Lista de obras - Kenneth Myers - Dominio Público Uruguay

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

artículo científico publicado en 2020

ADGRV1 is implicated in myoclonic epilepsy

artículo científico publicado en 2017

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

artículo científico publicado en 2010

Asphyxiation causing distinctive basal ganglia injury and generalized dystonia.

artículo científico publicado en 2011

Asymptomatic Tonsillar Herniation in a Neonate With Cleidocranial Dysplasia

scientific article published on 20 January 2014

Author Response: Teaching Video NeuroImages: Pathologic Yawning: A Sign of Brainstem Involvement in Acute Disseminated Encephalomyelitis?

artículo científico publicado en 2021

Author response: Clinical utility of therapeutic drug monitoring of antiepileptic drugs

scientific article published on 01 February 2020

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

article

CLASP1 regulates endothelial cell branching morphology and directed migration

artículo científico publicado en 2017

Can academic satire exist in the age of "fake news?" Tracking the citation record of a "holiday review" paper

scientific article published on 16 December 2019

Cell Phone Saccades: Electroencephalographic Artifact for the Twenty-first Century

artículo científico publicado en 2016

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

artículo científico publicado en 2011

Childhood-onset generalized epilepsy in Bainbridge-Ropers syndrome

artículo científico publicado en 2018

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

artículo científico publicado el 14 de diciembre de 2010

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

scientific article published on 05 July 2019

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

scientific article published on 01 August 2020

Corrigendum to “Childhood-onset generalized epilepsy in Bainbridge-Ropers syndrome” [Epilepsy Res. 140 (2018) 166–170]

scientific article published on 10 August 2018

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

artículo científico publicado en 2017

Deletion ofAFG3L2associated with spinocerebellar ataxia type 28 in the context of multiple genomic anomalies

artículo científico publicado en 2014

Diabetic patients with psychiatric illness

artículo científico publicado en 2010

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

artículo científico publicado en 2022

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

artículo científico publicado en 2016

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

artículo científico publicado en 2017

Fragile Females: Case Series of Epilepsy in Girls With FMR1 Disruption

artículo científico publicado en 2019

GRIN2A-Related Speech Disorders and Epilepsy

artículo científico publicado en 1993

Genetic literacy series: genetic epilepsy with febrile seizures plus

scientific article published on 01 August 2018

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

scientific article published on 06 June 2018

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

artículo científico publicado en 2018

Hydrostatic Pressure Stimulation of Human Mesenchymal Stem Cells Seeded on Collagen-Based Artificial Extracellular Matrices

article

Hydrostatic pressure sensation in cells: integration into the tensegrity model

artículo científico publicado en 2007

Incorporation of fixation-removal with Fresnel glasses in a routine EEG protocol

scientific article published on 24 May 2019

Infantile ictal apneas in a child with williams-beuren syndrome

artículo científico publicado en 2013

Infraslow EEG changes in infantile spasms.

artículo científico publicado en 2014

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

artículo científico publicado en 2017

KANSL1 variation is not a major contributing factor in self-limited focal epilepsy syndromes of childhood

artículo científico publicado en 2018

KCNT1-related epilepsy: An international multicenter cohort of 27 pediatric cases

artículo científico publicado en 2020

Late-onset Leclercia adecarboxylata bacteraemia in a premature infant in the NICU.

artículo científico

Late-onset seropositive Isaacs' syndrome after Guillain-Barré syndrome

artículo científico publicado en 2009

Megalencephaly-Capillary Malformation-Polymicrogyria with Cerebral Venous Thrombosis

artículo científico publicado en 2020

Monocarboxylate transporter-1 deficiency results in severe metabolic acidosis with ketogenic diet in early onset absence epilepsy: Case report

artículo científico publicado en 2019

Mosaic uniparental disomy results in GM1 gangliosidosis with normal enzyme assay

artículo científico publicado en 2017

Myoclonic Absence Seizures in Dravet Syndrome

artículo científico publicado en 2017

Myoclonic absence seizures with complex gestural automatisms

artículo científico publicado en 2017

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

scientific article published on 09 December 2016

Osteoblast-like cells and fluid flow: cytoskeleton-dependent shear sensitivity.

artículo científico publicado en 2007

PLCB1 Biallelic Point Mutations Cause West Syndrome

scientific article published on 22 November 2018

Postictal Subcortical Restricted Diffusion in a Child With Focal Symptomatic Epilepsy

artículo científico publicado en 2014

Preadolescent Indomethacin-Responsive Headaches Without Autonomic Symptoms

scientific article published on 13 February 2013

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

artículo científico publicado en 2018

Response to Canadian Neurophysiology Laboratory COVID-19 Practice Guidelines

artículo científico publicado en 2020

Rhythmic Sawtooth EEG Waveforms in Neonatal Hypoxic-Ischemic/Hypoglycemic Encephalopathy

artículo científico publicado en 2018

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

artículo científico publicado en 2021

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

scientific article published on 09 September 2020

Significance of BDNF Val66Met Polymorphism in Brain Plasticity of Children

artículo científico publicado en 2016

Spontaneous Multilevel Cerebrospinal Fluid Leak in Marfan Syndrome

artículo científico publicado en 2020

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

artículo científico publicado en 2018

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

artículo científico publicado en 2017

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

artículo científico publicado en 2019

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

artículo científico publicado en 2017

TUBA1A Mutation Associated With Eye Abnormalities in Addition to Brain Malformation

artículo científico publicado en 2015

Teaching NeuroImages: MRI findings in X-linked adrenoleukodystrophy.

artículo científico publicado en 2015

Teaching Video Neuroimages: Pathologic yawning: A sign of brainstem involvement in acute disseminated encephalomyelitis?

scientific article published on 04 May 2020

The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures

scientific article published on 01 December 2019

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

artículo científico publicado en 2017

Thoracic Myelopathy Secondary to Seizure Following Scoliosis Surgery

scientific article published on 02 December 2011

Torpedo Maculopathy Associated with NEXMIF Mutation

artículo científico publicado en 2019

Transcriptome analysis of a ring chromosome 20 patient cohort

artículo científico publicado en 2020

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

artículo científico publicado en 2014

Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation.

artículo científico publicado en 2014

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

artículo científico publicado en 2019

Lista de obras de Kenneth Myers

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

ADGRV1 is implicated in myoclonic epilepsy

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

Asphyxiation causing distinctive basal ganglia injury and generalized dystonia.

Asymptomatic Tonsillar Herniation in a Neonate With Cleidocranial Dysplasia

Author Response: Teaching Video NeuroImages: Pathologic Yawning: A Sign of Brainstem Involvement in Acute Disseminated Encephalomyelitis?

Author response: Clinical utility of therapeutic drug monitoring of antiepileptic drugs

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

CLASP1 regulates endothelial cell branching morphology and directed migration

Can academic satire exist in the age of "fake news?" Tracking the citation record of a "holiday review" paper

Cell Phone Saccades: Electroencephalographic Artifact for the Twenty-first Century

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

Childhood-onset generalized epilepsy in Bainbridge-Ropers syndrome

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

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

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

Corrigendum to “Childhood-onset generalized epilepsy in Bainbridge-Ropers syndrome” [Epilepsy Res. 140 (2018) 166–170]

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

Deletion ofAFG3L2associated with spinocerebellar ataxia type 28 in the context of multiple genomic anomalies

Diabetic patients with psychiatric illness

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

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

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

Fragile Females: Case Series of Epilepsy in Girls With FMR1 Disruption

GRIN2A-Related Speech Disorders and Epilepsy

Genetic literacy series: genetic epilepsy with febrile seizures plus

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

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

Hydrostatic Pressure Stimulation of Human Mesenchymal Stem Cells Seeded on Collagen-Based Artificial Extracellular Matrices

Hydrostatic pressure sensation in cells: integration into the tensegrity model

Incorporation of fixation-removal with Fresnel glasses in a routine EEG protocol

Infantile ictal apneas in a child with williams-beuren syndrome

Infraslow EEG changes in infantile spasms.

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

KANSL1 variation is not a major contributing factor in self-limited focal epilepsy syndromes of childhood

KCNT1-related epilepsy: An international multicenter cohort of 27 pediatric cases

Late-onset Leclercia adecarboxylata bacteraemia in a premature infant in the NICU.

Late-onset seropositive Isaacs' syndrome after Guillain-Barré syndrome

Megalencephaly-Capillary Malformation-Polymicrogyria with Cerebral Venous Thrombosis

Monocarboxylate transporter-1 deficiency results in severe metabolic acidosis with ketogenic diet in early onset absence epilepsy: Case report

Mosaic uniparental disomy results in GM1 gangliosidosis with normal enzyme assay

Myoclonic Absence Seizures in Dravet Syndrome

Myoclonic absence seizures with complex gestural automatisms

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

Osteoblast-like cells and fluid flow: cytoskeleton-dependent shear sensitivity.

PLCB1 Biallelic Point Mutations Cause West Syndrome

Postictal Subcortical Restricted Diffusion in a Child With Focal Symptomatic Epilepsy

Preadolescent Indomethacin-Responsive Headaches Without Autonomic Symptoms

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

Response to Canadian Neurophysiology Laboratory COVID-19 Practice Guidelines

Rhythmic Sawtooth EEG Waveforms in Neonatal Hypoxic-Ischemic/Hypoglycemic Encephalopathy

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

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

Significance of BDNF Val66Met Polymorphism in Brain Plasticity of Children

Spontaneous Multilevel Cerebrospinal Fluid Leak in Marfan Syndrome

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

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

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

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

TUBA1A Mutation Associated With Eye Abnormalities in Addition to Brain Malformation

Teaching NeuroImages: MRI findings in X-linked adrenoleukodystrophy.

Teaching Video Neuroimages: Pathologic yawning: A sign of brainstem involvement in acute disseminated encephalomyelitis?

The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures

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

Thoracic Myelopathy Secondary to Seizure Following Scoliosis Surgery

Torpedo Maculopathy Associated with NEXMIF Mutation

Transcriptome analysis of a ring chromosome 20 patient cohort

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

Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation.

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