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Azlina Ahmad

Showing results (101-110 of 122) with videos related to

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The Lancet. Neurology|October 24, 2024
Uncovering the genetic basis of Parkinson's disease globally: from discoveries to the clinicShen-Yang Lim, Ai Huey Tan, Azlina Ahmad-Annuar, et al.
Journal of Movement Disorders|January 31, 2024
Loss-of-Function Variant in the SMPD1 Gene in Progressive Supranuclear Palsy-Richardson Syndrome Patients of Chinese AncestryShen-Yang Lim, Ai Huey Tan, Jia Nee Foo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 9, 2021
Association study of MCCC1/LAMP3 and DGKQ variants with Parkinson's disease in patients of Malay ancestryJia Lun Lim, Ebonne Yulin Ng, Shen-Yang Lim, et al.
Journal of Parkinson'S Disease|February 20, 2025
New insights from a Malaysian real-world deep brain stimulation cohortAlfand Marl F Dy Closas, Ai Huey Tan, Yi Wen Tay, et al.
Parkinsonism & Related Disorders|May 20, 2023
Genetic study of early-onset Parkinson's disease in the Malaysian populationYi Wen Tay, Ai Huey Tan, Jia Lun Lim, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 24, 2025
A Complex FGF14 (TTC)/(TGC) Repeat Expansion in Parkinson's DiseaseXiaosheng Zheng, Zhidong Cen, Xinhui Chen, et al.
Human Molecular Genetics|February 26, 2014
Analysis of non-synonymous-coding variants of Parkinson's disease-related pathogenic and susceptibility genes in East Asian populationsJia Nee Foo, Louis C Tan, Herty Liany, et al.
NPJ Parkinson'S Disease|February 23, 2025
Clinical and functional evidence for the pathogenicity of the LRRK2 p.Arg1067Gln variantShen-Yang Lim, Tzi Shin Toh, Jia Wei Hor, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2024
Team Science Approaches to Unravel Monogenic Parkinson's Disease on a Global ScaleJohanna Junker, Lara M Lange, Eva-Juliane Vollstedt, et al.
BMC Research Notes|May 1, 2015
The first Malay database toward the ethnic-specific target molecular variationHashim Halim-Fikri, Ali Etemad, Ahmad Zubaidi Abdul Latif, et al.
Pageof 13

Showing results (101-110 of 122) with videos related to

Sort By:
Pageof 13
The Lancet. Neurology|October 24, 2024
Uncovering the genetic basis of Parkinson's disease globally: from discoveries to the clinicShen-Yang Lim, Ai Huey Tan, Azlina Ahmad-Annuar, et al.
Journal of Movement Disorders|January 31, 2024
Loss-of-Function Variant in the SMPD1 Gene in Progressive Supranuclear Palsy-Richardson Syndrome Patients of Chinese AncestryShen-Yang Lim, Ai Huey Tan, Jia Nee Foo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 9, 2021
Association study of MCCC1/LAMP3 and DGKQ variants with Parkinson's disease in patients of Malay ancestryJia Lun Lim, Ebonne Yulin Ng, Shen-Yang Lim, et al.
Journal of Parkinson'S Disease|February 20, 2025
New insights from a Malaysian real-world deep brain stimulation cohortAlfand Marl F Dy Closas, Ai Huey Tan, Yi Wen Tay, et al.
Parkinsonism & Related Disorders|May 20, 2023
Genetic study of early-onset Parkinson's disease in the Malaysian populationYi Wen Tay, Ai Huey Tan, Jia Lun Lim, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 24, 2025
A Complex FGF14 (TTC)/(TGC) Repeat Expansion in Parkinson's DiseaseXiaosheng Zheng, Zhidong Cen, Xinhui Chen, et al.
Human Molecular Genetics|February 26, 2014
Analysis of non-synonymous-coding variants of Parkinson's disease-related pathogenic and susceptibility genes in East Asian populationsJia Nee Foo, Louis C Tan, Herty Liany, et al.
NPJ Parkinson'S Disease|February 23, 2025
Clinical and functional evidence for the pathogenicity of the LRRK2 p.Arg1067Gln variantShen-Yang Lim, Tzi Shin Toh, Jia Wei Hor, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2024
Team Science Approaches to Unravel Monogenic Parkinson's Disease on a Global ScaleJohanna Junker, Lara M Lange, Eva-Juliane Vollstedt, et al.
BMC Research Notes|May 1, 2015
The first Malay database toward the ethnic-specific target molecular variationHashim Halim-Fikri, Ali Etemad, Ahmad Zubaidi Abdul Latif, et al.
Pageof 13