Accès ouvert
2026
article
OpenAlex
Aurélie Lebrun, Yann Leprince, Pauline Olivieri, Martin Moussion et autres
Alzheimer's disease (AD) and limbic-predominant age-related TDP-43 encephalopathy (LATE) are two neurodegenerative diseases underpinned by distinct proteinopathies, which share a similar initial amnestic clinical phenotype but have a different clinical course. Some pathophysiological models suggest a role for white matter (WM) fiber …
fr
(code pays fourni par la source)
Accès ouvert
2025
preprint
OpenAlex
Aurélie Lebrun, Yann Leprince, Pauline Olivieri, Martin Moussion et autres
Abstract Alzheimer’s disease (AD) and limbic-predominant age-related TDP-43 encephalopathy (LATE) are two neurodegenerative diseases underpinned by distinct proteinopathies, which share a similar initial amnestic clinical phenotype but have a different clinical course. Some pathophysiological models suggest a role for white matter (WM) …
fr
(code pays fourni par la source)
Accès ouvert
2024
article
OpenAlex
Aurélie Lebrun, Yann Leprince, Julien Lagarde, Pauline Olivieri et autres
INTRODUCTION: Typical Alzheimer's disease (AD) and limbic-predominant age-related TAR DNA-binding protein 43 (TDP-43) encephalopathy (LATE) are two neurodegenerative diseases that present with a similar initial amnestic clinical phenotype but are associated with distinct proteinopathies. METHODS: We investigated white matter (WM) fiber bundle …
fr
(code pays fourni par la source)
Accès ouvert
2024
article
OpenAlex
Julien Lagarde, Pauline Olivieri, Mattéo Tonietto, Camille Noiray et autres
BACKGROUND: The locus coeruleus (LC) and the nucleus basalis of Meynert (NBM) are altered in early stages of Alzheimer's disease (AD). Little is known about LC and NBM alteration in limbic-predominant age-related TDP-43 encephalopathy (LATE) and frontotemporal dementia (FTD). The aim of …
fr
(code pays fourni par la source)
Accès ouvert
2024
article
OpenAlex
Gaël Nicolas, Aline Zaréa, Morgane Lacour, Olivier Quenez et autres
PURPOSE: To assess the likely pathogenic/pathogenic (LP/P) variants rates in Mendelian dementia genes and the moderate-to-strong risk factors rates in patients with Alzheimer disease (AD). METHODS: We included 700 patients in a prospective study and performed exome sequencing. A panel of 28 …
fr
(code pays fourni par la source)
Accès ouvert
2023
article
OpenAlex
Pauline Dodet, Camille Noiray, Smaranda Leu‐Semenescu, Etienne Lefevre et autres
STUDY OBJECTIVES: To evaluate sleep, sleepiness, and excessive need for sleep in patients with craniopharyngioma (a suprasellar tumor which can affect sleep-wake systems). METHODS: A retrospective study of all adult patients living with craniopharyngioma referred to the sleep clinic, who received a …
fr, ca
(code pays fourni par la source)
Accès ouvert
2022
article
OpenAlex
Catherine Schramm, Camille Charbonnier, Aline Zaréa, Morgane Lacour et autres
BACKGROUND: Alzheimer disease (AD) is a common complex disorder with a high genetic component. Loss-of-function (LoF) SORL1 variants are one of the strongest AD genetic risk factors. Estimating their age-related penetrance is essential before putative use for genetic counseling or preventive trials. …
fr
(code pays fourni par la source)
2021
article
OpenAlex
Milan Nigam, Inès Ayadi, Camille Noiray, Ana Brás et autres
BACKGROUND: Hyposmia and isolated REM sleep behavior disorder are well-established features of prodromal Parkinson's disease (PD). OBJECTIVES: The objective of the present study was to evaluate whether taste loss (reported in PD and possibly suggesting brain stem involvement) is present at the …
fr, ca, pt, es
(code pays fourni par la source)
Accès ouvert
2018
article
OpenAlex
Guilhem Carle, Alexandre Morin, Camille Noiray, Perrine Roy-Joly et autres
fr
(code pays fourni par la source)