Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Christiane Elpers"'
Autor:
Aziza Miriam Belkheir, Janine Reunert, Christiane Elpers, Lambert van den Heuvel, Richard Rodenburg, Anja Seelhöfer, Stephan Rust, Astrid Jeibmann, Michael Frosch, Thorsten Marquardt
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
ßIV-spectrin is a protein of the spectrin family which is involved in the organization of the cytoskeleton structure and is found in high quantity in the axon initial segment and the nodes of Ranvier. Together with ankyrin G, ßIV-spectrin is respon
Externí odkaz:
https://doaj.org/article/5ea2c2d167bc4ff88f141e7678fb8989
Autor:
Stefan J. Troche, Tugba Kapanci, Thomas H. Rammsayer, Carl P. A. Kesseler, Martin Georg Häusler, Tobias Geis, Mareike Schimmel, Christiane Elpers, Jonas H. Kreth, Charlotte Thiels, Kevin Rostásy
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Background: For adult multiple sclerosis (MS) patients, impaired temporal processing of simultaneity/successiveness has been frequently reported although interval timing has been investigated in neither adult nor pediatric MS patients. We aim to exte
Externí odkaz:
https://doaj.org/article/c6dc7a04cb784272b143168ea3c38c6c
Autor:
Nina V. Fuchs, Maximilian Schieck, Michaela Neuenkirch, Christiane Tondera, Heike Schmitz, Lena Wendeburg, Doris Steinemann, Christiane Elpers, Frank Rutsch, Renate König
Publikováno v:
Stem Cell Research, Vol 43, Iss , Pp - (2020)
Aicardi-Goutières syndrome (AGS) is a hereditary early onset encephalopathy. AGS patients display variable clinical manifestations including intracranial calcification, cerebral atrophy, white matter abnormalities and characteristic leukocytosis as
Externí odkaz:
https://doaj.org/article/045c20fd937f4828a9c70550046d4de4
Publikováno v:
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
Externí odkaz:
https://doaj.org/article/a3dd7ec06a7c41a3945914f36b082e2a
Autor:
Tilman Schneider-Hohendorf, Hema Mohan, Christian G. Bien, Johanna Breuer, Albert Becker, Dennis Görlich, Tanja Kuhlmann, Guido Widman, Sebastian Herich, Christiane Elpers, Nico Melzer, Klaus Dornmair, Gerhard Kurlemann, Heinz Wiendl, Nicholas Schwab
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-14 (2016)
Rasmussen Encephalitis is a rare neurological disease accompanied by inflammation and T cell infiltration in the brain. Here the authors show that the severity of this disease correlates with clonal CD8 T cell expansion.
Externí odkaz:
https://doaj.org/article/628a86018f024cc3bd4d4ee72d33b5f0
Autor:
Julien H Park, Ulrika Nordström, Konstantinos Tsiakas, Isil Keskin, Christiane Elpers, Manoj Mannil, Raoul Heller, Melinda Nolan, Salam Alburaiky, Per Zetterström, Maja Hempel, Ulrike Schara-Schmidt, Saskia Biskup, Petra Steinacker, Markus Otto, Jochen Weishaupt, Andreas Hahn, René Santer, Thorsten Marquardt, Stefan L Marklund, Peter M Andersen
Superoxide dismutase-1 is a ubiquitously expressed antioxidant enzyme. Mutations in SOD1 can cause amyotrophic lateral sclerosis, probably via a toxic gain-of-function involving protein aggregation and prion-like mechanisms. Recently, homozygosity fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::503bd7fd2df67d84f154ec39b0ac77d1
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-208224
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-208224
Autor:
Maximilian Schieck, Lena Wendeburg, Michaela Neuenkirch, Doris Steinemann, Heike Schmitz, Christiane Elpers, Christiane Tondera, Nina V. Fuchs, Renate König, Frank Rutsch
Publikováno v:
Stem cell research, 43:101697
Stem Cell Research, Vol 43, Iss, Pp-(2020)
Stem Cell Research, Vol 43, Iss, Pp-(2020)
Aicardi-Goutières syndrome (AGS) is a hereditary early onset encephalopathy. AGS patients display variable clinical manifestations including intracranial calcification, cerebral atrophy, white matter abnormalities and characteristic leukocytosis as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfa32deeb8be20f5ab5c27a118ef054c
https://repository.publisso.de/resource/frl:6432588
https://repository.publisso.de/resource/frl:6432588
Autor:
U Grenzebach, Oliver Schwartz, Christiane Elpers, Amler S, Sven G. Meuth, Gerd Kurlemann, Barbara Fiedler, T Allkemper
Publikováno v:
Neonatal and Pediatric Medicine.
Isolated optic neuritis in adults (ON) is the most common initial manifestation of multiple sclerosis (MS). Conversion to MS after childhood ON is not well determined. We aimed to identify risk factors predicting MS following ON and to develop risk p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29de10302cd697b48e6e4d44a26ba56f
https://doi.org/10.4172/2572-4983.1000s1003
https://doi.org/10.4172/2572-4983.1000s1003