Výsledky vyhledávání - Ohlraun, Stephanie

Efficacy of Vitamin D Supplementation in Multiple Sclerosis (EVIDIMS Trial): study protocol for a randomized controlled trial Autor Dörr, Jan, Ohlraun, Stephanie, Skarabis, Horst, Paul, Friedemann

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Trichuris suis ova in relapsing-remitting multiple sclerosis and clinically isolated syndrome (TRIOMS): study protocol for a randomized controlled trial Autor Rosche, Berit, Wernecke, Klaus-Dieter, Ohlraun, Stephanie, Dörr, Jan-Markus, Paul, Friedemann

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Pregnancy in Multiple Sclerosis: A Questionnaire Study Autor Borisow, Nadja, Paul, Friedemann, Ohlraun, Stephanie, Pach, Daniel, Fischer, Felix, Dörr, Jan

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CARbon DIoxide for the treatment of Febrile seizures: rationale, feasibility, and design of the CARDIF-study Autor Ohlraun, Stephanie, Wollersheim, Tobias, Weiß, Claudia, Martus, Peter, Weber-Carstens, Steffen, Schmitz, Dietmar, Schuelke, Markus

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Efficacy of vision restoration therapy after optic neuritis (VISION study): study protocol for a randomized controlled trial Autor Schinzel, Johann, Schwarzlose, Lina, Dietze, Holger, Bartusch, Karolina, Weiss, Susanne, Ohlraun, Stephanie, Paul, Friedemann, Dörr, Jan

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Tracking the timely dissemination of clinical studies. Characteristics and impact of 10 tracking variables Autor Strech, Daniel, Sievers, Sören, Märschenz, Stefanie, Riedel, Nico, Wieschowski, Susanne, Meerpohl, Jörg, Langhof, Holger, Müller-Ohlraun, Stephanie, Dirnagl, Ulrich

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Assessing the Organizational Climate for Translational Research with a New Survey Tool Autor Simons, Arno, Riedel, Nico, Toelch, Ulf, Hendriks, Barbara, Müller-Ohlraun, Stephanie, Liebenau, Lisa, Ambrasat, Jens, Dirnagl, Ulrich, Reinhart, Martin

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The DTNBP1 (Dysbindin) Gene Contributes to Schizophrenia, Depending on Family History of the Disease Autor Van Den Bogaert, Ann, Schumacher, Johannes, Schulze, Thomas G., Otte, Andreas C., Ohlraun, Stephanie, Kovalenko, Svetlana, Becker, Tim, Freudenberg, Jan, Jönsson, Erik G., Mattila-Evenden, Marja, Sedvall, Göran C., Czerski, Piotr M., Kapelski, Pawel, Hauser, Joanna, Maier, Wolfgang, Rietschel, Marcella, Propping, Peter, Nöthen, Markus M., Cichon, Sven

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Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage... Autor Etain, Bruno, Mathieu, Flavie, Rietschel, Marcella, Maier, Wolfgang, Albus, Margot, Mckeon, Patrick, Roche, S., Kealey, Carmel, Blackwood, Douglas, Muir, Walter, Bellivier, Franc, Henry, C., Dina, Christian, Gallina, Sophie, Gurling, H., Malafosse, Alain, Preisig, Martin, Ferrero, François, Cichon, Sven, Schumacher, J., Ohlraun, Stéphanie, Borrmann-Hassenbach, M., Propping, Peter, Abou Jamra, Rami, Schulze, Thomas G., Marusic, Andrej, Dernovsek, Mojca Z., Giros, Bruno, Bourgeron, Thomas, Lemainque, Arnaud, Bacq, Delphine, Betard, Christine, Charon, Céline, Nöthen, Markus M., Lathrop, Mark, Leboyer, Marion

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Genomewide Scan and Fine-Mapping Linkage Studies in Four European Samples with Bipolar Affective Disorder Suggest a New Susceptibility Locus on Chromosome 1p35-p36 and Provides Fur... Autor Schumacher, Johannes, Kaneva, Radka, Jamra, Rami Abou, Diaz, Guillermo Orozco, Ohlraun, Stephanie, Milanova, Vihra, Lee, Young-Ae, Rivas, Fabio, Mayoral, Fermin, Fuerst, Robert, Flaquer, Antonia, Windemuth, Christine, Gay, Eudoxia, Sanz, Sebastian, González, Maria José, Gil, Susana, Cabaleiro, Francisco, del Rio, Francisco, Perez, Fermin, Haro, Jesus, Kostov, Christian, Chorbov, Vesselin, Nikolova-Hill, Amelia, Stoyanova, Vessela, Onchev, George, Kremensky, Ivo, Strauch, Konstantin, Schulze, Thomas G., Nürnberg, Peter, Gaebel, Wolfgang, Klimke, Ansgar, Auburger, Georg, Wienker, Thomas F., Kalaydjieva, Luba, Propping, Peter, Cichon, Sven, Jablensky, Assen, Rietschel, Marcella, Nöthen, Markus M.

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