Publications by authors named "Nabil Hasasna"

To investigate the therapeutic potential of mebendazole (MBZ)-loaded nanostructured lipid carriers (NLCs). NLC-MBZ was prepared and characterized to evaluate the and anticancer effects and the inhibitory effect on RanGTP and its potential as an antimetastatic treatment . NLC-MBZ exhibited a size and charge of 155 ± 20 nm and -27 ± 0.

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Article Synopsis
  • Multiparametric flow cytometry (MFC) is used for diagnosing and managing B-cell acute lymphoblastic leukemia (B-ALL) by monitoring leukemic cell characteristics and minimal residual disease (MRD) during treatment.
  • This study investigated the role of the myeloid marker CD371 in MRD detection for patients diagnosed with CD371-positive B-ALL, analyzing data from 238 patients over critical treatment periods.
  • Findings showed that 8.4% of B-ALL patients were CD371-positive, with specific associations to age and other leukemic markers, suggesting that CD371 status in patients may provide critical insights for future research and treatment approaches.
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Anti-programmed death-ligand 1 (PD-L1) treatments can improve colorectal carcinoma (CRC) survival; however, there is still controversy regarding the relationship between PD-L1 expression and the outcome of immunotherapeutic treatment and survival. The discrepancies are partly caused by the lack of a unified scoring system. This retrospective, cross-sectional study evaluated PD-L1 by immunohistochemistry in 127 CRC cases and compared the 3 scoring systems used to assess PD-L1: Tumor Percentage Score (TPS), Combined Positive Score (CPS), and immune cell (IC) score.

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Glomus tumors are rare and usually benign. The malignant form (glomangiosarcoma) comprises <1% of all glomus tumors. There are limited reports that describe glomus tumors in the nasal cavity.

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Aim: Diffuse midline glioma (DMG) H3 K27M-mutant is a specific entity that, as the name indicates, tends to occur in midline structures including the thalamus, brainstem, and spinal cord. DMG predominates in children, is an aggressive tumor with poor prognosis, and is considered a WHO grade IV tumor regardless of histological features. The exact frequency of these mutations in adults diagnosed with glioma in the midline is unknown.

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