Gene deletions of glutathione S-transferase and iron status in sickle cell patients by Paula Juliana Antoniazzo Zamaro

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Comparing electrophoresis at alkaline pH and high performance liquid chromatography to diagnose Hb S-like hemoglobin by Renan Gracia de Oliveira, Paula Juliana Antoniazzo Zamaro, Claudia Regina Bonini-Domingos

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Diagnóstico laboratorial de hemoglobinas semelhantes à HbS by Paula Juliana Antoniazzo Zamaro, Andréia A. Canalli, Wilson Araujo da Silva Júnior, Claudia Regina Bonini Domingos

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The Neonatal Screening Program in Brazil, Focus on Sickle Cell Disease (SCD) by Ana C. Silva-Pinto, Maria Cândida Alencar de Queiroz, Paula Juliana Antoniazzo Zamaro, Miranete Arruda, Helena Pimentel dos Santos

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