- A case of Creutzfeldt-Jakob disease
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Cha JK, Kim MH, Oh SJ, Hong EK
- KMID: 1421866
- J Korean Med Sci.
- 1991 Sep;6(3):273-278.
- doi: 10.3346/jkms.1991.6.3.273
Creutzfeldt-Jakob disease (CJD) is presumably caused by a slow infectious pathogen or prion. The principal clinical features of Creutzfeldt-Jakob disease are dementia, pyramidal and extrapyramidal symptoms and signs, cerebellar dysfunction,... -
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- New Variant Creutzfeldt-Jakob Disease
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Jeon BS
- KMID: 2348129
- J Korean Med Assoc.
- 2001 May;44(5):483-493.
- doi: 10.5124/jkma.2001.44.5.483
No abstract available. -
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- Creutzfeldt-Jakob Disease Mimicking a Stroke as Initial Manifestation
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Cho GN, Jeong HY, Noh SW, Lee SY, Kim YJ, Kim SJ
- KMID: 2191546
- J Korean Neurol Assoc.
- 2012 Nov;30(4):374-376.
No abstract available. -
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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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- Familial Creutzfeldt-Jakob Disease with M232R Mutation Progressed Slowly like Alzheimer's Disease
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Lee S, Bae HW, Yang Y
- KMID: 2442823
- Dement Neurocogn Disord.
- 2017 Sep;16(3):91-93.
- doi: 10.12779/dnd.2017.16.3.91
No abstract available. -
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- Familial Creutzfeldt-Jakob Disease with V180I Mutation Presented with Broca's Aphasia
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Kim J, Lee DS, Park KW
- KMID: 2435849
- J Korean Neurol Assoc.
- 2018 Nov;36(4):345-349.
- doi: 10.17340/jkna.2018.4.15
Familial Creutzfeldt-Jakob Disease (fCJD) is characteristic with older age onset, relatively low occurrence rate, slower progression and lower possibility of developing myoclonus, cerebellar, pyramidal signs and visual disturbance compared with... -
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- Anesthetic management in patients suspected of Creutzfeldt-Jakob disease -A case report-
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In CB, Choi YS, Park EY, Chang DJ, Lee SK, Choi H, Moon HS
- KMID: 2031318
- Korean J Anesthesiol.
- 2011 Sep;61(3):262-264.
- doi: 10.4097/kjae.2011.61.3.262
Creutzfeldt-Jakob disease (CJD) is a fatal neurodegenerative disorder in which accumulation of the pathogenic prion protein induces neuronal damage and results in distinct pathologic features. This abnormal prion is an... -
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- Neurosyphilis Mimicking Limbic Encephalitis and Creutzfeldt-Jakob Disease
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Lee DH, Lee SJ, Jeong DE
- KMID: 2464161
- J Korean Neurol Assoc.
- 2019 Nov;37(4):442-443.
- doi: 10.17340/jkna.2019.4.26
No abstract available. -
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- A Case of Creutzfeldt-Jakob Disease Presented as Rapid Progressive Parkinsonism
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Park Y, Lee CN
- KMID: 2466759
- Dement Neurocogn Disord.
- 2019 Dec;18(4):152-156.
- doi: 10.12779/dnd.2019.18.4.152
No abstract available. -
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- Probable Creutzfeldt-Jakob Disease Presenting as Progressive Supranuclear Palsy
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Kang SH, Kim M, Lee HM, Kwon KY, Lee SM, Koh SB
- KMID: 2343551
- J Korean Neurol Assoc.
- 2014 Nov;32(4):272-274.
- doi: 10.0000/jkna.2014.32.4.272
Progressive supranuclear palsy (PSP) is a clinical syndrome comprising vertical supranuclear palsy, parkinsonism, postural instability, and mild dementia. Other disorders can present with similar clinical pictures. In this report we... -
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- A Case of Creutzfeldt-Jakob Disease Presenting Mainly with Abnormal Eye Movements
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Kang YJ, Kim JH, Kim TE, Park SA, Lee TK
- KMID: 1910485
- Res Vestib Sci.
- 2014 Jun;13(2):53-56.
Creutzfeldt-Jakob disease (CJD) is a human prion disease with rapidly progressive neurodegeneration. The major clinical manifestations of CJD include mental deterioration, myoclonus, cerebellar dysfunction, and neuro-ophthalmic symptoms and signs. However,... -
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- White Matter Lesions in a Patient With Creutzfeldt-Jakob Disease
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Lee HS, Park HY, Chang H
- KMID: 2188244
- J Korean Geriatr Soc.
- 2013 Dec;17(4):259-262.
- doi: 10.4235/jkgs.2013.17.4.259
This is a report of a patient with Creutzfeldt-Jakob disease. The 67-year-old male first developed partial and secondary generalized tonic-clonic seizures. He was disoriented and could not perform calculations nor... -
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- Mad Cow Disease and New Variant Creutzfeldt Jacob Disease
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Kim YS
- KMID: 2253762
- J Korean Acad Fam Med.
- 2004 Jul;25(7):509-518.
No abstract available. -
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- A Case of Acute Onset Progressive Dementia Suggestive of a Creutzfeldt-Jakob disease
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Lee DK, Do JK
- KMID: 2342546
- J Korean Neurol Assoc.
- 1996 Jun;14(2):662-668.
Creutzfeldt-Jakob disease (CJD) is a rare dementing illness that usually affects older adults and is characterized by a rapidly progressive dementia, ataxia, and myoclonus. The disease is due to an... -
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- Thrombolytic Therapy of Pulmonary Thromboembolism in Probable Sporadic Creutzfeldt-Jakob Disease
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Chang JY, Jung JH, Chang YH, Kim SY
- KMID: 2191926
- J Korean Neurol Assoc.
- 2009 Nov;27(4):405-408.
The effect of intravenous recombinant tissue plasminogen activator for patients with Creutzfeldt-Jakob disease (CJD) has yet to be determined. A woman with rapidly progressive cognitive decline, cerebellar dysfunction, and extrapyramidal... -
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- Molecular analysis of prion protein gene (PRNP) in Korean patients with Creutzfeldt-Jakob disease
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Jeong BH, Ju WK, Huh K, Lee EA, Choi IS, Im JH, Choi EK, Kim YS
- KMID: 1745544
- J Korean Med Sci.
- 1998 Jun;13(3):234-240.
- doi: 10.3346/jkms.1998.13.3.234
Creutzfeldt-Jakob disease (CJD), a relatively uncommon human dementia, is caused by an unconventional slow infectious agent. Several cases of CJD, clinically or histopathologically diagnosed, have been reported in Korea.... -
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- Chorea in Sporadic Creutzfeldt-Jakob Disease
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Tan AH, Toh TH, Low SC, Fong SL, Chong KK, Lee KW, Goh KJ, Lim SY
- KMID: 2438833
- J Mov Disord.
- 2018 Sep;11(3):149-151.
- doi: 10.14802/jmd.18017
No abstract available. -
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- Rapidly Aggravated Creutzfeldt-Jacob Disease: Autopsy-Proven Case
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Park SH, Kang HK, Yu H, Lee SC
- KMID: 1582622
- J Korean Radiol Soc.
- 2005 Nov;53(5):331-335.
- doi: 10.3348/jkrs.2005.53.5.331
Creutzfeldt-Jakob disease (CJD) is one of the transmissible spongiform encephalopathies, which is mediated by what has been known as "prion". It is a rare and fatal progressive neurodegenerative disease that... -
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- Four Cases of Probable Creutzfeldt-Jacob Disease with High Signals in Cerebral Cortex on Diffusion Weighted MR Imaging
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Kwak YT, Bang OY, Kim OJ, Kim WJ
- KMID: 1636119
- J Korean Neurol Assoc.
- 2006 Dec;24(6):596-600.
A high signal in the cerebral cortex and/or basal ganglia on a diffusion-weighted MRI (DWI) has been described as a good diagnostic marker for sporadic Creutzfeldt-Jakob disease (sCJD). We report... -
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- Diffusion-Weighted MR Imaging in Biopsy-Proven Creutzfeldt-Jakob Disease
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Kim HC, Chang KH, Song IC, Lee SH, Kwon BJ, Han MH, Kim SY
- KMID: 754087
- Korean J Radiol.
- 2001 Dec;2(4):192-196.
- doi: 10.3348/kjr.2001.2.4.192
OBJECTIVE: To compare conventional and diffusion-weighted MR imaging in terms of their depiction of the abnormalities occurring in Creutzfeldt-Jakob disease. MATERIALS AND METHODS: We retrospectively analyzed the findings of conventional... -
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