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Centromedian thalamic nuclei deep brain stimulation and Anakinra treatment for FIRES – Two different outcomes

European journal of paediatric neurology, 2019-09, Vol.23 (5), p.749-754

2019

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

Brain (London, England : 1878), 2013-05, Vol.136 (Pt 5), p.1578-1591

2013

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Low frequency centromedian thalamic nuclei deep brain stimulation for the treatment of super refractory status epilepticus: A case report and a review of the literature

Brain stimulation, 2021-03, Vol.14 (2), p.226-229

2021

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Incorporating epilepsy genetics into clinical practice: a 360°evaluation

Npj genomic medicine, 2018-05, Vol.3 (1), p.13-11, Article 13

2018

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The L1624Q Variant in SCN1A Causes Familial Epilepsy Through a Mixed Gain and Loss of Channel Function

Frontiers in pharmacology, 2021-12, Vol.12, p.788192-788192

2021

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Archaeological Collecting at the Museum of Northern Arizona: From Past to Present

Collections (Walnut Creek, Calif.), 2021-03, Vol.17 (1), p.46-53

Hughes, Elaine

2021

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Education Collections: Case Study in Their Use to Replace Permanent Collection Objects

Collections (Walnut Creek, Calif.), 2020-09, Vol.16 (3), p.344-354

Hughes, Elaine

2020

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Encephalopathy and SCN1A mutations

Epilepsia (Copenhagen), 2011-04, Vol.52 (4), p.e26-e30

2011

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The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits

Neurobiology of disease, 2005-12, Vol.20 (3), p.799-804

2005

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Paroxysmal disorders in infancy: a diagnostic challenge

Developmental medicine and child neurology, 2010-11, Vol.52 (11), p.980-981

2010

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Epilepsy deaths in children: Improvements driven by data and surveillance in pediatrics

Epilepsy & behavior, 2020-02, Vol.103 (Pt B), p.106493-106493, Article 106493

2020

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Cannabidiol in patients with seizures associated with Lennox-Gastaut syndrome (GWPCARE4): a randomised, double-blind, placebo-controlled phase 3 trial

The Lancet (British edition), 2018-03, Vol.391 (10125), p.1085-1096

2018

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Intolerance to quinidine in a n-of-1 trial for KCNT1 associated epilepsy of infancy with migrating focal seizures

Seizure (London, England), 2022-12, Vol.103, p.46-50

2022

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Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: a randomised, double-blind, placebo-controlled trial

The Lancet (British edition), 2019-12, Vol.394 (10216), p.2243-2254

2019

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Local Anesthetic Systemic Toxicity: Ensuring Sustained Nursing Knowledge in a High-Volume Outpatient Surgery Center

Journal of perianesthesia nursing, 2024-03

2024

Volltextzugriff (PDF)

Trihexyphenidyl for acute life-threatening episodes due to a dystonic movement disorder in Rett syndrome

Movement disorders, 2010-02, Vol.25 (3), p.385-389

2010

Volltextzugriff (PDF)

Learning and Thinking Styles: An analysis of their interrelationship and influence on academic achievement

Educational psychology (Dorchester-on-Thames), 2000-12, Vol.20 (4), p.413-430

2000

Volltextzugriff (PDF)

Paediatric autoimmune encephalopathies: clinical features, laboratory investigations and outcomes in patients with or without antibodies to known central nervous system autoantigens

Journal of neurology, neurosurgery and psychiatry, 2013-07, Vol.84 (7), p.748-755

2013

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Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

Nature genetics, 2013-09, Vol.45 (9), p.1067-1072

2013

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Epilepsy and cannabidiol: a guide to treatment

Epileptic disorders, 2020-02, Vol.22 (1), p.1-14

2020

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Virtual fracture clinic reduces patient X-ray volume for common wrist and ankle fractures

Irish journal of medical science, 2022-10, Vol.191 (5), p.2117-2121

2022

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Correction to: Virtual fracture clinic reduces patient X‑ray volume for common wrist and ankle fractures

Irish journal of medical science, 2022-12, Vol.191 (6), p.2843-2843

2022

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N‐methyl‐D‐aspartate receptor antibody‐associated movement disorder without encephalopathy

Developmental medicine and child neurology, 2014-02, Vol.56 (2), p.190-193

2014

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Nurses' perceptions of continuing professional development

Nursing standard, 2005-07, Vol.19 (43), p.41

Hughes, Elaine

2005

Volltextzugriff (PDF)

Clinical spectrum of STX1B -related epileptic disorders

Neurology, 2019-03, Vol.92 (11), p.e1238

2019

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Centromedian thalamic nuclei deep brain stimulation and Anakinra treatment for FIRES – Two different outcomes

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

Low frequency centromedian thalamic nuclei deep brain stimulation for the treatment of super refractory status epilepticus: A case report and a review of the literature

Incorporating epilepsy genetics into clinical practice: a 360°evaluation

The L1624Q Variant in SCN1A Causes Familial Epilepsy Through a Mixed Gain and Loss of Channel Function

Archaeological Collecting at the Museum of Northern Arizona: From Past to Present

Education Collections: Case Study in Their Use to Replace Permanent Collection Objects

Encephalopathy and SCN1A mutations

The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits

Paroxysmal disorders in infancy: a diagnostic challenge

Epilepsy deaths in children: Improvements driven by data and surveillance in pediatrics

Cannabidiol in patients with seizures associated with Lennox-Gastaut syndrome (GWPCARE4): a randomised, double-blind, placebo-controlled phase 3 trial

Intolerance to quinidine in a n-of-1 trial for KCNT1 associated epilepsy of infancy with migrating focal seizures

Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: a randomised, double-blind, placebo-controlled trial

Local Anesthetic Systemic Toxicity: Ensuring Sustained Nursing Knowledge in a High-Volume Outpatient Surgery Center

Trihexyphenidyl for acute life-threatening episodes due to a dystonic movement disorder in Rett syndrome

Learning and Thinking Styles: An analysis of their interrelationship and influence on academic achievement

Paediatric autoimmune encephalopathies: clinical features, laboratory investigations and outcomes in patients with or without antibodies to known central nervous system autoantigens

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

Epilepsy and cannabidiol: a guide to treatment

Virtual fracture clinic reduces patient X-ray volume for common wrist and ankle fractures

Correction to: Virtual fracture clinic reduces patient X‑ray volume for common wrist and ankle fractures

N‐methyl‐D‐aspartate receptor antibody‐associated movement disorder without encephalopathy

Nurses' perceptions of continuing professional development

Clinical spectrum of STX1B -related epileptic disorders

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