Chronic Serotonergic Overstimulation Mimicking Panic Attacks in a Patient with Parkinson’s Disease Receiving Additional Antidepressant Treatment with Moclobemide

Autor: Martin E. Keck, Lukas Werle, Stefan Kloiber, S. Nischwitz, Timo Schiele, Janina Kuffer, Marc Praetner

Publikováno v: Case Reports in Psychiatry, Vol 2021 (2021)
Case Reports in Psychiatry

Background. The pharmacological treatment options of Parkinson’s disease (PD) have considerably evolved during the last decades. However, therapeutic regimes are complicated due to individual differences in disease progression as well as the occurr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c6926b69d089ebbdad4a25821dc8823
https://doaj.org/article/5e1f55709e404adbac37e1796a545b8e

MALDI imaging mass spectrometry analysis—A new approach for protein mapping in multiple sclerosis brain lesions

Autor: Sören-Oliver Deininger, F. König, Joachim Hornung, Christoph W. Turck, Frank Weber, Giuseppina Maccarrone, S. Nischwitz, Christine Stadelmann

Publikováno v: Journal of Chromatography B. 1047:131-140

Multiple sclerosis is a disease of the central nervous system characterized by recurrent inflammatory demyelinating lesions in the early disease stage. Lesion formation and mechanisms leading to lesion remyelination are not fully understood. Matrix A

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::945d6abe40c38e0a881a602dcd2a2775
https://doi.org/10.1016/j.jchromb.2016.07.001

GAD antibody-associated limbic encephalitis in a young woman with APECED

Autor: S. Nischwitz, Tania Kümpfel, Matthias K. Auer, Günter K. Stalla, Anna Kopczak, Adrian-Minh Schumacher

Publikováno v: Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-4 (2017)
Endocrinology, Diabetes & Metabolism Case Reports

Summary The autoimmune polyendocrinopathy–candidiasis–ectodermal dystrophy (APECED) syndrome is a genetic disorder caused by a mutation in the autoimmune regulator (AIRE) gene. Immune deficiency, hypoparathyroidism and Addison’s disease due to

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4b31bdcb3ce6b2661b4e475afad7cb4
https://doi.org/10.1530/edm-17-0010

Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation

Autor: Uwe K. Zettl, Michael Pütz, Rajesh Rawal, Frauke Zipp, Martin Stangel, Ulf Schminke, Marcus Ising, Martina Müller-Nurasyid, Heinz Wiendl, Jürgen Haas, Thomas Meitinger, Michael Hecker, Wolfgang Lieb, Magdalena Zoledziewska, Tania Carrillo-Roa, Ulf Ziemann, S. Nischwitz, Stefan Herms, Maristella Pitzalis, Stefan Kloiber, Frank Weber, Hayrettin Tumani, Bertram Müller-Myhsok, Sven G. Meuth, Georg Homuth, Ralf Gold, M. Knop, Antonella Mulas, Christina M. Lill, Henry Völzke, Antonios Bayas, Francesco Cucca, Eleonora Porcu, Andrew T. Chan, Janine Arloth, Lukas Bechmann, Darina Czamara, Dorothea Buck, Klaus Berger, Peter Lichtner, Jürgen Wellmann, Susanne Moebus, Andre Franke, Florian Then Bergh, Peter Weber, Thomas Bettecken, Ilenia Zara, Till F. M. Andlauer, Volker Limmroth, Achim Berthele, Ralf A. Linker, Tobias Ruck, Anke Salmen, Matthias Laudes, Gisela Antony, Christiane Graetz, Christian Gieger, Konstantin Strauch, Astrid Petersmann, Elisabeth B. Binder, Melanie Waldenberger, Christiane Gasperi, Carlo Sidore, Brigitte Wildemann, Friedemann Paul, Felix Luessi, Bernhard Hemmer, Klarissa Hanja Stürner, Karl-Heinz Jöckel, Milena Radivojkov-Blagojevic, Björn Tackenberg, Tim Kacprowski, Lars Bertram, Clemens Warnke, Markus O. Scheinhardt, Theresa Dankowski, Verena Loleit, Tania Kümpfel, Carmen Infante-Duarte, Susanne Lucae, Markus M. Nöthen, Jan-Patrick Stellmann, Mark Mühlau, Andreas Ziegler

Publikováno v: Sci. Adv. 2:e1501678 (2016)
Science advances
Andlauer, Till F M; Buck, Dorothea; Antony, Gisela; Bayas, Antonios; Bechmann, Lukas; Berthele, Achim; Chan, Andrew; Gasperi, Christiane; Gold, Ralf; Graetz, Christiane; Haas, Jürgen; Hecker, Michael; Infante-Duarte, Carmen; Knop, Matthias; Kümpfel, Tania; Limmroth, Volker; Linker, Ralf A; Loleit, Verena; Luessi, Felix; Meuth, Sven G; ... (2016). Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation. Science Advances, 2(6), e1501678. American Association for the Advancement of Science 10.1126/sciadv.1501678
Science Advances

Genome-wide study in Germans identifies four novel multiple sclerosis risk genes and confirms already known gene loci.
We conducted a genome-wide association study (GWAS) on multiple sclerosis (MS) susceptibility in German cohorts with 4888 case

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09024c9b9a0412f283b1b4db24ebb8ef
http://hdl.handle.net/10044/1/39479

More CLEC16A gene variants associated with multiple sclerosis

Autor: S. Nischwitz, F. Müller-Sarnowski, Christiane Wolf, Bertram Müller-Myhsok, Hildegard Pfister, Thomas Bettecken, Marcus Ising, Peter Rieckmann, M. Knop, Frank Weber, Florian Holsboer, Antje Kroner, Sabine Cepok, Manfred Uhr, Bernhard Hemmer

Publikováno v: Acta Neurologica Scandinavica. 123:400-406

Nischwitz S, Cepok S, Kroner A, Wolf C, Knop M, Muller-Sarnowski F, Pfister H, Rieckmann P, Hemmer B, Ising M, Uhr M, Bettecken T, Holsboer F, Muller-Myhsok B, Weber F. More CLEC16A gene variants associated with multiple sclerosis. Acta Neurol Scand:

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::296d222d3fd626c5736bab18d7c59712
https://doi.org/10.1111/j.1600-0404.2010.01421.x