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Electroclinical pattern in the transition from West to Lennox-Gastaut syndrome

Epilepsy research, 2020-11, Vol.167, p.106446-106446, Article 106446

2020

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Rasmussen syndrome: absence seizures may be induced by oxcarbazepine

Epileptic disorders, 2019-02, Vol.21 (1), p.108-111

2019

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Real-World Evidence of Factors Affecting Cannabidiol Exposure in Children with Drug-Resistant Developmental and Epileptic Encephalopathies

Pharmaceutics, 2023-08, Vol.15 (8), p.2120

2023

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Rasmussen syndrome: an atypical presentation in ten patients

Epileptic disorders, 2018-12, Vol.20 (6), p.468-478

2018

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Long-term effectiveness and adverse effects of ketogenic diet therapy in infants with drug-resistant epilepsy treated at a single center in Argentina

Epilepsy research, 2021-12, Vol.178, p.106793-106793, Article 106793

2021

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West syndrome: A study of 26 patients receiving short-term therapy

Epilepsy & behavior, 2021-01, Vol.114 (Pt A), p.107235-107235, Article 107235

2021

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Purified cannabidiol as add-on therapy in children with treatment-resistant infantile epileptic spasms syndrome

Seizure (London, England), 2024-02, Vol.115, p.94-99

2024

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Non-epileptic stimulus-sensitive myoclonus in a newborn with developmental and epileptic encephalopathy associated with the SCN8A gene

Epileptic disorders, 2024-10

2024

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Late-onset childhood neuronal ceroid lipofuscinosis: Early clinical and electroencephalographic markers

Epilepsy research, 2018-08, Vol.144, p.49-52

2018

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Cannabidiol in children with treatment-resistant epilepsy with myoclonic-atonic seizures

Epilepsy & behavior, 2023-06, Vol.143, p.109245-109245, Article 109245

2023

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Use of sulthiame as add-on therapy in children with myoclonic atonic epilepsy: A study of 35 patients

Epilepsy & behavior, 2022-06, Vol.131 (Pt A), p.108702-108702, Article 108702

2022

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Benign rolandic epilepsy and generalized paroxysms: A study of 13 patients

Seizure (London, England), 2018-04, Vol.57, p.27-31

2018

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An Ultrafast Ultrahigh-Performance Liquid Chromatography Coupled With Tandem Mass Spectrometry Method for Cannabidiol Monitoring in Pediatric Refractory Epilepsy

Therapeutic drug monitoring, 2021-10, Vol.43 (5), p.712-717

2021

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The ketogenic diet in two paediatric patients with refractory myoclonic status epilepticus

Epileptic disorders, 2015-12, Vol.17 (4), p.491-495

2015

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Ketonemia variability through menstrual cycle in patients undergoing classic ketogenic diet

Frontiers in nutrition (Lausanne), 2023-07, Vol.10, p.1188055-1188055

2023

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Cannabidiol-enriched medical cannabis as add-on therapy in children with treatment-resistant West syndrome: A study of eight patients

Seizure (London, England), 2021-11, Vol.92, p.238-243

2021

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Single-Epileptic Spasms with or without Hypsarrhythmia: A Study of 16 Patients

Journal of pediatric epilepsy, 2017-09, Vol.6 (3), p.149-155

2017

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The Contribution of Argentine Neurologists to the Description of Infantile Epileptic Spasms Syndrome and Related Epileptic and Nonepileptic Neurological Conditions

Journal of pediatric epilepsy, 2023-12, Vol.12 (4), p.117-121

2023

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CDKL5-associated developmental and epileptic encephalopathy: A long-term, longitudinal electroclinical study of 22 cases

Epilepsy research, 2023-02, Vol.190, p.107098-107098, Article 107098

2023

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Vigabatrin-associated brain abnormalities on MRI and other neurological symptoms in patients with West syndrome

Epilepsy & behavior, 2022-04, Vol.129, p.108606-108606, Article 108606

2022

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Sulthiame add-on therapy in children with Lennox-Gastaut syndrome: A study of 44 patients

Seizure (London, England), 2018-11, Vol.62, p.55-58

2018

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Erratum: Single-Epileptic Spasms with or without Hypsarrhythmia: A Study of 16 Patients

Journal of pediatric epilepsy, 2017-09, Vol.6 (3), p.e1-e1

2017

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Epilepsias focales autolimitadas de la infancia

Medicina (Buenos Aires), 2023-10, Vol.83 (suppl 4), p.57-62

2023

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Immunogenicity and tolerability of a multicomponent meningococcal serogroup B (4CMenB) vaccine in healthy adolescents in Chile: a phase 2b/3 randomised, observer-blind, placebo-controlled study

The Lancet (British edition), 2012-02, Vol.379 (9816), p.617-624

2012

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Evidence of the active participation of women in the intergroup conflict based on the use of aggression and cooperation

Scientific reports, 2023-10, Vol.13 (1), p.17742-17742, Article 17742

2023

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Electroclinical pattern in the transition from West to Lennox-Gastaut syndrome

Rasmussen syndrome: absence seizures may be induced by oxcarbazepine

Real-World Evidence of Factors Affecting Cannabidiol Exposure in Children with Drug-Resistant Developmental and Epileptic Encephalopathies

Rasmussen syndrome: an atypical presentation in ten patients

Long-term effectiveness and adverse effects of ketogenic diet therapy in infants with drug-resistant epilepsy treated at a single center in Argentina

West syndrome: A study of 26 patients receiving short-term therapy

Purified cannabidiol as add-on therapy in children with treatment-resistant infantile epileptic spasms syndrome

Non-epileptic stimulus-sensitive myoclonus in a newborn with developmental and epileptic encephalopathy associated with the SCN8A gene

Late-onset childhood neuronal ceroid lipofuscinosis: Early clinical and electroencephalographic markers

Cannabidiol in children with treatment-resistant epilepsy with myoclonic-atonic seizures

Use of sulthiame as add-on therapy in children with myoclonic atonic epilepsy: A study of 35 patients

Benign rolandic epilepsy and generalized paroxysms: A study of 13 patients

An Ultrafast Ultrahigh-Performance Liquid Chromatography Coupled With Tandem Mass Spectrometry Method for Cannabidiol Monitoring in Pediatric Refractory Epilepsy

The ketogenic diet in two paediatric patients with refractory myoclonic status epilepticus

Ketonemia variability through menstrual cycle in patients undergoing classic ketogenic diet

Cannabidiol-enriched medical cannabis as add-on therapy in children with treatment-resistant West syndrome: A study of eight patients

Single-Epileptic Spasms with or without Hypsarrhythmia: A Study of 16 Patients

The Contribution of Argentine Neurologists to the Description of Infantile Epileptic Spasms Syndrome and Related Epileptic and Nonepileptic Neurological Conditions

CDKL5-associated developmental and epileptic encephalopathy: A long-term, longitudinal electroclinical study of 22 cases

Vigabatrin-associated brain abnormalities on MRI and other neurological symptoms in patients with West syndrome

Sulthiame add-on therapy in children with Lennox-Gastaut syndrome: A study of 44 patients

Erratum: Single-Epileptic Spasms with or without Hypsarrhythmia: A Study of 16 Patients

Epilepsias focales autolimitadas de la infancia

Immunogenicity and tolerability of a multicomponent meningococcal serogroup B (4CMenB) vaccine in healthy adolescents in Chile: a phase 2b/3 randomised, observer-blind, placebo-controlled study

Evidence of the active participation of women in the intergroup conflict based on the use of aggression and cooperation

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