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Medrxiv : the Preprint Server for Health Sciences|June 22, 2026
Multi-ancestry analysis of POLG variants in Parkinson's diseaseYi Wen Tay, Inas Elsayed, Dennis Yeow, et al.Annals of Clinical and Translational Neurology|February 26, 2025
Targeted Long-Read Sequencing as a Single Assay Improves the Diagnosis of Spastic-Ataxia DisordersLaura Ivete Rudaks, Igor Stevanovski, Dennis Yeow, et al.Movement Disorders Clinical Practice|February 24, 2026
MDSGene Systematic Review of Common Forms of Dominant Hereditary Spastic Paraplegia: Novel InsightsCe Kang, Rajasumi Rajalingam, Zachary Walls, et al.Nature Communications|November 24, 2025
Targeted sequencing and iterative assembly of near-complete genomesHasindu Gamaarachchi, Igor Stevanovski, Jillian M Hammond, et al.Parkinsonism & Related Disorders|May 21, 2024
Genome sequencing reanalysis increases the diagnostic yield in dystoniaAvi Fellner, Gurusidheshwar M Wali, Neil Mahant, et al.Nature Communications|July 4, 2026
Targeted long-read sequencing enables comprehensive analysis of the genetic and epigenetic landscape of inherited myopathiesDennis Yeow, Andre L M Reis, Igor Stevanovski, et al.Annals of Neurology|June 9, 2026
Monoallelic POLR3A Variants Cause Early-Onset Peripheral NeuropathyLuiza L P Ramos, Jevin M Parmar, Robin Wijngaard, et al.Pageof 2