Childhood arterial ischaemic stroke incidence, presenting features, and risk factors: a prospective population-based study

Andrew A. Mallick, Vijeya Ganesan, Fenella J. Kirkham, +9

The Lancet Neurology

HypertensionVascular DiseaseCerebrovascular DiseaseThrombosisStroke +14

Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis

H. Christian Martin, Grace Kim, A. T. Pagnamenta, +29

Human Molecular Genetics

EngineeringGeneticsDisease Gene IdentificationGenomicsPotassium Channel +19

Vigabatrin with hormonal treatment versus hormonal treatment alone (ICISS) for infantile spasms: 18-month outcomes of an open-label, randomised controlled trial

Finbar O’Callaghan, Stuart W. Edwards, Fabienne Dietrich Alber, +221

The Lancet Child & Adolescent Health

Pain DisordersHormonal TreatmentPediatricsInfantile SpasmsPain Management +4

Diagnostic delays in paediatric stroke

Andrew A. Mallick, Vijeya Ganesan, Fenella J. Kirkham, +8

Journal of Neurology Neurosurgery & Psychiatry

<i>GNAO1</i> encephalopathy

Federica Rachele Danti, Serena Galosi, Marta Romani, +18

Neurology Genetics

Early use of high‐dose riboflavin in a case of Brown–Vialetto–Van Laere syndrome

Geetha Anand, Hasan Nadeem, Sathiya S K Jayapal, +6

Developmental Medicine & Child Neurology

Generalized Muscle WeaknessHigh‐dose RiboflavinEarly UseDiaphragmatic ParalysisSurgery +5

Outcome and recurrence 1 year after pediatric arterial ischemic stroke in a population‐based cohort

Andrew A. Mallick, Vijeya Ganesan, Fenella J. Kirkham, +10

Annals of Neurology

Subdural haematoma and non-accidental head injury in children

Aparna Hoskote, Peter G. Richards, Philip Anslow, +1

Child s Nervous System

PediatricsIntracranial PressurePediatric Traumatic Brain InjuryBrain InjuryNeurology +2

Subdural effusions and lack of early pontocerebellar hypoplasia in siblings with RARS2 mutations

Katherina Kastrissianakis, Geetha Anand, Gerardine Quaghebeur, +5

Archives of Disease in Childhood

Cerebral AtrophyNeurological DisorderGeneticsRars2 MutationEarly Pontocerebellar Hypoplasia +15

Milder phenotypes of glucose transporter type 1 deficiency syndrome

Geetha Anand, Anuruddha Padeniya, Donncha Hanrahan, +12

Developmental Medicine & Child Neurology