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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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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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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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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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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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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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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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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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Seizures and early onset dementia: D2HGA1 inborn error of metabolism in adults

Annals of clinical and translational neurology, 2020-10, Vol.7 (10), p.2052-2056

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

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

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

Precision medicine for epilepsies: are we there yet?

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

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)

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?

Somatic Variants and Surgical Epilepsies: Search and You Will Find

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

Seizures and early onset dementia: D2HGA1 inborn error of metabolism in adults

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