SEARCH

SEARCH BY CITATION

REFERENCES

  • 1
    Pippard MJ. Functions of the spleen. In: CuschieriA, ForbesCD, editors. Disorders of the spleen. London, UK: Blackwell Scientific Publications; 1994. p 2550.
  • 2
    Neiman RS, Orazi A. Functions of the spleen. In: Disorders of the spleen 2nd edition. Philadelphia, PA: W.B. Saunders Company; 1999. p 838.
  • 3
    Neiman RS, Orazi A. Non-neoplastic disorders of erythrocytes, granulocytes and platelets. In: Disorders of the spleen. 2nd edition. Philadelphia, PA: W.B. Saunders Company; 1999. p 147166.
  • 4
    Pearson HA, Spencer RP, Cornelius EA. Functional asplenia in sickle anemia. N Engl J Med 1969; 282: 923926.
  • 5
    Adekile AD, McKie KM, Adeodu OO, Sulzer AJ, McKie VC, Kutlar F, Ramachandra M, Kaine W, Akenzua GI, Okolo AA, Asindi AA, Obinyan EA, Ogala WN, Ibrahim M, Huisman THJ. The spleen in sickle cell anemia: comparative studies of Nigerian and US patients. Am J Hematol 1993; 42: 316.
  • 6
    Adekile AD, Gu L-H, Baysal E, Haider MZ, Al-Fuzae L, Aboobacker KC, Al-Rashied A, Huisman THJ. Molecular characterization of α-thalassaemia determinants, β-thalassaemia alleles and βS haplotypes among Kuwaiti Arabs. Acta Haematol 1994; 92: 176181.
  • 7
    Miller BA, Olivieri N, Salameh M, Ahmed M, Antognetti G, Huisman THJ, Nathan DG, Orkin SH. Molecular analysis of the high-hemoglobin-F phenotype in Saudi Arabian sickle cell anemia. N Engl J Med 1987; 316: 244250.
  • 8
    Adekile AD, Haider MZ. Morbidity, βS haplotype and α-globin gene patterns in SS Patients from Kuwait. Acta Haematol 1996; 96: 150154.
  • 9
    Owunwanne A, Halker R, Al-Rasheed A, Abubacker KC, Abdel-Dayem H. Radionuclide imaging of the spleen with heat-denatured technetium-99m RBC when the splenic reticuloendothelial system seems impaired. J Nucl Med 1988; 29: 320323.
  • 10
    Adekile AD, Tuli M, Haider MZ, AL-Zaabi K, Mohannadi S, Owunwanne A. Influence of α-thal trait on spleen function in sickle cell anemia patients with high Hb F. Am J Hematol 1996; 53: 15.
  • 11
    Aburano T, Katada R, Shuke N, Aburano T, Katada R, Shuke N, Yamamoto W, Kawakami T, Makino I, Sato J, Ishikawa Y. Discordant splenic uptake of Tc-99m colloid and Tc-99m denatured RBC in candidiasis-endocrinopathy syndrome. Ann Nucl Med 1997; 11: 335338.
  • 12
    Graves DS, Stadalnik RC. Anatomic and functional asplenia- absence of the splenic image during colloid scintigraphy. Semin Nucl Med 1982; 12: 9596.
  • 13
    Spencer RP, Dhawan V, Suresh K, Antar MA, Sziklas JJ, Wasserman I. Causes and temporal sequence of onset of functional asplenia in adults. Clin Nucl Med 1978; 3: 1718.
  • 14
    Klausner MA, Hirsch LJ, Leblond PF, Chamberlain JK, Klempterer MR, Segel GB. Contrasting splenic mechanisms in the blood clearance of blood cells and colloidal particles. Blood 1975; 46: 965976.
  • 15
    Atkins HL, Thomas SR, Buddenmeyer U, Chervu LR. MIRD dose estimate report No. 14: radiation absorbed dose from technetium-99m-labeled red blood cells. J Nucl Med 1990; 31: 378380.
  • 16
    Product Information: Amerscan hepatate II technetium agent for liver/spleen scintigraphy. Amersham International Buckinghamshire, UK 1990.
  • 17
    Righetti PG. Practical application of isoelectric focusing in hemoglobin separation and identification. In: HuismanTHJ, editor. The hemoglobinopathies. Methods in hematology series, Vol. 15. Edinburgh: Churchill Livingstone; 1986. p 4770.
  • 18
    Bissé E, Wieland H. High-performance liquid chromatographic separation of human hemoglobins. Simultaneous quantitation of fetal and glycated hemoglobins. J Chromatogr 1988; 434: 95110.
  • 19
    Poncz M, Solowiejczyk D, Harpel B, Mory Y, Schwartz E, Surrey S. Construction of human gene libraries from small amounts of peripheral blood: analysis of βS-like globin genes. Hemoglobin 1982; 6: 2736.
  • 20
    Baysal E, Huisman THJ. Detection of common deletional α-thalassemia-2 determinants by PCR. Am J Hematol 1994; 46: 208213.
  • 21
    Dimovski AJ, Öner C, Agarwal S, Gu Y-C, Kutlar F, Lanclos KD, Huisman THJ. Certain mutations observed in the 5′ sequences of the Gγ- and Aγ-globin genes of S chromosomes are specific for chromosomes with major haplotypes. Acta Haematol 1991; 85: 7987.
  • 22
    Steinberg MH, Rosenstock W, Coleman MB, Adams JG, Platt O, Cedano M, Reider RF, Wilson JT, Milner P, West S, The Cooperative Study Group of Sickle Cell Disease. Effects of thalassemia and microcytosis on the hematologic and vaso-occlusive severity of sickle cell anemia. Blood 1984; 63: 1353.
  • 23
    Adams RJ, Kutlar A, McKie V, Carl E, Nichols FT, Liu JC, McKie K, Clary A. α-Thalassemia and stroke risk in sickle cell anemia. Am J Hematol 1994; 45: 279.