نتایج جستجو برای: onset type eoad

تعداد نتایج: 1494578  

2002
ENG HOCK ANGUS MACDONALD

We analyse, in a probabilistic setting, Newcombe's (1981) life table method of estimating rates of onset of high-penetrance single-gene disorders, and extend this to a counting process model for individual life histories, including movement between risk groups arising from genetic testing and onset in relatives. A key result is that estimates of rates of onset at any age x must be conditioned o...

2008
Hyun-Kyung Park Duk Lyul Na Jae-Hong Lee Jong-Won Kim Chang-Seok Ki

Although mutations in three genes, amyloid precursor protein (APP), presenilin 1 (PSEN1), and presenilin 2 (PSEN2), have been identified as genetic causes of early-onset Alzheimer s disease (EOAD), there has been a single report on a PSEN1 mutation in Koreans. In the present study, we performed a genetic analysis of six Korean patients with EOAD. Direct sequencing analysis of the APP, PSEN1 and...

2018
Jurre den Haan Sarah F. Janssen Jacoba A. van de Kreeke Philip Scheltens Frank D. Verbraak Femke H. Bouwman

Introduction The retina may reflect Alzheimer's disease (AD) neuropathological changes and is easily visualized with optical coherence tomography (OCT). Retinal thickness decrease has been correlated to AD, however, without information on amyloid status. We correlated retinal (layer) thickness to AD biomarkers in amyloid-positive early-onset AD (EOAD) patients and amyloid-negative controls. M...

2017
Massimo Filippi Silvia Basaia Elisa Canu Francesca Imperiale Alessandro Meani Francesca Caso Giuseppe Magnani Monica Falautano Giancarlo Comi Andrea Falini Federica Agosta

OBJECTIVE To investigate functional brain network architecture in early-onset Alzheimer disease (EOAD) and behavioral variant frontotemporal dementia (bvFTD). METHODS Thirty-eight patients with bvFTD, 37 patients with EOAD, and 32 age-matched healthy controls underwent 3D T1-weighted and resting-state fMRI. Graph analysis and connectomics assessed global and local functional topologic network...

Journal: :Dementia and geriatric cognitive disorders 2014
Edmond Teng Tritia R Yamasaki Michelle Tran Julia J Hsiao David L Sultzer Mario F Mendez

BACKGROUND/AIMS Accurate diagnosis of sporadic early-onset Alzheimer's disease (EOAD) can be challenging, and cerebrospinal fluid (CSF) biomarkers may assist in this process. We compared CSF indices between three EOAD subtypes: amnestic, logopenic progressive aphasia (LPA), and posterior cortical atrophy (PCA). METHODS We identified 21 amnestic EOAD, 20 LPA, and 12 PCA patients with CSF data,...

2015
Shima Mehrabian Panagiotis Alexopoulos Marion Ortner Latchezar Traykov Timo Grimmer Alexander Kurz Hans Förstl Horst Bickel Janine Diehl-Schmid

INTRODUCTION Cerebrospinal fluid (CSF) biomarkers improve the diagnostic accuracy for Alzheimer's disease (AD), even at the predementia stage of the disease. The ε4-allele of apolipoprotein E (ApoE ε4), female sex, and older age are well-known risk factors for AD. It is unclear how these risk factors affect the CSF biomarkers in patients with AD. AIM The objective of this study was to investi...

Journal: :Neurobiology of Aging 2015
Elise Cuyvers Julie van der Zee Karolien Bettens Sebastiaan Engelborghs Mathieu Vandenbulcke Caroline Robberecht Lubina Dillen Céline Merlin Nathalie Geerts Caroline Graff Håkan Thonberg Huei-Hsin Chiang Pau Pastor Sara Ortega-Cubero Maria A. Pastor Janine Diehl-Schmid Panagiotis Alexopoulos Luisa Benussi Roberta Ghidoni Giuliano Binetti Benedetta Nacmias Sandro Sorbi Raquel Sanchez-Valle Albert Lladó Ellen Gelpi Maria Rosário Almeida Isabel Santana Jordi Clarimon Alberto Lleó Juan Fortea Alexandre de Mendonça Madalena Martins Barbara Borroni Alessandro Padovani Radoslav Matěj Zdenek Rohan Agustín Ruiz Giovanni B. Frisoni Gian Maria Fabrizi Rik Vandenberghe Peter P. De Deyn Christine Van Broeckhoven Kristel Sleegers

Meta-analysis of existing genome-wide association studies on Alzheimer's disease (AD) showed subgenome-wide association of an intronic variant in the sequestosome 1 (SQSTM1) gene with AD. We performed targeted resequencing of SQSTM1 in Flanders-Belgian AD patients selected to be enriched for a genetic background (n = 435) and geographically matched nonaffected individuals (n = 872) to investiga...

Journal: :Alzheimers & Dementia 2023

Background The evaluation of similarities and differences between mouse models human Alzheimer’s disease (AD) provides invaluable insights on pathophysiology. We compared hippocampal transcriptomic profiles late-onset AD (LOAD) early-onset (EOAD) individuals with three (hAβ-KI, APP/PS1 5xFAD) in an exploratory analysis. Afterwards, we validated the intersection genes consistently altered all gr...

Journal: :Journal of Alzheimer's disease : JAD 2016
Samrah Ahmed Ian Baker Masud Husain Sian Thompson Christopher Kipps Michael Hornberger John R Hodges Christopher R Butler

Posterior cortical atrophy (PCA) is characterized by core visuospatial and visuoperceptual deficits, and predominant atrophy in the parieto-occipital cortex. The most common underlying pathology is Alzheimer's disease (AD). Existing diagnostic criteria suggest that episodic memory is relatively preserved. The aim of this study was to examine memory performance at initial clinical presentation i...

2017
Elisa Canu Federica Agosta Gorana Mandic-Stojmenovic Tanja Stojković Elka Stefanova Alberto Inuggi Francesca Imperiale Massimiliano Copetti Vladimir S. Kostic Massimo Filippi

This prospective study explored whether an approach combining structural [cortical thickness and white matter (WM) microstructure] and resting state functional MRI can aid differentiation between 62 early onset Alzheimer's disease (EOAD) and 27 behavioural variant of frontotemporal dementia (bvFTD) patients. Random forest and receiver operator characteristic curve analyses assessed the ability ...

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