K. Myers

发表

Clinical utility of therapeutic drug monitoring of antiepileptic drugs: Systematic review.

A. Ramanakumar, Zanab Al-Roubaie, E. Guadagno, 2020, Neurology. Clinical practice.

The epileptology of Koolen‐de Vries syndrome: Electro‐clinico‐radiologic findings in 31 patients

I. Scheffer, B. D. de Vries, E. Rushing, 2017, Epilepsia.

Heart rate variability measurement in epilepsy: How can we move from research to clinical practice?

P. Perucca, K. Myers, Shobi Sivathamboo, 2018, Epilepsia.

TUBA1A Mutation Associated With Eye Abnormalities in Addition to Brain Malformation.

X. Wei, A. Innes, L. Bello-Espinosa, 2015, Pediatric neurology.

Genetic Epilepsy Syndromes

K. Myers, 2022, Continuum.

DEPDC5 as a potential therapeutic target for epilepsy

I. Scheffer, K. Myers, 2017, Expert opinion on therapeutic targets.

Epilepsy in children with cerebral palsy: a data linkage study

M. Shevell, M. Dorais, M. Oskoui, 2021, Developmental medicine and child neurology.

The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures

I. Scheffer, H. Mefford, R. Burgess, 2019, Annals of neurology.

Randomized Controlled Trial of Melatonin for Sleep Disturbance in Dravet Syndrome: The DREAMS Study.

I. Scheffer, Paul A Lightfoot, M. Ching, 2018, Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine.

The spectrum of indomethacin-responsive headaches in children and adolescents

M. Kabbouche, A. Hershey, C. Saint-Martin, 2022, Cephalalgia : an international journal of headache.

Clinical utility of multigene panel testing in adults with epilepsy and intellectual disability

D. Andrade, F. Filloux, K. Myers, 2019, Epilepsia.

Copy number variation in genetic epilepsy with febrile seizures plus.

S. Chénier, M. Shevell, C. Vincelette, 2020, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Asymptomatic Tonsillar Herniation in a Neonate With Cleidocranial Dysplasia

X. Wei, Morris H. Scantlebury, K. Myers, 2014, Pediatrics.

Genetic Generalized Epilepsy and Intrafamilial Phenotypic Variability with Distal 7q11.23 Deletion

K. Myers, Veronica Birca, 2022, Child neurology open.

Myoclonic Absence Seizures in Dravet Syndrome.

I. Scheffer, K. Myers, 2017, Pediatric neurology.

Vibration therapy tolerated in children with Duchenne muscular dystrophy: a pilot study.

Aneal Khan, B. Ramage, J. Mah, 2014, Pediatric neurology.

Stiripentol efficacy and safety in Dravet syndrome: a 12‐year observational study

I. Scheffer, J. Cross, Paul A Lightfoot, 2018, Developmental medicine and child neurology.

A 12-Year Observational Study of Stiripentol Efficacy and Safety in Dravet Syndrome

I. Scheffer, J. Cross, Paul A Lightfoot, 2018 .

Fatal Cerebral Edema With Status Epilepticus in Children With Dravet Syndrome: Report of 5 Cases

I. Scheffer, M. Mackay, R. Kalnins, 2017, Pediatrics.

De novo SCN1A pathogenic variants in the GEFS+ spectrum: Not always a familial syndrome

I. Scheffer, S. Berkovic, R. Burgess, 2017, Epilepsia.

A proposed guideline for vagus nerve stimulator handling in palliative care and after death

M. Keezer, J. Atkinson, K. Myers, 2020, Epilepsia.

Behavioral effects of cocaine: interactions with D1 dopaminergic antagonists and agonists in mice and squirrel monkeys.

T. Kopajtic, J. Katz, K. Myers, 1999, The Journal of pharmacology and experimental therapeutics.

H. Otsubo, L. Lingappa, T. Hershkovitz, 2020, Epilepsia.

Preadolescent Indomethacin‐Responsive Headaches Without Autonomic Symptoms

K. Myers, Kimberly Smyth, Kim A. Smyth, 2013, Headache.

Self-limited focal epilepsy and childhood apraxia of speech with WAC pathogenic variants.

I. Scheffer, A. Morgan, K. Myers, 2020, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Asphyxiation Causing Distinctive Basal Ganglia Injury and Generalized Dystonia

X. Wei, Katie M. Wiltshire, K. Myers, 2011, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Late-onset seropositive Isaacs’ syndrome after Guillain–Barré syndrome

S. Baker, K. Myers, 2009, Neuromuscular Disorders.

Megalencephaly–Capillary Malformation–Polymicrogyria with Cerebral Venous Thrombosis

C. Sabapathy, O. Fortin, K. Myers, 2020, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

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

Jeremy T. Moreau, F. Dubeau, B. Rosenblatt, 2022, Journal of child neurology.

Diagnostic utility of specific abnormal EEG patterns in children for determining epilepsy phenotype and presence of structural brain abnormalities

C. Poulin, S. Berrahmoune, K. Myers, 2022, Heliyon.

Myoclonic absence seizures with complex gestural automatisms.

I. Scheffer, K. Myers, 2017, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Epilepsy genetics: Current knowledge, applications, and future directions

D. Dyment, K. Myers, D. Johnstone, 2018, Clinical genetics.

PLCB1 Biallelic Point Mutations Cause West Syndrome.

K. Myers, 2019, Pediatric neurology.

Seizures in Sotos syndrome: Phenotyping in 49 patients

I. Scheffer, S. Berrahmoune, C. Vincelette, 2021, Epilepsia open.

Phenotypic Spectrum of Seizure Disorders in MBD5-Associated Neurodevelopmental Disorder

G. Carvill, I. Scheffer, H. Mefford, 2021, Neurology: Genetics.

Sudden unexpected death in GEFS+ families with sodium channel pathogenic variants

M. Shevell, G. Sébire, K. Myers, 2019, Epilepsy Research.

I. Scheffer, K. Myers, 2016 .

Optic neuropathy in the context of leukemia or lymphoma: diagnostic approach to a neuro-oncologic emergency.

M. Brundler, F. Costello, E. Weis, 2017, Neuro-oncology practice.

ADGRV1 is implicated in myoclonic epilepsy

P. Lockhart, I. Scheffer, A. Boys, 2018, Epilepsia.

Torpedo Maculopathy Associated with NEXMIF Mutation

A. Khan, K. Myers, T. Alarcon-Martinez, 2019, Molecular Syndromology.

Cerebral edema in maple syrup urine disease despite newborn screening diagnosis and early initiation of treatment.

Aneal Khan, X. Wei, K. Myers, 2012, JIMD reports.

Spontaneous Multilevel Cerebrospinal Fluid Leak in Marfan Syndrome

C. Saint-Martin, K. Myers, A. Mirchi, 2020, Annals of Neurology.

Addison disease presenting with acute neurologic deterioration: a rare presentation yields new lessons from old observations in primary adrenal failure.

G. Kline, K. Myers, 2010, Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists.

Cigarette smoking: an underused tool in high-performance endurance training

K. Myers, 2010, Canadian Medical Association Journal.

Familial Congenital Facial Synkinesis Due to 12q Duplication: A Case Report and Literature Review

A. Innes, J. Mah, K. Myers, 2016, Pediatrics.

SUDEP risk and autonomic dysfunction in genetic epilepsies

M. Shevell, Ahmed N. Sahly, L. Sadleir, 2021, Autonomic Neuroscience.

Cerebral white matter abnormalities associated with chromosome 18q duplication

C. Saint-Martin, Jiayin Huang, Guergana Tchakarska, 2022, Brain and Development.

Deletion of AFG3L2 associated with spinocerebellar ataxia type 28 in the context of multiple genomic anomalies

Lijia Huang, K. Boycott, K. Myers, 2014, American journal of medical genetics. Part A.

Transcriptome analysis of a ring chromosome 20 patient cohort

I. Scheffer, S. Berkovic, M. Bahlo, 2020, Epilepsia.

X-Linked Familial Focal Epilepsy Associated With Xp22.31 Deletion.

C. Saint-Martin, K. Myers, E. Simard-Tremblay, 2020, Pediatric neurology.

Homozygous THAP1 pathogenic variant causes early onset multifocal dystonia with severe oromandibular/laryngeal dysfunction

K. Myers, Miranda F. Bird, 2022, American journal of medical genetics. Part A.

Heart Rate Variability in Insulo-Opercular Epilepsy

P. Rainville, M. Keezer, P. Pouliot, 2021, Brain sciences.

Heart rate variability in epilepsy: A potential biomarker of sudden unexpected death in epilepsy risk

I. Scheffer, J. Buchhalter, S. Zuberi, 2018, Epilepsia.

Sudden Death After Febrile Seizure Case Report: Cerebral Suppression Precedes Severe Bradycardia

J. Buchhalter, K. Myers, R. Clegg, 2017, Pediatrics.

Contribution of rare genetic variants to drug response in absence epilepsy

I. Scheffer, S. Berkovic, M. Bahlo, 2021, Epilepsy Research.

Hemiconvulsion-hemiplegia-epilepsy evolving to contralateral hemi-Lennox-Gastaut-like phenotype

I. Scheffer, J. Archer, K. Myers, 2018, Brain and Development.

Hemiconvulsion‐Hemiplegia‐Epilepsy in a girl with cobalamin C deficiency

M. Srour, Roy W R Dudley, K. Myers, 2018, Epileptic disorders : international epilepsy journal with videotape.

WWOX developmental and epileptic encephalopathy: Understanding the epileptology and the mortality risk

I. Scheffer, H. Mefford, M. Bahlo, 2023, Epilepsia.

The phenotypic spectrum of epilepsy associated with periventricular nodular heterotopia

F. Dubeau, M. Srour, S. Berrahmoune, 2023, Journal of Neurology.

Aspiring to freedom : commentaries on John Paul II's encyclical The Social concerns of the Church

P. Berger, K. Myers, C. Pope, 1988 .

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

J. Garfinkle, K. Myers, K. Paquette, 2022, Clinical EEG and neuroscience.

A retrospective analysis of memantine use in a pediatric neurology clinic

C. Poulin, S. Berrahmoune, K. Myers, 2021, Brain and Development.

Blake's pouch cyst in 13q deletion syndrome: Posterior fossa malformations may occur due to disruption of multiple genes

M. Newton, M. Wallis, G. Fitt, 2017, American journal of medical genetics. Part A.

Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability Syndrome.

M. M. Morrow, M. Shinawi, D. Chitayat, 2021, Pediatric neurology.

Childhood-onset generalized epilepsy in Bainbridge-Ropers syndrome

I. Scheffer, A. Fry, S. Mohammed, 2018, Epilepsy Research.

De Novo GLI3 Pathogenic Variants May Cause Hypotonia and a Range of Brain Malformations Without Skeletal Abnormalities.

E. Sherr, E. Argilli, K. Myers, 2022, Pediatric neurology.

Significance of BDNF Val66Met Polymorphism in Brain Plasticity of Children.

A. Kirton, M. Hill, K. Myers, 2017, Pediatric neurology.

Systematic review of MRI findings in children with developmental delay or cognitive impairment

X. Wei, K. Murias, K. Myers, 2017, Brain and Development.

MT‐TA pathogenic variants may cause developmental and epileptic encephalopathy without myopathy

Ahmed N. Sahly, K. Myers, D. Buhas, 2022, American journal of medical genetics. Part A.

Infraslow EEG Changes in Infantile Spasms

X. Wei, Morris H. Scantlebury, L. Bello-Espinosa, 2014, Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society.

Xq26 duplications lead to undergrowth or overgrowth via competing pathways including GPC3/GPC4

K. Myers, Gaurav K Karna, 2020, Annals of human genetics.

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

I. Scheffer, M. Srour, Ahmed N. Sahly, 2023, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

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

P. Kwan, P. Perucca, K. Myers, 2023, Epilepsia open.

Is a microRNA‐328 binding site in PAX6 associated with Rolandic epilepsy?

I. Scheffer, S. Berkovic, S. Petrovski, 2017, Annals of clinical and translational neurology.

Mosaic uniparental disomy results in GM1 gangliosidosis with normal enzyme assay

I. Scheffer, M. Bahlo, S. Mandelstam, 2018, American journal of medical genetics. Part A.

Severe DNM1 encephalopathy with dysmyelination due to recurrent splice site pathogenic variant

M. Srour, J. St‐Onge, Ahmed N. Sahly, 2020, Human Genetics.

Ataxia and Diplopia

K. Myers, A. Laliberté, 2023, Neurology: Genetics.

SCN1A as a therapeutic target for Dravet syndrome

K. Myers, 2023, Expert opinion on therapeutic targets.