Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Sylvia Stemberger"'
Autor:
Sylvia Stemberger, Angelika Jamnig, Nadia Stefanova, Günter Lepperdinger, Markus Reindl, Gregor K Wenning
Publikováno v:
PLoS ONE, Vol 6, Iss 5, p e19808 (2011)
Mesenchymal stem cells (MSC) are currently strong candidates for cell-based therapies. They are well known for their differentiation potential and immunoregulatory properties and have been proven to be potentially effective in the treatment of a larg
Externí odkaz:
https://doaj.org/article/b575624d72e4474a8c15218df48bd7a0
Publikováno v:
Experimental Neurology
Multiple system atrophy (MSA) is a rare neurodegenerative disease of undetermined cause manifesting with progressive autonomic failure (AF), cerebellar ataxia and parkinsonism due to neuronal loss in multiple brain areas associated with (oligodendro)
Autor:
Daniela, Kuzdas, Sylvia, Stemberger, Stefano, Gaburro, Nadia, Stefanova, Nicolas, Singewald, Gregor K, Wenning
Publikováno v:
Experimental Neurology
Multiple system atrophy (MSA) is a fatal, rapidly progressive neurodegenerative disease with limited symptomatic treatment options. Discrimination of MSA from other degenerative disorders crucially depends on the presence of early and severe cardiova
Autor:
Philipp Mahlknecht, Johannes Rainer, Werner Poewe, Markus Reindl, Christoph Grabmer, Sylvia Stemberger, Gregor K. Wenning, Eva Hametner, Rudolf Kirchmair, Christoph Scherfler, Fabienne Sprenger, Klaus Seppi
Publikováno v:
Proteome Science
Proteome Science, Vol 10, Iss 1, p 71 (2012)
Proteome Science, Vol 10, Iss 1, p 71 (2012)
Background Microarray technology may offer a new opportunity to gain insight into disease-specific global protein expression profiles. The present study was performed to apply a serum antibody microarray to screen for differentially regulated cytokin
Autor:
Ana P.L. Abdala, David H. Adams, Marlies Alvarenga, Amy C. Arnold, Felicia B. Axelrod, Franca Barbic, Peter J. Barnes, Deborah Bauer, Christopher Bell, Eduardo E. Benarroch, Elizabeth M. Berry-Kravis, Luciano Bernardi, Italo Biaggioni, Lori Birder, Virginia L. Brooks, Joan Heller Brown, Geoffrey Burnstock, Michael Camilleri, J.Preston Campbell, Robert M. Carey, Marc G. Caron, Calvin Carter, Priscila A. Cassaglia, Javier G. Castillo, Mark W. Chapleau, Nisha Charkoudian, P. David Charles, Gisela Chelimsky, Thomas Chelimsky, Pei-Wen Cheng, Gilles Clément, Pietro Cortelli, Allen W. Cowley, Leslie Crews, Stephen N. Davis, Thomas L. Davis, William C. de Groat, Vincent G. DeMarco, André Diedrich, Donald J. DiPette, Debra I. Diz, Marcus J. Drake, Rachel C. Drew, Matthias Dütsch, Graeme Eisenhofer, Florent Elefteriou, Fernando Elijovich, Brett A. English, Murray Esler, John Y. Fang, Robert D. Fealey, Stanley Fernandez, Gregory D. Fink, John S. Floras, Roy Freeman, Qi Fu, Liang-Wu Fu, Raffaello Furlan, Alfredo Gamboa, Emily M. Garland, Christopher H. Gibbons, Michael P. Gilbey, Janice L. Gilden, Sid Gilman, David S. Goldstein, Diego A. Golombek, Robert M. Graham, Guido Grassi, Mark D. Grier, Jan T. Groothuis, Blair P. Grubb, Maureen K. Hahn, Julian P.J. Halcox, Robert W. Hamill, Kenneth R. Hande, Yadollah Harati, David G. Harrison, Emma C. Hart, Jacqui Hastings, Luke A. Henderson, Max J. Hilz, Robert Hoeldtke, Shung Tai Ho, Peter Hunter, Keith Hyland, Lauren Hyland, Shahram Izadyar, Joseph L. Izzo, Edwin K. Jackson, Giris Jacob, Wilfrid Jänig, Megan S. Johnson, Carrie K. Jones, James F.X. Jones, Karen M. Joos, Jens Jordan, Michael J. Joyner, Stephen G. Kaler, Sergey Kasparov, Horacio Kaufmann, David Kaye, Ramesh K. Khurana, Chun-Hyung Kim, Kwang-Soo Kim, Kazuto Kobayashi, Nancy L. Kuntz, Tomas Konecny, Andrew Kontak, Cheryl L. Laffer, Andre H. Lagrange, Nora Laiken, Gavin Lambert, Jacques W.M. Lenders, Benjamin D. Levine, Lewis A. Lipsitz, Julian H. Lombard, John C. Longhurst, David A. Low, Phillip A. Low, Chih Cherng Lu, James M. Luther, Vaughan G. Macefield, Belinda H. McCully, James G. McLeod, William M. Manger, Tadaaki Mano, Paul J. Marvar, Eliezer Masliah, Christopher J. Mathias, Mark R. Melson, Douglas F. Milam, Marion C. Mohl, Yaroslav I. Molkov, Margaret Morris, Shaun F. Morrison, Toshiharu Nagatsu, Charles D. Nichols, Lucy Norcliffe-Kaufmann, Vera Novak, Luis E. Okamoto, John W. Osborn, Brian A. Parsons, Julian F.R. Paton, Pallavi P. Patwari, Cecile L. Phan, Fenna T. Phibbs, Nanduri R. Prabhakar, Amanda C. Peltier, Sean M. Peterson, Anthony E Pickering, J.Howard Pratt, Kamal Rahmouni, Satish R. Raj, Casey M. Rand, Heinz Reichmann, Jeff Richards, L.Jackson Roberts, David W. Robertson, Rose Marie Robertson, Michael Robinson, Ilya A. Rybak, Elaine Sanders-Bush, Paola Sandroni, Kyoko Sato, Takayuki Sato, Irwin J. Schatz, Ernesto L. Schiffrin, Ronald Schondorf, Rosemary Schwarz, Gino Seravalle, Robert E. Shapiro, Cyndya Shibao, Virend Somers, Michaela Stampfer, C.Michael Stein, Sylvia Stemberger, Julian Stewart, Lawrence I. Sinoway, James R. Sowers, Sirisha Srikakarlapudi, Kenji Sunagawa, Scott C. Supowit, Palmer Taylor, Jane Thompson, Roland D. Thijs, Rhian M Touyz, Daniel Tranel, Subbulaxmi Trikudanathan, Ching-Jiunn Tseng, Che-Se Tung, Kiren Ubhi, Nikhil Urs, Joseph G. Verbalis, Steven Vernino, Ronald G. Victor, Margaret A. Vizzard, Wanpen Vongpatanasin, B.Gunnar Wallin, Tobias Wang, Qin Wang, Andrew A. Webster, Debra E. Weese-Mayer, Gregor K. Wenning, Adam Whaley-Connell, Wouter Wieling, Gordon H. Williams, Scott Wood, Michael G. Ziegler, Daniel B. Zoccal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::339751ee66d6eee5a7316633f4b04b2f
https://doi.org/10.1016/b978-0-12-386525-0.00149-9
https://doi.org/10.1016/b978-0-12-386525-0.00149-9
Autor:
Gregor K. Wenning, Sylvia Stemberger
Publikováno v:
Journal of neural transmission (Vienna, Austria : 1996). 118(5)
Multiple system atrophy (MSA) is a fatal late-onset α-synucleinopathy that presents with features of ataxia, Parkinsonism, and pyramidal dysfunction in any combination. Over the last decade, efforts have been made to develop preclinical MSA testbeds
Publikováno v:
Neurobiology of Aging
Multiple system atrophy (MSA) is a fatal oligodendrogliopathy characterized by prominent α-synuclein inclusions resulting in a neuronal multisystem degeneration. Until recently MSA was widely conceived as a nongenetic disorder. However, during the l