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Journal Abstract Search

184 related items for PubMed ID: 28276593

  • 1. Association between sickle cell anemia and alpha thalassemia reveals a high prevalence of the α3.7 triplication in congolese patients than in worldwide series.
    Mikobi TM, Lukusa PT, Aloni MN, Lumaka A, Akilimali PZ, Devriendt K, Matthijs G, Mbuyi Muamba JM, Race V.
    J Clin Lab Anal; 2018 Jan; 32(1):. PubMed ID: 28276593
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  • 2. alpha-thalassemia in Bantu population from Congo-Brazzaville: its interaction with sickle cell anemia.
    Mouélé R, Pambou O, Feingold J, Galactéros F.
    Hum Hered; 2000 Jan; 50(2):118-25. PubMed ID: 10799970
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  • 3. Serum Soluble Transferrin Receptor Concentrations Are Elevated in Congolese Children with Glucose-6-Phosphate Dehydrogenase Variants, but Not Sickle Cell Variants or α-Thalassemia.
    Barker MK, Henderson AM, Naguib K, Vercauteren SM, Devlin AM, Albert AY, Bahizire E, Tugirimana PL, Akilimali PZ, Boy E, Green TJ, Karakochuk CD.
    J Nutr; 2017 Sep; 147(9):1785-1794. PubMed ID: 28768839
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  • 4. The clinical characteristics of Congolese children and adolescents suffering from sickle-cell anemia are marked by the high frequencies of epistaxis compared to Western series.
    Kazadi AL, Ngiyulu RM, Gini-Ehungu JL, Mbuyi-Muamba JM, Aloni MN.
    Pediatr Hematol Oncol; 2019 Aug; 36(5):267-276. PubMed ID: 31339399
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  • 5. Influence of alpha thalassemia on clinical and laboratory parameters among nigerian children with sickle cell anemia.
    Olatunya OS, Albuquerque DM, Adekile A, Costa FF.
    J Clin Lab Anal; 2019 Feb; 33(2):e22656. PubMed ID: 30129219
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  • 6. The co-inheritance of alpha-thalassemia and sickle cell anemia is associated with better hematological indices and lower consultations rate in Cameroonian patients and could improve their survival.
    Rumaney MB, Ngo Bitoungui VJ, Vorster AA, Ramesar R, Kengne AP, Ngogang J, Wonkam A.
    PLoS One; 2014 Feb; 9(6):e100516. PubMed ID: 24978191
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  • 7. Prevalence of sickle cell disease in a pediatric population suffering from severe infections: a Congolese experience.
    Kondani DA, Gini-Ehungu JL, Bodi JM, Ekulu PM, Kunuanunua TS, Aloni MN.
    Hemoglobin; 2014 Feb; 38(4):225-9. PubMed ID: 25023084
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  • 11. Prevalence and Genetic Analysis of α- and β-Thalassemia and Sickle Cell Anemia in Southwest Iran.
    Nezhad FH, Nezhad KH, Choghakabodi PM, Keikhaei B.
    J Epidemiol Glob Health; 2018 Dec; 8(3-4):189-195. PubMed ID: 30864762
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  • 14. Clinical phenotypes and the biological parameters of Congolese patients suffering from sickle cell anemia: A first report from Central Africa.
    Mikobi TM, Lukusa Tshilobo P, Aloni MN, Akilimali PZ, Mvumbi-Lelo G, Mbuyi-Muamba JM.
    J Clin Lab Anal; 2017 Nov; 31(6):. PubMed ID: 28116772
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  • 16. Challenge of managing sickle cell disease in a pediatric population living in kinshasa, democratic republic of congo: a sickle cell center experience.
    Aloni MN, Nkee L.
    Hemoglobin; 2014 Nov; 38(3):196-200. PubMed ID: 24669956
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  • 17. High rate of sickle cell anaemia in Sub-Saharan Africa underlines the need to screen all children with severe anaemia for the disease.
    Kadima BT, Gini Ehungu JL, Ngiyulu RM, Ekulu PM, Aloni MN.
    Acta Paediatr; 2015 Dec; 104(12):1269-73. PubMed ID: 25982693
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  • 18. Alpha thalassemia and stroke risk in sickle cell anemia.
    Adams RJ, Kutlar A, McKie V, Carl E, Nichols FT, Liu JC, McKie K, Clary A.
    Am J Hematol; 1994 Apr; 45(4):279-82. PubMed ID: 8178798
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