- Two Cases of Primary Sjogren's Syndrome Presenting as Relapsing-Remitting Multiple Sclerosis
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Cho JH, Kim SM, Kim JH, Chu CK, Lee MH, Shin HW, Doh WY, Sunwoo IN
- KMID: 2343096
- J Korean Neurol Assoc.
- 2004 Aug;22(4):410-413.
Sjogren's syndrome is a slowly progressive autoimmune disorder that predominantly affects major exocrine glands, and may also involve the central nervous system (CNS). It is sometimes very difficult to differentiate... -
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- Two Cases of Discontinuation Syndrome Following Cessation of Cholinesterase Inhibitors
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Kwak YT
- KMID: 2343089
- J Korean Neurol Assoc.
- 2004 Aug;22(4):386-388.
Discontinuation syndrome is a cluster of symptoms that appear when a patient terminates long-term medication. We report 2 patients with Alzheimer's disease who developed significant behavioral disturbances after the cessation... -
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- Genetic Basis of Parkinson Disease
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Jung KH, Jeon BS
- KMID: 2343073
- J Korean Neurol Assoc.
- 2004 Aug;22(4):281-289.
Parkinson disease (PD) is a neurodegenerative disease characterized by the selective loss of dopaminergic neurons from the substantia nigra pars compacta leading to the impairment of motor functions. Recent genetic... -
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- A Case of Cryptococcal Meningitis Presenting as Multiple Cerebral Infarctions
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Hong JM, Kim HS, Kim WJ, Lee KY
- KMID: 2343088
- J Korean Neurol Assoc.
- 2004 Aug;22(4):382-385.
Cryptococcal meningitis is one of the common fungal infections of the central nervous system, usually developed in immunocompromised patients. Cerebral infarction has been reported as one of the late complications... -
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- A Case of Successful Treatment During Migraine Aura Using Isometheptene Compound
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Park TH, Kwon OS
- KMID: 2343093
- J Korean Neurol Assoc.
- 2004 Aug;22(4):399-401.
Taking medication early on for aborting migraines has proved to be more effective, but trials using triptans during the aura phase have not shown significant effectiveness. Isometheptene compounds are popularly... -
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- Forntal Lobe Epilepsy Presenting with Blinking and Leg Jerking
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Song YM, Lee SK, Roh JK
- KMID: 2343090
- J Korean Neurol Assoc.
- 2004 Aug;22(4):389-391.
Eye blinking is a rare semiology in frontal lobe epilepsy. However, eye blinking with leg jerking as a manifestation of simple partial seizure has not been reported. We report a... -
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- Convergence-related Nystagmus in a Patient with Hydrocephalus from Shunt Malfunction
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Kim JS, Han DH, Moon SY, Park SH
- KMID: 2343091
- J Korean Neurol Assoc.
- 2004 Aug;22(4):392-395.
We report a 30-year-old woman with neurocysticercosis, who showed convergence and convergence-retraction nystagmus, V-bobbing, and typical findings of pretectal syndrome due to shunt malfunction. The symptoms and signs improved with... -
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- Tumarkin's Otolithic Crisis
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Kim JS, Moon SY, Jung SM, Park SH, Koo JW
- KMID: 2343092
- J Korean Neurol Assoc.
- 2004 Aug;22(4):396-398.
Tumarkin's otolithic crisis refers to drop attacks of vestibular origins. It usually occurs without warning in patients with late or end-stage endolymphatic hydrops. However, drop attacks of vestibular origins may... -
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- Clinical Feature and Outcome in Spontaneous Cerebellar Hemorrhage: Determination of Treatment Strategies
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Lee SM, Jung B, Lee KY, Lee YJ, Cheong JH, Kim JM
- KMID: 2343074
- J Korean Neurol Assoc.
- 2004 Aug;22(4):290-294.
BACKGROUND: Cerebellar hemorrhage may present with a wide spectrum of clinical manifestations, from a benign course with little to no neurological deficit to a rapidly fatal course with hydrocephalus and... -
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- Ondine's Curse Consequent to Recurrent Respiratory Failure in a Man with Leber Hereditary Optic Neuropathy
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Ha S, An SG, Lee SA
- KMID: 2343097
- J Korean Neurol Assoc.
- 2004 Aug;22(4):414-417.
Leber's hereditary optic neuropathy (LHON) is a disease due to mitochondrial DNA mutations. We report a man with LHON, who presented with four episodes of respiratory failure. In the last... -
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- A Case of Probable Creutzfeldt-Jakob Disease with Coexistence of the Features of Hashimoto Encephalopathy
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Cho YJ, Park CH, Paik JW, Shin HW, Park CW, Park S, Kim HO, Kim YS
- KMID: 2343095
- J Korean Neurol Assoc.
- 2004 Aug;22(4):406-409.
Hashimoto encephalopathy shares common clinical features with Creutzfeldt-Jakob disease and must be regarded as a differential diagnosis because of its good prognosis. We report a case of Hashimoto encephalopathy, which... -
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- A Case of Bilateral Sciatic Neuropathy Caused by Lotus Position
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Kim D, Kwon OY, Kim Y, Hye KS, Son S, Park KJ, Choi NC, Lim BH
- KMID: 2343098
- J Korean Neurol Assoc.
- 2004 Aug;22(4):418-420.
The prolonged pressure against the buttock or posterior thigh may cause the stretch or direct compression of the sciatic nerve. A sixty-year old man fell asleep, heavily inebriated in the... -
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- Complicated Spastic Paraparesis with Thin Corpus Callosum
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Lee JH, Park YE, Choi KD, Park KP, Kim DS, Jung DS, Park KH
- KMID: 2343094
- J Korean Neurol Assoc.
- 2004 Aug;22(4):402-405.
Autosomal recessive hereditary spastic paraparesis (AR-HSP) associated with a thin corpus callosum (TCC) has recently been described in Japan. It is characterized by slowly progressive spastic paraparesis, mental retardation, and... -
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- Efficacy of Buspirone Hydrochloride in Migraineurs with Anxiety: a Randomized Double Blind, Parallel Group, Placebo-controlled Study
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Lee ST, Kim M
- KMID: 2343080
- J Korean Neurol Assoc.
- 2004 Aug;22(4):328-333.
BACKGROUND: Migraine is commonly associated with anxiety disorder. However, whether anxiolytic medicine or changes in anxiety levels affect the migraine attack is unclear. Buspirone, the agonist for 5-HT1A receptor, is... -
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- The Bcl-2 and NeuN Expressions and Morphological Changes in Organotypic Explant Culture of Rat Hippocampus
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Youn YC, Kwon OS, Chae SA
- KMID: 2343086
- J Korean Neurol Assoc.
- 2004 Aug;22(4):368-374.
BACKGROUND: Bcl-2 protein is essential for neurodevelopment and it is implicated in various neurodegenerative diseases. However, little is known about the normal developmental expression of Bcl-2 and NeuN protein in... -
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- The Clinical Properties of Deep Small Basal Ganglia Infarctions: Lacune or Small Striatocapsular Infarction?
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Jung S, Kwon SB, Hwang SH
- KMID: 2343075
- J Korean Neurol Assoc.
- 2004 Aug;22(4):295-301.
BACKGROUND: Small subcortical infarctions of basal ganglia can be divided into either lacunes or striatocapsular infarctions by size of lesion. However, there are some controversies concerning the size criteria of... -
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- Development of `Korean Version of Caregiver Activity Survey (CAS-K)' in Caregivers of Community Dwelling Elderly with Dementia
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Kim JM, Shin IS, Kim SW, Yang SJ, Jeong SK, Yoon JS
- KMID: 2343079
- J Korean Neurol Assoc.
- 2004 Aug;22(4):322-327.
BACKGROUND: The Caregiver Activity Survey (CAS) has been designed to collect information about the time caregivers spend providing care during a typical 24-hour period. This study aimed to develop the... -
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- Effect of Antiepileptic Drugs on Bone Mineral Density and Bone Metabolism in Epileptic Patients
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Park SW, Cho YW, Her JH, Shin YE, Yi HA, Lee J, Lee H, Lim JG, Yi SD
- KMID: 2343077
- J Korean Neurol Assoc.
- 2004 Aug;22(4):310-314.
BACKGROUND: Bone mineral density (BMD) is influenced by genetic, hormonal, and environmental factors. Long-term antiepileptic drug (AED) use also causes osteopenia or osteoporosis that have been most extensively described in... -
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- Abnormal Cerebral Glucose Metabolism in Patients with Narcolepsy
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Joo EY, Tae WS, Kim JH, Han SJ, Cho YW, Kim L, Yun CH, Kim MH, Kim BT, Hong SB
- KMID: 2343082
- J Korean Neurol Assoc.
- 2004 Aug;22(4):340-344.
BACKGROUND: The purpose of this study was to investigate the differences of cerebral glucose metabolism between narcoleptic patients and normal controls. METHODS: We enrolled 24 patients with narcolepsy who underwent... -
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- Comparison of Nerve Conduction Studies between the Patients with Hereditary Neuropathy with Liability to Pressure Palsies and Charcot-Marie-Tooth1A
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Lee JY, Sunwoo IN, Choi BO, Cho JH, Kim JH, Jung YK, Kim SW, Kim SM
- KMID: 2343083
- J Korean Neurol Assoc.
- 2004 Aug;22(4):345-351.
BACKGROUND: Hereditary neuropathy with liability to pressure palsy (HNPP) and Charcot-Marie-Tooth1A (CMT1A) are autosomal dominant inherited demyelinating neuropathy associated with the deletion or duplication of 17p11.2-p12 segments including the gene... -
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