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    <title>DSpace Collection:</title>
    <link>http://localhost:8080/xmlui/handle/123456789/9697</link>
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    <pubDate>Sat, 18 Apr 2026 03:48:52 GMT</pubDate>
    <dc:date>2026-04-18T03:48:52Z</dc:date>
    <item>
      <title>Role of regulatory T cells and T helper 17 cells in the pathogenesis of hypertension: a review</title>
      <link>http://localhost:8080/xmlui/handle/123456789/9707</link>
      <description>Title: Role of regulatory T cells and T helper 17 cells in the pathogenesis of hypertension: a review
Authors: Sakti Muliawan, Hary; Dwi Putra, Swastya; Zulkifli Amin, Hilman; Widyantoro, Bambang
Abstract: The discovery of autoantibodies in artery samples from cadavers with hypertension&#xD;
over 50 years ago suggested a potential link between the immune system and&#xD;
hypertension. Since then, research exploring the role of the immune system in&#xD;
hypertension has emerged. Animal studies have demonstrated a strong correlation&#xD;
between regulatory T cells (Tregs) and T helper 17 (Th17) cells in hypertension&#xD;
development, yet studies on human hypertension remain limited. Tregs produce&#xD;
inhibitory cytokines such as interleukin (IL)-10 and transforming growth factor-β&#xD;
to act as anti-inflammatory cells that protect against hypertension. In contrast,&#xD;
Th17 cells, by producing IL-17A, function as pro-inflammatory cells that promote&#xD;
hypertension. Recently, a subset of cells known as IL-17A+FOXP3+Treg cells have&#xD;
been identified, which can produce IL-17 and act as inflammatory cells under certain&#xD;
conditions. Understanding the basic mechanisms by which the immune system&#xD;
influences hypertension could lead to targeted immunotherapies for hypertension in&#xD;
the future. Thus, we highlighted the role of Tregs and Th17 cells in the development&#xD;
of hypertension and their potential as targets for therapy. Our findings confirmed the&#xD;
role of Tregs and Th17 cells in the pathogenesis of hypertension.&#xD;
KEYWORDS hypertension, immune system, regulatory T cell, T helper 17 cell</description>
      <pubDate>Mon, 01 Jan 2024 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://localhost:8080/xmlui/handle/123456789/9707</guid>
      <dc:date>2024-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Intracranial dural arteriovenous fistula presenting like longitudinally extensive transverse myelitis</title>
      <link>http://localhost:8080/xmlui/handle/123456789/9706</link>
      <description>Title: Intracranial dural arteriovenous fistula presenting like longitudinally extensive transverse myelitis
Authors: Yuliatri, Nia; Ayke Widjaya, Ingrid; Aditiara Wibawa, Gibran; Harlyjoy, Alphadenti; Satyanegara, Satyanegara
Abstract: Intracranial dural arteriovenous fistula (DAVF) that drains into spinal perimedullary&#xD;
veins can generate longitudinally extensive transverse myelitis (LETM)-like lesion,&#xD;
which often represents a significant diagnostic and therapeutic challenge. This is a case&#xD;
report of a 50-year-old male referred with all extremity weaknesses. Despite receiving&#xD;
high-dose intravenous steroids for suspected myelitis, no improvement was recorded.&#xD;
Spinal imaging showed abnormal hyperintensity extending from the T6 vertebral level&#xD;
to the medulla, and a flow void lesion from the cervicomedullary junction up to the&#xD;
L3 level. Angiography confirmed a Cognard type V spinal DAVF, which was treated&#xD;
with transarterial embolization of the feeding vessel. Follow-up angiography showed&#xD;
complete occlusion of the fistula without any backflow. Flow voids are no longer&#xD;
visible on MRI conducted 3 weeks post-procedure. Unfamiliarity with these disorders&#xD;
often leads to delays in diagnosis and treatment. Therefore, it is essential to consider&#xD;
intracranial DAVF as a differential diagnosis for LETM-like lesions.&#xD;
KEYWORDS endovascular procedures, dural arteriovenous fistula, transverse myelitis</description>
      <pubDate>Mon, 01 Jan 2024 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://localhost:8080/xmlui/handle/123456789/9706</guid>
      <dc:date>2024-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Multimodal approach in the diagnosis and management of Eales disease: a case report</title>
      <link>http://localhost:8080/xmlui/handle/123456789/9705</link>
      <description>Title: Multimodal approach in the diagnosis and management of Eales disease: a case report
Authors: Andayani Adriono, Gitalisa; Rasyid Mahfudz, Sausan; Fauzi Triyoga, Ichsan
Abstract: Eales disease is a rare idiopathic occlusive retinal vasculitis with low prevalence in&#xD;
the general population. Its infrequent occurrence limits diagnostic and treatment&#xD;
guidelines, emphasizing the need for ongoing reports to establish effective protocols.&#xD;
This case report describes a patient presenting with symptoms of bilateral retinal&#xD;
vasculitis. Fundus examination revealed vitreous hemorrhage (VH) and peripheral&#xD;
retinal vasculitis. Laboratory and imaging tests were performed to exclude differential&#xD;
diagnoses, leading to Eales disease as the primary diagnosis. Pars plana vitrectomy,&#xD;
panretinal laser photocoagulation, intravitreal anti-vascular endothelial growth&#xD;
factor, and anti-tuberculosis therapy were administered. Long-term follow-up showed&#xD;
satisfactory outcomes. This report suggested Eales disease to be a diagnosis of&#xD;
consideration for ophthalmologists encountering male patients with recurrent VH.&#xD;
Clinical suspicion, including appropriate laboratory testing and imaging, is essential&#xD;
to developing a holistic approach to diagnosis and management, aiming to prevent&#xD;
progression and achieve optimal visual outcomes.&#xD;
KEYWORDS periphlebitis, rare diseases, retinal vasculitis, vitreous hemorrhage</description>
      <pubDate>Mon, 01 Jan 2024 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://localhost:8080/xmlui/handle/123456789/9705</guid>
      <dc:date>2024-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Stand-alone middle meningeal artery embolization in chronic subdural hematoma patient presenting cognitive decline: a case report</title>
      <link>http://localhost:8080/xmlui/handle/123456789/9704</link>
      <description>Title: Stand-alone middle meningeal artery embolization in chronic subdural hematoma patient presenting cognitive decline: a case report
Authors: Galindra, Yusmahenry; Rilianto, Beny; Gusanto Kurniawan, Ricky; Tri Prasetyo, Bambang
Abstract: Chronic subdural hematoma (cSDH) is a neurological disorder that commonly occurs in&#xD;
the elderly with high morbidity and mortality. Current treatment for cSDH consists of&#xD;
conservative therapy, surgical evacuation, and endovascular therapy, or a combination&#xD;
of all the methods. Endovascular therapy for cSDH management involving middle&#xD;
meningeal artery embolization (MMAE) has become a promising therapeutic option&#xD;
for clinicians as it offers a minimally invasive, safe, and effective choice with a low&#xD;
recurrence rate. MMAE using particles can also be performed in frail elderly patients&#xD;
who cannot undergo large craniotomy procedures. We presented a case of a subdural&#xD;
hematoma patient with cognitive decline using a therapeutic strategy of stand-alone&#xD;
MMAE, which resulted in cognitive function improvement.&#xD;
KEYWORDS chronic subdural hematoma, cognitive impairment, MMA embolization</description>
      <pubDate>Mon, 01 Jan 2024 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://localhost:8080/xmlui/handle/123456789/9704</guid>
      <dc:date>2024-01-01T00:00:00Z</dc:date>
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