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Severe Epileptic Encephalopathies in Infant and Children

Hwang KG

  • KMID: 2137180
  • J Korean Child Neurol Soc.
  • 2001 May;9(1):201-209.
No abstract available.
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Overview of Epileptogenisis

Moon HK

  • KMID: 2137179
  • J Korean Child Neurol Soc.
  • 2001 May;9(1):192-200.
No abstract available.
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Benign Childhood Epilepsy: Do We Know All about It?

Ko TS

  • KMID: 2137181
  • J Korean Child Neurol Soc.
  • 2001 May;9(1):210-216.
No abstract available.
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Mitochondrial Disorders

Chae JH

  • KMID: 2137157
  • J Korean Child Neurol Soc.
  • 2001 May;9(1):13-24.
No abstract available.
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Electro Pysiological in Approach in Human Hippocampus

Choi BJ

  • KMID: 2137156
  • J Korean Child Neurol Soc.
  • 2001 May;9(1):1-12.
No abstract available.
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Classification of Epileptic Seizures and Syndromes: Historical Review and Changes in Terms and Concepts

Chung SJ

  • KMID: 2137178
  • J Korean Child Neurol Soc.
  • 2001 May;9(1):178-191.
No abstract available.
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Recent Advances in Epilepsy Research in the Developing Brain

Swann JW

  • KMID: 2137182
  • J Korean Child Neurol Soc.
  • 2001 May;9(1):217-227.
No abstract available.
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Treatment Principles of Atiepileptic Drug Therapy and Rational Polypharmacy Including new antiepileptic Drugs

Kim YC

  • KMID: 2137183
  • J Korean Child Neurol Soc.
  • 2001 May;9(1):228-238.
No abstract available.
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The Case of Tuberous Sclerosis Occured in Mother and Two Daughters

Ko MJ, Ji GH, Ha CW, Hwang TG

  • KMID: 2137173
  • J Korean Child Neurol Soc.
  • 2001 May;9(1):146-151.
Tuberous sclerosis is an autosomal dominant disorder of cellular differentiation that affect the brain, skin, heart, kidney and other organs. We experienced three cases of tuberous sclerosis that affect multiple...
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A Case of Neurocutaneous Giant Melanosis Associated with Dandy-Walker Syndrome

Hong SY, Ban JE, Rhu JH, Choi SS, Hwang KG

  • KMID: 2137177
  • J Korean Child Neurol Soc.
  • 2001 May;9(1):171-177.
Neurocutaneous melanosis is a rare congenital phacomatosis, characterized by the presence of multiple pigmented skin nevi at birth. Meningeal melanosis tending to become malignant and seizure. Dandy-Walker syndrome is a...
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A Case of Acute Necrotizing Encephalopathy

Kim JH, Yun HJ, Kim DS, Ko TS, Choi CG

  • KMID: 2137171
  • J Korean Child Neurol Soc.
  • 2001 May;9(1):134-139.
Acute necrotizing encephalopathy is a recently established disease entity, proposed by Mizuguchi et al in 1995, that shows a characteristic symmetric and multifocal involvement of both thalamus, brainstem tegmentum, cerebral...
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A Case of Suspected Autosomal Dominant Nocturnal Frontal Lobe Epilepsy

Kim SY, Park JC, Kim HD, Chung HJ

  • KMID: 2137170
  • J Korean Child Neurol Soc.
  • 2001 May;9(1):129-133.
Autosomal dominant nocturnal frontal lobe epilepsy(ADNFLE) is a recently identified partial epilepsy. This disorder is characterized by a variable age of onset(mostly in childhood), autosomal dominant inheritance, clusters of brief...
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The Effect of Valproic Acid on Ovary of Pubertal Child

Moon EK, Lim HK, Yoo JH, Lee KS

  • KMID: 2137165
  • J Korean Child Neurol Soc.
  • 2001 May;9(1):86-94.
PURPOSE: Valproic acid is effective and safe in adults and children for the treatment of a variety of seizure types. But, according to the recent reports, this drug induce hyperandrogenism,...
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Growth Pattern of Children on Medication with Anticonvulsants

Park SS, Lee JI, Bae SN, Nam SO, Park HJ

  • KMID: 2137166
  • J Korean Child Neurol Soc.
  • 2001 May;9(1):95-102.
PURPOSE: This study was performed to investigate the growth pattern of epileptic children on medication with anticonvulsants. METHODS: We measured the weight, height and head circumference of 219 epileptic children on...
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Visual Field Defect in the Vigabatrin-treated Pediatric Patients

Kim JS, Lee SL

  • KMID: 2137164
  • J Korean Child Neurol Soc.
  • 2001 May;9(1):80-85.
PURPOSE: Vigabatrin has proved to be a successful and well tolerated drug used for the treatment of epilepsy of partial onset and for infantile spasms(West's syndrome). It is a selective...
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A Case of Alternating Hemiplegia of Childhood

Bae SN, Jeong PJ, Nam SO

  • KMID: 2137172
  • J Korean Child Neurol Soc.
  • 2001 May;9(1):140-145.
Alternating hemiplegia of childhood(AHC) is a rare but clinically distinct syndrome characterized by onset before 18 months of age, frequent attacks of alternating paralysis, nystagmus transient ocular palsies, other autonomic...
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Ectrodactyly-Ectodermal Dysplasia-Clefting(EEC) Syndrome with Ocular Defects and Nevus Lipomatosus Cutaneous Superficialis

Lee SM, Chae KY

  • KMID: 2137175
  • J Korean Child Neurol Soc.
  • 2001 May;9(1):159-163.
The ectrodactyly-ectodermal dysplasia-clefting(EEC) syndrome is a rare autosomal dominant disease which has multiple congenital anomalies characterized by ectodermal dysplasia, distal limb anomaly, cleft lip and palate, and lacrimal duct anomalies....
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Comparative Analysis of Magnetic Resonance Angiography and 4-Vessel Angiography in the Diagnosis of Pediatric Moyamoya Disease

Lee KW, Kim SH

  • KMID: 2137168
  • J Korean Child Neurol Soc.
  • 2001 May;9(1):111-121.
PURPOSE: Conventional 4-vessel cerebral angiography has been considered as a gold standard for the diagnosis of Moyamoya disease. However, it is an invasive procedure requiring general anesthesia and various neurologic...
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Cutis Verticis Gyrata-Mental Deficiency Syndrome : A Patient with Generalized Epidermal Nevus

Chae KY, Nam YH, Song KY

  • KMID: 2137174
  • J Korean Child Neurol Soc.
  • 2001 May;9(1):152-158.
We report a case of cutis verticis gyrata-mental deficiency syndrome associated with generalized epidermal nevus. The clinical features of the patient included severe mental retardation, drug resistant epilepsy, short stature,...
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Correlation between the Handedness and Clinical Findings in Children with Epilepsy

Kim PJ, Nam SO, Park HJ

  • KMID: 2137167
  • J Korean Child Neurol Soc.
  • 2001 May;9(1):103-110.
PURPOSE: Some reports left handedness is more common in epileptic patients compared with normal populations, but the study on this topics are rare. This can be due to epilepsy itself...
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