Search Results - "Medhaffar, M"

PB2095: RELAPSED AND REFRACTORY DIFFUSE LARGE B CELL LYMPHOMA: EXPERIENCE OF A LOW‐INCOME CENTER IN TIME OF NEW DRUGS by Charfi, M., Abichou, G., Kallel, F., Ben amor, I., Khelifa, L., Frikha, I., Fakhfekh, Y., Kassar, O., Medhaffar, M., Hdiji, S., Elloumi, M.

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PB2029: MULTIPLE MYELOMA AND SPINAL CORD COMPRESSION: THE EXPERIENCE OF THE HEMATOLOGY DEPARTMENT OF SFAX by Kallel, F., Siala, N., Mezghani, K., Charfi, M., Ghorbel, L., Ben Salah, H., Fakhfekh, Y., Kassar, O., Khelifa, L., Hadiji, S., Frikha, I., Ben Amor, I., Daoued, J., Medhaffar, M., Elloumi, M.

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PB1842: EARLY DEATH IN NEWLY DIAGNOSED ADULT ACUTE MYELOID LEUKEMIA by Siala, N., Fakhfekh, Y., Ben Amor, I., Kallel, F., Frikha, I., Kassar, O., Chaari, M., Louati, N., Sennana, H., Khelifa, L., Charfi, M., Hadiji, S., Medhaffar, M., 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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PB1767: OUTCOME OF RELAPSED CHILDHOOD ACUTE LYMPHOBLASTIC LEUKEMIA IN THE SOUTH OF TUNISIA SINGLE CENTER EXPERIENCE by Siala, N., Frikha, I., Medhaffar, M., Ben Amor, I., Turki, I., Ben Abdejallil, N., Fakhfekh, Y., Louati, N., kassar, O., Charfi, M., Kallel, F., Khelifa, L., hadiji, S., mnif, H., Ben Othmen, T., Elloumi, M.

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PB2017: YOUNG PATIENTS WITH NEWLY DIAGNOSED MULTIPLE MYELOMA AND RENAL IMPAIRMENT: A TUNISIAN SINGLE‐CENTER EXPERIENCE by Kallel, F., Mezghani, K., Siala, N., Fakhfekh, Y., Khalifa, L., Hadiji, S., Kassar, O., Frikha, I., Ben Amor, I., Charfi, M., Balloumi, D., Torjmen, L., Kammoun, K., Ben Hamida, M., Ben Othmen, T., Medhaffar, M., Elloumi, M.

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PB2093: DIFFUSE LARGE B CELL LYMPHOMA IN THE ELDERLY by Abichou, G., Charfi, M., Kassar, O., Kallel, F., Saguem, I., Feki, W., Ben amor, I., Ben kridis, W., Frikha, I., Khelifa, L., fakhfekh, Y., Toumi, N., Medhaffar, M., Hdiji, S., Boudawara, T., Mnif, Z., Elloumi, M.

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A probably isolated subclavicular lymphadenopathy in acute leukemia: An unusual localisation of cryptococcosis by Harrabi, H., Medhaffar, M., Kammoun, L., Maaloul, I., Ayadi, L., Elloumi, M.

“…Cryptococcus neoformans ( C.  neoformans) is a fungal opportunistic pathogen which infects immunocompromised patients, especially those who are seropositive…”
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Isolated extramedullary adnexal relapse of acute lymphoblastic leukemia: a case report by Bellaaj, H, Moussa, A, Gouiaa, N, Maazoun, K, Frikha, I, Medhaffar, M, Hdiji, S, Elloumi, M, Souissi, T

“…The occurrence of an isolated ovarian or pelvic relapse of acute lymphoblastic leukemia (ALL) in complete remission after chemotherapy has rarely been…”
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Evaluation of a prospective therapeutic protocol in adult patients with nonsevere aplastic anemia in South Tunisia by Bellaaj, H, Kallel, C, Elloumi, M, Rekik, H, Kassar, O, Hdiji, S, Medhaffar, M, Souissi, T

“…Immunosuppressive drugs are usually used in the treatment of acquired aplastic anemia (AAA). The aim of this study was to evaluate the efficiency of a…”
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Congenital factor XIII deficiency in the south of Tunisia by Medhaffar, M, Elloumi, M, Guermazi, S, Kallel, C, Mseddi, S, Bellaaj, H, Makni, F, Souissi, T

“…Factor XIII deficiency is a rare autosomal recessive congenital disorder of haemostasis characterised by a plasmatic factor XIII level less than 1% in…”
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Rechute extramédullaire annexielle isolée d’une leucémie aiguë lymphoblastique : à propos d’un cas by Bellaaj, H., Moussa, A., Gouiaa, N., Maazoun, K., Frikha, I., Medhaffar, M., hdiji, S., Elloumi, M., Souissi, T.

“…La survenue d’une rechute ovarienne isolée d’une leucémie aiguë lymphoblastique (LAL), en rémission complète après une chimiothérapie est une situation…”
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Evaluation of anxiety in children with acute leukemia: A prospective study of 20 cases by Baccouche, K., Walha, A., Medhaffar, M., Kammoun, W., Ayadi, H., Moalla, Y., Elloumi, M., Ghribi, F.

“…The occurrence of acute leukemia (AL) in childhood causes a profound upheaval in the child itself and also within his family. Exposure to this test could…”
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Évaluation d’un protocole thérapeutique prospectif des aplasies médullaires acquises non sévères de l’adulte dans le Sud tunisien by Bellaaj, H., Kallel, C., Elloumi, M., Rekik, H., Kassar, O., Hdiji, S., Medhaffar, M., Souissi, T.

“…Les immunosuppresseurs sont habituellement indiqués dans le traitement de première ligne des formes non sévères de l’aplasie médullaire acquise (AMA). Le but…”
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Facteurs prédictifs de lésions digestives et stratégie d’exploration chez les patients ayant une anémie by Chtourou, L., Sellami, W., Smaoui, M.A., Amouri, A., Medhaffar, M., Elloumi, M., Tahri, N.

“…L’anémie ferriprive est une maladie multifactorielle dont les étiologies digestives sont assez fréquentes. Identifier les facteurs prédictifs de la présence de…”
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Syndrome de Budd–Chiari associé à un POEMS syndrome by Fakhfakh, Y., Chtourou, L., Smaoui, H., Medhaffar, M., Tahri, N., Elloumi, M.

“…Le POEMS syndrome est une maladie multisystémique caractérisée par des manifestations cliniques diverses. Les thromboses vasculaires, artérielles ou veineuses,…”
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Évaluation des pratiques à propos de la réactivation virale B chez les patients recevant un traitement immunosuppresseur by Amouri, A., Chtourou, L., Kallel, F., Medhaffar, M., Gdoura, H., Boudabous, M., Mnif, L., Elloumi, M., Tahri, N.

“…La réactivation du virus de l’hépatite B (VHB) est une situation de plus en plus fréquente avec l’utilisation plus large des immunosuppresseurs et des…”
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Déficit congénital en facteur XIII de la coagulation dans le sud tunisien by Medhaffar, M., Elloumi, M., Guermazi, S., Kallel, C., Mseddi, S., Bellaaj, H., Makni, F., Souissi, T.

“…Le déficit congénital en facteur XIII de la coagulation est une affection rare de l'hémostase à transmission autosomique récessive, s'exprimant à l'état…”
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Autoimmune lymphoproliferative syndrome caused by homozygous FAS mutations with normal or residual protein expression by Agrebi, Nourhen, PhD, Mansour, Lamia Ben, MD, Medhaffar, Moez, MD, Hadiji, Sondes, MD, Fedhila, Faten, MD, Ben-Ali, Meriem, MD, Mekki, Najla, MD, Hachicha, Mongia, MD, Barsaoui, Sihem, MD, Barbouche, Mohamed-Ridha, MD, PhD, Ben-Mustapha, Imen, MD

“…Capsule summary : The identification of homozygous FAS mutations with normal or residual protein expression expands the spectrum of autoimmune…”
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