Amyloid angiopathy and variability in amyloid beta deposition is determined by mutation position in presenilin-1-linked Alzheimer's disease.
about
CLAC: a novel Alzheimer amyloid plaque component derived from a transmembrane precursor, CLAC-P/collagen type XXVThe genetics and neuropathology of Alzheimer's diseaseDense-core senile plaques in the Flemish variant of Alzheimer's disease are vasocentricClinical phenotypic heterogeneity of Alzheimer's disease associated with mutations of the presenilin-1 geneQuantitative amyloid imaging using image-derived arterial input functionQuantitative Amyloid Imaging in Autosomal Dominant Alzheimer's Disease: Results from the DIAN Study GroupNeurological manifestations of autosomal dominant familial Alzheimer's disease: a comparison of the published literature with the Dominantly Inherited Alzheimer Network observational study (DIAN-OBS).Regional variability of imaging biomarkers in autosomal dominant Alzheimer's diseaseGenetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathiesComparison of Abeta levels in the brain of familial and sporadic Alzheimer's disease.Autosomal-dominant Alzheimer's disease: a review and proposal for the prevention of Alzheimer's disease.Early onset of hypersynchronous network activity and expression of a marker of chronic seizures in the Tg2576 mouse model of Alzheimer's disease.Cerebral amyloid angiopathy: pathogenesis and effects on the ageing and Alzheimer brain.Amyloid deposition begins in the striatum of presenilin-1 mutation carriers from two unrelated pedigreesGenetic counseling and testing for Alzheimer disease: joint practice guidelines of the American College of Medical Genetics and the National Society of Genetic CounselorsSporadic cerebral amyloid angiopathy: pathology, clinical implications, and possible pathomechanisms.Mechanism of cerebral beta-amyloid angiopathy: murine and cellular models.Presenilin-1 280Glu-->Ala mutation alters C-terminal APP processing yielding longer abeta peptides: implications for Alzheimer's diseaseCerebral amyloid angiopathy: pathogenetic mechanisms and link to dense amyloid plaques.Neuropathology of Autosomal Dominant Alzheimer Disease in the National Alzheimer Coordinating Center Database.Cerebral amyloid angiopathy and its relationship to Alzheimer's disease.Hereditary and sporadic forms of abeta-cerebrovascular amyloidosis and relevant transgenic mouse modelsSubjects harboring presenilin familial Alzheimer's disease mutations exhibit diverse white matter biochemistry alterations.Early onset familial Alzheimer Disease with spastic paraparesis, dysarthria, and seizures and N135S mutation in PSEN1.Genetic animal models of cerebral vasculopathies.Correlating familial Alzheimer's disease gene mutations with clinical phenotype.Review: sporadic cerebral amyloid angiopathy.Alzheimer's silent partner: cerebral amyloid angiopathy.Symptom onset in autosomal dominant Alzheimer disease: a systematic review and meta-analysis.Familial Presenilin Mutations and Sporadic Alzheimer's Disease Pathology: Is the Assumption of Biochemical Equivalence Justified?Interference with splicing of Presenilin transcripts has potent dominant negative effects on Presenilin activity.The usefulness of biological and neuroimaging markers for the diagnosis of early-onset Alzheimer's disease.Cerebral microbleeds in familial Alzheimer's diseaseAtaxic variant of Alzheimer's disease caused by Pro117Ala PSEN1 mutation.Neuropathology of the recessive A673V APP mutation: Alzheimer disease with distinctive features.Neuropathological and clinical phenotype of an Italian Alzheimer family with M239V mutation of presenilin 2 gene.Alzheimer's disease: A matter of blood-brain barrier dysfunction?Cytoskeletal alterations differentiate presenilin-1 and sporadic Alzheimer's disease.Familial cases presenting very early onset autosomal dominant Alzheimer's disease with I143T in presenilin-1 gene: implication for genotype-phenotype correlation.Thymoquinone prevents β-amyloid neurotoxicity in primary cultured cerebellar granule neurons.
P2860
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P2860
Amyloid angiopathy and variability in amyloid beta deposition is determined by mutation position in presenilin-1-linked Alzheimer's disease.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
2001年论文
@zh
2001年论文
@zh-cn
name
Amyloid angiopathy and variabi ...... -1-linked Alzheimer's disease.
@ast
Amyloid angiopathy and variabi ...... -1-linked Alzheimer's disease.
@en
type
label
Amyloid angiopathy and variabi ...... -1-linked Alzheimer's disease.
@ast
Amyloid angiopathy and variabi ...... -1-linked Alzheimer's disease.
@en
prefLabel
Amyloid angiopathy and variabi ...... -1-linked Alzheimer's disease.
@ast
Amyloid angiopathy and variabi ...... -1-linked Alzheimer's disease.
@en
P2093
P2860
P1476
Amyloid angiopathy and variabi ...... -1-linked Alzheimer's disease.
@en
P2093
A Takeuchi
Members of the Familial Alzheimer's Disease Pathology Study Group
T Iwatsubo
P2860
P304
P356
10.1016/S0002-9440(10)64688-3
P407
P577
2001-06-01T00:00:00Z