相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。A multifactorial model of pathology for age of onset heterogeneity in familial Alzheimer's disease
Diego Sepulveda-Falla et al.
ACTA NEUROPATHOLOGICA (2021)
Depression in Alzheimer's Disease: A Delphi Consensus on Etiology, Risk Factors, and Clinical Management
Luis Aguera-Ortiz et al.
FRONTIERS IN PSYCHIATRY (2021)
The Italian Version of the Test Your Memory (TYM-I): A Tool to Detect Mild Cognitive Impairment in the Clinical Setting
Maria Rosaria Barulli et al.
FRONTIERS IN PSYCHOLOGY (2021)
Identification of a RarePSEN1Mutation (Thr119Ile) in Late-Onset Alzheimer's Disease With Early Presentation of Behavioral Disturbance
Shouzi Zhang et al.
FRONTIERS IN PSYCHIATRY (2020)
Late-onset presentation and phenotypic heterogeneity of the rareR377W PSEN1mutation
M. Scarioni et al.
EUROPEAN JOURNAL OF NEUROLOGY (2020)
Global, regional, and national burden of Alzheimer's disease and other dementias, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016
Emma Nichols et al.
LANCET NEUROLOGY (2019)
Molecular genetics of early-onset Alzheimer's disease revisited
Rita Cacace et al.
ALZHEIMERS & DEMENTIA (2016)
Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer's disease: a case series
Natalie S. Ryan et al.
LANCET NEUROLOGY (2016)
Genetic determinants of white matter hyperintensities and amyloid angiopathy in familial Alzheimer's disease
Natalie S. Ryan et al.
NEUROBIOLOGY OF AGING (2015)
Sampling the conformational space of the catalytic subunit of human γ-secretase
Xiao-chen Bai et al.
ELIFE (2015)
Symptom onset in autosomal dominant Alzheimer disease A systematic review and meta-analysis
Davis C. Ryman et al.
NEUROLOGY (2014)
The mechanism of γ-Secretase dysfunction in familial Alzheimer disease
Lucia Chavez-Gutierrez et al.
EMBO JOURNAL (2012)
The French Series of Autosomal Dominant Early Onset Alzheimer's Disease Cases: Mutation Spectrum and Cerebrospinal Fluid Biomarkers
David Wallon et al.
JOURNAL OF ALZHEIMERS DISEASE (2012)
The diagnosis of dementia due to Alzheimer's disease: Recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease
Guy M. McKhann et al.
ALZHEIMERS & DEMENTIA (2011)
Worldwide distribution of PSEN1 Met146Leu mutation A large variability for a founder mutation
A. C. Bruni et al.
NEUROLOGY (2010)
Depression and psychiatric symptoms preceding onset of dementia in a family with early-onset Alzheimer disease with a novel PSEN1 mutation
Kensaku Kasuga et al.
JOURNAL OF NEUROLOGY (2009)
Forecasting the global burden of Alzheimer's disease
Ron Brookmeyer et al.
ALZHEIMERS & DEMENTIA (2007)
Putting presenilins centre stage - Introduction to the Talking Point on the role of presenilin mutations in Alzheimer disease
John Hardy
EMBO REPORTS (2007)
Clinical phenotypic heterogeneity of Alzheimer's disease associated with mutations of the presenilin-1 gene
AJ Larner et al.
JOURNAL OF NEUROLOGY (2006)
Molecular diagnosis of autosomal dominant early onset Alzheimer's disease:: an update
G Raux et al.
JOURNAL OF MEDICAL GENETICS (2005)
Female preclinical presenilin-1 mutation carriers unaware of their genetic status have higher levels of depression than their non-mutation carrying kin
JM Ringman et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2004)
Early onset familial Alzheimer's disease - Mutation frequency in 31 families
JC Janssen et al.
NEUROLOGY (2003)
Amyloid angiopathy and variability in amyloid β deposition is determined by mutation position in presenilin-1-linked Alzheimer's disease
DMA Mann et al.
AMERICAN JOURNAL OF PATHOLOGY (2001)
Presenilin structure, function and role in Alzheimer disease
PE Fraser et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2000)