Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Thorsten Schulte"'
Autor:
Valerie Apell, Thorsten Schulte
Publikováno v:
CSR in Hessen ISBN: 9783662630037
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d298c8d47cf7a43c3246b1bd57e8cbaf
https://doi.org/10.1007/978-3-662-63004-4_16
https://doi.org/10.1007/978-3-662-63004-4_16
Autor:
Thorsten Schulte
Marketing ist Krieg! Krieg um das knappe Gut Aufmerksamkeit beim Kunden. Der Feind ist der Wettbewerb und der Kunde ist das Terrain, welches es zu erobern gilt. Guerilla Krieg ist eine echte strategische Alternative! Dieses Buch liefert Ihnen das nö
Autor:
Thorsten Schulte
Dieses Buch ist ein Warnruf an alle Europäer! Kurt Tucholsky schrieb 1931:'Das Volk versteht das meiste falsch; aber es fühlt das meiste richtig.'Immer mehr Menschen fühlen, dass die Zukunft Deutschlands und Europas in Gefahr ist, verstehen jedoch
Autor:
Thomas Müller, Horst Przuntek, Kerstin Hellwig, Thorsten Schulte, Birgit Voss, Franz Josef Stein
Publikováno v:
CNS Drugs. 18:105-111
Objective: In some countries, such as Germany, there has been a move towards the treatment of patients with Parkinson’s disease in specialised inpatient units. However, data on patient outcome and the daily costs of antiparkinsonian drugs in these
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3a786247c701c1da1e9b372a12b96c8
https://doi.org/10.2165/00023210-200418020-00004
https://doi.org/10.2165/00023210-200418020-00004
Autor:
Klaus Berger, Jörg T. Epplen, C. Fischer, Horst Przuntek, Stefan Böhringer, Thorsten Schulte, Rejko Krüger, Thomas Müller, Olaf Riess, Ludger Schöls
Publikováno v:
Scopus-Elsevier
Aspartyl protease Cathepsin D (CTSD) has been suggested to play a role in the pathogenesis of sporadic Alzheimer's disease (AD) due to interference with protein degradation mechanisms. A C224T (A38V) polymorphism in exon 2 of the CTSD gene is reporte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6b1f5fd809e8db341538fef996fbb53
https://doi.org/10.1007/s00702-003-0832-x
https://doi.org/10.1007/s00702-003-0832-x
Autor:
Ingrid Bauer, Katrin Bürk, Christina Kölmel, Olaf Riess, Ludger Schöls, Peter Bauer, Horst Przuntek, Christine Zühlke, Thorsten Schulte, Helge Topka
Publikováno v:
Annals of Neurology. 54:110-115
To evaluate the significance of expanded CTG repeats at the SCA8 locus, we analyzed the allele distribution in 1,262 German ataxia patients. We found intermediate and expanded CTG repeats with similar frequencies in ataxia patients with and without e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7890d71d7feebbfef0f0b698e9d2eb48
https://doi.org/10.1002/ana.10608
https://doi.org/10.1002/ana.10608
Autor:
Thorsten Schulten, Torsten Müller
Publikováno v:
Italian Labour Law e-Journal, Vol 14, Iss 1, Pp 1-19 (2021)
In autumn 2020, the European Commission published a proposal for a "Directive on adequate minimum wages in the European Union". For the first time in the history of the EU, draft legislation is on the table which explicitly aims not only to significa
Externí odkaz:
https://doaj.org/article/f9a099af4cf14b30b60c540906c5bfbf
Publikováno v:
Neuroscience Letters. 326:70-72
Several lines of evidence indicate that immune mechanisms are involved in the pathogenesis of neurodegenerative disorders. Activated immunocompetent cells and inflammatory cytokines are present in affected brain regions in patients with Alzheimer's (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f6eb4dd45ce1e11b76e9eda6c1b56b4
https://doi.org/10.1016/s0304-3940(02)00301-4
https://doi.org/10.1016/s0304-3940(02)00301-4
Autor:
Kathrin, Grundmann, Ulrike, Laubis-Herrmann, Dirk, Dressler, Juliane, Vollmer-Haase, Peter, Bauer, Manfred, Stuhrmann, Thorsten, Schulte, Ludger, Schöls, Helge, Topka, Olaf, Riess
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 19(11)
Primary dystonias represent a clinically and genetically heterogeneous group of movement disorders. Mutations in the epsilon-sarcoglycan (SGCE) gene have been found recently to cause myoclonus-dystonia (MD). Considerable clinical variation of SGCE mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4bf0713c5b9ac3ea16e0f0e1b7bb1775
https://pubmed.ncbi.nlm.nih.gov/15390016
https://pubmed.ncbi.nlm.nih.gov/15390016