家族性脳アミロイド血管症
WordNet
- 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
- of or relating to the cerebrum or brain; "cerebral hemisphere"; "cerebral activity"
- involving intelligence rather than emotions or instinct; "a cerebral approach to the problem"; "cerebral drama" (同)intellectual
- (pathology) a waxy translucent complex protein resembling starch that results from degeneration of tissue
- a non-nitrogenous food substance consisting chiefly of starch; any substance resembling starch
- any disease of the blood vessels or lymph ducts
PrepTutorEJDIC
- 家族の,家族特有の / 違伝的な,血統にあらわれる
- 大脳の,脳の / 頭脳的な,知的な
UpToDate Contents
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English Journal
- Two distinct β-sheet structures in Italian-mutant amyloid-beta fibrils: a potential link to different clinical phenotypes.
- Hubin E1,2,3, Deroo S4, Schierle GK5, Kaminski C5, Serpell L6, Subramaniam V1,7, van Nuland N2,3, Broersen K8, Raussens V4, Sarroukh R9.
- Cellular and molecular life sciences : CMLS.Cell Mol Life Sci.2015 Dec;72(24):4899-913. doi: 10.1007/s00018-015-1983-2. Epub 2015 Jul 21.
- Most Alzheimer's disease (AD) cases are late-onset and characterized by the aggregation and deposition of the amyloid-beta (Aβ) peptide in extracellular plaques in the brain. However, a few rare and hereditary Aβ mutations, such as the Italian Glu22-to-Lys (E22K) mutation, guarantee the developmen
- PMID 26190022
- Genetic determinants of white matter hyperintensities and amyloid angiopathy in familial Alzheimer's disease.
- Ryan NS1, Biessels GJ2, Kim L3, Nicholas JM4, Barber PA5, Walsh P6, Gami P6, Morris HR7, Bastos-Leite AJ8, Schott JM5, Beck J9, Mead S9, Chavez-Gutierrez L10, de Strooper B10, Rossor MN5, Revesz T6, Lashley T6, Fox NC5.
- Neurobiology of aging.Neurobiol Aging.2015 Dec;36(12):3140-51. doi: 10.1016/j.neurobiolaging.2015.08.026. Epub 2015 Sep 4.
- Familial Alzheimer's disease (FAD) treatment trials raise interest in the variable occurrence of cerebral amyloid angiopathy (CAA); an emerging important factor in amyloid-modifying therapy. Previous pathological studies reported particularly severe CAA with postcodon 200 PSEN1 mutations and amyloid
- PMID 26410308
- Oxidative stress and mitochondria-mediated cell death mechanisms triggered by the familial Danish dementia ADan amyloid.
- Todd K1, Ghiso J2, Rostagno A3.
- Neurobiology of disease.Neurobiol Dis.2015 Oct 13;85:130-143. doi: 10.1016/j.nbd.2015.10.003. [Epub ahead of print]
- Familial Danish Dementia (FDD), an early-onset non-amyloid-β (Aβ) cerebral amyloidosis, is neuropathologically characterized by widespread cerebral amyloid angiopathy, parenchymal amyloid and preamyloid deposits, as well as neurofibrillary degeneration indistinguishable to that seen in Alzheimer's
- PMID 26459115
Japanese Journal
- 遺伝性ATTRアミロイドーシスの治療の現状と今後の展望
- 古典型脳表ヘモジデリン沈着症を呈したVal30Metホモ接合体家族性アミロイドポリニューロパチーの1例
- 古典型脳表ヘモジデリン沈着症を呈したVal30Metホモ接合体家族性アミロイドポリニューロパチーの1例
Related Links
- Hereditary cerebral amyloid angiopathy is a condition that can cause a progressive loss of intellectual function ... cerebral amyloid angiopathy, familial cerebral amyloid angiopathy, genetic HCHWA Related Information How are ...
- Background Advances in genetic technology have revealed that variation in the same gene can cause both rare familial and common sporadic forms of the same disease. Cerebral amyloid angiopathy (CAA), a common ...
Related Pictures
★リンクテーブル★
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- 英
- familial cerebral amyloid angiopathy
[★]
- 関
- brain、cerebri、cerebro、cerebrum、encephalic、encephalo、encephalon
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- 関
- family、family member、household、kindred
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アミロイド
- 関
- amyloid fibril、amyloid protein
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- 同
- アミロイド・アンギオパチー