Skip Navigation
Skip to contents
Filter

ARTICLE TYPE

PUBLICATION DATE

33 results
Display

No title in English

No authors listed

  • KMID: 2177149
  • J Korean Child Neurol Soc.
  • 1998 May;5(2):449-454.
No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
No title in English

No authors listed

  • KMID: 2177148
  • J Korean Child Neurol Soc.
  • 1998 May;5(2):436-448.
No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
No title in English

No authors listed

  • KMID: 2177147
  • J Korean Child Neurol Soc.
  • 1998 May;5(2):431-435.
No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
No title in English

No authors listed

  • KMID: 2177146
  • J Korean Child Neurol Soc.
  • 1998 May;5(2):422-430.
No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
No title in English

No authors listed

  • KMID: 2177145
  • J Korean Child Neurol Soc.
  • 1998 May;5(2):412-429.
No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
No title in English

No authors listed

  • KMID: 2177144
  • J Korean Child Neurol Soc.
  • 1998 May;5(2):403-411.
No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Septo-Optic Dysplasia

Cho YS, Jang EY, Cha BH, Lim BK

  • KMID: 2177143
  • J Korean Child Neurol Soc.
  • 1998 May;5(2):393-397.
Septo-optic dysplasia, as first described by de Morsier, is a rare developmental anomaly of absent or hypoplastic septum pellucidum, a primitive optic vesicle, and dysplasia of the optic nerve, chiasm,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Battered Child Syndrome with Subdural hemorrhage

Song YJ, Kim WS, Han HS, Chae SA

  • KMID: 2177142
  • J Korean Child Neurol Soc.
  • 1998 May;5(2):388-392.
The diagnosis of a Battered Child Syndrome is made by the pediatrician, surgeon and the radiologist because almost parents deny the diagnosis or refuse to answer the doctor's questions. The...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of 13 Ring Chromosome Syndrome

Park CJ, Lim BI, Cho HJ, Song KY, Kim KW

  • KMID: 2177141
  • J Korean Child Neurol Soc.
  • 1998 May;5(2):383-387.
We have experienced a case of 13 ring chromosome in a 40-month-old girl who demonstrated psychomotor retardation with delayed speech, growth retardation, hearing loss(left), microcephaly, trigonocephaly with flat occiput, hypertelorism,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Relapsed Acute Disseminated Encephalomyelitis

Park JH, Lee JS, Coe CJ, Yoon CS

  • KMID: 2177140
  • J Korean Child Neurol Soc.
  • 1998 May;5(2):377-382.
Acute disseminated encephalomyelitis(ADEM) and acute relapsing disseminated encephalomyelitis(ARDEM) are representative demyelination diseases that occur among young children with a fulminant onset similar to encephalitis or meningitis. The diseases often occur...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Reversible brain MRI Finding in Hypertensive Encephalopathy with Poststreptococcal Acute Glomerulonephritis

Park KW, Kim GM, Woo YJ

  • KMID: 2177139
  • J Korean Child Neurol Soc.
  • 1998 May;5(2):372-376.
Hypertensive encephalopathy is characterized by an acute, severe rise in blood pressure associated with headache, nausea, vomiting, altered mental status, and focal neurologic deficits, and rapid improvement after control of...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Acute Encephlopathy with Bilateral Thalamotegmental Involvement

Kim JH, Park WI, Lee HJ, Lee GJ

  • KMID: 2177138
  • J Korean Child Neurol Soc.
  • 1998 May;5(2):367-371.
We experienced an unusual case of acute encephalopathy in a 4 month-old boy He was admitted to our hospital because of lethargy and seizures after preceding symptoms of upper respiratory...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case Of Cerebellar Hemorrhage Associated with Cavernous Hemangioma and Developmental Venous Anomaly

Lee JY, Kim SH, Yoon SH

  • KMID: 2177137
  • J Korean Child Neurol Soc.
  • 1998 May;5(2):361-366.
Developmental venous anomalies are congenital anomalies of the intracranial venous drainage and clinically asymptomatic. Cavernous hemangiomas are vascular malformations composed of dilated vascular channels lined with a single layer of...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Congenital Myotonic Dystrophy Diagnosed by Molecular Genetics

Kim HK, Kim JH, Lee YA, Ko TS, Kim KS, Yoo HW, Pi SY, Lee BJ

  • KMID: 2177136
  • J Korean Child Neurol Soc.
  • 1998 May;5(2):356-360.
Congenital myotonic dystrophy is an inherited, autosomal dominant disease that results in a progressive wasting of the skeletal muscle, and sometimes heart and smooth muscles in human. In the newborn...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Miller-Bicker Syndrome

Kim SJ, Lee YK, Choi BJ, Lee IG, Lee IJ, Whang KT

  • KMID: 2177135
  • J Korean Child Neurol Soc.
  • 1998 May;5(2):351-355.
Miller-Dieter syndrome consists of severe type I lissencephaly, abnormal facial appearance, and sometimes other birth defects. Lissencephaly is a brain malformation manifested by a smooth cerebral surface, thickened cortical mantle,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Epidermal Nevus Syndrome with Infantile Spasm

Kim HS, Shin YK, Lee KH, Eun BL, Park SH, Kim IH

  • KMID: 2177134
  • J Korean Child Neurol Soc.
  • 1998 May;5(2):346-350.
Epidermal nevus syndrome is a rare congenital malformation clinically characterized by the association of epidermal nevi with multiple abnormalities of the skin, skeletal system, central nervous system, eyes, cardiovascular system,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Dyke-Davidoff-Masson Syndrome with Infantile Spasm

Jang EY, Cha BH, Lim BK

  • KMID: 2177133
  • J Korean Child Neurol Soc.
  • 1998 May;5(2):342-345.
Dyke-Davidoff-Masson syndrome is a rare clinical syndrome consisting of hemiatrophy of cerebral hemisphere, enlargement of ventricles and prominent pneumatization of petrous pyramid of the temporal bone. Its clinical manifestations are...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Dysembryoplastic Neuroepithelial Tumors in Children with Intractable Seizures: Report of Two Cases

Lee MH, Hong SC, Suh YL, Yoon HK, Kim BK

  • KMID: 2177132
  • J Korean Child Neurol Soc.
  • 1998 May;5(2):334-341.
We report 2 cases of pediatric DNTs which presented with intractable seizures and no other associated neurologic abnormalities. They showed typical appearance of DNTs on neuroimaging and histopathology. Most patients...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
No title in English

No authors listed

  • KMID: 2177131
  • J Korean Child Neurol Soc.
  • 1998 May;5(2):328-333.
No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Analysis of Usefulness of Biochemical Enzyme Assay and MR Spectroscopy(MRS) in Leigh Syndrome

Choi BH, Robinson B, Kim JH, Kim HM, Choi CK, Yoo HW, Ko TS

  • KMID: 2177130
  • J Korean Child Neurol Soc.
  • 1998 May;5(2):319-327.
PURPOSE: Leigh syndrome is a kind of mitochondrial disease with a pathological production of lactate and variable clinical manifestations. Recently biochemical assay of the mitochondrial enzyme activity and MRS are...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2021 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr