, Timothy S. Fisher, Herbert J. Meiselman, Michael C. K. Khoo, Thomas D. Coates

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Burkitt's lymphoma and sickle cell trait. od Malcolm C. Pike, Richard H. Morrow, A. Kisuule, J Mafigiri

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ACSM and CHAMP Summit on Sickle Cell Trait od Francis G. O’Connor, Michael F. Bergeron, Joyce A. Cantrell, Philippe Connes, Kimberly G. Harmon, Edward Donnell Ivy, John A. Kark, DAVE KLOSSNER, Peter Lisman, BRYCE K. MEYERS, Karen O’Brien, Kwaku Ohene‐Frempong, Alexis A. Thompson, James R. Whitehead, Patricia A. Deuster

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Sickle cell trait and the risk of venous thromboembolism among blacks od Harland Austin, Nigel S. Key, Jane M. Benson, Cathy Lally, Nicole F. Dowling, Carolyn Whitsett, W. Craig Hooper

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Impaired Antibody Response to Intravenous Immunization in Sickle Cell Anemia od Allen D. Schwartz, Howard A. Pearson

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Epidemiological profile of common haemoglobinopathies in Arab countries od Hanan Hamamy, Nasir Al‐Allawi

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Renal Medullary Carcinoma Response to Chemotherapy: a Referral Center Experience in Brazil od Marina Cavalcanti Maroja Silvino, Camila Motta Venchiarutti Moniz, Gustavo Henrique Munhoz Piotto, Sheila Aparecida Coelho Siqueira, Ariel Galapo Kann, Carlos Dzik

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Anaesthesia in Sickle-cell States: A Plea for Simplicity od Kwadwo A. Oduro, J.F. Searle

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Alpha chain hemoglobins with electrophoretic mobility similar to that of hemoglobin S in a newborn screening program od Marcilene Rezende Silva, Shimene Mascarenhas Sendin, Isabela Couto de Oliveira Araujo, Fernanda Silva Pimentel, Marcos Borato Viana

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Effects of alpha-thalassemia and sickle polymerization tendency on the urine-concentrating defect of individuals with sickle cell trait. od Aakash Gupta, K A Kirchner, Rosie Nicholson, Junius G. Adams, Alan N. Schechter, CT Noguchi, Martin H. Steinberg

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