Search Results - "Hend Ben Neji"

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  1. 1

    Acquired FVII Deficiency and Acute Myeloid Leukemia: A Case Report and Literature Review by Hammami, Emna, Borgi, Wijden El, Lakhal, Fatma Ben, Salem, Sarra Fekih, Neji, Hend Ben, Gouider, Emna

    Published in Laboratory medicine (01-09-2022)
    “…Abstract Factor VII (FVII) deficiency is the most common among all rare inherited bleeding disorders. However, acquired FVII deficiency (aFVIID) is uncommon…”
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    Journal Article
  2. 2

    SMARCA4-deficient thoracic sarcoma revealed by metastasis to the small intestine: a diagnostic dilemma by Khanchel, Fatma, Hedhili, Raweh, Zenaidi, Hakim, Helal, Imen, Yahmadi, Abdelwahed, Ben Néji, Hend, Ksontini, Feryel, Ben Brahim, Ehsen, Jouini, Raja, Chadli, Aschraf

    “…SMARCA4-deficient thoracic sarcoma (SMARCA4-DTS) is a recently identified aggressive subtype of sarcoma. We present the case of a 44-year-old man who underwent…”
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    Journal Article
  3. 3

    Blastic plasmacytoid dendritic cell neoplasm or CD4+ CD56+ acute myeloid leukemia: A case report by Neji, Sameh, Lakhal, Fatma Ben, Salem, Sarra Fekih, Ghali, Ons, Neji, Hend Ben, Achour, Meriem, El Borgi, Wijdene, Gouider, Emna

    Published in Annales de biologie clinique (Paris) (19-09-2024)
    “…Blastic plasmacytoid dendritic-cell neoplasm (BPDCN) is an extremely rare disease that originates from dendritic cells, characterized by co-expression of CD4…”
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    Journal Article
  4. 4

    Predictive factors of all-trans-retinoic acid related complications during induction therapy for acute promyelocytic leukemia by Jeddi, Ramzi, Kacem, Karima, Ben Neji, Hend, Mnif, Samia, Gouider, Emna, Aissaoui, Lamia, Ben Amor, Ramzi, Ben Lakhal, Raihane, Ben Abid, Hela, Belhadjali, Zaher, Meddeb, Balkis

    Published in Hematology (01-06-2008)
    “…The combination of all-trans-retinoic acid (ATRA) and chemotherapy has made acute promyelocytic leukemia (APL) a highly curable leukemia. However, several…”
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    Echanges plasmatiques au cours des purpuras thrombotiques thrombocytopéniques by Jabr, Dorra, Hsasna, Roua, Kefi, Salma, Kharrat, Rachid, Ben Neji, Hend, Ben Lakhal, Raihane

    Published in Tunisie Medicale (01-06-2023)
    “…Introduction: Le purpura thrombotique thrombocytopénique (PTT) est une pathologie hématologique rare mais potentiellement fatale en l’absence d’une prise en…”
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    Journal Article
  8. 8

    The Glanzmann's Thrombasthenia in Tunisia: A Cohort Study by Elmahmoudi, Hejer, Achour, Meriem, Belhedi, Nejla, Ben Neji, Hend, Zahra, Kaouther, Meddeb, Balkis, Gouider, Emna

    Published in Journal of hematology (01-09-2017)
    “…The Glanzmann's thrombasthenia (GT) is a rare autosomal-recessive bleeding disorder with uncommon neonatal revelation. It is due to abnormalities of…”
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    Journal Article
  9. 9
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    Bronchiolitis Obliterans After Allogeneic Stem Cell Transplantation: a Single Center Retrospective Study of Risk Factors by Neji, Hend Ben, Dromer, Claire, Tabrizi, Reza, Vigouroux, Stephane, Guenard, Herve, Pigneux, Arnaud, Leguay, Thibaut, Dilhuydy, Marie-Sarah, Bouabdallah, Krimo, Schmitt, Anna, Marit, Gerald, Milpied, Noel

    Published in Blood (19-11-2010)
    “…Abstract 4507 Bronchiolitis obliterans (BO) is a late-onset pulmonary complication occurring after stem cell transplantation as a manifestation of chronic…”
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    Journal Article
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    Treatment of acute promyelocytic leukemia with PETHEMA LPA 99 protocol: a Tunisian single center experience by Jeddi, Ramzi, Ghédira, Héla, Menif, Samia, Ben Neji, Hend, Ben Amor, Ramzi, Kacem, Karima, Aissaoui, Lamia, Bouteraâ, Walid, Abdennebi, Yosr, Raihane, Ben Lakhal, Gouider, Emna, Raouf, Hafsia, Hèla, Ben Abid, Saad, Ali, Zaher, Belhadjali, Meddeb, Balkis

    Published in Hematology (01-08-2010)
    “…Acute promyelocytic leukemia (APL) has now become the most curable of all subtypes of acute myeloid leukemia. A cure rate of 75-80% can be anticipated with a…”
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    Journal Article
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    Echanges plasmatiques au cours des purpuras thrombotiques thrombocytopéniques by Jabr, Dorra, Hsasna, Roua, Kéfi, Salma, Kharrat, Rachid, Ben Néji, Hend, Ben Lakhal, Raihane

    Published in Tunisie Medicale (30-05-2024)
    “…Introduction : Le purpura thrombotique thrombocytopénique (PTT) est une pathologie hématologique rare mais potentiellement fatale en l’absence d’une prise en…”
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    Journal Article