Search Results - "Jo M Wilmshurst"
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The ILAE classification of seizures and the epilepsies: Modification for seizures in the neonate. Position paper by the ILAE Task Force on Neonatal Seizures
Published in Epilepsia (Copenhagen) (01-03-2021)“…Seizures are the most common neurological emergency in the neonatal period and in contrast to those in infancy and childhood, are often provoked seizures with…”
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Subacute sclerosing panencephalitis: clinical phenotype, epidemiology, and preventive interventions
Published in Developmental medicine and child neurology (01-10-2019)“…Subacute sclerosing panencephalitis (SSPE) is a preventable condition reported in 6.5 to 11 per 100 000 cases of measles, and highest in children who…”
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Timing of referral to evaluate for epilepsy surgery: Expert Consensus Recommendations from the Surgical Therapies Commission of the International League Against Epilepsy
Published in Epilepsia (Copenhagen) (01-10-2022)“…Epilepsy surgery is the treatment of choice for patients with drug‐resistant seizures. A timely evaluation for surgical candidacy can be life‐saving for…”
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Clinical practice applicability and relevance to non-specialists of a paediatric EEG online learning tool
Published in BMC medical education (31-01-2024)“…Paediatric electroencephalography (EEG) training is inadequate amongst healthcare practitioners and technicians managing children with epilepsy in sub-Saharan…”
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Editorial: Insights in pediatric neurology: 2021
Published in Frontiers in neurology (01-11-2022)Get full text
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Dravet syndrome: A systematic literature review of the illness burden
Published in Epilepsia open (01-12-2023)“…We performed a systematic literature review and narrative synthesis according to a pre‐registered protocol (Prospero: CRD42022376561) to identify the evidence…”
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Establishing criteria for pediatric epilepsy surgery center levels of care: Report from the ILAE Pediatric Epilepsy Surgery Task Force
Published in Epilepsia (Copenhagen) (01-12-2020)“…Presurgical evaluation and surgery in the pediatric age group are unique in challenges related to caring for the very young, range of etiologies, choice of…”
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Hereditary peripheral neuropathies of childhood: An overview for clinicians
Published in Neuromuscular disorders : NMD (01-11-2011)“…Abstract This review focuses on the “pure” hereditary peripheral neuropathies where peripheral nerve disease is the main manifestation and does not address…”
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A Comparison of Parenteral Phenobarbital vs. Parenteral Phenytoin as Second-Line Management for Pediatric Convulsive Status Epilepticus in a Resource-Limited Setting
Published in Frontiers in neurology (15-05-2019)“…Pediatric convulsive status epilepticus (CSE) which is refractory to first-line benzodiazepines is a significant clinical challenge, especially within…”
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Neuropsychiatric and Neurocognitive Manifestations in HIV-Infected Children Treated With Efavirenz in South Africa-A Retrospective Case Series
Published in Frontiers in neurology (09-07-2019)“…Efavirenz is associated with transient neuropsychiatric manifestations but the impact on neurocognition in children is unknown. Genetically slow metabolizers…”
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The mutational profile in a South African cohort with inherited neuropathies and spastic paraplegia
Published in Frontiers in neurology (29-08-2023)“…Limited diagnostics are available for inherited neuromuscular diseases (NMD) in South Africa and (excluding muscle disease) are mainly aimed at the most…”
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Medical treatment in infants and young children with epilepsy: Off‐label use of antiseizure medications. Survey Report of ILAE Task Force Medical Therapies in Children
Published in Epilepsia open (01-03-2023)“…Objective Antiseizure medications (ASMs) remain the mainstay of epilepsy treatment. These ASMs have mainly been tested in trials in adults with epilepsy, which…”
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Skin cells for use in an alternate diagnostic method for Duchenne muscular dystrophy
Published in Neuromuscular disorders : NMD (01-07-2018)“…•Confirmed the feasibility of cultured skin cells for RNA-based diagnosis of DMD.•Skin biopsies are safer and cheaper than muscle biopsies for RNA-based…”
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RyR1 Deficiency in Congenital Myopathies Disrupts Excitation-Contraction Coupling
Published in Human mutation (01-07-2013)“…ABSTRACT In skeletal muscle, excitation–contraction (EC) coupling is the process whereby the voltage‐gated dihydropyridine receptor (DHPR) located on the…”
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Clinical Application of Epilepsy Genetics in Africa: Is Now the Time?
Published in Frontiers in neurology (02-05-2018)“…Over 80% of people with epilepsy live in low- to middle-income countries where epilepsy is often undiagnosed and untreated due to limited resources and poor…”
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Neurologic Complications of Pediatric Human Immunodeficiency Virus: Implications for Clinical Practice and Management Challenges in the African Setting
Published in Seminars in pediatric neurology (01-03-2014)“…Approximately 3.4 million children worldwide are affected with human immunodeficiency virus (HIV)/AIDS with more than 90% of them residing in sub-Saharan…”
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Peripheral nerve disease secondary to systemic conditions in children
Published in Therapeutic Advances in Neurological Disorders (01-08-2019)“…This review is an overview of systemic conditions that can be associated with peripheral nervous system dysfunction. Children may present with neuropathic…”
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The Challenges of Managing Children With Epilepsy in Africa
Published in Seminars in pediatric neurology (01-03-2014)“…Children with epilepsy who reside in the African continent are faced with some of the greatest challenges of receiving adequate care. The burden of disease is…”
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International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood: Position paper by the ILAE Task Force on Nosology and Definitions
Published in Epilepsia (Copenhagen) (01-06-2022)“…The 2017 International League Against Epilepsy classification has defined a three‐tier system with epilepsy syndrome identification at the third level…”
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