Santhi D. Puvanarajah
Kuala Lumpur, Malaysia
Last Updated: 09/26/2026
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Found 17 publications
Identifying factors in the provision of intravenous stroke thrombolysis in Malaysia: a multiple case study from the healthcare providers' perspective.
Journal: BMC health services research
Published: July 12, 2023
Stroke thrombolysis in a middle-income country: A case study exploring the determinants of its implementation.
Journal: Frontiers in neurology
Published: September 20, 2022
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
Association study of MCCC1/LAMP3 and DGKQ variants with Parkinson's disease in patients of Malay ancestry.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: May 29, 2020
PINK1 p.Leu347Pro mutations in Malays: Prevalence and illustrative cases.
Journal: Parkinsonism & related disorders
Published: May 29, 2020
Validation of Malay brief screening instrument for ascertainment of epilepsy.
Journal: Epilepsy & behavior : E&B
Published: February 23, 2019
LRRK2 N551K and R1398H variants are protective in Malays and Chinese in Malaysia: A case-control association study for Parkinson's disease.
Journal: Molecular genetics & genomic medicine
Published: October 26, 2018
Conventional and unconventional therapies in typical and atypical chronic inflammatory demyelinating polyneuropathy with different clinical course of progression.
Journal: Journal of the peripheral nervous system : JPNS
Published: May 08, 2018
Outcome in chronic inflammatory demyelinating polyneuropathy from a Malaysian centre over sixteen years.
Journal: Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
Published: July 04, 2017
Guillain-Barré Syndrome, variants & forms fruste: Reclassification with new criteria.
Journal: Clinical neurology and neurosurgery
Published: March 07, 2017
Coupling Genotyping and Computational Modeling in Prediction of Anti-epileptic Drugs that cause Stevens Johnson Syndrome and Toxic Epidermal Necrolysis for Carrier of HLA-B*15:02.
Journal: Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques
Published: April 21, 2016
Last Updated: 09/26/2026