Sickle-cell disease
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference93 articles.
1. Structural analysis of the 5' flanking region of the (3-globin gene in African sickle cell anemia patients: further evidence for three origins of the sickle cell mutation in Africa;Chebloune;Proc Natl Acad Sci USA,1988
2. Geographical survey of βs-globin gene haplotypes: evidence for an independent Asian origin of the sickle-cell; mutation;Kulozik;Am J Hum Genet,1986
3. Recurrent folic acid deficiency in sickle cell disease;Lopez;Am J Dis Child,1973
4. Outbreak of aplastic crises in sickle cell anaemia associated with parvovirus-like agent;Serjeant;Lancet,1981
5. Prevention of pneumococcal infection in children with homozygous sickle cell disease;John;BMJ,1984
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1. Urine concentration impairment in sickle cell anemia: genuine nephrogenic diabetes insipidus or osmotic diuresis?;American Journal of Physiology-Renal Physiology;2024-02-01
2. Red Blood Cell Exchange as a Valid Therapeutic Approach for Pregnancy Management in Sickle Cell Disease: Three Explicative Cases and Systematic Review of Literature;Journal of Clinical Medicine;2023-11-16
3. Subperiosteal Orbital Hematoma: A Rare Clinical Manifestation of Sickle Cell Disease - A Case Report;Case Reports in Ophthalmology;2023-08-18
4. A Comprehensive Review of Pregnancy in Sickle Cell Disease;Cureus;2023-06-30
5. Prevalence of orofacial alterations in patients with sickle-cell disease: Systematic review and meta-analysis;Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology;2023-05
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