Search Results - "Rittey, Christopher"
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Vagus nerve stimulation for drug‐resistant epilepsy: A European long‐term study up to 24 months in 347 children
Published in Epilepsia (Copenhagen) (01-10-2014)“…Summary Objective To gain insight into the long‐term impact of vagus nerve stimulation (with VNS Therapy) in children with drug‐resistant epilepsy, we…”
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Outcome of children with hyperventilation‐induced high‐amplitude rhythmic slow activity with altered awareness
Published in Developmental medicine and child neurology (01-11-2012)“…Hyperventilation‐induced high‐amplitude rhythmic slow activity with altered awareness (HIHARS) is increasingly being identified in children and is thought to…”
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Neonatal hypertonia – a diagnostic challenge
Published in Developmental medicine and child neurology (01-07-2015)“…In comparison to hypotonia, hypertonia is less commonly expressed in the neonatal period. The scientific literature on the causes of neonatal hypertonia is…”
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Movement disorders associated with complex regional pain syndrome in children
Published in Developmental medicine and child neurology (01-07-2009)“…The aim of the present study was to review the history, clinical course, treatment, and outcome of movement disorders in children and young people with complex…”
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Reversible Parainfectious Bilateral “Striatal Necrosis”
Published in Pediatric neurology (2012)“…Abstract Bilateral striatal necrosis is usually associated with either endogenous or exogenous toxins, and with poor neurodevelopmental outcomes. We describe…”
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The infant with seizures (excluding neonatal)
Published in Paediatrics and child health (01-05-2009)“…Abstract Seizures in infancy are common. Although there are a number of clearly defined epilepsy syndromes which begin or occur in infancy many infants cannot…”
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Skull base osteomyelitis leading to lateral medullary syndrome in a child
Published in European journal of paediatric neurology (01-03-2007)“…Abstract Skull base osteomyelitis (SBO) arising from the sphenoidal paranasal air sinus infection without associated external otitis is rare. Initially SBO may…”
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A novel distinctive cerebrovascular phenotype is associated with heterozygous Arg179 ACTA2 mutations
Published in Brain (London, England : 1878) (01-08-2012)“…Mutations in the ACTA2 gene lead to diffuse and diverse vascular diseases; the Arg179His mutation is associated with an early onset severe phenotype due to…”
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Juvenile neuronal ceroid-lipofuscinosis: developmental progress after supplementation with polyunsaturated fatty acids
Published in Developmental medicine and child neurology (01-07-1994)“…Six patients with juvenile neuronal ceroid-lipofuscinosis (NCL) who were demonstrated to have abnormally low levels of membrane phospholipids were treated by…”
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Pediatric sciatic neuropathy presenting as painful leg: A case report and review of literature
Published in Journal of pediatric neurosciences (01-05-2013)“…Introduction: Mononeuropathies, in general, are very uncommon in childhood. Sciatic neuropathy (SN) is probably underappreciated in childhood and likely to…”
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Phenotypic Comparison of Two Scottish Families with Mutations in Different Genes Causing Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
Published in Epilepsia (Copenhagen) (01-04-2003)“…Purpose: Mutations in genes coding for the α4 and β2 subunits of the neuronal nicotinic acetylcholine receptor receptor (CHRN) are known to cause autosomal…”
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Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection
Published in Nature genetics (01-08-2006)“…Aicardi-Goutières syndrome (AGS) is an autosomal recessive neurological disorder, the clinical and immunological features of which parallel those of congenital…”
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Pediatric sciatic neuropathy presenting as painful leg: A case report and review of literature
Published in Journal of pediatric neurosciences (01-05-2013)“…INTRODUCTIONMononeuropathies, in general, are very uncommon in childhood. Sciatic neuropathy (SN) is probably underappreciated in childhood and likely to…”
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Neonatal Seizures
Published in Archives of Disease in Childhood (01-04-1991)Get full text
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