Ok H. Kim
Incheon, Republic of Korea
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 publications
Imaging findings in pediatric interferonopathies.
Journal: Pediatric radiology
Published: January 31, 2026
A Case of Familial Spondyloenchondrodysplasia with Immune Dysregulation Masquerading as Moyamoya Syndrome.
Journal: Journal of clinical neurology (Seoul, Korea)
Published: January 25, 2019
Regarding Camurati-Engelmann Disease: In Reply.
Journal: Clinics in orthopedic surgery
Published: March 23, 2018
Orthopedic Manifestations of Type I Camurati-Engelmann Disease.
Journal: Clinics in orthopedic surgery
Published: September 01, 2016
Acromicric Dysplasia Caused by a Novel Heterozygous Mutation of FBN1 and Effects of Growth Hormone Treatment.
Journal: Annals of laboratory medicine
Published: May 03, 2016
Acromesomelic dysplasia, type maroteaux caused by novel loss-of-function mutations of the NPR2 gene: Three case reports.
Journal: American journal of medical genetics. Part A
Published: June 15, 2015
Novel COL2A1 variant (c.619G>A, p.Gly207Arg) manifesting as a phenotype similar to progressive pseudorheumatoid dysplasia and spondyloepiphyseal dysplasia, Stanescu type.
Journal: Human mutation
Published: April 02, 2015
Showing 1-8 of 8
Last Updated: 09/26/2026