Calcifying Aponeurotic Fibroma: Case Report with Radiographic and MR Features

por Kim, Ok Hwa, Kim, Yeon Mee
Publicado 2014

The First Korean Patient with Potocki-Shaffer Syndrome: A Rare Cause of Multiple Exostoses

por Sohn, Young Bae, Yim, Shin-Young, Cho, Eun-Hae, Kim, Ok-Hwa
Publicado 2015

Identification of p.Glu131Lys Mutation in the IHH Gene in a Korean Patient With Brachydactyly Type A1

por Jang, Mi-Ae, Kim, Ok-Hwa, Kim, Sun Wook, Ki, Chang-Seok
Publicado 2015

Identification of the Mutations in the Prostaglandin Transporter Gene, SLCO2A1 and Clinical Characterization in Korean Patients with Pachydermoperiostosis

por Lee, Sihoon, Park, So Young, Kwon, Hyun Jin, Lee, Chul-Ho, Kim, Ok-Hwa, Rhee, Yumie
Publicado 2016

Carcinoma Mixed within Milk of Calcium in a Breast: a Case Report

por Park, Ji-Sung, Park, Young-Mi, Kim, Eun-Kyung, Lee, Jin-Hwa, Kim, Ok-Hwa, Ryu, Ji-Hwa
Publicado 2008

Effect of Zoledronic Acid on Acro-Osteolysis and Osteoporosis in a Patient with Hajdu-Cheney Syndrome

por Hwang, Sena, Shin, Dong Yoeb, Moon, Seong Hwan, Lee, Eun Jig, Lim, Sung-Kil, Kim, Ok Hwa, Rhee, Yumie
Publicado 2011

Spinal Meningeal Melanocytoma with Benign Histology Showing Leptomeningeal Spread: Case Report

por Kim, Ok Hwa, Kim, Seon Jeong, Choo, Hye Jung, Lee, Sun Joo, Lee, In Sook, Kim, Ji Yeon, Kim, Hoon
Publicado 2013

Comparison of Clinico-Radiological Features between Congenital Cystic Neuroblastoma and Neonatal Adrenal Hemorrhagic Pseudocyst

por Eo, Hong, Kim, Ji Hye, Jang, Kyung Mi, Yoo, So-Young, Lim, Gye-Yeon, Kim, Myung-Joon, Kim, Ok-Hwa
Publicado 2011

Extending the phenotype of BMPER-related skeletal dysplasias to ischiospinal dysostosis

por Kuchinskaya, Ekaterina, Grigelioniene, Giedre, Hammarsjö, Anna, Lee, Hye-Ran, Högberg, Lotta, Grigelionis, Gintautas, Kim, Ok-Hwa, Nishimura, Gen, Cho, Tae-Joon
Publicado 2016

Acromicric Dysplasia Caused by a Novel Heterozygous Mutation of FBN1 and Effects of Growth Hormone Treatment

por Jin, Hyung Suk, Song, Ho young, Cho, Sung Yoon, Ki, Chang-Seok, Yang, Song Hyun, Kim, Ok-Hwa, Kim, Su Jin
Publicado 2017

Biallelic novel mutations of the COL27A1 gene in a patient with Steel syndrome

por Kim, Jong Seop, Jeon, Hyoungseok, Lee, Hyeran, Ko, Jung Min, Kim, Yonghwan, Choi, Murim, Nishimura, Gen, Kim, Ok-Hwa, Cho, Tae-Joon
Publicado 2021

Identification of a GDF5 Mutation in a Korean Patient with Brachydactyly Type C without Foot Involvement

por Seo, Soo Hyun, Park, Mi Jung, Kim, Shin-Hye, Kim, Ok-Hwa, Park, Seungman, Cho, Sung Im, Park, Sung Sup, Seong, Moon-Woo
Publicado 2013

Desmoplastic Fibroma of Bone in a Toe: Radiographic and MRI Findings

por Kim, Ok Hwa, Kim, Seon Jeong, Kim, Ji Yeon, Ryu, Ji Hwa, Choo, Hye Jung, Lee, Sun Joo, Lee, In Sook, Suh, Kyung Jin
Publicado 2013

Novel COL9A3 mutation in a family diagnosed with multiple epiphyseal dysplasia: a case report

por Jeong, Changhoon, Lee, Jae Young, Kim, Jiyeon, Chae, Hyojin, Park, Hae-il, Kim, Myungshin, Kim, Ok-Hwa, Kim, Paul, Lee, Young Kee, Jung, Jongsun
Publicado 2014

Autosomal Recessive Multiple Epiphyseal Dysplasia in a Korean Girl Caused by Novel Compound Heterozygous Mutations in the DTDST (SLC26A2) Gene

por Cho, Tae-Joon, Kim, Ok-Hwa, Lee, Hye-Ran, Shin, Sung Jin, Yoo, Won Joon, Park, Woong Yang, Park, Sung Sup, Cho, Sung Im, Choi, In Ho
Publicado 2010

A Case of Familial Spondyloenchondrodysplasia with Immune Dysregulation Masquerading as Moyamoya Syndrome

por Lee, Jin Sook, Lim, Byung Chan, Kim, Ki Joong, Kim, Seung-Ki, Kim, Ok-Hwa, Kim, Joong Gon, Park, Sung-Gyoo, Cho, Tae-Joon, Chae, Jong-Hee
Publicado 2019

Orthopedic Manifestations of Type I Camurati-Engelmann Disease

por Yuldashev, Alisher J., Shin, Chang Ho, Kim, Yong Sung, Jang, Woo Young, Park, Moon Seok, Chae, Jong Hee, Yoo, Won Joon, Choi, In Ho, Kim, Ok Hwa, Cho, Tae-Joon
Publicado 2017

Regarding Camurati-Engelmann Disease: In Reply

por Yuldashev, Alisher J., Shin, Chang Ho, Kim, Yong Sung, Jang, Woo Young, Park, Moon Seok, Chae, Jong Hee, Yoo, Won Joon, Choi, In Ho, Kim, Ok Hwa, Cho, Tae-Joon
Publicado 2018

Clinical, biochemical, and genetic analysis of two Korean patients with Trichorhinophalangeal syndrome type I and growth hormone deficiency

por Sohn, Young Bae, Ki, Chang-Seok, Park, Sung Won, Cho, Sung-Yoon, Ko, Ah-Ra, Kwon, Min-Jung, Kim, Ji-Youn, Park, Hyung-Doo, Kim, Ok-Hwa, Jin, Dong-Kyu
Publicado 2013

Novel loss-of-function variants of TRAPPC2 manifesting X-linked spondyloepiphyseal dysplasia tarda: report of two cases

por Won, Joon Yeon, Kim, Dayeon, Park, Seon Young, Lee, Hye Ran, Lim, Jong-Seok, Park, Jong Hoon, Song, Mi Hyun, Song, Hae Ryong, Kim, Ok-Hwa, Kim, Yonghwan, Cho, Tae-Joon
Publicado 2019