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Long‐term outcome in children with infantile spasms treated with vigabatrin: A cohort of 180 patients

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Prospective study of outcome of infants with infantile spasms treated during controlled studies of ACTH and prednisone
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The United Kingdom Infantile Spasms Study comparing vigabatrin with prednisolone or tetracosactide at 14 days: a multicentre, randomised controlled trial
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Reversibility of vigabatrin-induced visual-field defect
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Long-term outcome of patients with West syndrome
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Vigabatrin as Initial Therapy for Infantile Spasms: A European Retrospective Survey
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Developmental and epilepsy outcomes at age 4 years in the UKISS trial comparing hormonal treatments to vigabatrin for infantile spasms: a multi-centre randomised trial
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Severe persistent visual field constriction associated with vigabatrin: FIG 1
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Guideline for prescribing vigabatrin in children has been revised
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Vigabatrin as a First-Choice Drug in the Treatment of West Syndrome
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Neurodevelopmental and Epilepsy Outcomes in a North American Cohort of Patients With Infantile Spasms
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Therapeutic Trial of Vigabatrin in Refractory Infantile Spasms
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Randomized trial of vigabatrin in patients with infantile spasms

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Infantile Epileptic Spasms Syndrome in Chinese Cohort Southern China: The Clinical Practice Based on the 2017 and 2022 ILAE Classification
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Torin 1 partially corrects vigabatrin‐induced mitochondrial increase in mouse
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Combination Therapy With Vigabatrin and Prednisolone Versus Vigabatrin Alone for Infantile Spasms
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Prenatal betamethasone–postnatal N‐methyl‐D‐aspartic acid model of spasms: Update on mechanisms and treatments
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Fast sleep spindles as a potential prognostic marker of developmental outcome in infantile epileptic spasms syndrome
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Impact of vigabatrin on risk of relapse of infantile spasms
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Preclinical tissue distribution and metabolic correlations of vigabatrin, an antiepileptic drug associated with potential use‐limiting visual field defects
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Infantile Spasms: Outcome in Clinical Studies
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Etiology of Infantile Epileptic Spasms Syndrome and Clinical Response With Vigabatrin as the First Treatment
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What is the optimal duration for vigabatrin monotherapy in patients with infantile spasms: 6 months or longer?
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Diagnosis and management of infantile epileptic spasms syndrome (IESS) in Gulf Cooperation Council (GCC) countries: Expert consensus statement
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Effectiveness of vigabatrin for infantile epileptic spasm syndrome categorized by etiologies
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Alpha-ERSP as a prognostic biomarker in infantile epileptic spasms syndrome: Insights from quantitative EEG analysis
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Epilepsy may be the major risk factor of mental retardation in children with tuberous sclerosis: A retrospective cohort study
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Long‐term outcome in children with infantile spasms treated with vigabatrin: A cohort of 180 patients
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In response to: Long‐term outcome in children with infantile spasms treated with vigabatrin: A cohort of 180 patients
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Response to second treatment after initial failed treatment in a multicenter prospective infantile spasms cohort
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Heterozygous GABAA receptor β3 subunit N110D knock‐in mice have epileptic spasms
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Fifteen years of real‐world data on the use of vigabatrin in individuals with infantile epileptic spasms syndrome
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Epileptic Spasms Predict Poor Epilepsy Outcomes After Perinatal Stroke
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Epileptic Encephalopathies in Infants and Children
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