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

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

2011

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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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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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Sex-specific disease modifiers in juvenile myoclonic epilepsy

Scientific reports, 2022-02, Vol.12 (1), p.2785-2785, Article 2785

2022

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22q11.2 deletion syndrome lowers seizure threshold in adult patients without epilepsy

Epilepsia (Copenhagen), 2017-06, Vol.58 (6), p.1095-1101

2017

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Prevalence of hypocalcaemia and its associated features in 22q11·2 deletion syndrome

Clinical endocrinology (Oxford), 2014-08, Vol.81 (2), p.190-196

2014

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Mitochondrial Encephalopathy With Lactic Acidosis and Stroke-like Episodes (MELAS) May Respond to Adjunctive Ketogenic Diet

Pediatric neurology, 2014-05, Vol.50 (5), p.498-502

2014

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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

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

2023

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Imaging in medically refractory epilepsy at 3 Tesla: a 13-year tertiary adult epilepsy center experience

Insights into imaging, 2022-06, Vol.13 (1), p.99-99, Article 99

2022

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Excluding Digenic Inheritance of PGAP2 and PGAP3 Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with PGAP2 Gene Variants in Hyperphosphatasia with Mental Retardation Syndrome-3 (HPMRS3)

Genes, 2023-01, Vol.14 (2), p.359

2023

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Myopathic dysphagia caused by thyrotoxicosis: a case report and review of the literature

Endocrinology, diabetes & metabolism case reports, 2022-11, Vol.2022 (1), p.1-4

2022

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Deep brain stimulation of the anterior nucleus of the thalamus: Effects of electrical stimulation on pilocarpine-induced seizures and status epilepticus

Epilepsy research, 2008-02, Vol.78 (2), p.117-123

2008

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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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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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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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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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Epilepsy Transition: Let’s start planting the seed

European journal of paediatric neurology, 2016-07, Vol.20 (4), p.684-685

2016

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Daily listening to Mozart reduces seizures in individuals with epilepsy: A randomized control study

Epilepsia open, 2020-06, Vol.5 (2), p.285-294

2020

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Genetic Mechanisms Behind Severe Psychotic Reactions to Levetiracetam

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

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

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

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

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

Sex-specific disease modifiers in juvenile myoclonic epilepsy

22q11.2 deletion syndrome lowers seizure threshold in adult patients without epilepsy

Prevalence of hypocalcaemia and its associated features in 22q11·2 deletion syndrome

Mitochondrial Encephalopathy With Lactic Acidosis and Stroke-like Episodes (MELAS) May Respond to Adjunctive Ketogenic Diet

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

Imaging in medically refractory epilepsy at 3 Tesla: a 13-year tertiary adult epilepsy center experience

Excluding Digenic Inheritance of PGAP2 and PGAP3 Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with PGAP2 Gene Variants in Hyperphosphatasia with Mental Retardation Syndrome-3 (HPMRS3)

Myopathic dysphagia caused by thyrotoxicosis: a case report and review of the literature

Deep brain stimulation of the anterior nucleus of the thalamus: Effects of electrical stimulation on pilocarpine-induced seizures and status epilepticus

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

A systematic review of adults with Dravet syndrome

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

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

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

Epilepsy Transition: Let’s start planting the seed

Daily listening to Mozart reduces seizures in individuals with epilepsy: A randomized control study

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