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Farah Qaiser

Showing results (1-10 of 10) with videos related to

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Current Neurology and Neuroscience Reports|August 14, 2020
Genetics of Epileptic Networks: from Focal to Generalized Genetic EpilepsiesFarah Qaiser, Ryan K C Yuen, Danielle M Andrade
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|March 4, 2026
Frequency of Impaired Oral Glucose Tolerance Test Results in Women with Polycystic Ovary SyndromeSana Zahid, Rabeea Sadaf, Nadia Rani, et al.
Epilepsy & Behavior : E&B|July 25, 2025
Genetic Epilepsies: Clinical pearls for early career epileptologistsDanielle M Andrade, Victor S T Lira, Farah Qaiser, et al.
Orphanet Journal of Rare Diseases|January 7, 2021
Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotypeFarah Qaiser, Yue Yin, Carolyn B Mervis, et al.
Neurology. Genetics|November 27, 2024
Adult Phenotype of <i>CHD2</i>-Associated DisordersMarlene Rong, Quratulain Zulfiqar Ali, Angel Aledo-Serrano, et al.
Neurology. Genetics|December 4, 2023
Adult Phenotype of <i>SYNGAP1</i>-DEEMarlene Rong, Tim Benke, Quratulain Zulfiqar Ali, et al.
Brain Communications|October 8, 2021
Genome sequencing identifies rare tandem repeat expansions and copy number variants in Lennox-Gastaut syndromeFarah Qaiser, Tara Sadoway, Yue Yin, et al.
Epilepsia|March 14, 2025
Variants in ATP6V0C are associated with Dravet-like developmental and epileptic encephalopathyMarlene Rong, Paula T Marques, Quratulain Zulfiqar Ali, et al.
Epilepsy Research|August 21, 2024
Do germline genetic variants influence surgical outcomes in drug-resistant epilepsy?Paula Marques, Patrick B Moloney, Caihong Ji, et al.
Epilepsia|March 4, 2025
Dravet syndrome: From neurodevelopmental to neurodegenerative disease?Arunan Selvarajah, Andrea Sabo, Carolina Gorodetsky, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Current Neurology and Neuroscience Reports|August 14, 2020
Genetics of Epileptic Networks: from Focal to Generalized Genetic EpilepsiesFarah Qaiser, Ryan K C Yuen, Danielle M Andrade
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|March 4, 2026
Frequency of Impaired Oral Glucose Tolerance Test Results in Women with Polycystic Ovary SyndromeSana Zahid, Rabeea Sadaf, Nadia Rani, et al.
Epilepsy & Behavior : E&B|July 25, 2025
Genetic Epilepsies: Clinical pearls for early career epileptologistsDanielle M Andrade, Victor S T Lira, Farah Qaiser, et al.
Orphanet Journal of Rare Diseases|January 7, 2021
Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotypeFarah Qaiser, Yue Yin, Carolyn B Mervis, et al.
Neurology. Genetics|November 27, 2024
Adult Phenotype of <i>CHD2</i>-Associated DisordersMarlene Rong, Quratulain Zulfiqar Ali, Angel Aledo-Serrano, et al.
Neurology. Genetics|December 4, 2023
Adult Phenotype of <i>SYNGAP1</i>-DEEMarlene Rong, Tim Benke, Quratulain Zulfiqar Ali, et al.
Brain Communications|October 8, 2021
Genome sequencing identifies rare tandem repeat expansions and copy number variants in Lennox-Gastaut syndromeFarah Qaiser, Tara Sadoway, Yue Yin, et al.
Epilepsia|March 14, 2025
Variants in ATP6V0C are associated with Dravet-like developmental and epileptic encephalopathyMarlene Rong, Paula T Marques, Quratulain Zulfiqar Ali, et al.
Epilepsy Research|August 21, 2024
Do germline genetic variants influence surgical outcomes in drug-resistant epilepsy?Paula Marques, Patrick B Moloney, Caihong Ji, et al.
Epilepsia|March 4, 2025
Dravet syndrome: From neurodevelopmental to neurodegenerative disease?Arunan Selvarajah, Andrea Sabo, Carolina Gorodetsky, et al.
Pageof 1