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Journal Article
Wolf, Dominik, Tuescher, Oliver, Teipel, Stefan, Mierau, Andreas 
ORCID: 0000-0002-6305-3260, Strueder, Heiko, Drzezga, Alexander, Baier, Bernhard, Binder, Harald ORCID: 0000-0002-5666-8662 and Fellgiebel, Andreas
(2018).
Mechanisms and modulators of cognitive training gain transfer in cognitively healthy aging: study protocol of the AgeGain study.
Trials, 19.
LONDON:
BMC.
ISSN 1745-6215
Konstantinides, Stavros V., Barco, Stefano ORCID: 0000-0002-2618-347X, Rosenkranz, Stephan, Lankeit, Mareike ORCID: 0000-0001-5211-7997, Held, Matthias, Gerhardt, Felix, Bruch, Leonard, Ewert, Ralf, Faehling, Martin, Freise, Julia, Ghofrani, Hossein-Ardeschir, Gruenig, Ekkehard, Halank, Michael, Heydenreich, Nadine, Hoeper, Marius M., Leuchte, Hanno H., Mayer, Eckhard, Meyer, F. Joachim, Neurohr, Claus, Opitz, Christian, Pinto, Antonio, Seyfarth, Hans-Juergen, Wachter, Rolf ORCID: 0000-0003-2231-2200, Zaepf, Bianca, Wilkens, Heinrike ORCID: 0000-0002-7789-8563, Binder, Harald ORCID: 0000-0002-5666-8662 and Wild, Philipp S.
(2016).
Late outcomes after acute pulmonary embolism: rationale and design of FOCUS, a prospective observational multicenter cohort study.
J. Thromb. Thrombolysis, 42 (4).
S. 600 - 610.
DORDRECHT:
SPRINGER.
ISSN 1573-742X
Vogt, Johannes ORCID: 0000-0003-2439-8247, Yang, Jenq-Wei, Mobascher, Arian, Cheng, Jin, Li, Yunbo, Liu, Xingfeng, Baumgart, Jan ORCID: 0000-0003-1996-4267, Thalman, Carine, Kirischuk, Sergei, Unichenko, Petr, Horta, Guilherme, Radyushkin, Konstantin, Stroh, Albrecht, Richers, Sebastian, Sahragard, Nassim, Distler, Ute ORCID: 0000-0002-8031-6384, Tenzer, Stefan ORCID: 0000-0003-3034-0017, Qiao, Lianyong, Lieb, Klaus, Tuescher, Oliver, Binder, Harald ORCID: 0000-0002-5666-8662, Ferreiros, Nerea, Tegeder, Irmgard ORCID: 0000-0001-7524-8025, Morris, Andrew J., Gropa, Sergiu, Nuernberg, Peter, Toliat, Mohammad R., Winterer, Georg, Luhmann, Heiko J. ORCID: 0000-0002-7934-8661, Huai, Jisen and Nitsch, Robert
(2016).
Molecular cause and functional impact of altered synaptic lipid signaling due to a prg-1 gene SNP.
EMBO Mol. Med., 8 (1).
S. 25 - 39.
HOBOKEN:
WILEY.
ISSN 1757-4684