Author:
El-Tagui Mona,Tawfik Sameh,Al-Hussain AbdulGawad Eman,Gad Alaa,El Sherbiny Mohamed,Saad Nassim Mariam
Publisher
Springer Science and Business Media LLC
Reference35 articles.
1. Rees DC, Williams TN, Gladwin MT (2010) Sickle-cell disease. Lancet 376:2018–2031
2. Ajinkpang S, Anim-Boamah O, Bimpong KA, Kanton FJ, Pwavra JB, Abdul-Mumin A (2022) Sickle cell disease in children: knowledge and home-based management strategies among caregivers at a Tertiary facility in Northern Ghana. BioMed Res Int
3. Kim SK, Miller JH (2002) Natural history and distribution of bone and bone marrow infarction in sickle hemoglobinopathies. J Nucl Med 43:896–900
4. Neonato MG, Guilloud-Bataille M, Beauvais P, Begue P, Belloy M, Benkerrou M, Ducrocq R, Maier-Redelsperger M, de Montalembert M, Quinet B et al (2000) Acute clinical events in 299 homozygous sickle cell patients living in France. Eur J Haematol 65:155–164
5. Ebong WW (1987) Septic arthritis in patients with sickle-cell disease. Br J Rheumatol 26:99–102