- A case of neuronal carotid-lipofuscinosis with characteristic photic evoke spikes in EEG
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Han JH, Oh JW, Shin JH, Seol IJ, Koh YH, Park MH
- KMID: 1691352
- J Korean Pediatr Soc.
- 1992 Feb;35(2):252-256.
No abstract available. -
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- A Case of Late Infantile Neuronal Ceroid Lipofuscinosis that was Diagnosed by Characteristic EEG Findings
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Kim JR, Bang HI, Lee CW
- KMID: 2333382
- J Korean Epilepsy Soc.
- 2002 Jun;6(1):53-56.
Neuronal ceroid lipofuscinoses (NCL) are the most common childhood neurodegenerative disorders. Clinical features include seizures, blindness, psychomotor deterioration, the age of onset differ for each NCL type. Diagnosis of late... -
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- CLN6 Mutation in a Patient with Progressive Myoclonus Epilepsy
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Lee HG, Yoon BA, Kim YO, Kim MK, Woo YJ
- KMID: 2435249
- J Korean Child Neurol Soc.
- 2018 Jun;26(2):123-127.
- doi: 10.26815/jkcns.2018.26.2.123
Neuronal ceroid lipofuscinoses (NCLs) are inherited neurodegenerative disorders, which are caused by the accumulation of lipopigment in lysosomes. Variant forms of late infantile NCLs (vLINCLs) characterized by a later onset... -
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- A Case of Early Juvenile Neuronal Ceroid Lipofuscinosis
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Kim OJ, Jun SI, Huh K
- KMID: 2066026
- J Korean Neurol Assoc.
- 1995 Dec;13(4):1011-1016.
The neuronal ceroid-lipofuscinosis (NCL) is a group of progressive,. Inherited neurodegenerative diseases characterized by the deposition of large numbers o autofluorescent cytosomes in most tissues. Based on the age at... -
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- A Case of Adult Neuronal Ceroid-Lipofuscinosis, Proven by Brain Biopsy
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Lee SK, Kang JK, Lee SA, Lee JK, Kang SK
- KMID: 1812915
- J Korean Neurol Assoc.
- 2001 Jan;19(1):45-48.
A 20-year-old woman was admitted because of intractable seizures, myoclonus, gait ataxia, and severe intellectual deterioration with age of onset at 16 years. She had no family history of neurological... -
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