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Current Opinion in Neurology|May 21, 2025
Barriers to clinical genetic testing in movement disordersDennis Yeow, Laura I Rudaks, Kishore R KumarPediatric Neurology|May 29, 2012
Novel clinical features in pontine tegmental cap dysplasiaLaura I Rudaks, Sandeep Patel, Christopher P BarnettPediatric Cardiology|March 1, 2012
Hypertrophic cardiomyopathy with cardiac rupture and tamponade caused by congenital disorder of glycosylation type IaLaura I Rudaks, Chad Andersen, T Y Khong, et al.Pediatric Neurology|August 10, 2011
Novel TSEN54 mutation causing pontocerebellar hypoplasia type 4Laura I Rudaks, Lynette Moore, Karen L Shand, et al.Tremor and Other Hyperkinetic Movements (New York, N.Y.)|January 15, 2024
Genetic Testing of Movements Disorders: A Review of Clinical UtilityDennis Yeow, Laura I Rudaks, Sue-Faye Siow, et al.Genes|September 28, 2023
Outcome Measures and Biomarkers for Clinical Trials in Hereditary Spastic Paraplegia: A Scoping ReviewSue-Faye Siow, Dennis Yeow, Laura I Rudaks, et al.American Journal of Medical Genetics. Part A|April 8, 2022
Decompensation of cardiorespiratory function and emergence of anemia during pregnancy in a case of mitochondrial myopathy, lactic acidosis, and sideroblastic anemia 2 with compound heterozygous YARS2 pathogenic variantsLaura I Rudaks, Eloise Watson, Carly Oboudiyat, 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.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.Pageof 2