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A prospective study of the presentation and management of dancing eye syndrome/opsoclonus-myoclonus syndrome in the United Kingdom.
The incidence, mode of presentation and management of Dancing Eye Syndrome/Opsoclonus-Myoclonus Syndrome (DES/OMS) was prospectively evaluated in 20 United Kingdom (UK) paediatric neurology centresExpand
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Fracture prevalence in Duchenne muscular dystrophy.
The objective of this study was to determine the prevalence, circumstances, and outcome of fractures in males with Duchenne muscular dystrophy (DMD) attending neuromuscular clinics. Three hundred andExpand
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Paediatric acquired demyelinating syndromes: incidence, clinical and magnetic resonance imaging features
Objective: Changing trends in multiple sclerosis (MS) epidemiology may first be apparent in the childhood population affected with first onset acquired demyelinating syndromes (ADSs). We aimed toExpand
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Herpes simplex encephalitis with relapse.
Three children are described in whom herpes simplex encephalitis (HSE) followed a clearly biphasic course. The secondary deterioration may be due to a resurgence of the viral infection and calls intoExpand
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Acquired transverse myelopathy in children in the United Kingdom--a 2 year prospective study.
AIMS To define the incidence, describe presentation, management and outcome and identify prognostic factors in Acquired Transverse Myelopathy (ATM) in children under 16 years. METHODS A prospectiveExpand
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Paediatric neuromyelitis optica: clinical, MRI of the brain and prognostic features
Background Neuromyelitis Optica (NMO) is a severe and rare inflammatory condition, where relapses are predictive of disability. Methods We describe a national paediatric NMO cohort's clinical, MRI,Expand
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Fatal infantile neuromuscular presentation of glycogen storage disease type IV
Glycogen storage disease type IV or Andersen disease is an autosomal recessive disorder due to deficiency of glycogen branching enzyme. Typically, glycogen storage disease type IV presents withExpand
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The changing face of paediatric hydrocephalus: A decade’s experience
All 253 children receiving neurosurgical intervention for hydrocephalus (HCP) at a single British Neurosurgical Unit over a decade were investigated by retrospective case note review. Referral ratesExpand
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Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters
Neurexin 1 (NRXN1) is a cell adhesion protein, the normal function of which is critical for effective neurotransmission. It forms a trans‐synaptic complex in the central nervous system withExpand
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Renal vascular disease in neurofibromatosis type 2: association or coincidence?
Neurofibromatosis type 2 (NF2) remains a challenging diagnosis in childhood where there may be no neurological involvement. A 12‐month‐old male in whom NF2 was suspected because of characteristicExpand
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