- 関
- CJD、Creutzfeldt-Jakob disease、Creutzfeldt-Jakob syndrome、new variant Creutzfeldt-Jakob disease、subacute spongiform encephalopathy
WordNet
- an impairment of health or a condition of abnormal functioning
- relating to or having the characteristics of a family; "children of the same familial background"; "familial aggregation"
- occurring among members of a family usually by heredity; "an inherited disease"; "familial traits"; "genetically transmitted features" (同)genetic, hereditary, inherited, transmitted, transmissible
- caused by or altered by or manifesting disease or pathology; "diseased tonsils"; "a morbid growth"; "pathologic tissue"; "pathological bodily processes" (同)morbid, pathologic, pathological
PrepTutorEJDIC
- (体の)『病気』,疾患 / (精神・道徳などの)病気,病弊
- 女性の話術芸人 =diseur
- 家族の,家族特有の / 違伝的な,血統にあらわれる
- 病気にかかった / 病的な,不健全な(morbid)
UpToDate Contents
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- 1. クロイツフェルト・ヤコブ病 creutzfeldt jakob disease
- 2. プリオンの生物学および遺伝学 biology and genetics of prions
- 3. プリオンによる中枢神経系疾患 diseases of the central nervous system caused by prions
- 4. 供血者の病歴 blood donor medical history
English Journal
- Creutzfeldt-Jakob disease and blood transfusion: updated results of the UK Transfusion Medicine Epidemiology Review Study.
- Urwin PJ1, Mackenzie JM1, Llewelyn CA2, Will RG1, Hewitt PE3.
- Vox sanguinis.Vox Sang.2015 Dec 28. doi: 10.1111/vox.12371. [Epub ahead of print]
- BACKGROUND AND OBJECTIVES: This paper reports the results to 31 May 2015 of an ongoing UK study to look for additional cases of variant Creutzfeldt-Jakob disease (vCJD) transmission by blood transfusion, and to seek evidence whether other subtypes of Creutzfeldt-Jakob disease (CJD) may be transmissi
- PMID 26709606
- Prion Diseases.
- Geschwind MD.
- Continuum (Minneapolis, Minn.).Continuum (Minneap Minn).2015 Dec;21(6 Neuroinfectious Disease):1612-38. doi: 10.1212/CON.0000000000000251.
- PURPOSE OF REVIEW: This article presents an update on the clinical aspects of human prion disease, including the wide spectrum of their presentations.RECENT FINDINGS: Prion diseases, a group of disorders caused by abnormally shaped proteins called prions, occur in sporadic (Jakob-Creutzfeldt disease
- PMID 26633779
- Early-onset spastic paraparesis as presenting sign of familial Creutzfeldt-Jakob disease.
- Conte F1, Giordano A2, Tortora F3, Caiazzo G4, Ladogana A5, Tedeschi G6, Tessitore A7.
- Parkinsonism & related disorders.Parkinsonism Relat Disord.2015 Dec;21(12):1479-80. doi: 10.1016/j.parkreldis.2015.10.004. Epub 2015 Oct 22.
- PMID 26578040
Japanese Journal
- プリオン病 : 本邦の特徴と診断のポイント
- 三條 伸夫,水澤 英洋
- 臨床神経学 50(5), 287-300, 2010-05-01
- NAID 10026900121
- Familial Creutzfeldt-Jakob disease with a V180I mutation: comparative analysis with pathological findings and diffusion-weighted images.
- Mutsukura Kazuo,Satoh Katsuya,Shirabe Susumu,Tomita Itsuro,Fukutome Takayasu,Morikawa Minoru,Iseki Masachika,Sasaki Kensuke,Shiaga Yusei,Kitamoto Tetsuyuki,Eguchi Katsumi
- Dementia and geriatric cognitive disorders 28(6), 550-557, 2009-12
- … BACKGROUND: Diffusion-weighted imaging (DWI) has been reported to be a useful technique for diagnosing Creutzfeldt-Jakob disease (CJD). … The present study reported DWI results in cases of familial CJD with a V180I mutation (CJD180) in the prion protein gene as well as neurological findings. …
- NAID 120002219591
Related Links
- The spectrum of neuropsychological features of familial Creutzfeldt-Jakob disease (CJD) have seldom been reported, possibly because of (a) the rarity of this he ... On the day of JD's admission, the neurology team requested a ...
- 1. Dement Geriatr Cogn Disord. 2009;28(6):550-7. doi: 10.1159/000254842. Epub 2009 Dec 30. Familial Creutzfeldt-Jakob disease with a V180I mutation: comparative analysis with pathological findings and diffusion ...
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★リンクテーブル★
| リンク元 | 「家族性クロイツフェルト・ヤコブ病」「new variant Creutzfeldt-Jakob disease」「subacute spongiform encephalopathy」 |
| 関連記事 | 「disease」「familial」「Jakob」 |
「家族性クロイツフェルト・ヤコブ病」
- 英
- familial Creutzfeldt-Jakob disease
- 関
- クロイツフェルトヤコブ病、クロイツフェルト・ヤコブ病、新変異型クロイツフェルト・ヤコブ病、クロイツフェルト・ヤコブ症候群、亜急性海綿状脳症
「new variant Creutzfeldt-Jakob disease」
新変異型クロイツフェルト・ヤコブ病、新型クロイツフェルト・ヤコブ病
- 関
- CJD、Creutzfeldt-Jakob disease、Creutzfeldt-Jakob syndrome、familial Creutzfeldt-Jakob disease、subacute spongiform encephalopathy
「subacute spongiform encephalopathy」
- 関
- CJD、Creutzfeldt-Jakob disease、Creutzfeldt-Jakob syndrome、familial Creutzfeldt-Jakob disease、new variant Creutzfeldt-Jakob disease
「disease」
- n.
- 疾患：illnessより厳密な概念。「ある臓器に明確な障害が確認され、それによって症状が出ているとはっきり説明できる場合」 (PSY.9)
- 特定の原因、病態生理、症状、経過、予後、病理組織所見が全てそろった場合 (PSY.9)
- something that is very wrong with people's attitudes, way of life or with society.
- 注意
「familial」
- adj.
- 家族性の、家系性の、家族の