- Guideline
- Nutrition
- Clinical practice guideline for the diagnosis and treatment of pediatric obesity: recommendations from the Committee on Pediatric Obesity of the Korean Society of Pediatric Gastroenterology Hepatology and Nutrition
-
Dae Yong Yi, Soon Chul Kim, Ji Hyuk Lee, Eun Hye Lee, Jae Young Kim, Yong Joo Kim, Ki Soo Kang, Jeana Hong, Jung Ok Shim, Yoon Lee, Ben Kang, Yeoun Joo Lee, Mi Jin Kim, Jin Soo Moon, Hong Koh, JeongAe You, Young-Sook Kwak, Hyunjung Lim, Hye Ran Yang
-
Clin Exp Pediatr. 2019;62(1):3-21. Published online December 27, 2018
-
|
The Committee on Pediatric Obesity of the Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition newly developed the first Korean Guideline on the Diagnosis and Treatment of Obesity in Children and Adolescents to deliver an evidence-based systematic approach to childhood obesity in South Korea. The following areas were systematically reviewed, especially on the basis of all available references published in... |
-
-
- Review Article
- Neurology
- Epilepsy syndromes during the first year of life and the usefulness of an epilepsy gene panel
-
Eun Hye Lee
-
Clin Exp Pediatr. 2018;61(4):101-107. Published online April 23, 2018
-
|
Recent advances in genetics have determined that a number of epilepsy syndromes that occur in the first year of life are associated with genetic etiologies. These syndromes range from benign familial epilepsy syndromes to early-onset epileptic encephalopathies that lead to poor prognoses and severe psychomotor retardation. An early genetic diagnosis can save time and overall cost by reducing the amount... |
-
-
- Original Article
- Early postictal electroencephalography and correlation with clinical findings in children with febrile seizures
-
Kyung A Jeong, Myung Hee Han, Eun Hye Lee, Sajun Chung
-
Clin Exp Pediatr. 2013;56(12):534-539. Published online December 20, 2013
-
|
Purpose Electroencephalography (EEG) is frequently ordered for patients with febrile seizures despite its unclear diagnostic value. We evaluated the prevalence of abnormal EEGs, the association between clinical findings and abnormal EEGs, and the predictive value of EEG for the recurrence of febrile seizures. MethodsData were collected on 230 children who were treated for febrile seizures at Kyung Hee University Medical Center from... |
-
-
- Short term outcomes of topiramate monotherapy as a first-line treatment in newly diagnosed West syndrome
-
Gyu Min Lee, Kyung Suk Lee, Eun Hye Lee, Sajun Chung
-
Clin Exp Pediatr. 2011;54(9):380-384. Published online September 30, 2011
-
|
Purpose To investigate the efficacy of topiramate monotherapy in West syndrome prospectively. MethodsThe study population included 28 patients (15 male and 13 female children aged 2 to 18 months) diagnosed with West syndrome. After a 2-week baseline period for documentation of the frequency of spasms, topiramate was initiated at 2 mg/kg/day. The dose was increased by 2 mg/kg every week to a... |
-
-
- Case Report
- A case of Bartter syndrome type I with atypical presentations
-
Eun Hye Lee, Ju Sun Heo, Hyun Kyung Lee, Kyung Hee Han, Hee Gyung Kang, Il Soo Ha, Yong Choi, Hae Il Cheong
-
Clin Exp Pediatr. 2010;53(8):809-813. Published online August 31, 2010
-
|
Bartter syndrome (BS) is an autosomal recessively inherited rare renal tubular disorder characterized by hypokalemic metabolic alkalosis and hyperreninemic hyperaldosteronism with normal to low blood pressure due to a renal loss of sodium. Genetically, BS is classified into 5 subtypes according to the underlying genetic defects, and BS is clinically categorized into antenatal BS and classical BS according to onset... |
-
-
- Original Article
- Genotype and clinical features of Korean patients with methylmalonic aciduria and propionic aciduria
-
Eun Hye Lee, Jung Min Ko, Jae-Min Kim, Han-Wook Yoo
-
Clin Exp Pediatr. 2008;51(9):964-970. Published online September 15, 2008
-
|
Purpose : Methylmalonic aciduria (MMA) and propionic aciduria (PA) are inborn errors in the catabolism of branched-chain amino acids. The study was undertaken to investigate the genotypes and clinical features of Korean patients with MMA and PA.
Methods : This study examined 12 patients with MMA and eight with PA. We analyzed various clinical features, laboratory findings, treatments, and neuro-developmental outcomes.... |
-
-
|