Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

PUBLICATION DATE

10 results
Display

Platybasia in 22q11.2 Deletion Syndrome Is Not Correlated with Speech Resonance

Spruijt NE, Kon M, Mink van der Molen AB

BACKGROUND: An abnormally obtuse cranial base angle, also known as platybasia, is a common finding in patients with 22q11.2 deletion syndrome (22q11DS). Platybasia increases the depth of the velopharynx and...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Cerebellar Ectopia Associated with Unilateral Agenesis of Posterior Arch of Atlas

Kim YZ, Song YJ, Kim HD

  • KMID: 1822224
  • J Korean Neurosurg Soc.
  • 2004 Aug;36(2):157-159.
Chiari type I malformation(CM-I) is a congenital disorder recognized by caudal displacement of the cerebellar tonsils through the foramen magnum and into the cervical canal. Though bony anomalies associated with...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Relationship Between Findings on Brain MRI and Prognosis in Patients With Spontaneous Intracranial Hypotension

Park MH, Kim BC, Choi SM, Kim DE, Choi KH, Kim JT, Yoon W, Nam TS, Lee SH, Park MS, Kim MK, Cho KH

  • KMID: 1708057
  • J Korean Neurol Assoc.
  • 2014 Feb;32(1):14-18.
BACKGROUND: The outcome of spontaneous intracranial hypotension (SIH) is unpredictable and some patients have persistent and often incapacitating symptoms. This study was aimed to investigate whether abnormalities on initial magnetic...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Acrodysostosis Associated with Symptomatic Cervical Spine Stenosis

Ko JM, Kwack KS, Kim SH, Kim HJ

  • KMID: 2184480
  • J Genet Med.
  • 2010 Dec;7(2):145-150.
Acrodysostosis is an extremely rare disorder characterized by short fingers and toes with peripheral dysostosis, nasal hypoplasia, and mental retardation. We report a 16-year-old Korean boy with acrodysostosis who had...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Basilar Impression

Suh JK, Chu JW

  • KMID: 2019758
  • J Korean Neurosurg Soc.
  • 1987 Jun;16(2):513-522.
A case of basilar impression surgically treated in a female patient aged 22 years is presented. A myriad of abnormal neurologic findings were present that were secondary to compression of...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Stereological and Morphometric Analysis of MRI Chiari Malformation Type-1

Alkoc OA, Songur A, Eser O, Toktas M, Gonul Y, Esi E, Haktanir A

OBJECTIVE: In this study, we aimed to investigate the underlying ethiological factors in chiari malformation (CM) type-I (CMI) via performing volumetric and morphometric length-angle measurements. METHODS: A total of 66 individuals...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Surgical Experience of Basilar Invagination by Transoral Transpharyngeal Approach

Rim DC, Cho YJ, Ahn MS

  • KMID: 2067941
  • J Korean Neurosurg Soc.
  • 1992 Sep;21(9):1160-1167.
Basilar invagination or basilar impression involves the upward displacement of the margins of the foramen magnum into the base of the skull. That this entity may be asymptomatic or associated...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Tuberculosis of the Craniovertebral Junction with Basilar Impression: A Case Report

Hong JM, Lee SG, Park CW, Yoo CJ, Kim WK

  • KMID: 2288427
  • Korean J Spine.
  • 2010 Jun;7(2):103-106.
We report a rare case of tuberculosis as a cause of secondary basilar impression. A 35-year-old man was admitted to our hospital complaining of severe neck pain and motor weakness...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Surgical Treatment of Klippel-Feil Syndrome with Cervical Spondylosis

Park KS, Lee KS, Kim YS, Kuh SU

  • KMID: 2010649
  • J Korean Neurosurg Soc.
  • 2004 Jan;35(1):116-118.
We report a case of Klippel-Feil syndrome. The patient was a 37-year-old man who developed progressive motor weakness and on C4-5 and C6-7 segments combined with severe cervical stenosis, basilar...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Arnold-Chiari Malformation Type I Associated with Syringomyelia and Atlantoaxial Instability: A Case Report

Kim EJ, Kim MS, Lee JY, Whang JW, Yoon TS

The Arnold-Chiari Malformation is a cognenital disorder with symptoms such as ataxia, dissociated sensory loss, extremity pain, and frequently associated with other malformations of the same kind, including syringomyelia, basilar...
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