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English Journal
- [The clinical and genetic studies in a family of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].
- Zhang LF, Yang XS, Wang YF, Pei LT.SourceDepartment of Neurology, Central South University, Changsha, People's Republic of China.
- Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.Zhonghua Yi Xue Yi Chuan Xue Za Zhi.2009 Apr;26(2):187-90. doi: 10.3760/cma.j.issn.1003-9406.2009.02.015.
- OBJECTIVE: To investigate the clinical features and genetic diagnostic method of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).METHODS: A systematic study on the clinical manifestations, neuroimaging characteristics, therapeutic measures and mol
- PMID 19350513
- Behavioral alterations and vascular dementia.
- Moretti R, Torre P, Antonello RM, Cazzato G.SourceDipartimento di Fisiologia e Patologia, Ambulatorio Disturbi Cognitivi, Università degli Studi di Trieste, Trieste, Italy. moretti@univ.trieste.it
- The neurologist.Neurologist.2006 Jan;12(1):43-7.
- BACKGROUND: Vascular dementia is one of the most frequent forms of dementia, where behavioral and cognitive symptoms coexist. Negative signs, such as apathy, abulia, opposition, and agnosia, are badly tolerated and dramatically experienced by caregivers, even worse than the other signs of cognitive
- PMID 16547446
- Diffusion magnetic resonance histograms as a surrogate marker and predictor of disease progression in CADASIL: a two-year follow-up study.
- Holtmannspötter M, Peters N, Opherk C, Martin D, Herzog J, Brückmann H, Sämann P, Gschwendtner A, Dichgans M.SourceAbteilung für Neuroradiologie, Klinikum Grosshadern, Ludwig-Maximilians-Universität, Munich, Germany.
- Stroke; a journal of cerebral circulation.Stroke.2005 Dec;36(12):2559-65. Epub 2005 Nov 3.
- BACKGROUND AND PURPOSE: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a cerebral small vessel disease caused by mutations in the NOTCH3 gene. MRI is sensitive in detecting preclinical involvement and changes over time. However, little is know
- PMID 16269644
Japanese Journal
- 石窪 力,古川 泰司,相原 弘之,合原 進二,竹井 真一郎,Shuto Chio,有馬 美和子,多田 正弘
- 自治医科大学医学部紀要 27, 155-160, 2004-12-01
- 多発性脳梗塞の74歳女性にpull法による内視鏡的胃瘻造設術(PEG)を施行した。5ヶ月後、PEGチューブが事故的に抜去され入院となった。チューブ再挿入後造影したところ、横行結腸が造影され皮膚結腸瘻と診断された。保存的治療で瘻孔は自然に閉鎖し、腹膜炎は発症しなかった。経皮的経食道胃管挿入術を施行後退院とした。PEG造設1週間後の造影検査でPEGチューブの先端は横行結腸ガス像の辺縁にあった。PEG造 …
- NAID 110006452444
- Urinary and gait disturbances as markers for early multiinfarct dementia
Related Links
- MID; Dementia - multi-infarct; Dementia - post-stroke; Multi-infarct dementia Images Central nervous system and peripheral nervous system References Apostolova LG, DeKosky ST, Cummings JL. Dementias. In: Daroff RB6th ed ...
- What is Multi-Infarct Dementia? Multi-infarct dementia (MID) is a common cause of memory loss in the elderly. MID is caused by multiple strokes (disruption of blood flow to the brain). Disruption of blood flow leads to ...
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