Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Ewald Auer"'
Autor:
Naira P Martínez Vera, Reinhold Schmidt, Klaus Langer, Iavor Zlatev, Robert Wronski, Ewald Auer, Daniel Havas, Manfred Windisch, Hagen von Briesen, Sylvia Wagner, Julia Stab, Motti Deutsch, Claus Pietrzik, Franz Fazekas, Stefan Ropele
Publikováno v:
PLoS ONE, Vol 9, Iss 3, p e92068 (2014)
This study was performed to explore the feasibility of tracing nanoparticles for drug transport in the healthy rat brain with a clinical MRI scanner. Phantom studies were performed to assess the R1 ( = 1/T1) relaxivity of different magnetically label
Externí odkaz:
https://doaj.org/article/d4e3429bf71e4b1b9db56514734a1b24
Publikováno v:
Molecular Genetics and Metabolism. 138:107014
Publikováno v:
Molecular Genetics and Metabolism. 138:107307
Autor:
Tina Loeffler, Livia Breznik, Ewald Auer, Irene Schilcher, Birgit Hutter-Paier, Manuela Prokesch
Publikováno v:
Molecular Genetics and Metabolism. 135:S75
Publikováno v:
Molecular Genetics and Metabolism. 132:S65-S66
Autor:
Joerg Neddens, Vera Niederkofler, Magdalena Temmel, Victoria Schiffer, Birgit Hutter-Paier, Ewald Auer
Publikováno v:
Molecular Genetics and Metabolism. 129:S116-S117
Publikováno v:
Molecular Genetics and Metabolism. 132:S30
Autor:
Joerg Neddens, Balázs Dobrovich, Robert Zimmermann, Birgit Hutter-Paier, Stefanie Flunkert, Meritxell Aguilo, Ewald Auer
Publikováno v:
Alzheimer's & Dementia. 14
Publikováno v:
Molecular Genetics and Metabolism. 126:S108-S109
Gaucher disease is the most prevalent lysosomal storage disorder and is caused by autosomal recessive mutations in the glucocerebrosidase gene. Glucocerebrosidase (GCase) hydrolyses the sphingolipid glucoceramide to glucose and ceramide. Deficiency i
Autor:
Roland Rabl, David Amschl, Birgit Hutter-Paier, Ewald Auer, Joerg Neddens, Stephan Duller, Vera Niederkofler, Stefanie Flunkert
Publikováno v:
Molecular Genetics and Metabolism. 123:S46-S47