A brain extraction algorithm for infant T2 weighted magnetic resonance images based on fuzzy c-means thresholding

por Bae, Inyoung, Chae, Jong-Hee, Han, Yeji
Publicado 2021

Pediatric Stroke

por Jeong, Goun, Lim, Byung Chan, Chae, Jong-Hee
Publicado 2015

A compound heterozygous mutation in the FMO3 gene: the first pediatric case causes fish odor syndrome in Korea

por Kim, Ji Hyun, Cho, Sung Min, Chae, Jong-Hee
Publicado 2017

The Common NF-κB Essential Modulator (NEMO) Gene Rearrangement in Korean Patients with Incontinentia Pigmenti

por Song, Min-Jung, Chae, Jong-Hee, Park, Eun-Ae, Ki, Chang-Seok
Publicado 2010

The Clinical Characteristics of Optic Neuritis in Korean Children

por Jo, Dong Hyun, Kim, Seong-Joon, Chae, Jong Hee, Yu, Young Suk
Publicado 2011

Successful Pallidal Deep Brain Stimulation in a Patient with Childhood-Onset Generalized Dystonia with ANO3 Mutation

por Yoo, Dallah, Kim, Han-Joon, Chae, Jong-Hee, Paek, Sun Ha, Jeon, Beomseok
Publicado 2019

A case of Rubinstein-Taybi Syndrome with a CREB-binding protein gene mutation

por Kim, Se Hee, Lim, Byung Chan, Chae, Jong Hee, Kim, Ki Joong, Hwang, Yong Seung
Publicado 2010

A 6-Month-Old Girl with Incontinentia Pigmenti Presenting as Status Epilepticus

por Seo, Moon Young, You, Su Jeong, Kim, Soung Hee, Cho, Woo Ho, Chae, Jong Hee
Publicado 2017

Whole genomic approach in mutation discovery of infantile spasms patients

por Lee, Seungbok, Jang, Sesong, Kim, Jong-Il, Chae, Jong Hee, Kim, Ki Joong, Lim, Byung Chan
Publicado 2022

Angiography-negative childhood primary angiitis of the central nervous system diagnosed by open brain biopsy: a case report

por Kang, Dayun, Kim, Soo Yeon, Chae, Jong Hee, Kim, Ki Joong, Park, Sung-Hye, Lim, Byung Chan
Publicado 2022

A Familial Case of Childhood Ataxia with Leukodystrophy Due to Novel POLR1C Mutations

por Han, Ji Yeon, Kim, Soo Yeon, Cheon, Jung-Eun, Choi, Murim, Lee, Jin Sook, Chae, Jong-Hee
Publicado 2020

Pediatric Miller Fisher Syndrome; Characteristic Presentation and Comparison with Adult Miller Fisher Syndrome

por Jang, Yeonji, Choi, Jae-Hwan, Chae, Jong Hee, Lim, Byung Chan, Kim, Seong-Joon, Jung, Jae Ho
Publicado 2020

Genetic and clinical heterogeneity in Korean patients with Rubinstein–Taybi syndrome

por Choi, Naye, Kim, Hwa Young, Lim, Byung Chan, Chae, Jong‐Hee, Kim, Soo Yeon, Ko, Jung Min
Publicado 2021

FOXG1 Mutation is a Low-Incidence Genetic Cause in Atypical Rett Syndrome

por Byun, Christine K., Lee, Jin Sook, Lim, Byung Chan, Kim, Ki Joong, Hwang, Yong Seung, Chae, Jong-Hee
Publicado 2015

A Case of Multiple Mitochondrial Dysfunctions Syndrome 4 with Novel ISCA2 Variants, Mimicking Post-Infectious Encephalitis

por Chin, Hyungjin, Cho, Jaeso, Kim, Woo Joong, Kim, Soo Yeon, Lim, Byung Chan, Kim, Ki Joong, Chae, Jong Hee
Publicado 2023

Development of Korean Rare Disease Knowledge Base

por Seo, Heewon, Kim, Dokyoon, Chae, Jong-Hee, Kang, Hee Gyung, Lim, Byung Chan, Cheong, Hae Il, Kim, Ju Han
Publicado 2012

Predictive Value of Electroencephalography for Seizure Outcome Following Corpus Callosotomy in Children

por Jeong, Go-Un, Kim, Hunmin, Lim, Byung Chan, Chae, Jong-Hee, Kim, Ki Joong, Hwang, Yong Seung, Hwang, Hee
Publicado 2011

Home Mechanical Ventilation in Childhood-Onset Hereditary Neuromuscular Diseases: 13 Years’ Experience at a Single Center in Korea

por Han, Young Joo, Park, June Dong, Lee, Bongjin, Choi, Yu Hyeon, Suh, Dong In, Lim, Byung Chan, Chae, Jong-Hee
Publicado 2015

The extended clinical and genetic spectrum of CTNNB1-related neurodevelopmental disorder

por Lee, Seungbok, Jang, Se Song, Park, Soojin, Yoon, Jihoon G., Kim, Soo Yeon, Lim, Byung Chan, Chae, Jong Hee
Publicado 2022

Expansion of clinico-genetic spectrum of PRDX3 disease: a literature review with two additional cases

por Cho, Jaeso, Yoon, Jihoon G, Lee, Seungbok, Kim, Sheehyun, Kim, Soo Yeon, Kim, Man Jin, Moon, Jangsup, Chae, Jong-Hee
Publicado 2023