1. Modell B, Darlison M. Global epidemiology of haemoglobin disorders and derived service indicators. Bull World Health Organ. 2008; 86:480–487.
Article
2. Little JA, McGowan VR, Kato GJ, et al. Combination erythropoietin-hydroxyurea therapy in sickle cell disease: experience from the National Institutes of Health and a literature review. Haematologica. 2006; 91:1076–1083.
3. Kaddam L, Fadl-Elmula I, Eisawi OA, et al. Gum Arabic as novel anti-oxidant agent in sickle cell anemia, phase II trial. BMC Hematol. 2017; 17:4.
Article
4. Pandey S, Sharma A, Dahia S, et al. Biochemical indicator of sickle cell disease: preliminary report from India. Indian J Clin Biochem. 2012; 27:191–195.
Article
5. Kotila T, Adedapo K, Adedapo A, Oluwasola O, Fakunle E, Brown B. Liver dysfunction in steady state sickle cell disease. Ann Hepatol. 2005; 4:261–263.
Article
6. Nduka N, Kazem Y, Saleh B. Variation in serum electrolytes and enzyme concentrations in patients with sickle cell disease. J Clin Pathol. 1995; 48:648–651.
Article
7. Yahaya IA. Biochemical features of hepatic dysfunction in Nigerians with sickle cell anaemia. Niger Postgrad Med J. 2012; 19:204–207.
8. Oparinde DP, Oghagbon EK, Okesina AB, Olatunji PO, Ojuawo AO. Role of hepatic enzymes in the biochemical assessment of the severity of sickle cell anemia. Trop Gastroenterol. 2006; 27:118–121.
9. Wright JG, Malia R, Cooper P, Thomas P, Preston FE, Serjeant GR. Protein C and protein S in homozygous sickle cell disease: does hepatic dysfunction contribute to low levels? Br J Haematol. 1997; 98:627–631.
Article
10. Thompson J, Reid M, Hambleton I, Serjeant GR. Albuminuria and renal function in homozygous sickle cell disease: observations from a cohort study. Arch Intern Med. 2007; 167:701–708.
Article
11. Aloni MN, Ngiyulu RM, Gini-Ehungu JL, et al. Renal function in children suffering from sickle cell disease: challenge of early detection in highly resource-scarce settings. PLoS One. 2014; 9:e96561.
Article
12. Morgan AG, Serjeant GR. Renal function in patients over 40 with homozygous sickle-cell disease. Br Med J (Clin Res Ed). 1981; 282:1181–1183.
Article
13. Gurkan S, Scarponi KJ, Hotchkiss H, Savage B, Drachtman R. Lactate dehydrogenase as a predictor of kidney involvement in patients with sickle cell anemia. Pediatr Nephrol. 2010; 25:2123–2127.
Article
14. Agoreyo FO, Nwanze N. Plasma sodium and potassium changes in sickle cell patients. Int J Genet Mol Biol. 2010; 2:14–19.
15. De Ceulaer K, Morgan AG, Choo-Kang E, Wilson WA, Serjeant GR. Serum urate concentrations in homozygous sickle cell disease. J Clin Pathol. 1981; 34:965–969.
Article
16. Walker BR, Alexander F. Uric acid excretion in sickle cell anemia. JAMA. 1971; 215:255–258.
Article
17. Rothschild BM, Sienknecht CW, Kaplan SB, Spindler JS. Sickle cell disease associated with uric acid deposition disease. Ann Rheum Dis. 1980; 39:392–395.
Article
18. Morgan AG, De Ceulaer K, Serjeant GR. Glomerular function and hyperuricaemia in sickle cell disease. J Clin Pathol. 1984; 37:1046–1049.
Article
19. Ali BH, Al-Husseni I, Beegam S, et al. Effect of gum arabic on oxidative stress and inflammation in adenine-induced chronic renal failure in rats. PLoS One. 2013; 8:e55242.
Article
20. Al-Majed AA, Abd-Allah AR, Al-Rikabi AC, Al-Shabanah OA, Mostafa AM. Effect of oral administration of arabic gum on cisplatin-induced nephrotoxicity in rats. J Biochem Mol Toxicol. 2003; 17:146–153.
Article
21. Kaddam L, FdleAlmula I, Eisawi OA, et al. Gum arabic as fetal hemoglobin inducing agent in sickle cell anemia; in vivo study. BMC Hematol. 2015; 15:19.
Article
22. Palmer SM, Kaufman RA, Salamone SJ, et al. Cobas Integra: clinical laboratory instrument with continuous and random-access capabilities. Clin Chem. 1995; 41:1751–1760.
Article
23. Gamal el-din AM, Mostafa AM, Al-Shabanah OA, Al-Bekairi AM, Nagi MN. Protective effect of arabic gum against acetaminophen-induced hepatotoxicity in mice. Pharmacol Res. 2003; 48:631–635.
Article
24. Ali BH, Ziada A, Blunden G. Biological effects of gum arabic: a review of some recent research. Food Chem Toxicol. 2009; 47:1–8.
Article
25. Ross AH, Eastwood MA, Brydon WG, Anderson JR, Anderson DM. A study of the effects of dietary gum arabic in humans. Am J Clin Nutr. 1983; 37:368–375.
Article
26. Ali BH, Beegam S, Al-Lawati I, Waly MI, Al Za'abi M, Nemmar A. Comparative efficacy of three brands of gum acacia on adenine-induced chronic renal failure in rats. Physiol Res. 2013; 62:47–56.
Article
27. Nasir O, Artunc F, Saeed A, et al. Effects of gum arabic (Acacia senegal) on water and electrolyte balance in healthy mice. J Ren Nutr. 2008; 18:230–238.
Article
28. Khalid SA, Musa AM, Saeed AM, et al. Manipulating dietary fibre: Gum arabic making friends of the colon and the kidney. Bioactive carbohydr Diet Fibre. 2014; 3:71–76.
Article
29. Al Mosawi AJ. The use of acacia gum in end stage renal failure. J Trop Pediatr. 2007; 53:362–365.
Article
30. Nasir O, Umbach AT, Rexhepaj R, et al. Effects of gum arabic (Acacia senegal) on renal function in diabetic mice. Kidney Blood Press Res. 2012; 35:365–372.
Article