Science Journal of Clinical Medicine

Volume 13, Issue 4, December 2024

  • Research Article

    Decreased Collagen Xii Expression and Increased Reactive Oxygen Species Production in Levofloxacin-Treated Tendon

    Takashi Kobayashi, Tsuyoshi Sato, Yuta Isozaki, Masahiko Okubo, Seiji Asoda, Toshinori Iwai, Shinnosuke Nogami, Ko Ito*

    Issue: Volume 13, Issue 4, December 2024
    Pages: 63-70
    Received: 30 October 2024
    Accepted: 15 November 2024
    Published: 29 November 2024
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    Abstract: Background: Levofloxacin (LVFX) is widely used for many respiratory, urinary, and oral infections. Although rare, tendinopathy and tendon rupture have been reported in patients treated with LVFX as adverse effect. However, the exact mechanism is not fully elucidated. In this study, we investigated the effects of LVFX on tendon cells and tendon tiss... Show More
  • Review Article

    ‘Risala Tahaffuz Min al-Nazla’, Al-Rāzi’s Legacy in Cold Remedy and Prevention

    Ashfaque Ahmad*

    Issue: Volume 13, Issue 4, December 2024
    Pages: 71-75
    Received: 23 October 2024
    Accepted: 9 November 2024
    Published: 13 December 2024
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    Abstract: Nazla (Catarrh) is a condition in Unani medicine that involves the flow of catarrhal fluids, or mucus, from the brain downwards into the throat and chest, leading to symptoms similar to what we consider a cold today. This condition is characterized by congestion, irritation in the respiratory pathways, and in some cases, can progress to more seriou... Show More
  • Case Report

    Pulmonary Alveolar Microlithiasis: An Incidental Case Report from Jordan with Literature Review

    Basheer Radi Alakhras*, Omar Habashneh, Ahmad Basim Yaghi, Abdallah Daseh, Adham Alkilani

    Issue: Volume 13, Issue 4, December 2024
    Pages: 76-80
    Received: 4 November 2024
    Accepted: 21 November 2024
    Published: 16 December 2024
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    Abstract: Pulmonary alveolar microlithiasis (PAM) is one of the rare lung diseases, in which an otherwise healthy individual develops diffuse alveolar calcifications. It is reported to be caused by mutation of the SLC34A2 gene. Patients who are eventually diagnosed with PAM usually present late when progression to cor pulmonale has already developed, or for ... Show More