Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Bettina Göricke"'
Autor:
Payam Dibaj, Jana Zschüntzsch, Heinz Steffens, Jörg Scheffel, Bettina Göricke, Jochen H Weishaupt, Karim Le Meur, Frank Kirchhoff, Uwe-Karsten Hanisch, Eike D Schomburg, Clemens Neusch
Publikováno v:
PLoS ONE, Vol 7, Iss 8, p e43963 (2012)
Mutations in SOD1 cause hereditary variants of the fatal motor neuron disease amyotrophic lateral sclerosis (ALS). Pathophysiology of the disease is non-cell-autonomous, with toxicity deriving also from glia. In particular, microglia contribute to di
Externí odkaz:
https://doaj.org/article/2e89c0240a874299be60915d21fe406b
Autor:
Albert C Ludolph, Joachim Schuster, Johannes Dorst, Luc Dupuis, Jens Dreyhaupt, Jochen H Weishaupt, Jan Kassubek, Ulrike Weiland, Susanne Petri, Thomas Meyer, Julian Grosskreutz, Berthold Schrank, Matthias Boentert, Alexander Emmer, Andreas Hermann, Daniel Zeller, Johannes Prudlo, Andrea S Winkler, Torsten Grehl, Michael T Heneka, Siw Wollebæk Johannesen, Bettina Göricke, Andreas Funke, Dagmar Kettemann, Robert Meyer, Kai Gruhn, Peter Schwenkreis, Philipp Stude, Delia Kurzwelly, Alexander Storch, Nicole Richter, Tobias Frank, Katharina Hein, Frank Hanisch, Dagmar Hanke, Torsten Kraya, Andreas Posa, Martina Romanakova, Susanne Schilling, Susanne Abdulla, Sebastian Böselt, Claas Janssen, Imken Lange, Xenia Kobeleva, Sonja Körner, Katja Kollewe, Alma Osmanovic, Nicole Scharn, Klaus J Rath, Christiane Dahms, Anne Gunkel, Bianka Heiling, Thomas Ringer, Uta Smesny, Sarah Baumeister, Achim Berthele, Sarah Bublitz, Esra Akova-Öztürk, Bianca Stubbe-Dräger, Alexandra Rahmann, Charlotte Young, Peter Young, Dobri Baldaranov, Ulrich Bogdahn, Andrei Khomenko, Wilhelm Schulte-Mattler, Christina Stadler, Susanne Husung, Simone Tesar, Nigar Dargah-Zaden, Christina Last, Eva Langer, Ann-Sophie Lauenstein, Eckard Lensch, Carolyn Mc Farlane, Heike Fischer-Brasse, Klara Orbán, Bertold Schrank, Sonja Schürger, Stephan Klebe, Peter Kraft, Thomas Musacchio, Carola Seiler
Publikováno v:
The Lancet Neurology
The Lancet Neurology, Elsevier, 2018, 17 (8), pp.681-688. ⟨10.1016/S1474-4422(18)30176-5⟩
The Lancet Neurology, 2018, 17 (8), pp.681-688. ⟨10.1016/S1474-4422(18)30176-5⟩
The Lancet Neurology, Elsevier, 2018, 17 (8), pp.681-688. ⟨10.1016/S1474-4422(18)30176-5⟩
The Lancet Neurology, 2018, 17 (8), pp.681-688. ⟨10.1016/S1474-4422(18)30176-5⟩
International audience; Background: Rasagiline, a monoamine oxidase B inhibitor with neuroprotective potential in Parkinson's disease, has shown a disease-modifying effect in the SOD1-Gly93Ala low-expressing mouse model of amyotrophic lateral scleros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b70e9f6bbf70e7d2a063a95b23e7ffaa
https://doi.org/10.1016/s1474-4422(18)30176-5
https://doi.org/10.1016/s1474-4422(18)30176-5
Autor:
Christoph van Riesen, Vesna Malinova, Dorothee Mielke, Meike Bettina Göricke, Hanna J. Eisenberg, Mathias Bähr
Publikováno v:
Movement Disorders Clinical Practice
Movement disorders clinical practice 8(1), 142-144 (2021). doi:10.1002/mdc3.13076
Movement disorders clinical practice 8(1), 142-144 (2021). doi:10.1002/mdc3.13076
ADCY5 mutations cause early-onset hyperkinetic movement disorders.1 A wide range of phenotypic presentations has been described in pediatric and adult patients including delayed psychomotor development and axial hypotonia as well as generalized myocl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3540c25b953a9b1707a589fd7c785e50
http://europepmc.org/articles/PMC7780953
http://europepmc.org/articles/PMC7780953
Autor:
Adrienne Heyduck, Bettina Göricke, Deike Adamske, Matthias Weidenmüller, Tobias Frank, Arno Olthoff
Publikováno v:
Journal of oral rehabilitationReferences. 48(9)
Background Dysphagia as a sequel and possible early sign of amyotrophic lateral sclerosis (ALS) is caused by progressive impaired bulbar motor function. Objective To evaluate bulbar motor dysfunction in patients suffering from ALS compared to a healt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::429632910e25efe00b489a74b0dba082
https://pubmed.ncbi.nlm.nih.gov/34185922
https://pubmed.ncbi.nlm.nih.gov/34185922
Autor:
Christian Kubisch, Sibylle Jablonka, Petra Baum, Karin M Danzer, Susana Pinto, Stephan Zierz, Bettina Göricke, Daniel Zeller, Jürgen Winkler, Johannes Dorst, Ulrich Bogdahn, Markus Weber, Heiko Braak, Joachim Weis, Kathrin Muller, Susanne Petri, Peter M. Andersen, Kornelia Günther, Mamede de Carvalho, Markus Otto, Wolfgang Ruf, Angela Rosenbohm, Berthold Schrank, Christoph Neuwirth, Kelly Del Tredici, Thomas Meitinger, Axel Freischmidt, Julian Grosskreutz, Thomas F. Meyer, Antje Knehr, Ute Weyen, Albert C. Ludolph, Andreas Hermann, David A. Brenner, Peter Young, Jochen H. Weishaupt, Jan C. Koch, Patrick Weydt, Alexander E Volk, Torsten Grehl, Thomas Klopstock, Joachim Schuster, Berit Jordan, Tim Hagenacker, Andrea Sylvia Winkler, Paul Lingor, Jan Kassubek, Joachim Wolf, Anne D. Sperfeld, Guntram Borck, Michael Sendtner, Rüstem Yilmaz, Annemarie Hübers, Kristl G. Claeys, Johannes Prudlo
Publikováno v:
Brain 142(12), e67-e67 (2019). doi:10.1093/brain/awz306
Reply : Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2aaab4bd734052271cfbd00205a0d265
https://pubmed.ncbi.nlm.nih.gov/31612903
https://pubmed.ncbi.nlm.nih.gov/31612903
Autor:
Rüstem Yilmaz, Kathrin Müller, David Brenner, Alexander E. Volk, Guntram Borck, Andreas Hermann, Thomas Meitinger, Tim M. Strom, Karin M. Danzer, Albert C. Ludolph, Peter M. Andersen, Jochen H. Weishaupt, Ute Weyen, Martin Regensburger, Jürgen Winkler, Ralf Linker, Beate Winner, Tim Hagenacker, Jan Christoph Koch, Paul Lingor, Bettina Göricke, Stephan Zierz, Berit Jordan, Petra Baum, Joachim Wolf, Andrea Winkler, Peter Young, Ulrich Bogdahn, Johannes Prudlo, Jan Kassubek
Publikováno v:
Neurobiology of aging 87, 139.e9-139.e15 (2020). doi:10.1016/j.neurobiolaging.2019.10.018
Several studies reported amyotrophic lateral sclerosis (ALS)-linked mutations in TBK1, OPTN, VCP, UBQLN2, and SQSTM1 genes encoding proteins involved in autophagy. SQSTM1 was originally identified by a candidate gene approach because it encodes p62,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c53dec8ded6f5d1039a7895c26f1b380
https://doi.org/10.1016/j.neurobiolaging.2019.10.018
https://doi.org/10.1016/j.neurobiolaging.2019.10.018
Autor:
Sergey Ryazanov, Song Shi, Hans A. Kretzschmar, Wolfgang Zinth, Andrei Leonov, Martin Fuhrmann, Carolin Miklitz, Armin Giese, Daniel Weckbecker, Dan Ehninger, Bettina Göricke, Anne Reiner, Julia Steffen, Jens Wagner, Jochen H. Weishaupt, Alexander Kleinknecht, Johannes Levin, Stefan Remy, Christian Griesinger, Sybille Krauss
Publikováno v:
Acta Neuropathologica
Acta neuropathologica 130(5), 619-631 (2015). doi:10.1007/s00401-015-1483-3
Acta neuropathologica 130(5), 619-631 (2015). doi:10.1007/s00401-015-1483-3
Pathological tau aggregation leads to filamentous tau inclusions and characterizes neurodegenerative tauopathies such as Alzheimer’s disease and frontotemporal dementia and parkinsonism linked to chromosome 17. Tau aggregation coincides with clinic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5d7327b3d660fae3c7d3a6ab97d5440
http://europepmc.org/articles/PMC4612332
http://europepmc.org/articles/PMC4612332
Autor:
Mathias Bähr, Herbert Desel, Bettina Göricke, David Liebetanz, Tobias Frank, Armin Schneider, Florian Klinker, Fred Lühder, Jochen H. Weishaupt, Björn H. Falkenburger, Hartmud Neurath, Rico Laage
Publikováno v:
Brain. 135:1914-1925
Recent proof-of-principle data showed that the haematopoietic growth factor granulocyte colony-stimulating factor (filgrastim) mediates neuroprotection in rodent models of Parkinson's disease. In preparation for future clinical trials, we performed a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8447b593b70054f5584b6e0ccea9ff3c
https://doi.org/10.1093/brain/aws054
https://doi.org/10.1093/brain/aws054
Autor:
Andreas Broocks, Guido Knapp, Carl Detlef Reimers, Iris Reuter, Barbara Tettenborn, Norbert Thürauf, Norbert Bachl, Mathias Bähr, Sophie Bischoff, Dorothea Frevel, Ansgar Felbecker, Tobias Frank, Marian Galovic, Katharina Gaudlitz, Markus Gerber, Burkhard Gess, Bettina Göricke, Manfred Holzgraefe, Andreas Janßen, Johannes Kornhuber, Herbert Löllgen, Mathias Mäurer, Anne K. Reimers, Niklas Reimers, Peter Rieckmann, Beate Schlotter-Weigel, Jens Schmidt, Sarah Schumacher, Wilfried Schupp, Arne Schwennicke, Marcel Sommer, Andreas Ströhle, Insa Wingendorf, Peter Young
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff0cf47a7d0ee02da9adab7ffc9136c3
https://doi.org/10.1016/b978-3-437-24265-6.01002-7
https://doi.org/10.1016/b978-3-437-24265-6.01002-7
The group of degenerative motor neuron diseases is characterized by a very heterogeneously caused degeneration of the first and/or second motor neuron. Disorders of this group are amyotrophic lateral sclerosis (ALS), postpoliomyelitis syndrome (PPS),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78ea2e958a6302ac0a347bab55acfe7f
https://doi.org/10.1016/b978-3-437-24265-6.00010-x
https://doi.org/10.1016/b978-3-437-24265-6.00010-x