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pro vyhledávání: '"Roy AM Haast"'
Autor:
Jordan DeKraker, Roy AM Haast, Mohamed D Yousif, Bradley Karat, Jonathan C Lau, Stefan Köhler, Ali R Khan
Publikováno v:
eLife, Vol 11 (2022)
Like neocortical structures, the archicortical hippocampus differs in its folding patterns across individuals. Here, we present an automated and robust BIDS-App, HippUnfold, for defining and indexing individual-specific hippocampal folding in MRI, an
Externí odkaz:
https://doaj.org/article/c9fb3012f2fd47079e8539125966ec77
Publikováno v:
NeuroImage, Vol 262, Iss , Pp 119553- (2022)
Tractography combined with regions of interest (ROIs) has been used to non-invasively study the structural connectivity of the cortex as well as to assess the reliability of these connections. However, the subcortical connectome (subcortex to subcort
Externí odkaz:
https://doaj.org/article/6c2c0bb015444bf8ad61198bf995402d
Publikováno v:
bioRxiv
The cholinergic innervation of the cortex originates almost entirely from populations of neurons in the basal forebrain. Structurally, the ascending basal forebrain cholinergic projections are highly branched, with individual cells targeting multiple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61618fe313bbe459c2b738f3f2daff6b
https://doi.org/10.1101/2023.05.26.541324
https://doi.org/10.1101/2023.05.26.541324
Autor:
Roy AM Haast, Benoit Testud, Julia Makhalova, Hugo Dary, Alexandre Cabane, Arnaud Le Troter, Jean-Philippe Ranjeva, Fabrice Bartolomei, Maxime Guye
Focal epilepsy is characterized by repeated spontaneous seizures that originate from cortical epileptogenic zone networks (EZN). More recently, analysis of intracerebral recordings showed that subcortical structures, and in particular the thalamus, p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfd420c65391a731f18bb1c0b3b96e98
https://doi.org/10.1101/2022.11.01.514655
https://doi.org/10.1101/2022.11.01.514655
Autor:
Roy AM. Haast, Irenaeus FM. De Coo, Dimo Ivanov, Ali R Khan, Jacobus FA. Jansen, Hubert JM. Smeets, Kâmil Uludağ
Mutations of the mitochondrial DNA are an important cause of inherited diseases that can severely affect the tissue’s homeostasis and integrity. The m.3243A>G mutation is the most commonly observed across mitochondrial disorders and is linked to mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad189615714b1f3b61634e52098df10b
https://doi.org/10.1101/2021.04.30.442091
https://doi.org/10.1101/2021.04.30.442091