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Journal of Pediatric Orthopedics|August 29, 2002
Deformity correction of knee and leg lengthening by Ilizarov method in hypophosphatemic rickets: outcomes and significance of serum phosphate levelIn Ho Choi, Jae Kwang Kim, Chin Youb Chung, et al.Journal of Pediatric Orthopedics|December 15, 2010
Transcultural adaptation and validation of the Korean version of the Pediatric Outcomes Data Collection Instrument (PODCI) in children and adolescentsDae Gyu Kwon, Chin Youb Chung, Kyoung Min Lee, et al.Journal of Pediatric Orthopedics|February 14, 2012
Medial and lateral crossed pinning versus lateral pinning for supracondylar fractures of the humerus in children: decision analysisKyoung Min Lee, Chin Youb Chung, Dae Kyu Gwon, et al.Skeletal Radiology|May 29, 2012
Metaphyseal chondromatosis combined with D-2-hydroxyglutaric aciduria in four patientsHye Jung Choo, Tae-Joon Cho, Junghan Song, et al.Journal of Korean Medical Science|July 2, 2010
Autosomal recessive multiple epiphyseal dysplasia in a Korean girl caused by novel compound heterozygous mutations in the DTDST (SLC26A2) geneTae-Joon Cho, Ok-Hwa Kim, Hye-Ran Lee, et al.American Journal of Medical Genetics. Part A|June 28, 2013
Osteogenesis imperfecta type V: clinical and radiographic manifestations in mutation confirmed patientsOk-Hwa Kim, Dong-Kyu Jin, Keisuke Kosaki, et al.Journal of Pediatric Orthopedics|April 8, 2014
Fibular lengthening for the management of translational talus instability in hereditary multiple exostoses patientsDong Yeon Lee, Joong Il Kim, Mi Hyun Song, et al.Human Mutation|July 18, 2015
Novel COL2A1 variant (c.619G>A, p.Gly207Arg) manifesting as a phenotype similar to progressive pseudorheumatoid dysplasia and spondyloepiphyseal dysplasia, Stanescu typeJulie Jurgens, Nara Sobreira, Peggy Modaff, et al.Journal of Pediatric Orthopedics|September 25, 2010
Clinical relevance of valgus deformity of proximal femur in cerebral palsyKyoung Min Lee, Jong Yeol Kang, Chin Youb Chung, et al.American Journal of Medical Genetics. Part A|March 23, 2017
Confirmation of CAGSSS syndrome as a distinct entity in a Danish patient with a novel homozygous mutation in IARS2Shahida Moosa, Annette Haagerup, Pernille Axel Gregersen, et al.Pageof 25