Search Results - "Menif, S"

P1549: NOVEL SLC4A1 GENE MUTATIONS IN HEREDITARY SPHEROCYTOSIS BAND 3 PROTEIN‐DEFICIENT TUNISIAN PATIENTS by TRABELSI, N., Kraiem, I., Menif, S., Abbes, S.

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5613458 BLOOD MICROPARTICLES: A TOOL OF EVALUATING THE EFFECT OF TRANSFUSION IN SICKLE CELL DISEASE PATIENTS by Khalfaoui, K., Chebbi, M., Safra, I., Barmate, M., Chaouechi, D., Benkhaled, M., Ouederni, M., Mellouli, F., Menif, S., Moumni, I.

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5613312 PLASMATIC MICROPARTICLES AS POTENTIAL BIOMARKERS IN THE PREVENTIVE DIAGNOSIS OF BETA THALASSEMIA by Chebbi, M., Khalfaoui, K., Saidani, S., Safra, I., Barmate, M., Chaouechi, D., Ben Khaled, M., Ouederni, M., Mellouli, F., Menif, S., Moumni, I.

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P105: BLOOD MICROVESICLES AS BIOMARKERS TO PREDICT VASO‐OCCLUSIVE CRISIS IN SICKLE CELL ANEMIA by Chebbi, M, Moumni, I, Khalfaoui, K, Safra, I, Barmate, M, Chaouechi, D, Benkhaled, M, Ouederni, M, Mellouli, F, Menif, S

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P‐077: POTENTIAL BIOMARKERS IN THE PREVENTIVE DIAGNOSIS OF ACUTE COMPLICATIONS IN SICKLE CELL DISEASE by I., MOUMNI, K., KHALFAOUI, M., CHEBBI, I., SAFRA, B., MBARKA, D., CHAOUACHI, M., BEN KHALED, M., OUEDERNI, F., MELLOULI, S., MENIF

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PB1812: CORE BINDING FACTOR ACUTE MYELOID LEUKEMIA IN PEDIATRIC POPULATION: THE RESULTS OF A MONOCENTRIC EXPERIENCE by Charfi, H., Kassar, O., Charfi, M., Fakhfakh, Y., Senanna, H., Menif, S., Kallel, F., Frikha, I., Ben Amor, I., Khalifa, L., Medhaffer, M., Hadiji, S., Elloumi, M.

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PB1843: ACUTE MYELOID LEUKEMIA WITH PHILADELPHIA CHROMOSOME: EXPERIENCE OF SFAX HEMATOLOGY DEPARTMENT by Siala, N., Khelifa, L., Frikha, I., Kallel, F., Sennana, H., Menif, S., Ben abdeljalil, N., Laddeb, S., Fakhfekh, Y., Ben Amor, I., Kassar, O., Hadiji, S., Charfi, M., Ben othmen, T., Medhaffar, M., Elloumi, M.

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P106: EARLY PREVENTIVE DIAGNOSIS OF HEMOLYTIC ANEMIA IN SICKLE CELL PATIENTS BY DETECTING THE TRIGGERING OF ERYPTOSIS by Khalfaoui, K, Moumni, I, Chebbi, M, Safra, I, Barmate, M, Chaouechi, D, Benkhaled, M, Ouederni, M, Mellouli, F, Menif, S

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Efficacy of imatinib in FIP1L1-PDGFRA positive hypereosinophilic syndrome by Menif, S, Ben Romdhane, N, Hafsia, R

“…Hypereosinophilic syndromes (HES) are a heterogeneous group of disorders characterized by marked peripheral blood and tissue eosinophilia resulting in organ…”
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Epidemiological and biological characteristics of G6PD deficiency in women in Tunisia by Chaabouni, S., Zanned, S., Sahli, E., Kasdallah, M., Chaouechi, D., Menif, S.

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Quantitative detection of bcr-abl transcripts in chronic myeloid leukemia by Menif, S., Zarrouki, S., Jeddi, R., Alaya, N. ben, Ali, Z. BelHadj, Abid, H. Ben, Hdeiji, S., Elloumi, M., Khlif, A., Meddeb, B., Dellagi, K.

“…The optimal management of malignant haematological disorders depend on the degree of tumor load reduction after therapy. Chronic myeloid leukemia constitutes a…”
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EZH2, new diagnosis and prognosis marker in acute myeloid leukemia patients by Mechaal, Amal, Menif, Samia, Abbes, Salem, Safra, Ines

“…Acute myeloid leukemia (AML) is a heterogeneous disease. The discovery of novel discriminative biomarkers remains of utmost value for improving outcome…”
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Efficacité de l’imatinib dans les syndromes hyperéosinophiliques associés au transcrit FIP1L1– PDGFRA by Menif, S., Ben Romdhane, N., Hafsia, R.

“…Le syndrome hyperéosinophilique est un diagnostic d’exclusion à évoquer devant une hyperéosinophilie importante et persistante pour laquelle aucune étiologie…”
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FIP1L1–PDGFRA positive chronic eosinophilic leukemia in Tunisian patients by Menif, S., Omri, H., Hafsia, R., Ben Romdhane, N., Turki, S., Meddeb, B., Dellagi, K.

“…Hypereosinophilic syndromes (HES) are a heterogenous group of rare disorders characterized by sustained and otherwise unexplained overproduction of eosinophils…”
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Eryptosis and circulating blood cells microparticules in sickle cell diseases by Moumni, I, Khalfaoui, K, Safra, I, Chebbi, M, Barmate, M, chaouechi, D, Ben khaled, M, Ouederni, M, Mellouli, F, Menif, S

“…Abstract Sickle cell disease(SCD)is a monogenic disease, in which the severity and symptoms vary widely.The sickle cell mutation is the origin of all…”
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P106: EARLY PREVENTIVE DIAGNOSIS OF HEMOLYTIC ANEMIA IN SICKLE CELL PATIENTS BY DETECTING THE TRIGGERING OF ERYPTOSIS by Khalfaoui, K, Moumni, I, Chebbi, M, Safra, I, Barmate, M, Chaouechi, D, Benkhaled, M, Ouederni, M, Mellouli, F, Menif, S

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Epidemiological Approach of Chronic Myeloid Leukemia. Algerian-Tunisian Study by Djouadi, K, Abdennebi, N, Harieche, F, Ahmed Nacer, R, Hamladji, RM, Bouchakour, A, Taoussi, S, Abad, MT, Touil, Fz, Hamdi, S, Bougherira, S, Grifi, F, Kerrar, C, Allam, I, Djidjik, O, Boudjerra, N, Belhani, M, Gherras, S, Graine, A, Ait Ali, H, Entasoltane, B, Brahimi, M, Bekadja, MA, Ben lakhal, R, Meddeb, B, Ouchenane, Z, Sidi Mansour, N, Kacha, F, Tibermacine, F, Saidi, M, Mehalhal, N, Brahimi, Fz, Touati, L, Lakhdari, N, Saber Cherif, D, Meddour, Y, Chaib, S, Ardjoun, Fz, Bellaaj, H, Taibi, K, Touhami, H, Manai, HZ, Benzineb, B, Mesli, N, Maghraoui, A, Hadjeb, S, Zouaoui, Z, Baghdad, S, Bachiri, A, Laatiri, MA, Attari, M, Lamara, D, Bendjabellah, B, Ghedira, H, Ben Youcef, Y, Trabzi, A, Menif, S, Ben Othman, T, Benakli, M

“…Introduction: Chronic myeloid leukemia (CML) accounts for 7%-15% of all leukemias affecting adults. The incidence in Algeria is 0.4/100,000 inhabitants in…”
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MANAGEMENT AND OUTCOME OF CML PATIENTS: A TUNISIAN MULTI-CENTER STUDY ABOUT 116 CASES by Ben Amor, R., Ben Lakhal, R., Ghedira, H., Belaaj, H., Laatiri, M., Ben Youssef, Y., Ben Romdhane, N., M'Saddek, F., Menif, S., Elloumi, M., Khelif, A., Meddeb, B.

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RT-PCR use for the diagnostic of chronic myeloid leukaemia by Menif, S, El Borgi, W, Jeddi, R, Belakhal, R, Elloumi, M, Laatiri, A, Meddeb, B, Dellagi, K

“…The molecular analysis of chromosomal abnormalities associated with hematological malignancies allowed the identification of genes involved in theses…”
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