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Open Access Macedonian Journal of Medical Sciences|December 19, 2018
"Two Stones on One Bird": A Case Report on Severe Biphasic Anaphylaxis Masquerading as Life-Threatening Acute AsthmaAlvin Oliver Payus, Azliza Ibrahim, Norlaila Mustafa
Journal of Cardiothoracic Surgery|January 19, 2023
The poorly understood yet potent risk of pulmonary artery thrombosis in-situ in Post-Acute COVID-19 syndromeAlvin Oliver Payus, Constance Liew Sat Lin, Azliza Ibrahim
Case Reports in Neurology|August 11, 2022
Sensory Predominant Guillain-Barré Syndrome Concomitant with Dengue Infection: A Case ReportAlvin Oliver Payus, Azliza Ibrahim, Constance Liew Sat Lin, et al.
Oxford Medical Case Reports|January 27, 2022
'Crescendo transient ischemic attack'-an uncommon presentation of a very common disease: a case report on capsular warning syndromeAlvin Oliver Payus, Azliza Ibrahim, Vinushini Chandra Sheaker, et al.
The American Journal of Case Reports|January 20, 2021
Myasthenic Crisis as the First Presentation of Myasthenia Gravis: A Case ReportAlvin Olivier Payus, Justin Leow Wen Hsiang, Jia Qian Leong, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 2, 2021
Immune-mediated neurological syndrome in SARS-CoV-2 infection: a review of literature on autoimmune encephalitis in COVID-19Alvin Oliver Payus, Mohammad Saffree Jeffree, May Honey Ohn, et al.
Plos One|December 31, 2020
Multi-strain probiotics (Hexbio) containing MCP BCMC strains improved constipation and gut motility in Parkinson's disease: A randomised controlled trialAzliza Ibrahim, Raja Affendi Raja Ali, Mohd Rizal Abdul Manaf, et al.
BMC Neurology|March 23, 2023
Immune-mediated necrotizing myopathy (NAM) related to SARS-Cov-2 infection: a case reportAzliza Ibrahim, Wan Syamimee Wan Ghazali, Anna Misyail, et al.
BMC Neurology|October 13, 2021
Longitudinal extensive transverse myelitis following ChAdOx1 nCOV-19 vaccine: a case reportWee Yong Tan, Abdul Hanif Khan Yusof Khan, Mohd Naim Mohd Yaakob, et al.
Frontiers in Genetics|January 20, 2023
Case report: Incomplete penetrance of autosomal dominant myotonia congenita caused by a rare CLCN1 variant c.1667T>A (p.I556N) in a Malaysian familyNurul Huda Musa, Karuppiah Thilakavathy, Nur Afiqah Mohamad, et al.
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