List of works - Amy McTague

Clinical and molecular characterization of KCNT1-related severe early-onset epilepsy

scientific article published in December 2017

Delineation of the movement disorders associated withFOXG1mutations: Table 1

scientific article

Episodic dyscontrol syndrome

scientific article published on 01 June 2010

GABRB3 mutations: a new and emerging cause of early infantile epileptic encephalopathy.

scientific article published on 9 December 2015

GNAO1 encephalopathy: Broadening the phenotype and evaluating treatment and outcome.

scientific article

Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis.

scientific article published on 18 March 2016

Intravenous levetiracetam in acute repetitive seizures and status epilepticus in children: Experience from a children's hospital ⬇️

scientific article published on June 19, 2012

Migrating partial seizures of infancy: expansion of the electroclinical, radiological and pathological disease spectrum.

scientific article published on 18 April 2013

Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizures

scientific article

Myoclonic epilepsy in a child with 17q22-q23.1 deletion

scientific article published on 21 June 2013

Navigating the genetic landscape of childhood epilepsy: a new perspective?

scientific article published on 10 March 2019

RARS2 mutations in a sibship with infantile spasms

scientific article published on 8 April 2016

SLC25A22 is a novel gene for migrating partial seizures in infancy.

scientific article

Severe infantile epileptic encephalopathy due to mutations in PLCB1: expansion of the genotypic and phenotypic disease spectrum

scientific article

The expanding spectrum of movement disorders in genetic epilepsies

scientific article published on 29 November 2019

The genetic landscape of the epileptic encephalopathies of infancy and childhood.

scientific article published on 16 November 2015

Treatment of epileptic encephalopathies

scientific article

VGKC-complex antibody mediated encephalitis presenting with psychiatric features and neuroleptic malignant syndrome - further expanding the phenotype

scientific article published on 12 March 2012

List of works by Amy McTague

Clinical and molecular characterization of KCNT1-related severe early-onset epilepsy

Delineation of the movement disorders associated withFOXG1mutations: Table 1

Episodic dyscontrol syndrome

GABRB3 mutations: a new and emerging cause of early infantile epileptic encephalopathy.

GNAO1 encephalopathy: Broadening the phenotype and evaluating treatment and outcome.

Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis.

Intravenous levetiracetam in acute repetitive seizures and status epilepticus in children: Experience from a children's hospital ⬇️

Migrating partial seizures of infancy: expansion of the electroclinical, radiological and pathological disease spectrum.

Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizures

Myoclonic epilepsy in a child with 17q22-q23.1 deletion

Navigating the genetic landscape of childhood epilepsy: a new perspective?

RARS2 mutations in a sibship with infantile spasms

SLC25A22 is a novel gene for migrating partial seizures in infancy.

Severe infantile epileptic encephalopathy due to mutations in PLCB1: expansion of the genotypic and phenotypic disease spectrum

The expanding spectrum of movement disorders in genetic epilepsies

The genetic landscape of the epileptic encephalopathies of infancy and childhood.

Treatment of epileptic encephalopathies

VGKC-complex antibody mediated encephalitis presenting with psychiatric features and neuroleptic malignant syndrome - further expanding the phenotype