UNIMAS Scholarhub

UNIMAS Open Access Repository

Managed by Perpustakaan Tun Abdul Rahman Ya'kub, Universiti Malaysia Sarawak

 

Communities in Scholarhub

Select a community to browse its collections.

Now showing 1 - 5 of 5
  • A digital repository community hosting research outputs, publications, and scholarly works related to Borneo studies, including culture, biodiversity, indigenous knowledge, and regional development. Managed by Institute of Borneo Studies, UNIMAS.
  • This community refers specifically to published works (journal articles, books, book chapters, and conference proceedings). For any inquiries, please contact the dedicated team at scholarhub-research@unimas.my. Managed by Academic Support Division.
  • The Special Collections at PeTARY comprise unique and valuable materials of historical, cultural, and academic significance. These collections preserve and provide access to rare books, personal archives, manuscripts, photographs, research materials, and documents related to distinguished individuals and the heritage of Borneo and UNIMAS.
  • This community refers specifically to UNIMAS theses and dissertation, final year project report and IMRAD collections. For any inquiries, please contact the dedicated team at repository@unimas.my. Managed by Metadata & Digital Section.
  • Archival collections, founding histories, and official publication records of UNIMAS, managed by the Archive and Conservation Unit.

Recent Submissions

Item
Disability, Identity and Impact of Impairments on The Survivors of Road Traffic Injuries (RTIs)
(UNIMAS Publisher, 2026) Juna Liau; Faculty of Social Sciences and Humanities
This paper examines the direct and vicarious impact of impairments on the lives of survivors of road traffic injuries (RTIs) and their families. Although the focus of analysis is at individual and household levels, in discussion it relates to social structures. Drawing on data from in-depth interviews and participant observation among survivors, caregivers and community leaders, this paper aims to provide a deeper understanding of disability and to critique ideas linked to lay aetiologies of RTIs, such as fate and individual irresponsibility. Before injury, survivors were living without disability and actively participating in their social world. The paper shows that after injury, survivors social and economic lives were altered, as they coped with changes in bodily functions, and physical capability, and in consequence, as they faced limited opportunities to engage in the social world. It investigates how types of disability affect people in different ways, in an effort to understand the links between their varied experiences, age, gender and ethnicity.
Item
Optimization of E-slot Applicator for Non-Invasive Hyperthermia Breast Cancer Treatment.
(Universiti Malaysia Sarawak, 2026) BIBI SARPINAH BINTI SHEIKH NAIMULLAH
Item
SMART IMAGING FOR AGRICULTURE DATA WITH ROAD DETECTION INTEGRATION
(UNIVERSITI MALAYSIA SARAWAK, 2025) OLIVER OH CHEN QI
Item
A Case of Placental Site Trophoblastic Tumour That Mimicked Missed Miscarriage
(MDPI, 2026) Joana Paula Artaiz-Pido; Mohd Hafiiz Mohamad Rizan; Chew Kah Teik; Wong Yin Ping; Tan Geok Chin; Faculty of Medicine and Health Sciences
Background and Clinical Significance: Placental site trophoblastic tumour (PSTT) is a malignant tumour of the implantation site intermediate trophoblasts. It has historically been described using terms such as atypical chorioepithelioma, atypical choriocarcinoma, syncytioma, and chorioepitheliosis. It belongs to one of the heterogeneous spectrums of gestational trophoblastic disease. It accounts for about 0.25 to 5% of all gestational trophoblastic neoplasia. The typical clinical presentation is alternating menorrhagia and amenorrhea, mildly elevated β-hCG, and radiological findings of a uterine mass. Case Presentation: A 32-year-old woman presented with a history of intermittent menorrhagia and amenorrhea, with a persistent mildly raised β-hCG level. Ultrasonography showed a hypoechoic lesion on the right side of the posterior wall of the uterus. She was diagnosed with a missed miscarriage, and an evacuation of the products of conception was performed. Histologically, the tissue fragments comprised cords and sheets of atypical intermediate trophoblast cells, with characteristic features of myometrial smooth muscle infiltration, vascular invasion, and vascular wall replaced by the neoplastic cells. Immunohistochemically, these cells are positive for β-hCG and GATA3, while negative for P63. Conclusions: PSTT is a rare form of gestational trophoblastic neoplasia. Early recognition of PSTT is essential because its clinical presentation may mimic benign pregnancy-related conditions, and diagnosis relies heavily on histopathological and immunohistochemical evaluation.