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Azlina Ahmad

Showing results (81-90 of 122) with videos related to

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Genome|July 5, 2016
Identification of the genomic mutation in Epha4(rb-2J/rb-2J) miceSiti W Mohd-Zin, Nor-Linda Abdullah, Aminah Abdullah, et al.
Parkinsonism & Related Disorders|August 30, 2020
PINK1 p.Leu347Pro mutations in Malays: Prevalence and illustrative casesAi Huey Tan, Katja Lohmann, Yi Wen Tay, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|September 18, 2003
No association with common Caucasian genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (DNCHC1) and familial motor neuron disordersAzlina Ahmad-Annuar, Paresh Shah, Majid Hafezparast, et al.
Neurogenetics|April 24, 2019
Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian familyShelisa Tey, Nortina Shahrizaila, Alexander P Drew, et al.
Neurobiology of Aging|October 20, 2018
Evaluation of novel Parkinson's disease candidate genes in the Chinese populationElaine Guo Yan Chew, Herty Liany, Louis C S Tan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 16, 2024
Identification of Genetic Variants in Progressive Supranuclear Palsy in Southeast AsiaAdeline Su Lyn Ng, Ai Huey Tan, Yi Jayne Tan, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 14, 2016
PARK16 is associated with PD in the Malaysian populationAroma Agape Gopalai, Azlina Ahmad-Annuar, Hui-Hua Li, et al.
BMC Research Notes|July 18, 2018
Cranial neural tube defect after trimethoprim exposureNor Linda Abdullah, Renuka Gunasekaran, Siti Waheeda Mohd-Zin, et al.
The Lancet. Neurology|June 9, 2019
Parkinson's disease in the Western Pacific RegionShen-Yang Lim, Ai Huey Tan, Azlina Ahmad-Annuar, et al.
Molecular Genetics & Genomic Medicine|September 6, 2019
LRRK2 N551K and R1398H variants are protective in Malays and Chinese in Malaysia: A case-control association study for Parkinson's diseaseAroma Agape Gopalai, Jia Lun Lim, Hui-Hua Li, et al.
Pageof 13

Showing results (81-90 of 122) with videos related to

Sort By:
Pageof 13
Genome|July 5, 2016
Identification of the genomic mutation in Epha4(rb-2J/rb-2J) miceSiti W Mohd-Zin, Nor-Linda Abdullah, Aminah Abdullah, et al.
Parkinsonism & Related Disorders|August 30, 2020
PINK1 p.Leu347Pro mutations in Malays: Prevalence and illustrative casesAi Huey Tan, Katja Lohmann, Yi Wen Tay, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|September 18, 2003
No association with common Caucasian genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (DNCHC1) and familial motor neuron disordersAzlina Ahmad-Annuar, Paresh Shah, Majid Hafezparast, et al.
Neurogenetics|April 24, 2019
Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian familyShelisa Tey, Nortina Shahrizaila, Alexander P Drew, et al.
Neurobiology of Aging|October 20, 2018
Evaluation of novel Parkinson's disease candidate genes in the Chinese populationElaine Guo Yan Chew, Herty Liany, Louis C S Tan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 16, 2024
Identification of Genetic Variants in Progressive Supranuclear Palsy in Southeast AsiaAdeline Su Lyn Ng, Ai Huey Tan, Yi Jayne Tan, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 14, 2016
PARK16 is associated with PD in the Malaysian populationAroma Agape Gopalai, Azlina Ahmad-Annuar, Hui-Hua Li, et al.
BMC Research Notes|July 18, 2018
Cranial neural tube defect after trimethoprim exposureNor Linda Abdullah, Renuka Gunasekaran, Siti Waheeda Mohd-Zin, et al.
The Lancet. Neurology|June 9, 2019
Parkinson's disease in the Western Pacific RegionShen-Yang Lim, Ai Huey Tan, Azlina Ahmad-Annuar, et al.
Molecular Genetics & Genomic Medicine|September 6, 2019
LRRK2 N551K and R1398H variants are protective in Malays and Chinese in Malaysia: A case-control association study for Parkinson's diseaseAroma Agape Gopalai, Jia Lun Lim, Hui-Hua Li, et al.
Pageof 13