Search Results - "Ouarlhent, Y"

Epidemiological Study of Aplastic Anemia in Algeria for 844 Cases over 10 Years (2007-2016) by Mehdid, F, Rekkab, N, Oukid, S, Abad, MT, Bradai, M, Hamdi, S, Boukhemia, F, Hamladji, RM, Ahmed Nacer, R, Allouda, M, Ait Ali, H, Benaichou, S, Zouaoui, Z, Boughrira, S, Grifi, F, Cherif, N, Bensenouci, A, Kaci, Z, Belhani, M, Boudjerra, N, Serradj, F, Bekadja, MA, Kehal, M, Touhami, H, Saidi, D, Gareh, B, Saidi, M, Sahraoui, L, Ardjoun, Fz, Belakehal, SE, Chichoune, S, Ouarlhent, Y, Bendahmane, F, Mesli, N, Benhalilou, M, Sidi Mansour, N, Benmoufek, N, Ladj, S, Hadji, W, Bensmaine, N, Hendel, N, Arbaoui, F, Mehalhal, N, Hadji, S, Bachiri, A, Touati, L, Lakhdari, N, Ferroudj, N, Nekkal, S, Boudiaf, H, Achir, M, Fafa, A, Benakli, Malek

“…Introduction: The aim of this work is to establish an epidemiological approach of aplastic anemia (AA) in Algeria, to identify the different therapeutic…”
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Epidemiological Study on β-Thalassemia in Algeria by Grifi, Fatiha, Djenouni, A, Bougherira, S, Abad, MT, Boucherit, C, Boudjerra, N, Zidani, N, Aboura, C, Aribi, A, Belhani, M, Nekkal, S, Bouaricha, H, Benhassine, Fz, Ahmed Nacer, R, Tensaout, F, Ait amer, N, Hamladji, RM, Hamdi, S, Zatout, S, Sidi Mansour, N, Ouchenane, Z, Belakehal, SE, Mansour, H, Ghassoul, Y, Djilali, M, Ardjoun, Fz, Lakhdari, N, Touati, L, Bouterfa, N, Fenghour, R, Ait Ali, H, Graine, A, Allouda, M, Bouacha, A, Saidi, D, Sfaoui, W, Touhami, H, Bouchair, N, Hamani, N, Saidi, M, Nacib, R, Bekache, A, Dridi, R, Mesli, N, Houti, N, Ouarlhent, Y, Chichoune, S, Mehalhal, N, Zouaoui, Z, Benallal, A, Bekadja, MA, Benakli, Malek

“…Introduction : Among genetic diseases in hematology, β Thalassemia ranks second after sickle cell disorders in Algeria. Given the seriousness and cost of the…”
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