Noguchi, CT

Hemoglobin S polymerization: primary determinant of the hemolytic and clinical severity of the sickling syndromes

Brittenham, G., Schechter, A., & Noguchi, C. (1985) · Blood

Hemoglobinopathies and Related DisordersHemoglobin structure and function

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Hydroxyurea increases fetal hemoglobin in cultured erythroid cells derived from normal individuals and patients with sickle cell anemia or beta-thalassemia

Fibach, E., Burke, L., Schechter, A., Noguchi, C., & Rodgers, G. (1993) · Blood

Hemoglobinopathies and Related DisordersHemoglobin structure and function

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Variation in fetal hemoglobin parameters and predicted hemoglobin S polymerization in sickle cell children in the first two years of life: Parisian Prospective Study on Sickle Cell Disease

Maier-Redelsperger, M., Noguchi, C., de Montalembert, M., Rodgers, G., Schechter, A., Gourbil, A., Blanchard, D., Jais, J., Ducrocq, R., & Peltier, J. (1994) · Blood

Hemoglobinopathies and Related DisordersHemoglobin structure and function

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