T. M. Mikobi

Correlation between the Lactate Dehydrogenase Levels with Laboratory Variables in the Clinical Severity of Sickle Cell Anemia in Congolese Patients

G. Matthijs, V. Racé, J. Muyembé-Tamfum, 2015, PloS one.

Protective BCL11A and HBS1L‐MYB polymorphisms in a cohort of 102 Congolese patients suffering from sickle cell anemia

K. Devriendt, G. Matthijs, A. Lumaka, 2018, Journal of clinical laboratory analysis.

Association between sickle cell anemia and alpha thalassemia reveals a high prevalence of the α3.7 triplication in congolese patients than in worldwide series

K. Devriendt, G. Matthijs, A. Lumaka, 2018, Journal of clinical laboratory analysis.

Homozygous Deletion Alpha-Thalassemia and Hereditary Persistence of Fetal Hemoglobin, Two Genetic Factors Predictive the Reduction of Morbidity and Mortality During Pregnancy in Sickle Cell Patients. A Report from the Democratic Republic of Congo

Prosper Lukusa, T. M. Mikobi, Jean-Marie Mbuyi Muamba, 2019, Mediterranean journal of hematology and infectious diseases.

Clinical phenotypes and the biological parameters of Congolese patients suffering from sickle cell anemia: A first report from Central Africa

M. Aloni, P. Akilimali, T. M. Mikobi, 2017, Journal of clinical laboratory analysis.

Sickle cell disease and pregnancy profile of complicated malaria in 982 pregnancies in Kinshasa

Prosper Lukusa, P. Akilimali, T. M. Mikobi, 2022, PloS one.

Clinical and biological profile of Sickle Cell Anemia children in a rural area in Central Africa.

K. Devriendt, G. Matthijs, A. Lumaka, 2023, Hematology.

Clinical and laboratory characterization of adult sickle cell anemia patients in Kinshasa

K. Devriendt, G. Matthijs, A. Lumaka, 2022, PloS one.