- No title in English
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No authors listed
- KMID: 2177149
- J Korean Child Neurol Soc.
- 1998 May;5(2):449-454.
No abstract available. -
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- No title in English
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No authors listed
- KMID: 2177148
- J Korean Child Neurol Soc.
- 1998 May;5(2):436-448.
No abstract available. -
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- No title in English
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No authors listed
- KMID: 2177147
- J Korean Child Neurol Soc.
- 1998 May;5(2):431-435.
No abstract available. -
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- No title in English
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No authors listed
- KMID: 2177146
- J Korean Child Neurol Soc.
- 1998 May;5(2):422-430.
No abstract available. -
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- No title in English
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No authors listed
- KMID: 2177145
- J Korean Child Neurol Soc.
- 1998 May;5(2):412-429.
No abstract available. -
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- No title in English
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No authors listed
- KMID: 2177144
- J Korean Child Neurol Soc.
- 1998 May;5(2):403-411.
No abstract available. -
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- A Case of Septo-Optic Dysplasia
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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,... -
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- A Case of Battered Child Syndrome with Subdural hemorrhage
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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... -
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- A Case of 13 Ring Chromosome Syndrome
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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,... -
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- A Case of Relapsed Acute Disseminated Encephalomyelitis
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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... -
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- Reversible brain MRI Finding in Hypertensive Encephalopathy with Poststreptococcal Acute Glomerulonephritis
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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... -
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- A Case of Acute Encephlopathy with Bilateral Thalamotegmental Involvement
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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... -
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- A Case Of Cerebellar Hemorrhage Associated with Cavernous Hemangioma and Developmental Venous Anomaly
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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... -
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- A Case of Congenital Myotonic Dystrophy Diagnosed by Molecular Genetics
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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... -
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- Miller-Bicker Syndrome
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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,... -
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- A Case of Epidermal Nevus Syndrome with Infantile Spasm
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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,... -
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- A Case of Dyke-Davidoff-Masson Syndrome with Infantile Spasm
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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... -
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- Dysembryoplastic Neuroepithelial Tumors in Children with Intractable Seizures: Report of Two Cases
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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... -
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- No title in English
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No authors listed
- KMID: 2177131
- J Korean Child Neurol Soc.
- 1998 May;5(2):328-333.
No abstract available. -
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- Analysis of Usefulness of Biochemical Enzyme Assay and MR Spectroscopy(MRS) in Leigh Syndrome
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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... -
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