関: CJD、Creutzfeldt-Jakob disease、Creutzfeldt-Jakob syndrome、familial Creutzfeldt-Jakob disease、new variant Creutzfeldt-Jakob disease

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less than acute; relating to a disease present in a person with no symptoms of it

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1. 小児における急性中毒性代謝性脳症 acute toxic metabolic encephalopathy in children
2. 成人における急性中毒性代謝性脳症 acute toxic metabolic encephalopathy in adults
3. 新生児脳症の病因および発症機序 etiology and pathogenesis of neonatal encephalopathy
4. 新生児脳症の臨床的特徴、診断、および治療 clinical features diagnosis and treatment of neonatal encephalopathy
5. 変異型クロイツフェルト・ヤコブ病 variant creutzfeldt jakob disease

Superficial bedside brain biopsy can be a safe and practical approach to confirm a rare form of prion disease in cerebellar ataxia: A case study.

Rusina R1, Netuka D2, Johanidesová S3, Smětáková M4, Mouchová Z5, Matěj R5.
Journal of the neurological sciences.J Neurol Sci.2017 Apr 15;375:73-75. doi: 10.1016/j.jns.2017.01.047. Epub 2017 Jan 16.
PMID 28320192

Reply to: The Letter to be published with the Letter, Amyotrophic lateral sclerosis with frontotemporal dementia (ALS-FTD) syndrome as a phenotype of Creutzfeldt-Jakob disease (CJD)? A case report.

Yaguchi H1, Takeuchi A2, Horiuchi K2, Takahashi I2, Shirai S2, Akimoto S2, Satoh K3, Moriwaka F4, Yabe I2, Sasaki H2.
Journal of the neurological sciences.J Neurol Sci.2017 Apr 15;375:490-491. doi: 10.1016/j.jns.2017.02.056. Epub 2017 Feb 27.
PMID 28259353

Reply to: Amyotrophic lateral sclerosis with frontotemporal dementia (ALS-FTD) syndrome as a phenotype of Creutzfeldt-Jakob disease (CJD)? A case report.

Hayashi Y1, Inuzuka T2.
Journal of the neurological sciences.J Neurol Sci.2017 Apr 15;375:489. doi: 10.1016/j.jns.2017.02.055. Epub 2017 Feb 24.
PMID 28258726

リンク元	「亜急性海綿状脳症」「new variant Creutzfeldt-Jakob disease」「familial Creutzfeldt-Jakob disease」
関連記事	「spongiform」