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Unexplained early onset epileptic encephalopathy: Exome screening and phenotype expansion

Epilepsia (Copenhagen), 2016-01, Vol.57 (1), p.e12-e17

2016

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Vagus nerve stimulation for refractory epilepsy in children: More to VNS than seizure frequency reduction

Epilepsia (Copenhagen), 2009-05, Vol.50 (5), p.1220-1228

2009

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The variable phenotypes of KCNQ‐related epilepsy

Epilepsia (Copenhagen), 2014-09, Vol.55 (9), p.e99-e105

2014

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Neurological involvement in children with hemolytic uremic syndrome

European journal of pediatrics, 2022-02, Vol.181 (2), p.501-512

2022

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Novel European SLC1A4 variant: infantile spasms and population ancestry analysis

Journal of human genetics, 2016-08, Vol.61 (8), p.761-764

2016

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Epileptic dyskinetic encephalopathy in KBG syndrome: Expansion of the phenotype

Epilepsy & behavior reports, 2024-01, Vol.25, p.100647, Article 100647

2024

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Typical absence seizures in children: Review with focus on EEG predictors of treatment response and outcome

Seizure (London, England), 2023-08, Vol.110, p.1-10

2023

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Monitoring the frequency and duration of epileptic seizures: “A journey through time”

European journal of paediatric neurology, 2021-07, Vol.33, p.168-178

2021

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The controversial association of ABCB1 polymorphisms in refractory epilepsy: An analysis of multiple SNPs in an Irish population

Epilepsy research, 2007-02, Vol.73 (2), p.192-198

2007

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The stigma experiences and perceptions of families living with epilepsy: Implications for epilepsy-related communication within and external to the family unit

Patient education and counseling, 2016-09, Vol.99 (9), p.1473-1481

2016

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Progressive myoclonic epilepsies: a review of genetic and therapeutic aspects

Lancet neurology, 2005-04, Vol.4 (4), p.239-248

2005

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Relationship Between Electroencephalography and Seizure Outcome in Typical Absence Seizures in Children

Pediatric neurology, 2023-11, Vol.148, p.56-64

2023

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“I don't want them to look at me and think of my illness, I just want them to look at me and see me”: Child perspectives on the challenges associated with disclosing an epilepsy diagnosis to others

Epilepsy & behavior, 2015-12, Vol.53, p.83-91

2015

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Assessing the Utility of Electroencephalography for Staring Episodes in Children with Autism

Irish medical journal, 2020-03, Vol.113 (3), p.37-37

2020

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The prevalence of seizures in comatose children in the pediatric intensive care unit: A prospective video‐EEG study

Epilepsia (Copenhagen), 2010-07, Vol.51 (7), p.1198-1204

2010

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Talking about epilepsy: Challenges parents face when communicating with their child about epilepsy and epilepsy-related issues

Epilepsy & behavior, 2016-04, Vol.57 (Pt A), p.9-15

2016

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Development and psychometric evaluation of the youth and parent versions of the Epilepsy Disclosure Scale (EDS)

Epilepsy & behavior, 2018-05, Vol.82, p.111-118

2018

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Sultiame revisited: treatment of refractory absence seizures

Epileptic disorders, 2016-09, Vol.18 (3), p.329-333

2016

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Maple syrup urine disease: Clinical outcomes, metabolic control, and genotypes in a screened population after four decades of newborn bloodspot screening in the Republic of Ireland

Journal of inherited metabolic disease, 2021-05, Vol.44 (3), p.639-655

2021

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Response to treatment and outcomes of infantile spasms in Down syndrome

Developmental medicine and child neurology, 2022-06, Vol.64 (6), p.780-788

2022

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Atypical presentation of ataxia–oculomotor apraxia type 1

Developmental medicine and child neurology, 2006-06, Vol.48 (6), p.529-532

2006

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Novel SMC 1A variant and epilepsy of infancy with migrating focal seizures: Expansion of the phenotype

Epilepsia (Copenhagen), 2017-07, Vol.58 (7), p.1301-1302

2017

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Parent perspectives of the challenging aspects of disclosing a child’s epilepsy diagnosis to others: Why don’t they tell?

Chronic illness, 2017-03, Vol.13 (1), p.28-48

2017

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The Temple Star Transitional Model of Care for epilepsy; the outcome of a quality improvement project

Epilepsy & behavior, 2018-02, Vol.79, p.4-8

2018

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Unexplained early onset epileptic encephalopathy: Exome screening and phenotype expansion

Vagus nerve stimulation for refractory epilepsy in children: More to VNS than seizure frequency reduction

The variable phenotypes of KCNQ‐related epilepsy

Neurological involvement in children with hemolytic uremic syndrome

Novel European SLC1A4 variant: infantile spasms and population ancestry analysis

Epileptic dyskinetic encephalopathy in KBG syndrome: Expansion of the phenotype

Typical absence seizures in children: Review with focus on EEG predictors of treatment response and outcome

Monitoring the frequency and duration of epileptic seizures: “A journey through time”

The controversial association of ABCB1 polymorphisms in refractory epilepsy: An analysis of multiple SNPs in an Irish population

The stigma experiences and perceptions of families living with epilepsy: Implications for epilepsy-related communication within and external to the family unit

Progressive myoclonic epilepsies: a review of genetic and therapeutic aspects

Relationship Between Electroencephalography and Seizure Outcome in Typical Absence Seizures in Children

“I don't want them to look at me and think of my illness, I just want them to look at me and see me”: Child perspectives on the challenges associated with disclosing an epilepsy diagnosis to others

Assessing the Utility of Electroencephalography for Staring Episodes in Children with Autism

The prevalence of seizures in comatose children in the pediatric intensive care unit: A prospective video‐EEG study

Talking about epilepsy: Challenges parents face when communicating with their child about epilepsy and epilepsy-related issues

Development and psychometric evaluation of the youth and parent versions of the Epilepsy Disclosure Scale (EDS)

Sultiame revisited: treatment of refractory absence seizures

Exploring the prevalence and profile of epilepsy across Europe using a standard retrospective chart review: Challenges and opportunities

Maple syrup urine disease: Clinical outcomes, metabolic control, and genotypes in a screened population after four decades of newborn bloodspot screening in the Republic of Ireland

Response to treatment and outcomes of infantile spasms in Down syndrome

Atypical presentation of ataxia–oculomotor apraxia type 1

Novel SMC 1A variant and epilepsy of infancy with migrating focal seizures: Expansion of the phenotype

Parent perspectives of the challenging aspects of disclosing a child’s epilepsy diagnosis to others: Why don’t they tell?

The Temple Star Transitional Model of Care for epilepsy; the outcome of a quality improvement project

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