Chin E. Ooi
Malaysia
Last Updated: 09/26/2026
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Found 11 publications
LRRK2 p.G2385R and p.R1628P variants in a multi-ethnic Asian Parkinson's Cohort: epidemiology and clinical insights.
Journal: NPJ Parkinson's disease
Published: August 09, 2025
Evaluation of a Mitochondrial Polygenic Score for Parkinson's Disease Across Ancestries.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: May 15, 2025
Very High Frequency of Early-Onset Parkinson's Disease and PRKN Mutations among Indigenous Patients in Sabah, Malaysia.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: April 22, 2025
Adult-onset Rasmussen's encephalitis with anti-AMPA receptor antibodies.
Journal: Practical neurology
Published: March 19, 2025
Anti-Myelin Oligodendrocyte Glycoprotein Antibodies and Acute Hemorrhagic Encephalomyelitis.
Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
Published: November 04, 2024
Uncovering the genetic basis of Parkinson's disease globally: from discoveries to the clinic.
Journal: The Lancet. Neurology
Published: March 26, 2024
Progressive ataxia, ophthalmoparesis, and hypogonadotropic hypogonadism in a family with a novel variant in the KIFBP gene.
Journal: Clinical genetics
Published: September 06, 2023
Relapsing GABA(A) Receptor Encephalitis After Stem Cell Transplant for Acute Myeloid Leukaemia.
Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
Published: July 12, 2023
Isolated bilateral lateral geniculate nuclei T2/FLAIR hyperintensities heralding the development of central pontine myelinolysis in osmotic demyelination syndrome: neuro-images.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: May 16, 2023
Genetic study of early-onset Parkinson's disease in the Malaysian population.
Journal: Parkinsonism & related disorders
Published: January 04, 2023
Glucocerebrosidase (GBA) gene variants in a multi-ethnic Asian cohort with Parkinson's disease: mutational spectrum and clinical features.
Journal: Journal of neural transmission (Vienna, Austria : 1996)
Published: August 13, 2021
Showing 1-11 of 11
Last Updated: 09/26/2026