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Azlina Ahmad

Showing results (91-100 of 122) with videos related to

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BMC Neurology|April 22, 2015
DRD and GRIN2B polymorphisms and their association with the development of impulse control behaviour among Malaysian Parkinson's disease patientsShahidee Zainal Abidin, Eng Liang Tan, Soon-Choy Chan, et al.
Frontiers in Neurology|July 29, 2022
Clinical Outcomes After Ventriculo-Peritoneal Shunting in Patients With Classic vs. Complex NPHEng Tah Goh, Christine Lock, Audrey Jia Luan Tan, et al.
Annals of the Academy of Medicine, Singapore|June 18, 2013
Lack of association between the LRRK2 A419V variant and Asian Parkinson's diseaseAroma Agape Gopalai, Shen Yang Lim, Zariah Abdul Aziz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 20, 2026
Ex Vivo LRRK2 Activation in Asian G2385R and R1628P Variant Carriers and Idiopathic Parkinson's DiseaseTzi Shin Toh, Lei Cheng Lit, Shen-Yang Lim, et al.
Neurology. Genetics|January 14, 2025
Global Perspectives on Returning Genetic Research Results in Parkinson DiseaseAi Huey Tan, Paula Saffie-Awad, Artur F Schumacher Schuh, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|November 15, 2021
Glucocerebrosidase (GBA) gene variants in a multi-ethnic Asian cohort with Parkinson's disease: mutational spectrum and clinical featuresJia Lun Lim, Katja Lohmann, Ai Huey Tan, et al.
Parkinsonism & Related Disorders|January 22, 2023
New insights from a multi-ethnic Asian progressive supranuclear palsy cohortShen-Yang Lim, Alfand Marl F Dy Closas, Ai Huey Tan, et al.
Biomed Research International|September 23, 2014
LRRK2 G2385R and R1628P mutations are associated with an increased risk of Parkinson's disease in the Malaysian populationAroma Agape Gopalai, Shen-Yang Lim, Jing Yi Chua, et al.
Journal of Parkinson'S Disease|February 20, 2025
Rare <i>SV2C</i> coding variants in Parkinson's disease riskChu Hua Chang, Elaine Guo Yan Chew, Michelle Mulan Lian, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 22, 2022
Underrepresented Populations in Parkinson's Genetics Research: Current Landscape and Future DirectionsArtur Francisco Schumacher-Schuh, Andrei Bieger, Olaitan Okunoye, et al.
Pageof 13

Showing results (91-100 of 122) with videos related to

Sort By:
Pageof 13
BMC Neurology|April 22, 2015
DRD and GRIN2B polymorphisms and their association with the development of impulse control behaviour among Malaysian Parkinson's disease patientsShahidee Zainal Abidin, Eng Liang Tan, Soon-Choy Chan, et al.
Frontiers in Neurology|July 29, 2022
Clinical Outcomes After Ventriculo-Peritoneal Shunting in Patients With Classic vs. Complex NPHEng Tah Goh, Christine Lock, Audrey Jia Luan Tan, et al.
Annals of the Academy of Medicine, Singapore|June 18, 2013
Lack of association between the LRRK2 A419V variant and Asian Parkinson's diseaseAroma Agape Gopalai, Shen Yang Lim, Zariah Abdul Aziz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 20, 2026
Ex Vivo LRRK2 Activation in Asian G2385R and R1628P Variant Carriers and Idiopathic Parkinson's DiseaseTzi Shin Toh, Lei Cheng Lit, Shen-Yang Lim, et al.
Neurology. Genetics|January 14, 2025
Global Perspectives on Returning Genetic Research Results in Parkinson DiseaseAi Huey Tan, Paula Saffie-Awad, Artur F Schumacher Schuh, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|November 15, 2021
Glucocerebrosidase (GBA) gene variants in a multi-ethnic Asian cohort with Parkinson's disease: mutational spectrum and clinical featuresJia Lun Lim, Katja Lohmann, Ai Huey Tan, et al.
Parkinsonism & Related Disorders|January 22, 2023
New insights from a multi-ethnic Asian progressive supranuclear palsy cohortShen-Yang Lim, Alfand Marl F Dy Closas, Ai Huey Tan, et al.
Biomed Research International|September 23, 2014
LRRK2 G2385R and R1628P mutations are associated with an increased risk of Parkinson's disease in the Malaysian populationAroma Agape Gopalai, Shen-Yang Lim, Jing Yi Chua, et al.
Journal of Parkinson'S Disease|February 20, 2025
Rare <i>SV2C</i> coding variants in Parkinson's disease riskChu Hua Chang, Elaine Guo Yan Chew, Michelle Mulan Lian, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 22, 2022
Underrepresented Populations in Parkinson's Genetics Research: Current Landscape and Future DirectionsArtur Francisco Schumacher-Schuh, Andrei Bieger, Olaitan Okunoye, et al.
Pageof 13