Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Jürgen, Menzel"'
Publikováno v:
Tempo e Argumento, Vol 8, Iss 18, Pp 470-487 (2016)
Jürgen e Uta Menzel nasceram em Berlim, na República Democrática Alemã (RDA), e por lá viveram mais de 30 anos, até a queda do Muro, em 9 de novembro de 1989 . Uta Menzel nasceu em 1957, formou-se em economia do povo e atualmente trabalha como
Autor:
Hans-Jürgen Menzel, Ulrich Schwevers, Christof Neumann, Peter Oberle, Mark Musall, Jochen Riesterer, Franz Nestmann, Boris Lehmann, Frank Seidel, Katrin Läkemäker, Beate Adam, Markus Faller, Stefan Gischkat, Henrik Hufgard, Sven Löwenberg, Nicola Mast
Publikováno v:
Biologische Durchgängigkeit von Fließgewässern ISBN: 9783658139896
Angesichts der Vielzahl bestehender Querbauwerke, die ein Wanderhindernis fur stromaufwarts ziehende Fisch e bilden, leistet der Bau funktionsfahiger Fisch auf stiegs anlagen einen wertvollen Beitrag zur okologischen Aufwertung der Fliesgewassersyste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac510e33cdda5c3cd12c8eb11aa093bc
https://doi.org/10.1007/978-3-658-13990-2_5
https://doi.org/10.1007/978-3-658-13990-2_5
Rahmenbedingungen für den Bau Europas größter Fischaufstiegsanlage am Nordufer des Wehres Geesthacht
Autor:
Hans-Jürgen Menzel, Ulrich Schwevers
Publikováno v:
WASSERWIRTSCHAFT. 102:12-17
Autor:
Ulrich Schwevers, Hans-Jürgen Menzel
Publikováno v:
WASSERWIRTSCHAFT. 102:58-63
Autor:
Judith Löffler, Helen Mundy, John Burn, Gerd Utermann, M Krajewska-Walasek, Gabriele Gillessen-Kaesbach, Udo Seedorf, Peter E. Clayton, Hans-Jürgen Menzel, Georg F. Hoffmann, Barbara U. Fitzky, Martina Witsch-Baumgartner, Elżbieta Ciara, Richard I. Kelley
Publikováno v:
European Journal of Human Genetics. 9:45-50
Smith-Lemli-Opitz syndrome/RSH (SLOS) is a multiple congenital anomaly syndrome caused by mutations in the gene for Delta7-sterol reductase (DHCR7) which catalyses the last step in the biosynthesis of cholesterol. SLOS is among the common recessive d
Autor:
Florian Kronenberg, Hans-Jürgen Menzel, Martina F. Kronenberg, Gregor K. Wenning, Gerd Utermann, Werner Poewe, E. Luginger, Martin Gollner, Gerhard Ransmayr, Georg Ebersbach
Publikováno v:
European Journal of Human Genetics. 7:397-400
Patients with idiopathic Parkinson's disease (IPD) are described as having markedly decreased novelty seeking characteristics. Since recent publications suggest an association between the dopamine D4 receptor polymorphism and novelty seeking, we inve
Publikováno v:
Human Molecular Genetics. 7:257-264
Lipoprotein(a) [Lp(a)] is a quantitative genetic trait in human plasma associated with atherothrombotic disease. The major determinant of Lp(a) concentration is the apolipoprotein(a) [apo(a)] gene locus. Variation in the number of kringle IV repeats
Autor:
Hans-Jürgen Menzel, Ole Faergeman, Maryvonne Rosseneu, I. C. Klausen, Viviane Nicaud, Ulrike Beisiegel
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 15:1001-1008
Abstract In the European Atherosclerosis Research Study, genetic and environmental markers of risk of premature coronary heart disease were compared in offspring of men with and without myocardial infarction before the age of 55 years. Cases were 682
Autor:
Bertil, Bouillon, Markus, Raum, Hagen, Fach, Bettina, Buchheister, Rolf, Lefering, Jürgen, Menzel, Norfried, Klug
Publikováno v:
Restorative neurology and neuroscience. 14(2)
Epidemiological data on the incidence, the prehospital and hospital care and the outcome of traumatic brain injury in Germany are scarce. It is therefore difficult to estimate the importance of this injury with respect to magnitude as well as effecti
Autor:
Laurence Tiret, P. de Knijff, Hans-Jürgen Menzel, H. Tenkanen, Maryvonne Rosseneu, Christian Ehnholm, L.M. Havekes
Publikováno v:
Atherosclerosis. 107:229-238
As a part of the EARS study we assessed the role of the common apo A-IV polymorphism in determining the hereditary predisposition to cardiovascular disease. The study population consisted of 1261 controls and 629 cases (students whose father had MI b