||EEG services for children in Africa: Pilot survey of capacity and needs.
||Practical aspects of the use of Ketogenic Diet in the management of Childhood Epilepsy - a review of experience from Scotland.
||Efficacy of Modified Atkins Diet (MAD) as Treatment for Intractable Epilepsy in Children - A Randomized Controlled Trial.
||Assessment of Oral Hygiene of Children with Epilepsy.
||Levels of Immunoglobulins, Complement and T Lymphocyte Subsets in the Peripheral Blood of Children with Convulsive Diseases and Their Signifiances
||Plasma Galanin and Neuropeptide Y Levels in Children with Convulsive Diseases and Their Signifiances.
||Classifying Electroencephalographic Diagnoses of Epilepsy without Epileptiform Discharges and Nonepileptic Paroxysmal Events Using Deep Convolutional Neural Networks.
||The clinical efficacy and follow-up study of ketogenic diet adding treatment for refractor epilepsy in children.
||The latest finding of genetic testing in Chinese patients with unexplained Epileptic encephalopathy(EE).
||Canonical transient receptor potential chan nel 3 contributes to recurrent febrile seizure s by inducing neuronal cell death and neuroi nflammation.
||Study of 15 patients with early infantile epileptic encephalopathy - treatable Neurometabolic causes.
||Factors associated with Electroencephalographic and Clinical Remission of Benign Childhood Epilepsy with Centrotemporal Spikes.
||Gaba Transaminase Deficiency Disorder in an Indian Family - Report of Two New Cases.
||Clinical features and efficiency of ketogenic diet of 106 Dravet syndrome patients.
||Analysis of clinical and genetic features of 30 patients with KCNQ2-related disorder.
||Electroencephalogram Features of Children with Type 1 Diabetes Mellitus.
||Perampanel and Brivaracetam: Efficacy and safety in pediatric refractory epilepsy.
||It's not all about seizures: Experience of Dravet Syndrome management in a Scottish Children's Hospital.
||First Complex Febrile Seizure â€“ do we need to investigate.
||Prevalence of Epilepsy and Inter-ictal Epileptiform discharges in children with Neurodevelopmental disorders.
||Clinico-Etiological Profile of Refractory Status Epilepticus in Children.
||Seizures in children with Zika Virus Congenital Syndrome.
||A critical analysis of lumbar puncture in the emergency management of febrile seizures: a cross-sectional study.
||Clinico-etiological Profile and Developmental Status of Infants Aged 1-24 months with Epilepsy in India.
||Ohtahara Syndrome due to unique Heterozygous PIGO mutation: Clinical and EEG features.
||Congenital Mirror Movements with epilepsy in association with KCNT1 gene mutation: A Case Report.
||National Surveillance of Mortality in Children with Epilepsy in the UK and Ireland.
||The absence of NIPA2 enhances neural excitability through BK channels.
||Pediatric status epilepticus. Cases admitted during years 2015-2016 at Hospital de niÃ±os Dr. O. Alassia de la ciudad de Santa Fe, Argentina.
||Evolution of epileptic zeisures iniciated during neonatal period in a long term follow up of 97 children.
||Febril status epilepticus in children. Series of cases of children admited at Dr. O Alassia Hospital, Santa Fe Argentina period 2015 to 2018.
||Absence epilepsy, the great masquerader.
||Not all that blinks is tics.
||Epileptic Spasms in Southern Africa.
||Autoimmunity of childhood epilepsy.
||Hemimegalencephaly with congenital facial lipoma-A Case Report.
||Evaluation of vitamin B12 levels in children with Infantile spasms and children with Global Developmental Delay without Infantile spasms: A cross sectional observational study.
||Ketogenic Diet in Zambia: Managing Refractory Epilepsy in a Low Income Country.
||The efficacy and safety of levetiracetam treating in pediatric epilepsy in different ages and seizure types.
||A Chinese boy with Malonyl-CoA decarboxylase deficiency and a novel mutation in the MLYCD gene.
||Nurse Lead Multi Levels Pediatric Epilepsy Education Initiatives.
||Experience with very high dose (8mg/kg/day, maximum 60mg/day) prednisolone for West syndrome in a resource limited setting.
||Comparison Of Electroencephalographic Sleep Stages With Bispectral Ä index Data an Children.
||Effects of ketogenic diet on plasma levels of valproic acid in children with epilepsy
||Cannabinoid receptor type 2 controls neuronal autophagy through regulation of mTOR signal pathway during the repair of hippocampal neurons in status epilepticus rats
||Comparison of Epileptic Seizure Classifications (ILAE-1981 and ILAE-2017) with A Modular Education Program Among Residents in Pediatrics
||Perampanel in paediatric population: experience in a regional hospital
||Risk of Recurrence after Withdrawal of Antiepileptic Medication in Children with Epilepsy
||WWOX related epileptic encephalopathy: A new autosomal recessively inherited disorder
||Analysis of curative effect and Â influence Â factors of small dose and short course of ACTH on 73 cases of IS
||Clinical and EEG characteristics of epilepsy of infancy with migrating focal seizures
||The value of mobile phone videos in increasing the diagnosis accuracy and saving cost of consultation for infant paroxysmal events: a prospective study in China
||Establishment and utility assessment of Posterior Reversible Encephalopathy Syndrome early warning scoring (PEWS) scale Establishment and utility assessment of PEWS scale
||First unprovoked seizure in children-Predictors of recurrence
||Clinical characteristics and genetic features of benign infantile epilepsy with PRRT2 mutation
||Adverse drug reactions of anti-epileptics in children-an observational studySundeep Kaushik, Suvasini Sharma, Deepti Chopra, Bijoy Patra, Satinder Aneja
||The latest finding of genetic testing in Chinese patients with unexplained Epileptic encephalopathy(EE).
||A unique variant of West Syndrome:Vitamin B12 responsive epileptic encephalopathy
||Clinical profile and short-term outcome of status epilepticus in children
||SYNDROMES AND ETIOLOGY IN PEDIATRIC EPILEPSY: EVALUATION OF INTERNATIONAL LEAGUE AGAINST EPILEPSY (ILAE) 1989, 2010 AND 2017 CLASSIFICATION OF EPILEPSY AT A TERTIARY CARE CENTRE IN INDIA
||Intravenous Fosphenytoin loading dose of 20 mg/kg in Status epilepticus: Is it enough in Indian children?
||DESCRIPTIVE EPIDEMIOLOGY OF â€œCONTINUOUS SPIKE AND SLOW WAVE IN SLEEP (CSWS)â€ EPILEPSY AT A TERTIARY CARE CENTRE IN INDIA
||ELECTROCLINICAL PROFILES OF CHILDREN WITH BENIGN EPILEPSY WITH CENTROTEMPORAL SPIKES (BECTS) AT A TERTIARY CARE CENTRE
||â€˜Prevent Neonatal hypoglycaemia, Prevent Infantile Spasms: Revealing findings from an etiological study on West Syndrome patients from North India
||A Practical Quality of Life Questionnaire for Children with Severe Intellectual Disability and Epilepsy: Comparing proxy reporting by Mothers and Fathers
||Effectiveness and tolerability of perampanel in children under 7 years old with refractory epilepsy: A single-center, retrospective study
||A case of KCNA2 encephalopathy presenting with various involuntary movements, severe psychomotor retardation, and sleep disturbance.
||Status Epilepticus in Pediatric Patients Severity Score (STEPSS): A clinical score to predict the outcome of status epilepticus in children.
||THE CLINICAL CASE OF EPILEPTIC ENCEPHALOPATHY IN ANGELMAN SYNDROME.
||Outcome of Rasmussen Encephalitis with conservative management
||Microbiological diagnostic challenges in a seasonal cluster of Rhombencephalitis
||Hemiconvulsion Hemiplegia Epilepsy Syndrome: A case Report
||Pediatric lamotrigine overdose resulting in generalized seizure and encephalopathy
||Improving triaging of Infantile Spasm EEG referrals in a large Canadian institution
||A case of De Novo NAA10 mutation presenting with eyelid myoclonias (AKA Jeavons syndrome)
||Significance of polyspikes on electroencephalogram in children with focal epilepsy
||Ketogenic Diet (KD) in children with epilepsy: Parental expectations and experiences
||Efficacy of adjunctive vagus nerve stimulation in patients with Dravet syndrome
||Evolution and Outcome of Epilepsy in Children with Neonatal Hypoglycemic Brain Injury
||Genotype and phenotype of epileptic patients with SCN2A mutations
||Infantile epilepsy with multifocal myoclonus caused by TBC1D24 mutations
||The electroclinical features of CHD2 mutation related epilepsy
||Clinicoetiological Profile of Childhood Seizures in a Tertiary Care Hospital: A Prospective Observational Study
||Does Ethnicity Affect the Clinical Presentation of Tuberous Sclerosis Complex?
||Semiological, Diagnostic and theraupetic challenges in Infantile onset epilepsy
||Clinical profile of patients with infantile spasms following Neonatal hypoglycemic brain injury: a retrospective study from India
||Simultaneous quantification of alpha-aminoadipic semialdehyde, piperideine-6-carboxylate, pipecolic acid and alpha-aminoadipic acid in pyridoxine-dependent epilepsy
||Some Neuropsychological factors as associated to cognitive functions of Mesial Temporal lobe epilepsy (MTLE) children.
||Low ratio ketogenic diet (KD) can achieve good seizure control in children with epilepsy
||Experience with Isoflurane in Paediatric Super Refractory Status Epilepticus
||Epilepsia Partialis Continua (EPC) in children: Clinical presentation and underlying aetiologies
||Protective effects of the ROCK inhibitor fasudil against cognitive dysfunction following status epilepticus in immature male rats
||A Study of Reasons for Poor Response/ Poor Control of Epilepsy in Children on Polytherapy
||Retrospective cohort of Dravet syndrome due to SCN gene mutation from Southern India
||Infantile tremor syndrome followed by West Syndrome: A case series
||EPILEPTIC ENCEPHALOPATHY DUE TO GABRG2 MUTATION
||systematic review of Perampanel in children and adolescent
||Comparison of 1981, 1989 and 2017 International League Against Epilepsy classification (ILAE)
||Mammalian Target of Rapamycin (mTOR) Inhibitors as an Effective Therapy for Refractory Epilepsy associated with Tuberous Sclerosis Complex: A Systematic Review
||Dandy Walker malformation with epileptic spasms
||Valproic Acid: A potion with caution
||Etiology of Epilepsy In a developing Country â€“ A study from a tertiary Pediatric Hospital
||X-LINKED EPILEPTIC INFANTILE ENCEPHALOPATHY OF UNUSUAL INHERITANCE
||Severe neonatal epileptic encephalopathy secondary to a mutation of the ATP1A3 gene
||Epilepsy in Children- Psychosocial and Emotional Impact on Their Siblings and Their Coping Skills
||Epidemiological Survey (three staged) of Pediatric Epilepsy in a rural suburb of Pune District
||Clinical and therapeutic profile of childhood epilepsy in an Onchocerciasis-endemic rural Area
||Prevalence of Seizures among children admitted with BRUE (Brief resolved unexplained event)
||Telephone based follow-up of children with Epilepsy aged 4 months to 18yrs: comparison of accuracy between a Specialty Nurse and a DM Pediatric Neurology Fellow to identify Critical Clinical Events requiring Face-to -Face evaluation
||Clinical Profile of Epilepsy in Neonatal Hypoglycemic Brain Injury.
||EFFECT OF LONG-TERM ANTIEPILEPTIC DRUGS ON BONE MINERAL METABOLISM AND THYROID PROFILE IN INDIAN CHILDREN:A CASE CONTROL STUDY
||SYNCOPE IN CHILDREN-CLINICO-ETIOLOGICAL CORRELATION
||Kabuki Syndrome and Effectiveness of Perampanel
||Asymptomatic malaria parasitaemia and seizure control in children with nodding syndrome; a cross sectional study
||Clinical spectrum and therapeutic outcomes of electrical status epilepticus during sleep in children
||Febrile Infection Related Epilepsy Syndrome (FIRES) â€“ A rare cause of super refractory status epilepticus
||Neonatal-onset epilepsy: Clinico-etiological spectrum and short-term outcome
||Clinicoetiological profile and outcome of convulsive status epilepticus in children
||Polypharmacy in childhood epilepsy syndrome management: overuse or underuse of a diagnostic tool?
||Continuous Spikes and Waves during Slow-Wave Sleep (CSWS) in Children: The Epilepsy Syndrome that Canâ€™t Stop, Wonâ€™t Stop
||An Exploration of Prescribing Practice and Parental Use of Emergency Rescue Medication to Prevent Status Epilepticus in Children
||Bones and brains: a prospective case-control study of seasonal vitamin D in childhood epilepsy
||Our experience with use of new 2017 ILAE classification in children with epilepsy
||Utility of short term video EEG recording in diagnosis of paroxysmal events in children
||LANGUAGE EVALUATION IN GENETIC EPILEPSY FEBRILE SEIZURES + SYNDROME â€“ A PROSPECTIVE CONTROLLED OBSERVATIONAL STUDY
||â€œMe and My Epilepsyâ€: A qualitative study of Childrenâ€™s Experiences and a novel child-centered animation about epilepsy
||Comparison between Melatonin and Diazepam for Prevention of Recurrent Simple Febrile Seizures: Randomized clinical trial.
||Magnitude of Co-Morbidities in Pediatric Epilepsy: Need for Neuropsychological Rehabilitation.
||Effect of Acth Combination Therapy Versus Acth Alone in West Syndrome: A Retrospective Study.
||Epilepsy burden in NHBI (Neonatal Hypoglycemic Brain Injury).
||Effectiveness and Safety of high-dose, Oral Pyridoxine as an adjunct to high-dose Adrenocorticotrophic hormone versus high-dose Adrenocorticotrophic hormone alone for the treatment of West Syndrome: An Open-Label, Randomized Control Trial
||Evolution of electroencephalogram findings in pontocerebellar hypoplasia type 2A
||Verbal Semantics and Social cognition in adolescents with drug resistant refractory epilepsy
||Two novel PCDH19 missense mutations in a mosaic male and a female epilepsy patients
||Assessment of quality of life in Omani children with epilepsy attending Sulatan Qaboos University Hospital
||SPECTRUM OF TUBEROUS SCLEROSIS COMPLEX - CLINICAL PROFILE IN A COHORT OF 48 CHILDREN
||Super Refractory Status Epilepticus in children : Etiological, electrophysiological, treatment and outcome profile
||A hot and jerky child
||Serum levels of both prolidase activity and oxidative stress in epileptic children
||Infantile epilepsy with prolonged focal myoclonic seizures: A distinctive syndrome associated with TBC1D24 mutation.
||Functional Hemispherotomy : patient characteristics and outcome in a series of 26 patients
||Efficacy of zinc supplementation in preventing recurrence of febrile seizure in Bangalore
||Vagal Nerve Stimulation treatment in children with pharmaco-resistant epilepsy: A single centre experience
||Clinical characteristics and epilepsy outcomes after surgery in children with focal cortical dysplasia type II
||Up-regulation of HMGB1-TLR4 Inflammatory Pathway in Focal Cortical Dysplasia Type II
||Effects rehabilitation with interactive metronome training on speech disorders and epilepsy patients.
||PHOTOSENSITIVITY AND CLINICAL CHARACTERISTICS FROM A SCOTTISH POPULATION COHORT
||Nitrazepam as first line treatment for Infantile Spasm-20 yearsâ€™ experience from Tertiary Paediatric Neurosciences Centre
||Outcome Following Febrile Seizures: A Scottish Population Cohort
||Yield of Laboratory Testing in Pediatric Ketogenic Diet Patients: Critical Assessment of Abnormal Results and Impact on Clinical Care.
||COMPARISON OF CALCIUM LEVELS IN CHILDREN WITH FEBRILE SEIZURES AND CHILDREN WITH FEVER AND NO SEIZURES
||Clinico-radiological and electrographic spectrum of children with Temporal lobe epilepsy: a retrospective cohort study
||Clinical and Molecular profile of First Indian cohort of Unclassified West Syndrome Patients
||KNOWLEDGE ATTITUDE PRACTICE (KAP) STUDY FOR THE CARE OF CHILDREN WITH EPILEPSY IN SCHOOLS
||Electrophysiological characteristics in children with Subacute sclerosing panencephalitis (SSPE): A study from a tertiary care hospital.
||Study of Drug Resistant Epilepsy at a Tertiary Care Centre in Western India 2018
||ETIOLOGICAL CLASSIFICATION (ILAE-2017) AND THERAPEUTIC REPONSE IN CHILDREN WITH EPILEPSY PRESENTING AT A TERTIARY CARE SPECIALIST EPILEPSY CLINIC.
||Achievement of camp in children with epilepsy
||Epilepsy Versus Chronic diseases: How different are parentâ€™s attitudes?
||Hypothyroidism and valproate: Is there a causal relationship?
||Clinical utility of next generation sequencing in Early-Onset Epileptic Encephalopathies.
||Profile of children with seizures and epilepsy presenting at a tertiary care specialist Paediatric epilepsy clinic.
||Association between clinical features and gene mutation in children with intractable epilepsy with unknown etiology.
||Profile of Childhood Epilepsy at a Tertiary Care Hospital in Southern India Janani R1, Saji James 2, Ranjith Kumar 3, 1 post Graduate, 2 Professor of Pediatrics, Department of Pediatrics, 3 Assistant Professor Paediatric Neurology Sri. Ramachandra Medical College.
||ketogenic diet in infant with intractable epilepsy.
||The role of sleep and awake EEGs in detection of epileptiform discharges in pediatric population.
||Lacosamide responsive ESES (electrical status epilepticus in slow wave sleep )â€“ 2 case reports.
||Experience of ketogenic diet as an adjuvant therapy in Febrile Infection Related Epilepsy Syndrome (FIRES).
||Parietal epilepsy presenting as eye flutter and absences.
||A clinical and electrophysiological profile of epileptic spasms - A tertiary care centre experience.
||EPEMA (encephalopathy,petechiae and ethylmalonic aciduria) â€“ a case series.
||Cohort of Clinical profile and Outcome of Pyridoxine dependent epilepsy.
||Features of Epilepsy and Cerebral Palsy in Children in Uzbekistan.
||A New Vegetative Sign Related to Anterior Insula Epilepsy: Ipsilateral Â€Œglove and Sockâ€ Skin Cyanosis
||Accelerated corticospinal tract maturation, as measured by neuronavigated transcranial magnetic stimulation (nTMS), corresponds to preserved IQ in girls, but not in boys, with focal epilepsy.
||Infantile spasms following Acquired brain injury - A tertiary Neuro-Rehabilitation centre experience.
||Oral Ketamine is an Effective and Safe Treatment for Non-Convulsive Status Epilepticus.
||A Prospective Study of Non-Epileptic Events in Children with Intractable Epileps.y
||Rigid spine syndrome: A report of 15 children.
||Childhood Onset Limb Girdle Muscular Dystrophies in Aegean Part of Turkey.
||Differentiation between inflammatory myopathies and genetic muscle disease.
||Diagnostic Potential of Next Generation Sequencing in Suspected Genetic Neuromuscular Disorders.
||Spinal Muscular Atrophy â€“ Lower Extremity Dominant Type 2 (SMALED2).
||Pain prevalence and characteristics in spinal muscular atrophy type II.
||Atypical childhood-onset neuroaxonal dystrophy in an Indian girl - case report.
||Neuromusclar transmission defect in FKRP congenital muscular dystrophy.
||Bone Health Monitoring In Boys With Duchenne Muscular Dystrophy: A Survey Of Clinical Practice In The United Kingdom NorthStar Clinical Network.
||The Efficacy of Acyclovir in Childhood Bellâ€™s Palsy.
||Received care by brazilian patients with Duchenne Muscular Dystrophy.
||Combination of Topiramate and Lacosamide is Effective for Paramyotonia Congenita with neurological symptoms.
||Impact of genetic results on treatment of CONGENITAL MYASTHENIC SYNDROME (CMS).
||A Toddler with Myasthenia Gravis Ocular.
Congenital Myasthenia Syndrome: Clinical Profile, Treatment Response, Electrodiagnostic Studies And Genetic Audit.
||Guillain-Barre Syndrome: Uncommon association to common pediatric diseases.
||Design of a phase 3 trial to evaluate the long-term efficacy and safety of ataluren in patients with nonsense mutation Duchenne muscular dystrophy
||Long-term Pulmonary Function Outcomes in Non-Ambulatory Patients with Nonsense Mutation Duchenne Muscular Dystrophy Treated with Ataluren: 240-Week Data from an Open-label Extension Study.
||Cardiopulmonary Assessment in Children with Duchenne Muscular Dystrophy.
||Late onset LAMA-2 Deficiency Congenital Muscular Dystrophy.
||Ragged red fibers in myopathy with white matter changes - mitochondrial disorder or a red herring?
||Multiplex ligation-dependent probe amplification based SMN1 deletion analysis in 150-Indian patients with spinal muscular atrophy.
||Spinal Muscular Atrophy, a single centre experience.
||Early Clinic-Elctrophysiological Predictors of Poor Functional Outcome in GBS.
||Duchenne Muscular Dystrophy a South Indian Perspective.
||Explore evaluation methods of treatment efficacy on spinal muscular atrophy.
||Double-blinded Randomized Placebo Controlled trial of Valproate and levocarnitine in Children with Spinal Muscular Atrophy (aged 2-15years).
||Prevalence of smooth muscle dysfunction among children with Duchenne muscular dystrophy.
||Case series - congenital myasthenia gravis genotype and phenotype co-relation.
||Hereditary Sensory and Autonomic Neuropathy Type VII- A Rare Presentation.
||Genetic evaluation of Congenital Myopathy (CM) and Congenital Muscular Dystrophy (CMD) in children : Slow Death of Muscle biopsies.
||Schwartz-Jampel syndrome responding positively to carbamazepine therapy: a case report and a novel mutation.
||Anti â€“HMG-Co A reductase antibodies associated with progressive necrotizing myositis and autophagosomes in a teenager.
||Clinical profile of three children with HSAN type 4 from South India.
||Abnormalities of Fatty Acid Oxidation as Potential Candidate Biomarker for Spinal Muscular Atrophy (SMA).
||Guillain-Barr Ã © syndrome in a pediatric tertiary center (last five years).
||McArdle disease: a diagnosis to suspect in the paediatric age.
||Clinical and genetic characteristics of congenital myasthenia syndrome with episodic apnea caused by CHAT gene mutation in China.
||Comparison of five different electrophysiological criteria for Childhood Guillian Barre Syndrome.
||A case series of hereditary sensory autonomic neuropathy in children.
||A Case of Congenital Myasthenia with False Positive Anti-acetylcholine Receptor antibody.
||Paediatric Gullain Barre syndrome and its variants â€“ observation of clinico-electrophysiological profile in a tertiary care hospital.
||Clinical and genetic characteristics of GDAP1 gene mutation in Charcot Marie Tooth disease.
||Factors influencing initial diagnosis of Guillain Barre syndrome: A retrospective analysis.
||Somatosensory Evoked Potential: a normative study in children.
||A pediatric case of anti-MuSK-antibody-positive ocular myasthenia gravis.
||Short Term Neurological Outcome of a Cohort of Acute Asymmetric Flaccid Myelitis.
||Disorders of Neuromuscular transmission in children: experience of a tertiary centre from North India.
||Collagen VI related myopathies: clinical variability of triple-helical domain mutations of COL6A mutations.
||Clinicopathological profile and treatment outcome of Inflammatory myopathies in children: a retrospective cohort study.
||Our experience in the management of diffuse axonal injury patients in pediatric population and the review of literature - an institutional study.
||Assessment of clinical follow-up and prognosis in acute neurological condition in pediatric patients managed in pediatric intensive care unit.
||Emergency room visits and admission rates of children with neuromuscular disorders: A 10-year experience in a medical center in Taiwan.
||Diagnostic Utility of Middle Cerebral Artery flow indices as a Non-invasive tool for detecting Raised Intracranial Pressure in Pediatric patients.
||Clinico-radiological profile of acute leucoencephalopathy with restricted diffusion - a novel cause of acute encephalopathy in children.
||Early Post-Traumatic Seizures in PediatricTraumatic Brain Injury.
||Big Black Brain.
||Native medicine use and lead poisoning in children.
||A prospective study on incidence of non-convulsive status epilepticus in children with acute encephalopathy.
||Brain Death Determination for Comatose Patients in The Pediatric Intensive Care Unit.
||Effect of Glucocorticoid Receptorâ€™s Function on Expression of MAOA by GC-KLF11-MAOA Pathway.
||The Ð¡Linical Case of Toxic Cranial Neuropathy in a Child With Neuroblastoma.