𝔖 Bobbio Scriptorium
✦   LIBER   ✦

α-Thalassemia among sickle cell anemia patients in various African populations

✍ Scribed by J. Pagnier; O. Dunda-Belkhodja; I. Zohoun; J. Teyssier; H. Baya; G. Jaeger; R. L. Nagel; D. Labie


Publisher
Springer
Year
1984
Tongue
English
Weight
229 KB
Volume
68
Category
Article
ISSN
0340-6717

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Influence of α-thalassemia trait on sple
✍ Adekile, A.D.; Tuli, M.; Haider, M.Z.; Al-Zaabi, K.; Mohannadi, S.; Owunwanne, A 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 614 KB

Spleen function was studied in a group of 20 Kuwaiti SS patients (aged 2-12 years), using 99mTc-labeled tin colloid scintigraphy. They were screened for the alpha-thalassemia determinants which are prevalent in the Arabian Peninsula [-alpha (3.7 kb) deletion, alpha2-globin gene polyadenylation signa

Functional characteristics of red cells
✍ Dr. E. C. Abraham; T. H. J. Huisman 📂 Article 📅 1980 🏛 John Wiley and Sons 🌐 English ⚖ 345 KB 👁 2 views

Oxygen equilibrium curves, red cell indices, 2,3-DPG levels, and the percentages of ISC and Hb F were determined for red cell fractions isolated by Dextran 40 density gradient centrifugation from blood of a sickle cell anemia (SS) patient, an SS patient with an additional homozygosity for ct-thalass

Determination of β-globin gene cluster h
✍ Arends, A.; Alvarez, M.; Velázquez, D.; Bravo, M.; Salazar, R.; Guevara, J.M.; C 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 32 KB 👁 1 views

Sickle cell anemia and ␣-thalassemia have a heterogeneous distribution in Venezuela with a high frequency in the coastal area (sea level) and few cases in the mountains. Most of our population is an ethnic admixture of Europeans (Spaniards colonists), Africans (slaves), and Amerindians. The purpose