## Abstract The diseases commonly confused with sickle cell anemia include sickle cellβ‐thalassemia in which synthesis of β^A^‐chains are completely suppressed (HbS‐β^O^‐thalassemia). We obtained hematologic measurements and studied globin biosynthesis in five patients with this disorder and compar
✦ LIBER ✦
Hyperkalemic hyperchloremic metabolic acidosis in a patient with sickle cell β-thalassemia
✍ Scribed by Moses Elisaf; Kostas Katopodis; Kostas Bouradas; Kostas C. Siamopoulos
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 239 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0361-8609
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