Zobrazeno 1 - 10
of 53
pro vyhledávání: '"C Elpers"'
Autor:
H. Wiendl, Nils C. Landmeyer, H. Omran, H. Lohmann, Andreas Johnen, Julia Krämer, Kerstin Göbel, P. Polzer, C. Elpers, Sven G. Meuth, Ester Riepl
Publikováno v:
European Journal of Paediatric Neurology. 23:783-791
Cognitive impairment (CI) is a critical feature for patients with childhood or juvenile multiple sclerosis (MS).To promote the understanding of CI and to address the impact of different pharmacological treatment strategies on cognitive performance in
Publikováno v:
Diabetes. 70
Background: In phase 3 trials, ultra rapid lispro (URLi) showed superior postprandial glucose control and non-inferior HbA1c reduction compared to Humalog® (Lispro). However, infusion site reactions (combined; ISRs) were more frequent with URLi. Met
Autor:
T. Geis, C. Elpers, Stefan J. Troche, Charlotte Thiels, Martin Häusler, Jonas H. Kreth, Kevin Rostasy, Tugba Kapanci, Mareike Schimmel
Publikováno v:
Kapanci, Tugba; Rostásy, Kevin; Häusler, Martin Georg; Geis, Tobias; Schimmel, Mareike; Elpers, Christiane; Kreth, Jonas H.; Tiehls, Charlotte; Troche, Stefan J. (2019). Evaluating the relationship between psychometric intelligence and cognitive functions in paediatric multiple sclerosis. Multiple sclerosis journal-experimental, translational and clinical, 5(4), p. 2055217319894365. Sage Publications 10.1177/2055217319894365
Multiple sclerosis journal-experimental, translational and clinical 5(4), 2055217319894365 (2019). doi:10.1177/2055217319894365
Multiple Sclerosis Journal-Experimental, Translational and Clinical
Multiple sclerosis journal-experimental, translational and clinical 5(4), 2055217319894365 (2019). doi:10.1177/2055217319894365
Multiple Sclerosis Journal-Experimental, Translational and Clinical
Background: Processing speed is frequently reduced in patients suffering from multiple sclerosis (MS). Reduced processing speed can also lead to impaired working memory capacity (WMC) in adult MS patients. Less is known about the interplay of cogniti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a57dc6b6b6b4c6f7d21c20a8f721bf2c
Autor:
Douglas R. Spitz, Marianne Grüneberg, Michael L. McCormick, Thorsten Marquardt, Stephan Rust, Julia Mohr, Janine Reunert, Saskia Biskup, C. Elpers, Oliver Schwartz, Anja Seelhöfer, Eugen Boltshauser, Ulrike Schara, Julien H Park
Publikováno v:
Brain
Superoxide dismutase 1 (SOD1) is the principal cytoplasmic superoxide dismutase in humans and plays a major role in redox potential regulation. It catalyses the transformation of the superoxide anion (O2•−) into hydrogen peroxide. Heterozygous va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44f0b5e56b81f1a853d0fd47e28a93eb
https://europepmc.org/articles/PMC6658856/
https://europepmc.org/articles/PMC6658856/
Publikováno v:
Brain. 143:e12-e12
Publikováno v:
Neuropediatrics. 46:292-295
Neuromyelitis optica (NMO) is a severe inflammatory demyelinating disease of the central nervous system and preferentially targets the optic nerves and spinal cord. NMO is rare in children and clinical course of the disease is highly variable as desc
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 20, Iss, Pp-(2019)
Molecular Genetics and Metabolism Reports, Vol 20, Iss, Pp-(2019)
Objectives: Multiple acyl-CoA dehydrogenase deficiency (MADD) is a severe inborn disorder of mitochondrial fatty acid oxidation. The only treatment option for MADD is the use of exogenous ketone bodies, like sodium β-hydroxybutyrate (NaβHB). Howeve
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Publikováno v:
Neuropediatrics. 47
Background: Optic neuritis (ON) is identified as one of the most frequent potential risk factor associated with future multiple sclerosis (MS). In children, conversion to MS after isolated ON is lower than in adults. Here, we aim to identify cerebros
Autor:
Sebastian Herich, Tilman Schneider-Hohendorf, Klaus Dornmair, Christian G. Bien, Johanna Breuer, Dennis Görlich, Nico Melzer, Nicholas Schwab, C. Elpers, Guido Widman, Gerhard Kurlemann, Heinz Wiendl, Tanja Kuhlmann, Hema Mohan, Albert J. Becker
Publikováno v:
Nature Communications
Nature Communications, Vol 7, Iss 1, Pp 1-14 (2016)
Nature Communications, Vol 7, Iss 1, Pp 1-14 (2016)
Rasmussen encephalitis (RE) is a rare paediatric epilepsy with uni-hemispheric inflammation and progressive neurological deficits. To elucidate RE immunopathology, we applied T-cell receptor (TCR) sequencing to blood (n=23), cerebrospinal fluid (n=2)