Kenneth Myers

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Assistant Professor

McGill University Health Centre

Canada

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About

Kenneth Myers is an Assistant Professor at McGill University Health Centre in Canada. His research focuses on neurologic conditions, particularly in the context of epilepsy and mitochondrial DNA depletion disorders. Recent publications include studies on vagus nerve stimulation responses, the impact of sociocultural factors on caregivers, and the safety of novel treatments for various neurodevelopmental disorders.

Recent Grants

Grant: Close

Pyrimidine Deoxynucleosides in Treatment of Mitochondrial DNA Depletion Disorders

Open Date: 2022-12-01

Close Date: 2024-12-01

Grant: Close

Open Label Trial of Deoxycytidine and Deoxythymidine for Mitochondrial DNA Depletion Disorders

Open Date: 2022-07-01

Close Date: 2023-06-01

Grant: Close

Phase I/II Trial of Deoxynucleotides for POLG-Related Disorders

Open Date: 2021-09-01

Close Date: 2023-08-01

Grant: Close

Improving the Care of Children with Genetic Epilepsy

Open Date: 2020-07-01

Close Date: 2024-06-01

Grant: Close

Evaluation of White Matter Organization in People with Koolen-de Vries Syndrome Using Diffusion Magnetic Resonance Imaging

Open Date: 2020-01-01

Close Date: 2021-01-01

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Collaborators (6)

Terence O'Brien

MONASH UNIVERSITY

AUSTRALIA

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Agnes Bloch-Zupan

Professeur des Universités - Praticien Hospitalier

University of Strasbourg

FRANCE

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Patrick Kwan

AUSTRALIA

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Katharina Schiller

McGill University

CANADA

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Piero Perucca

AUSTRALIA

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Juan Pablo Appendino

Clinical Associate Professor

University of Calgary

CANADA

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Kenneth Myers

Research Interests

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About

Recent Grants

Articles (27)

Response to vagus nerve stimulation in people with ring chromosome 20

Uncoupling in a child with tonic seizures

Myotonic Discharges in Infantile Sandhoff Disease

Comparative analysis of new-onset refractory status epilepticus in adult and pediatric patients: immunotherapy timing and functional outcomes

Investigating the safety and efficacy of deoxycytidine/deoxythymidine in mitochondrial DNA depletion disorders: phase 2 open-label trial

Recurrent status epilepticus and severe bifrontal hypometabolism in PGAP1‐related neurodevelopmental disorder

Eating habits and behaviors in children with Dravet syndrome: A case–control study

Mosaic CLTC pathogenic variant causing focal epilepsy with normal intelligence

Intrafamilial Phenotypic Variability in SYNE1‐Related Disorder

Safety and efficacy of deoxycytidine/deoxythymidine combination therapy in POLG-related disorders: 6-month interim results of an open-label, single arm, phase 2 trial

Acute encephalopathy with biphasic seizures and late reduced diffusion with concurrent transverse myelitis

Epilepsy in Legius syndrome: Coincidence or causation?

Understanding of Consciousness in Absence Seizures: A Literature Review

Sociocultural Factors Influence on Burden and Stress of Caregivers of Children with Epilepsy

Utility of genetic testing in the pre-surgical evaluation of children with drug-resistant epilepsy

Ictal asystole and increased ictal heart rate variability in PCDH19‐related epilepsy

Sleep and respiratory abnormalities in adults with developmental and epileptic encephalopathies using polysomnography and video‐EEG monitoring

Ataxia and Diplopia

Teaching NeuroImage: Low-Frequency Photoparoxysmal Response in a Patient With Neuronal Ceroid Lipofuscinosis Type 2

Awake Craniotomy Language Mapping in Children With Drug-Resistant Epilepsy due to Focal Cortical Dysplasia

SCN1A as a therapeutic target for Dravet syndrome

The epileptology of Wiedemann-Steiner syndrome: Electroclinical findings in five patients with KMT2A pathogenic variants

GenIDA, a participatory patient registry for genetic forms of intellectual disability provides detailed caregiver-reported information on 237 individuals with Koolen-de Vries syndrome

Objective Structured Clinical Examination: Underused Tool in Epilepsy Fellowship Programs?

Surgically Remediable Secondary Network Epileptic Encephalopathies With Continuous Spike Wave in Sleep: Lesions May Not Be Visible on Brain Magnetic Resonance Imaging (MRI)

Response to Hydrocortisone in an Extremely Preterm Neonate With Late-Onset Sepsis, Meningoencephalitis, and Drug-Resistant Seizures

Post-vaccination drug-resistant epileptic spasms associated with homozygous IFNAR2 pathogenic variant: Case report✰

Collaborators (6)

Terence O'Brien

Agnes Bloch-Zupan

Patrick Kwan

Katharina Schiller

Piero Perucca

Juan Pablo Appendino

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