Lista de obras -

A case of Rubinstein-Taybi Syndrome with a CREBbinding protein gene mutation ⬇️

artículo científico publicado el 23 de junio de 2010

A case of isodicentric chromosome 15 presented with epilepsy and developmental delay ⬇️

artículo científico publicado el 20 de diciembre de 2012

A case of mucolipidosis II presenting with prenatal skeletal dysplasia and severe secondary hyperparathyroidism at birth ⬇️

artículo científico publicado el 23 de noviembre de 2012

Association Analysis of Interleukin-1β, Interleukin-6, and HMGB1 Variants with Postictal Serum Cytokine Levels in Children with Febrile Seizure and Generalized Epilepsy with Febrile Seizure Plus

scientific article published on 01 October 2019

Chromosomal Microarray With Clinical Diagnostic Utility in Children With Developmental Delay or Intellectual Disability

scientific article published on 01 September 2018

Clinical Spectrum of Myelin Oligodendrocyte Glycoprotein-Immunoglobulin G-Associated Disease in Korean Children

scientific article published on 01 July 2020

Clinical and EEG risk factors for subsequent epilepsy in patients with complex febrile seizures ⬇️

artículo científico publicado el 16 de marzo de 2013

Clinical and Genetic Spectrum of ATP1A3-Related Disorders in a Korean Pediatric Population

scientific article published on 01 January 2020

Coexisting seizures in patients with infantile spasms confirmed by long-term video-electroencephalography monitoring ⬇️

artículo científico publicado el 28 de marzo de 2012

Comparison of flunarizine and topiramate for the prophylaxis of pediatric migraines ⬇️

artículo científico publicado el 27 de octubre de 2012

De Novo Interstitial Deletion of 3q22.3-q25.2 Encompassing FOXL2, ATR, ZIC1, and ZIC4 in a Patient With Blepharophimosis/Ptosis/Epicanthus Inversus Syndrome, Dandy-Walker Malformation, and Global Developmental Delay ⬇️

artículo científico publicado el 6 de abril de 2011

Development of the clinical assessment scale in autoimmune encephalitis

scientific article published on 10 February 2019

Diagnostic Challenges Associated with GLUT1 Deficiency: Phenotypic Variabilities and Evolving Clinical Features

artículo científico publicado en 2019

Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation ⬇️

artículo científico publicado el 12 de febrero de 2013

Electroencephalography in pediatric moyamoya disease: reappraisal of clinical value ⬇️

artículo científico publicado el 13 de agosto de 2013

Elevated Serum Uric Acid in Benign Convulsions with Mild Gastroenteritis in Children

scientific article published on 01 October 2019

Genetic diagnosis of Duchenne and Becker muscular dystrophy using next-generation sequencing technology: comprehensive mutational search in a single platform ⬇️

artículo científico publicado el 3 de octubre de 2011

Long-term effectiveness of ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy

artículo científico publicado el 3 de septiembre de 2011

Magnetoencephalography in Pediatric Lesional Epilepsy Surgery ⬇️

artículo científico publicado el 26 de mayo de 2012

Molecular diagnosis of congenital muscular dystrophies with defective glycosylation of alpha-dystroglycan using next-generation sequencing technology ⬇️

artículo científico publicado el 1 de marzo de 2013

Paroxysmal nonepileptic events in pediatric patients confirmed by long-term video-EEG monitoring — Single tertiary center review of 143 patients ⬇️

artículo científico publicado el 11 de mayo de 2012

Prevalence of antineuronal antibodies in patients with encephalopathy of unknown etiology: Data from a nationwide registry in Korea.

artículo científico publicado en 2016

Relapsing demyelinating CNS disease in a Korean pediatric population: Multiple sclerosis versus neuromyelitis optica ⬇️

artículo científico publicado el 21 de septiembre de 2010

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