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Functional Neuroimaging in Pediatric Epilepsy

No authors listed

  • KMID: 2329225
  • J Korean Child Neurol Soc.
  • 1997 Oct;5(1):184-185.
No abstract available.
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MRI in Pediatric Epilepsy

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  • KMID: 2329224
  • J Korean Child Neurol Soc.
  • 1997 Oct;5(1):181-183.
No abstract available.
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Epilepsy in Children and Vigabatrin: Experiences in the USA

Shields WD

  • KMID: 2329223
  • J Korean Child Neurol Soc.
  • 1997 Oct;5(1):180-180.
Many children with epilepsy remain medically intractable inspire of the best available therapies. One of the most difficult seizure types to treat is infantile spasms. Many children will respond to...
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Neonatal Seizures: An Epileptological Point of View

Watanabe K

  • KMID: 2329222
  • J Korean Child Neurol Soc.
  • 1997 Oct;5(1):177-179.
Neonatal seizures are only a manifestation of a variety of organic, metabolic or functional disorders of the neonatal brain. Most are caused by acute brain insults such as perinatal hypoxic-ischemic...
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A Case of Acute Transverse Myelitis Complicating Diffuse Spinal Cord Atrophy and Syrinx Formation

Cho NC, Jung JA, Hwang KG, Choi SS

  • KMID: 2329221
  • J Korean Child Neurol Soc.
  • 1997 Oct;5(1):167-171.
A 4-year-old girl developed acute motor, sensory impairment, lower abdominal pain and urinary dysfunction after URI. In acute stage of disease, MRI showed diffuse spinal cord swelling and high signal...
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A Case of Canavan Disease

Yoon SY, Kim JH, Ko TS, Choi CK, Kong KY

  • KMID: 2329220
  • J Korean Child Neurol Soc.
  • 1997 Oct;5(1):159-166.
Canavan disease(CD) is a rare autosomal recessive leukodystrophy caused by the deficiency of aspartoacylase and the accumulation in brain of N-acetylaspartate(NAA). CD has been reported mainly Ashkenazi Jews but also...
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A Case of Joubert Syndrome

Kim HS, Kim HD, Chung CY, Cho WH

  • KMID: 2329219
  • J Korean Child Neurol Soc.
  • 1997 Oct;5(1):153-158.
Joubert syndrome is a rare hereditary brain malformation and transmitted as an autosomal recessive tarit. This disorder is clinically characterized by episodic tachypnea and apnea, abnormal ocular movements, developmental delay...
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A Familial Case of Leigh Disease

Kim JH, Kim IJ, Kim IS, Yoon WS, Kim EY, Kim SH, Woo YJ

  • KMID: 2329218
  • J Korean Child Neurol Soc.
  • 1997 Oct;5(1):147-152.
In two female siblings, growth and developmental retardation, poor sucking, anorexia, floppiness and respiratory difficulty developed around 2 and 4 monthes of age in each, and the respiratory symptoms rapidly...
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A Two Cases of MELAS in Siblings

Yeon YY, Choi BJ, Kim YH, Kim JW, Park SS, Ji JG, Whang KT

  • KMID: 2329217
  • J Korean Child Neurol Soc.
  • 1997 Oct;5(1):138-146.
MELAS is the condition associated with mutant mtDNA that most closely mimics thrombotic cerebrovascular disease. It is characterized by mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes. These children develop short...
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A Case of Severe Myoclonic Epilepsy in Infancy

Koh YJ, Seol IJ

  • KMID: 2329216
  • J Korean Child Neurol Soc.
  • 1997 Oct;5(1):133-137.
Severe myoclonic epilepsy of infancy(SMEI) is a condition beginning with recurrent, prolonged febrile convulsion in normal children, followed within months to 4 years by generalized tonic clonic seizures, partial seizures,...
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No title in English

No authors listed

  • KMID: 2329215
  • J Korean Child Neurol Soc.
  • 1997 Oct;5(1):126-132.
No abstract available.
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Moyamoya Disease in Childen

Chin HJ, Lee JS, Coe CJ

  • KMID: 2329214
  • J Korean Child Neurol Soc.
  • 1997 Oct;5(1):119-125.
PURPOSE: Moyamoya disease is a primary vascular disease characterized by stenosis that is followed by occlusion of the intracranial portion of the internal carotid artery and other vessels of the...
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Accuracy of Denver II in Developmental Delay Screening

Jeon MC, Kim YH, Chung SY, Lee IG, Kim JW, Whang KT

  • KMID: 2329213
  • J Korean Child Neurol Soc.
  • 1997 Oct;5(1):111-118.
PURPOSE : Developmental screening tests are in widespread use, but few reliable and valid tests are available. One of the oldest and best known developmental screening test was recently restandardized...
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No title in English

No authors listed

  • KMID: 2329212
  • J Korean Child Neurol Soc.
  • 1997 Oct;5(1):106-110.
No abstract available.
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A Clinical Study of Recurrent Headaches in Children and An Application of International Headache Society Classification to Children

Park SS, Bae KY, Kim TH, Kim EJ, Hwang KG

  • KMID: 2329211
  • J Korean Child Neurol Soc.
  • 1997 Oct;5(1):95-105.
PURPOSE: Headache is a frequent symptom in pediatric practice, but the prevalence of chronic recurrent headache was estimated in several studies with wide variations, because of inadequate expression and differences...
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Benefits of High Dose Intravenous Gammaglobulin in Children with Severe Guillain-Barr Syndrome

Kim GM, Woo YJ

  • KMID: 2329210
  • J Korean Child Neurol Soc.
  • 1997 Oct;5(1):86-94.
To know the efficacy of intravenous gammaglobulin(IVGG) treatment and the resulting outcome at 18 months for acute Guillain-Barr syndrome (GBS) in children, clinical courses of 27 GBS patients who had...
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Electroencephalographic Findings in Moyamoya Disease

Kim JH, Ko TS

  • KMID: 2329209
  • J Korean Child Neurol Soc.
  • 1997 Oct;5(1):76-85.
BACKGROUND: "Rebuild-up" phenomenon, induced by hyperventilation, is a characteristic finding on EEG in children with Moyamoya disease. Its mechanism, however, remains obscure. In this study, we examined the relationship between...
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Hypothalamic Hamartoma : Clinical and MRI Features and Outcome

Han SK, Chae JH, Kim KJ, Hwang YS, Han TI, Kim IO

  • KMID: 2329208
  • J Korean Child Neurol Soc.
  • 1997 Oct;5(1):69-75.
PURPOSE: Hypothalamic hamartomas are non-neoplastic malformations which are composed of hyperplastic neuronal tissue of varying size. Clinically, they are characterized by gelastic seizure, precocious puberty, and behavioral and psychiatric disorders....
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No title in English

No authors listed

  • KMID: 2329207
  • J Korean Child Neurol Soc.
  • 1997 Oct;5(1):59-68.
No abstract available.
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Bone Mineral Density in Epileptic Children Who Received Long-term Anticonvulsant Drugs

Kim TJ, Suh ES

  • KMID: 2329206
  • J Korean Child Neurol Soc.
  • 1997 Oct;5(1):52-58.
OBJECTIVE : Bone mineral density is influenced by genetic, hormonal and exogenous factor that adversely affect peak mineral density include cigarette smoking, physical disability, poor calcium intake and certain medication...
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