Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

more+
SELECT FILTER
 
Close

PUBLICATION DATE

228 results
Display

Dysplasia Epiphyseal Multiple: A Case

Oh JD, Ihin JC, Kim ID

Dysplasia epiphysealis multiplex is a rare syndrome, first discribed by Fairbank in 1935, but numerous publications have made it a well-recognized entity. The syndrome is caused by a congenital developmental...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Bilateral Slipped Capital Femoral Epiphysis Due to Primary Hyperparathyroidism: A Case Report

Kim TS, Choi WS

Slippage of the upper femoral epiphysis can occur in association with endocrine disorder. A 14-year-old male patient, who complained of pain on multiple joints including both hips, was diagnosed with...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Acrodysostosis

Lee SH, Oh CW, Kim KS, Kim KB

  • KMID: 2208380
  • J Korean Pediatr Soc.
  • 1995 Jan;38(1):133-137.
Acrodysostosis is a rare multiple congenital malformation syndrome with peripheral dysostosis, nasal hypoplasia, mental retardation and growth failure. In 1968, Maroteaux and Malamut first described this disorder in three patients,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Study on the Growth of the Distal Tibio-Fibular Epiphysis in Poliomyelitis

Kang ES, Park BM, Kim NH, Chung IH, Shin JS, Lee KD

This study is concerned with a comparison of lower tibial and fibular epiphyseal growth and deformities of the ankles in normal and paralysed children. The data were based on 87...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Dysplasia Epiphysialis Punctata: A Case Report

Lee HB, Ha SH, Oh SK, Kang CJ, Kim YC

Dysplasia epiphysialis punctata is a rare congenital disorder of infancy affecting in particular cartilage, muscle, jointtcapsules and the eyes. A case of dysplasia epiphysialis punctata with involvement of all epiphyses...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Morquio's Syndrome: A Case Report

Choi KS, Choung ES, Yang CR

Morquio's syndrome is a very rare disease, which is characterized by dwarfism, flattening of the vertebral body, marked spinal kyphosis, widespread affection of the epiphyses and normal intelligence. The authors...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Traumatic Separation of Upper Femoral Epiphysis: A Case Report

Kim HS

Although separation of the epiphyses at the wrist, elbow, ankle, and knee, is a common injury in childhood, a traumatic separation of the upper femoral epiphysis in young children is...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
MR Evaluation of Pyo genic Osteomyelitis Involving the Epiphyses

Kim SG, Park JG, Lee YC, Cho YM, Kim HC, Kang HK

PURPOSE: The purpose of this study was to analyze of the MR findings of the pyogenic osteomyelitis involving the epiphyses of the long bones in childhood. MATERIALS AND METHODS: Eleven...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Trichorhinophalangeal Syndrome

Cho YH, Kim TH, Park KB, Song HR

  • KMID: 1930776
  • Korean J Dermatol.
  • 1994 Oct;32(5):920-925.
Trichorhinophalangeal syndiome, a rare genetic disease, is characterzed by the triad of slow growing, brittle hair with early loss, a pear-shaped nose with bulbous tip and long philtrum, and coneshaped...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Osteopoikilosis: Report of 6 cases

Kim Y, Kim YI, Moon MK

Osteopoikilosis is condensing or sclerosing osteopathy which is generally believed to be congenital anomalies and heriditary in nature. Osteopoikolosis or osteopathia condensans disseminata is a condition which is ralatively rare...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
MRI Findings of Dysplasia Epiphysealis Hemimelica: A Case Report

Seo YL, Nam ES

Dysplasia epiphysealis hemimelica, also known as Trevor's disease, is a rare disorder characterized by osteochondral overgrowth of one or more epiphyses and usually affecting the lower limbs. It typically presents...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Pathologic Separation of Capital Femoral Epiphysis due to an Osteosarcoma

Kim SL, Kim KW, Ko HS, Tae SK, Kim DH

In Korea, slipped capital femoral epiphysis is a rare disease. In which the capital femoral epiphysis migrate posteriorly and inferiorly against the neck portion. Sometimes it should be differentiated from...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Thiemann's Disease: a Case Report

Kim YH, Lee JY

Thiemann's disease is a form of idiopathic avascular necrosis of the immature epiphyses of the phalanges of the fingers and toes. Few cases of Thiemann's disease have been reported because...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Radiologic findings of epiphyseal metaphyseal dysplasia developed in one family

Lim DR, Shin HJ

The spondyloepiphseal dysplasia are chondrodystrohpies with selective and combine invovlement of vertebrae andlong bone epiphyses and metaphses. It is rare familial disease and transmitted autosomal dominant except X-linkedrecessive in SED...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Incidence of the Appearance of the Proximal Humeral Ossification Center of the Neonates and Infants on Plain Chest Radiograph

Kim SC, Lee YH, Choi YH, Kim TH, Kim SJ, Chang YP, Lee BH, Park HH, Yu PM

  • KMID: 2347075
  • J Korean Radiol Soc.
  • 1996 Feb;34(2):289-292.
PURPOSE: To ascertain the incidence of proximal humeral epiphyseal ossification centers, as shown on chest radiographs, in neonates and infants. MATERIALS AND METHODS: The distribution of corrected age(CA) of the infantswas...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Chondroblastoma of Temporal Bone

Kim SC, Moon IS, Kang HY, Lee WS

  • KMID: 2275874
  • Korean J Otolaryngol-Head Neck Surg.
  • 2002 Feb;45(2):174-177.
Chondroblastoma is an uncommon primary benign bone tumor that usually arises in the epiphyses of the long bones. Chondroblastoma of temporal bone is extremely rare. Its biological nature is often...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Trichorhinophalangeal Syndrome

Moon SH, Park BS, Suh DH, Eun HC

Trichorhinophalangeal syndrome is a genetic disease and divided into three differen types. Trichorhinophalangeal syndrome type I is characterixed by alopecia, a bulbous pear-shaped nose and cone-shaped epiphyses in the hand....
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Case Report of Imaging Analyses of the Dysplasia Epiphysealis Hemimelica (Trevor's Disease)

Suh JH, Cho KH

Trevor's disease, also known as dysplasia epiphysealis hemimelica, is a rare developmental disorder presented with epiphyseal overgrowth involving one or multiple epiphyses. Here we report the radiologic findings of two...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Trichorhinophalangeal Syndrome Type I

Son HS, Oh CK, Kim MB, Lee JB, Jang HS, Kwon KS

  • KMID: 2302983
  • Korean J Dermatol.
  • 2003 Jun;41(6):801-804.
Trichorhinophalangeal syndrome(TRPS) type I is characterized by sparse and slow-growing hairs, pear-shaped nose, elongated philtrum, thin upper lip, and bone deformities, especially, cone-shaped epiphyses of the phalanges. The syndrome is...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Bone Growth after Free Vascularized Grafting of the Upper Radius including its Epiphysis in Puppies

Hahn SB

The radius including the proximal epiphysis was transferred in puppies. Growth in the vascularized long bone grafts in growing animals was significantly greate than in the non-vascularized grafts, not equal...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr