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Precision medicine for epilepsies: are we there yet?

Journal of neurology, neurosurgery and psychiatry, 2021-10, Vol.92 (10), p.1032-1032

Andrade, Danielle M.

2021

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Third-generation computational approaches for genetic variant interpretation

Brain (London, England : 1878), 2023-02, Vol.146 (2), p.411-412

2023

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Teaching NeuroImage: Ictal Pouting Associated With Focal Cortical Dysplasia and Frontal Seizures on Stereotactic Depth Electrode EEG

Neurology, 2023-04, Vol.100 (14), p.683-684

2023

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Genetic Mechanisms Behind Severe Psychotic Reactions to Levetiracetam

Epilepsy currents, 2023-01, Vol.23 (1), p.29-31

Andrade, Danielle M.

2023

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Is There a Continuum Between Acute Symptomatic Seizures Secondary to Autoimmune Encephalitis and Autoimmune-Associated Epilepsy?

Epilepsy currents, 2023-09, Vol.23 (5), p.286-288

Andrade, Danielle M.

2023

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A systematic review of adults with Dravet syndrome

Seizure (London, England), 2021-04, Vol.87, p.39-45

2021

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Somatic Variants and Surgical Epilepsies: Search and You Will Find

Epilepsy currents, 2023-05, Vol.23 (3), p.196-198

Andrade, Danielle M.

2023

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Epilepsy gene panel yield and impact on outcomes for adults with unexplained seizures

Epilepsia (Copenhagen), 2020-08, Vol.61 (8), p.1797-1798

2020

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Global characterization of copy number variants in epilepsy patients from whole genome sequencing

PLoS genetics, 2018-04, Vol.14 (4), p.e1007285-e1007285

2018

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Time Is Brain: The Importance of an Accurate SCN1A Prediction Score in the Era of Precision Medicine

Epilepsy currents, 2022-07, Vol.22 (4), p.231-233

Andrade, Danielle M.

2022

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Tonic seizures: a diagnostic clue of anti-LGI1 encephalitis?

Neurology, 2011-04, Vol.76 (15), p.1355-1357

2011

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Prevalence of Pathogenic Copy Number Variation in Adults With Pediatric-Onset Epilepsy and Intellectual Disability

JAMA neurology, 2017-11, Vol.74 (11), p.1301

2017

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Frontal infraslow activity marks the motor spasms of anti-LGI1 encephalitis

Clinical neurophysiology, 2018-01, Vol.129 (1), p.59-68

2018

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Novel neuropathological findings in a long-term survivor of D-2-hydroxyglutaric aciduria type 1

Virchows Archiv : an international journal of pathology, 2024-07

2024

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Transition in epilepsy – A pilot study with patients in and outside of academic centers

Epilepsy & behavior, 2024-02, Vol.151, p.109624-109624, Article 109624

2024

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Starting stiripentol in adults with Dravet syndrome? Watch for ammonia and carnitine

Epilepsia (Copenhagen), 2020-11, Vol.61 (11), p.2435-2441

2020

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Antecollis and levodopa-responsive parkinsonism are late features of Dravet syndrome

Neurology, 2014-06, Vol.82 (24), p.2250-2251

2014

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Anterior Nucleus Deep Brain Stimulation for Refractory Epilepsy: Insights Into Patterns of Seizure Control and Efficacious Target

Neurosurgery, 2016-06, Vol.78 (6), p.802-811

2016

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Progressive Worsening of Gait and Motor Abnormalities in Older Adults With Dravet Syndrome

Neurology, 2022-05, Vol.98 (22), p.e2204

2022

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Practical guidelines for managing adults with 22q11.2 deletion syndrome

Genetics in medicine, 2015-08, Vol.17 (8), p.599-609

2015

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Adult motor phenotype differentiates Dravet syndrome from Lennox‐Gastaut syndrome and links SCN1A to early onset parkinsonian features

Epilepsia (Copenhagen), 2017-03, Vol.58 (3), p.e44-e48

2017

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Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature

Genetics in medicine, 2015-02, Vol.17 (2), p.149-157

2015

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Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability

American journal of human genetics, 2014-12, Vol.95 (6), p.721-728

2014

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Precision medicine for epilepsies: are we there yet?

Third-generation computational approaches for genetic variant interpretation

Teaching NeuroImage: Ictal Pouting Associated With Focal Cortical Dysplasia and Frontal Seizures on Stereotactic Depth Electrode EEG

Genetic Mechanisms Behind Severe Psychotic Reactions to Levetiracetam

Is There a Continuum Between Acute Symptomatic Seizures Secondary to Autoimmune Encephalitis and Autoimmune-Associated Epilepsy?

A systematic review of adults with Dravet syndrome

Somatic Variants and Surgical Epilepsies: Search and You Will Find

Epilepsy gene panel yield and impact on outcomes for adults with unexplained seizures

Global characterization of copy number variants in epilepsy patients from whole genome sequencing

Time Is Brain: The Importance of an Accurate SCN1A Prediction Score in the Era of Precision Medicine

Tonic seizures: a diagnostic clue of anti-LGI1 encephalitis?

Prevalence of Pathogenic Copy Number Variation in Adults With Pediatric-Onset Epilepsy and Intellectual Disability

Frontal infraslow activity marks the motor spasms of anti-LGI1 encephalitis

Novel neuropathological findings in a long-term survivor of D-2-hydroxyglutaric aciduria type 1

Transition in epilepsy – A pilot study with patients in and outside of academic centers

Starting stiripentol in adults with Dravet syndrome? Watch for ammonia and carnitine

Antecollis and levodopa-responsive parkinsonism are late features of Dravet syndrome

Anterior Nucleus Deep Brain Stimulation for Refractory Epilepsy: Insights Into Patterns of Seizure Control and Efficacious Target

Progressive Worsening of Gait and Motor Abnormalities in Older Adults With Dravet Syndrome

Practical guidelines for managing adults with 22q11.2 deletion syndrome

Epilepsy: Transition from pediatric to adult care. Recommendations of the Ontario epilepsy implementation task force

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1

Adult motor phenotype differentiates Dravet syndrome from Lennox‐Gastaut syndrome and links SCN1A to early onset parkinsonian features

Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature

Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability

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