Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Raimund, Kottke"'
Autor:
Antonio Giulio Gennari, Giulio Bicciato, Santo Pietro Lo Biundo, Raimund Kottke, Ilona Stefanos-Yakoub, Dorottya Cserpan, Ruth O’Gorman Tuura, Georgia Ramantani
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract Arterial spin labelling (ASL), an MRI sequence non-invasively imaging brain perfusion, has yielded promising results in the presurgical workup of children with focal cortical dysplasia (FCD)-related epilepsy. However, the interpretation of A
Externí odkaz:
https://doaj.org/article/0af06cff360344608feb02e9d5858f2d
Autor:
Anna Speckert, Hui Ji, Kelly Payette, Patrice Grehten, Raimund Kottke, Samuel Ackermann, Beth Padden, Luca Mazzone, Ueli Moehrlen, Spina Bifida Study Group Zurich, Andras Jakab
Publikováno v:
Data, Vol 9, Iss 9, p 107 (2024)
We present the Open Spina Bifida Aperta (OSBA) atlas, an open atlas and set of neuroimaging templates for spina bifida aperta (SBA). Traditional brain atlases may not adequately capture anatomical variations present in pediatric or disease-specific c
Externí odkaz:
https://doaj.org/article/ef9099e557f3487a831dfab8112cb4fb
Autor:
Alexandra De Silvestro, Bettina Reich, Sarah Bless, Julika Sieker, Willemijn Hollander, Karen de Bijl-Marcus, Cornelia Hagmann, Joppe Nijman, Walter Knirsch, the European Association Brain in Congenital Heart Disease, Mirielle N. Bekker, Manon J. N. L. Benders, Floris Groenendaal, Corine Koopman-Esseboom, Maaike Nijman, Raymond Stegeman, Alexandra Bonthrone, Andrew Chew, Serena J. Counsell, Daniel Cromb, Barat Gal-Er, Christopher J. Kelly, Kuberan Pushparajah, Rian Bosch, Sergei Chin On, Nicolaas J. G. Jansen, Valerie D. Slooff, Johannes M. P. J. Breur, Nathalie H. P. Claessens, Hitendu Dave, Maria Feldmann, Raimund Kottke, Beatrice Latal, Céline Steger, Monique C. Haak
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
BackgroundThe treatment of preterm and low birth weight (LBW) neonates born with congenital heart disease (CHD) requiring early cardiac intervention remains challenging. We aimed to analyze morbidity and mortality in this combined high-risk patient g
Externí odkaz:
https://doaj.org/article/b780ac00c8d94ec6a338901658b971ca
Autor:
Céline Steger, Charles Moatti, Kelly Payette, Alexandra De Silvestro, Thi Dao Nguyen, Seline Coraj, Ninib Yakoub, Giancarlo Natalucci, Raimund Kottke, Ruth Tuura, Walter Knirsch, Andras Jakab
Publikováno v:
Frontiers in Neuroscience, Vol 17 (2023)
IntroductionDespite established knowledge on the morphological and functional asymmetries in the human brain, the understanding of how brain asymmetry patterns change during late fetal to neonatal life remains incomplete. The goal of this study was t
Externí odkaz:
https://doaj.org/article/30128692ee6248d0bccf73455d462e20
Autor:
Antonio Giulio Gennari, Dorottya Cserpan, Ilona Stefanos-Yakoub, Raimund Kottke, Ruth O’Gorman Tuura, Georgia Ramantani
Publikováno v:
Insights into Imaging, Vol 14, Iss 1, Pp 1-11 (2023)
Key points 1. DTI derived indices may be a useful tool for FCD characterisation. 2. FA and MD discriminated between FCD and contralateral brain parenchyma (CBP). 3. Status epilepticus increased the FA difference values between FCD and CBP. 4. Type II
Externí odkaz:
https://doaj.org/article/61a3af8dc23448c18b18be7daf4ff733
Autor:
Kelly Payette, Priscille de Dumast, Hamza Kebiri, Ivan Ezhov, Johannes C. Paetzold, Suprosanna Shit, Asim Iqbal, Romesa Khan, Raimund Kottke, Patrice Grehten, Hui Ji, Levente Lanczi, Marianna Nagy, Monika Beresova, Thi Dao Nguyen, Giancarlo Natalucci, Theofanis Karayannis, Bjoern Menze, Meritxell Bach Cuadra, Andras Jakab
Publikováno v:
Scientific Data, Vol 8, Iss 1, Pp 1-14 (2021)
Measurement(s) regional part of brain • T2 (Observed)-Weighted Imaging Technology Type(s) Image Segmentation Sample Characteristic - Organism Homo sapiens Machine-accessible metadata file describing the reported data: https://doi.org/10.6084/m9.fig
Externí odkaz:
https://doaj.org/article/955b4c4a372743dc811da7c038c1a140
Autor:
Andras Jakab, Kelly Payette, Luca Mazzone, Sonja Schauer, Cécile Olivia Muller, Raimund Kottke, Nicole Ochsenbein-Kölble, Ruth Tuura, Ueli Moehrlen, Martin Meuli
Publikováno v:
European Radiology Experimental, Vol 5, Iss 1, Pp 1-10 (2021)
Abstract Magnetic resonance imaging (MRI) has become an essential diagnostic modality for congenital disorders of the central nervous system. Recent advancements have transformed foetal MRI into a clinically feasible tool, and in an effort to find pr
Externí odkaz:
https://doaj.org/article/31e6888f64f2477899fc40751ac8f532
Autor:
Bigna K. Bölsterli, Eugen Boltshauser, Luigi Palmieri, Johannes Spenger, Michaela Brunner-Krainz, Felix Distelmaier, Peter Freisinger, Tobias Geis, Andrea L. Gropman, Johannes Häberle, Julia Hentschel, Bruno Jeandidier, Daniela Karall, Boris Keren, Annick Klabunde-Cherwon, Vassiliki Konstantopoulou, Raimund Kottke, Francesco M. Lasorsa, Christine Makowski, Cyril Mignot, Ruth O’Gorman Tuura, Vito Porcelli, René Santer, Kuntal Sen, Katja Steinbrücker, Steffen Syrbe, Matias Wagner, Andreas Ziegler, Thomas Zöggeler, Johannes A. Mayr, Holger Prokisch, Saskia B. Wortmann
Publikováno v:
Nutrients, Vol 14, Iss 17, p 3605 (2022)
The mitochondrial malate aspartate shuttle system (MAS) maintains the cytosolic NAD+/NADH redox balance, thereby sustaining cytosolic redox-dependent pathways, such as glycolysis and serine biosynthesis. Human disease has been associated with defects
Externí odkaz:
https://doaj.org/article/b0f6a6745c114d6e995f41fa35173885
Autor:
Fatma Kivrak Pfiffner, Samuel Koller, Anika Ménétrey, Urs Graf, Luzy Bähr, Alessandro Maspoli, Annette Hackenberg, Raimund Kottke, Christina Gerth-Kahlert, Wolfgang Berger
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 13, p 7382 (2022)
Early infantile epileptic encephalopathy (EIEE) is a severe neurologic and neurodevelopmental disease that manifests in the first year of life. It shows a high degree of genetic heterogeneity, but the genetic origin is only identified in half of the
Externí odkaz:
https://doaj.org/article/cfaeb797a0d84b2b87b2e6d5c8ddb209
Autor:
Timothy Mueller, Sandra Laternser, Ana S. Guerreiro Stücklin, Nicolas U. Gerber, Sulayman Mourabit, Marion Rizo, Elisabeth J. Rushing, Raimund Kottke, Michael Grotzer, Niklaus Krayenbühl, Javad Nazarian, Sabine Mueller
Publikováno v:
European Journal of Cancer. 178:171-179
Children diagnosed with diffuse midline gliomas (DMG) have an extremely poor overall survival: 9-12 months from diagnosis with currently no curative treatment options. Given DMG molecular heterogeneity, surgical biopsies are needed for molecular prof
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b68b38fffe92663f5270002759ec38db
https://doi.org/10.1016/j.ejca.2022.10.014
https://doi.org/10.1016/j.ejca.2022.10.014