Area of Interest:

Biomedical Sciences

100%

Pharmacy

62%

Clinical Pharmacology

90%

Molecular Biology

75%

Genetics

55%

Research Publications in Numbers

Books
0

Chapters
0

Articles
20

Abstracts
0

Selected Publications

Ngor, S.R., D. Moustapha, K.P. Matar, D.J.P. Demba and B.N.O. Kesso et al., 2021. Influence of the genetic polymorphism of haptoglobin in the occurrence of retinopathy and nephropathy in diabetics subjects. Afr. J. Biochem. Res., 15: 9-14.
CrossRef | Direct Link |
Matar, K.P., D. Moustapha, B.N.O. Kesso, S.R. Ngor and T.N. Mareme, 2021. Association between uric acid and metabolic syndrome in homozygous sickle cell patients. Adv. Biol. Chem., 11: 142-148.
CrossRef | Direct Link |
Djite M., N.O.K. Barry, J.P.D. Diop, P.M. Kandji, E.H.M. Ndour, F. Gueye-Tall, N.F.C. Gueye, D. Doupa, R. Ndiaye-Dia, P.L. Sall, A. Cisse, P.A. Diop and P.M. Gueye, 2020. Haptoglobin polymorphism and hyperuricemia among stroke patients. American Journal of Biochemistry and Molecular Biology 10: 1-5.
CrossRef | Direct Link |
Barry, N.O.K., M. Djite, P.M. Kandji, F. Gueye-Tall, K. Hader, P. Lopez and P.M. Gueye, 2019. [Evaluation of the concordance of glycated hemoglobin values between the biochemistry D-10® (Biorad) and Minicap Flex piercing® (Sebia) systems]. Revue Francophone des Laboratoires, 2019: 19-23.
CrossRef | Direct Link |
Doupa, D., O. Boye, M. Ndiaye, M. Djite and P.M. Kandji et al., 2018. Prevalence of glucose-6-phosphate dehydrogenase (G6PD) deficiency (A-376/202) in homozygous sickle cell patients in Senegal and its clinical impact. Afr. J. Biochem. Res., 12: 55-62.
CrossRef | Direct Link |
Doupa, D., M. Djite, P.M Kandji, D. Makalou and S. Thiam et al., 2018. Polymorphism of the beta gene in homozygous sickle cell patients in senegal and its influence on the main complications of the disease. Adv. Biochem., 6: 19-25.
CrossRef | Direct Link |
Djite, M., N.O.K. Barry, J.P.D. Diop, F.B. Bah and P.M. Kandji et al., 2018. Haptoglobin polymorphism and disturbance of lipid parameters in victims of strokes. Adv. Biochem., 6: 47-52.
CrossRef |
Gueye, P.M., M. Djite, E.H.M. Ndour, F. Gueye-Tall and N.O.K. Barry et al., 2017. Haptoglobin polymorphism and cardiovascular risk factors in followed epileptic patients at Fann National University Hospital. Afr. J. Biochem. Res., 11: 43-48.
Doupa, D., M. Djite, P.M. Gueye, M. Seck and B.F. Faye et al., 2017. Biochemical and hematological profile of homozygous sickle cell patients in the stationary phase at the National Center for Blood Transfusion in Dakar. Int. J. Biol. Chem. Sci., 11: 1706-1715.
Gueye, P.M., M. Ndao, M. Djite, E.M. Ndour and B.F. Gueye-Tall et al., 2016. Evaluation of lipid profile and atherogenic index of plasma among stroke patients (AIP= Log TG/HDL-C). Asian J. Biochem. Pharm. Res., 6: 22-27.
Diouf, N.N., G. Lo, A. Sow-Ndoye, M. Djite, J.A.D. Tine and A. Diatta, 2014. Assessment of microalbuminuria and lipid profile in type 2 diabetics. Rev. Med. Brux., 35: 70-73.
Diouf, N.N., Y.F.O. Gaye, G. Lo, A.S. Ndoye, M. Djite, M. Diaw and S.C.T. Ndao, 2013. Proteinuria in pregnant women in the diagnosis of preeclampsia. Med. Black Afr., 60: 363-367.
Diouf, N.N., O. Boye, E.M. Saware, G. Lo, A.S. Ndoye, M. Djite and M.S. Niang, 2013. Prevalence of hyperuricemia in the Senegalese population. Med. Black Afr., 60: 437-440.