The Sickle Hemoglobinopathies—Genetic Analyses of Common Phenocopies and New Molecular Approaches to Treatment
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference20 articles.
1. The Clinical Features of Sickle Cell Disease;Serjeant,1974
2. The Thalassaemia Syndromes;Weatherall,1981
3. Sickle Cell Anemia. Molecular and cellular bases of therapeutic approaches;Dean;N Engl J Med,1978
4. Clinical implications of sickle cell trait and glucose-6-phosphate dehydrogenase deficiency in hospitalized black male patients;Heller;N Engl J Med,1979
5. Alpha-thalassaemia in adults with sickle cell trait;Steinberg;Br J Haematol,1975
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1. Overview of the current status of gene therapy for primary immune deficiencies (PIDs);Journal of Allergy and Clinical Immunology;2020-08
2. Cerebral blood flow velocity and language functioning in pediatric sickle cell disease;Journal of the International Neuropsychological Society;2010-02-03
3. Language Processing Deficits in Sickle Cell Disease in Young School-Age Children;Developmental Neuropsychology;2009-01-08
4. Chapter 45 Hematological diseases and stroke;Handbook of Clinical Neurology;2008
5. Neurobehavioral impact of sickle cell disease in early childhood;Journal of the International Neuropsychological Society;2007-10-18
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