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Diet in the Treatment of Epilepsy: What We Know So Far

Nutrients, 2020-08, Vol.12 (9), p.2645

2020

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The pharmacological management of Lennox-Gastaut syndrome and critical literature review

Seizure (London, England), 2018-12, Vol.63, p.17-25

2018

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Brain and eye involvement in McCune-Albright Syndrome: clinical and translational insights

Frontiers in endocrinology (Lausanne), 2023-05, Vol.14, p.1092252-1092252

2023

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Pharmacokinetics and Drug Interaction of Antiepileptic Drugs in Children and Adolescents

Paediatric drugs, 2018-10, Vol.20 (5), p.429-453

2018

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Ketogenic diet and childhood neurological disorders other than epilepsy: an overview

Expert review of neurotherapeutics, 2017-05, Vol.17 (5), p.461-473

2017

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The relationship between migraine and menstrual cycle: A growing evidence

European journal of paediatric neurology, 2020-05, Vol.26, p.3-3

2020

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The role of polytherapy in the management of epilepsy: suggestions for rational antiepileptic drug selection

Expert review of neurotherapeutics, 2020-02, Vol.20 (2), p.167-173

2020

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An update on brivaracetam for the treatment of pediatric partial epilepsy

Expert opinion on pharmacotherapy, 2021-07, Vol.22 (11), p.1387-1395

2021

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Intramuscular Midazolam for treatment of Status Epilepticus

Expert opinion on pharmacotherapy, 2021-01, Vol.22 (1), p.37-44

2021

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Pharmacokinetic considerations for anti-epileptic drugs in children

Expert opinion on drug metabolism & toxicology, 2019-03, Vol.15 (3), p.199-211

2019

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High-Dose Cytomegalovirus (CMV) Hyperimmune Globulin and Maternal CMV DNAemia Independently Predict Infant Outcome in Pregnant Women With a Primary CMV Infection

Clinical infectious diseases, 2020-09, Vol.71 (6), p.1491-1498

2020

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Anti-viral therapy for congenital cytomegalovirus infection: pharmacokinetics, efficacy and side effects

The journal of maternal-fetal & neonatal medicine, 2016-05, Vol.29 (10), p.1657-1664

2016

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Multiorgan mitochondrial dysfunction is not a main feature of MFN2 mutations (Reply to: CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder)

European journal of paediatric neurology, 2018-09, Vol.22 (5), p.892-893

2018

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New developments in the management of partial-onset epilepsy: role of brivaracetam

Drug design, development and therapy, 2017-01, Vol.11, p.643-657

2017

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Clinical and electroencephalographic features of epilepsy in patients with triple X syndrome: A case series

Seizure (London, England), 2022-11, Vol.102, p.32-35

2022

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Epilepsy, electroclinical features, and long‐term outcomes in Pitt–Hopkins syndrome due to pathogenic variants in the TCF4 gene

European journal of neurology, 2022-01, Vol.29 (1), p.19-25

2022

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Cessation of epilepsy therapy in children

Expert review of neurotherapeutics, 2016-05, Vol.16 (5), p.549-559

2016

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A novel homozygous MFN2 mutation associated with severe and atypical CMT2 phenotype

European journal of paediatric neurology, 2018-05, Vol.22 (3), p.563-567

2018

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Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up study

Epilepsy & behavior, 2020-02, Vol.103 (Pt A), p.106578-106578, Article 106578

2020

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A Case of Salt-Wasting Congenital Adrenal Hyperplasia with Triple Homozygous Mutation: Review of Literature

Journal of pediatric genetics (Birmingham, Ala.), 2021-03, Vol.10 (1), p.057-062

2021

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A Case of Salt-Wasting Congenital Adrenal Hyperplasia with Triple Homozygous Mutation: Review of Literature

Journal of pediatric genetics, 2021, Vol.10 (1), p.57-62

2021

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Myosteatosis is closely associated with sarcopenia and significantly worse outcomes in patients with cirrhosis

Journal of hepatology, 2024-05

2024

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Prevalence of hepatitis D virus infection in Central Italy has remained stable across the last 2 decades with dominance of subgenotypes 1 and characterized by elevated viral replication

International journal of infectious diseases, 2024-01, Vol.138, p.1-9

2024

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WED-203 - Stable temporal trend of HDV seroprevalence in central Italy across the last two decades with the circulation of HDV sub-genotypes 1 inducing different inflammatory stimuli

Journal of hepatology, 2023-06, Vol.78, p.S1122-S1123

2023

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Diet in the Treatment of Epilepsy: What We Know So Far

The pharmacological management of Lennox-Gastaut syndrome and critical literature review

Brain and eye involvement in McCune-Albright Syndrome: clinical and translational insights

Pharmacokinetics and Drug Interaction of Antiepileptic Drugs in Children and Adolescents

Ketogenic diet and childhood neurological disorders other than epilepsy: an overview

The relationship between migraine and menstrual cycle: A growing evidence

The role of polytherapy in the management of epilepsy: suggestions for rational antiepileptic drug selection

An update on brivaracetam for the treatment of pediatric partial epilepsy

Intramuscular Midazolam for treatment of Status Epilepticus

Pharmacokinetic considerations for anti-epileptic drugs in children

High-Dose Cytomegalovirus (CMV) Hyperimmune Globulin and Maternal CMV DNAemia Independently Predict Infant Outcome in Pregnant Women With a Primary CMV Infection

Anti-viral therapy for congenital cytomegalovirus infection: pharmacokinetics, efficacy and side effects

Multiorgan mitochondrial dysfunction is not a main feature of MFN2 mutations (Reply to: CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder)

New developments in the management of partial-onset epilepsy: role of brivaracetam

Clinical and electroencephalographic features of epilepsy in patients with triple X syndrome: A case series

Epilepsy, electroclinical features, and long‐term outcomes in Pitt–Hopkins syndrome due to pathogenic variants in the TCF4 gene

Cessation of epilepsy therapy in children

A PAK1 Mutational Hotspot Within the Regulatory CRIPaK Domain is Associated With Severe Neurodevelopmental Disorders in Children

A novel homozygous MFN2 mutation associated with severe and atypical CMT2 phenotype

Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up study

A Case of Salt-Wasting Congenital Adrenal Hyperplasia with Triple Homozygous Mutation: Review of Literature

A Case of Salt-Wasting Congenital Adrenal Hyperplasia with Triple Homozygous Mutation: Review of Literature

Myosteatosis is closely associated with sarcopenia and significantly worse outcomes in patients with cirrhosis

Prevalence of hepatitis D virus infection in Central Italy has remained stable across the last 2 decades with dominance of subgenotypes 1 and characterized by elevated viral replication

WED-203 - Stable temporal trend of HDV seroprevalence in central Italy across the last two decades with the circulation of HDV sub-genotypes 1 inducing different inflammatory stimuli

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