Inspiration is the major regulator of human CSF flow von Dreha-Kulaczewski, Steffi, Joseph, Arun A, Merboldt, Klaus-Dietmar, Ludwig, Hans-Christoph, Gärtner, Jutta, Frahm, Jens

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Trial of Fingolimod versus Interferon Beta-1a in Pediatric Multiple Sclerosis von Chitnis, Tanuja, Arnold, Douglas L, Banwell, Brenda, Brück, Wolfgang, Ghezzi, Angelo, Giovannoni, Gavin, Greenberg, Benjamin, Krupp, Lauren, Rostásy, Kevin, Tardieu, Marc, Waubant, Emmanuelle, Wolinsky, Jerry S, Bar-Or, Amit, Stites, Tracy, Chen, Yu, Putzki, Norman, Merschhemke, Martin, Gärtner, Jutta

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Deep breathing couples CSF and venous flow dynamics von Kollmeier, Jost M., Gürbüz-Reiss, Lukas, Sahoo, Prativa, Badura, Simon, Ellebracht, Ben, Keck, Mathilda, Gärtner, Jutta, Ludwig, Hans-Christoph, Frahm, Jens, Dreha-Kulaczewski, Steffi

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Therapy of highly active pediatric multiple sclerosis von Huppke, Peter, Huppke, Brenda, Ellenberger, David, Rostasy, Kevin, Hummel, Hannah, Stark, Wiebke, Brück, Wolfgang, Gärtner, Jutta

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Peroxisomal lactate dehydrogenase is generated by translational readthrough in mammals von Schueren, Fabian, Lingner, Thomas, George, Rosemol, Hofhuis, Julia, Dickel, Corinna, Gärtner, Jutta, Thoms, Sven

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Genetics of intellectual disability in consanguineous families von Hu, Hao, Kahrizi, Kimia, Musante, Luciana, Fattahi, Zohreh, Herwig, Ralf, Hosseini, Masoumeh, Oppitz, Cornelia, Abedini, Seyedeh Sedigheh, Suckow, Vanessa, Larti, Farzaneh, Beheshtian, Maryam, Lipkowitz, Bettina, Akhtarkhavari, Tara, Mehvari, Sepideh, Otto, Sabine, Mohseni, Marzieh, Arzhangi, Sanaz, Jamali, Payman, Mojahedi, Faezeh, Taghdiri, Maryam, Papari, Elaheh, Soltani Banavandi, Mohammad Javad, Akbari, Saeide, Tonekaboni, Seyed Hassan, Dehghani, Hossein, Ebrahimpour, Mohammad Reza, Bader, Ingrid, Davarnia, Behzad, Cohen, Monika, Khodaei, Hossein, Albrecht, Beate, Azimi, Sarah, Zirn, Birgit, Bastami, Milad, Wieczorek, Dagmar, Bahrami, Gholamreza, Keleman, Krystyna, Vahid, Leila Nouri, Tzschach, Andreas, Gärtner, Jutta, Gillessen-Kaesbach, Gabriele, Varaghchi, Jamileh Rezazadeh, Timmermann, Bernd, Pourfatemi, Fatemeh, Jankhah, Aria, Chen, Wei, Nikuei, Pooneh, Kalscheuer, Vera M., Oladnabi, Morteza, Wienker, Thomas F., Ropers, Hans-Hilger, Najmabadi, Hossein

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The expanding clinical and genetic spectrum of ATP1A3-related disorders von Rosewich, Hendrik, Ohlenbusch, Andreas, Huppke, Peter, Schlotawa, Lars, Baethmann, Martina, Carrilho, Inês, Fiori, Simona, Lourenço, Charles Marques, Sawyer, Sarah, Steinfeld, Robert, Gärtner, Jutta, Brockmann, Knut

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Efficacy and safety of ofatumumab in recently diagnosed, treatment-naive patients with multiple sclerosis: Results from ASCLEPIOS I and II von Gärtner, Jutta, Hauser, Stephen L, Bar-Or, Amit, Montalban, Xavier, Cohen, Jeffrey A, Cross, Anne H, Deiva, Kumaran, Ganjgahi, Habib, Häring, Dieter A, Li, Bingbing, Pingili, Ratnakar, Ramanathan, Krishnan, Su, Wendy, Willi, Roman, Kieseier, Bernd, Kappos, Ludwig

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Immune Sensing of Synthetic, Bacterial, and Protozoan RNA by Toll-like Receptor 8 Requires Coordinated Processing by RNase T2 and RNase 2 von Ostendorf, Thomas, Zillinger, Thomas, Andryka, Katarzyna, Schlee-Guimaraes, Thais Marina, Schmitz, Saskia, Marx, Samira, Bayrak, Kübra, Linke, Rebecca, Salgert, Sarah, Wegner, Julia, Grasser, Tatjana, Bauersachs, Sonja, Soltesz, Leon, Hübner, Marc P., Nastaly, Maximilian, Coch, Christoph, Kettwig, Matthias, Roehl, Ingo, Henneke, Marco, Hoerauf, Achim, Barchet, Winfried, Gärtner, Jutta, Schlee, Martin, Hartmann, Gunther, Bartok, Eva

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Interferon-driven brain phenotype in a mouse model of RNaseT2 deficient leukoencephalopathy von Kettwig, Matthias, Ternka, Katharina, Wendland, Kristin, Krüger, Dennis Manfred, Zampar, Silvia, Schob, Charlotte, Franz, Jonas, Aich, Abhishek, Winkler, Anne, Sakib, M. Sadman, Kaurani, Lalit, Epple, Robert, Werner, Hauke B., Hakroush, Samy, Kitz, Julia, Prinz, Marco, Bartok, Eva, Hartmann, Gunther, Schröder, Simone, Rehling, Peter, Henneke, Marco, Boretius, Susann, Alia, A., Wirths, Oliver, Fischer, Andre, Stadelmann, Christine, Nessler, Stefan, Gärtner, Jutta

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Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study von Rosewich, Hendrik, MD, Thiele, Holger, MD, Ohlenbusch, Andreas, PhD, Maschke, Ulrike, MD, Altmüller, Janine, MD, Frommolt, Peter, PhD, Zirn, Birgit, PhD, Ebinger, Friedrich, MD, Siemes, Hartmut, Prof, Nürnberg, Peter, Prof, Brockmann, Knut, Prof, Gärtner, Jutta, Prof

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The failure of microglia to digest developmental apoptotic cells contributes to the pathology of RNASET2‐deficient leukoencephalopathy von Hamilton, Noémie, Rutherford, Holly A., Petts, Jessica J., Isles, Hannah M., Weber, Thomas, Henneke, Marco, Gärtner, Jutta, Dunning, Mark J., Renshaw, Stephen A.

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Respiration and the watershed of spinal CSF flow in humans von Dreha-Kulaczewski, Steffi, Konopka, Mareen, Joseph, Arun A, Kollmeier, Jost, Merboldt, Klaus-Dietmar, Ludwig, Hans-Christoph, Gärtner, Jutta, Frahm, Jens

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Super-resolution imaging reveals the sub-diffraction phenotype of Zellweger Syndrome ghosts and wild-type peroxisomes von Soliman, Kareem, Göttfert, Fabian, Rosewich, Hendrik, Thoms, Sven, Gärtner, Jutta

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Activating de novo mutations in NFE2L2 encoding NRF2 cause a multisystem disorder von Huppke, Peter, Weissbach, Susann, Church, Joseph A., Schnur, Rhonda, Krusen, Martina, Dreha-Kulaczewski, Steffi, Kühn-Velten, W. Nikolaus, Wolf, Annika, Huppke, Brenda, Millan, Francisca, Begtrup, Amber, Almusafri, Fatima, Thiele, Holger, Altmüller, Janine, Nürnberg, Peter, Müller, Michael, Gärtner, Jutta

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Cognitive deficits including executive functioning in relation to clinical parameters in paediatric MS patients von Wuerfel, Eva, Weddige, Almuth, Hagmayer, York, Jacob, Rebecca, Wedekind, Lisa, Stark, Wiebke, Gärtner, Jutta

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Bi-allelic Mutations in NDUFA6 Establish Its Role in Early-Onset Isolated Mitochondrial Complex I Deficiency von Alston, Charlotte L., Heidler, Juliana, Dibley, Marris G., Kremer, Laura S., Taylor, Lucie S., Fratter, Carl, French, Courtney E., Glasgow, Ruth I.C., Feichtinger, René G., Delon, Isabelle, Pagnamenta, Alistair T., Dolling, Helen, Lemonde, Hugh, Aiton, Neil, Bjørnstad, Alf, Henneke, Lisa, Gärtner, Jutta, Thiele, Holger, Tauchmannova, Katerina, Quaghebeur, Gerardine, Houstek, Josef, Sperl, Wolfgang, Raymond, F. Lucy, Prokisch, Holger, Mayr, Johannes A., McFarland, Robert, Poulton, Joanna, Ryan, Michael T., Wittig, Ilka, Henneke, Marco, Taylor, Robert W.

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Spinal CSF flow in response to forced thoracic and abdominal respiration von Aktas, Gökmen, Kollmeier, Jost M, Joseph, Arun A, Merboldt, Klaus-Dietmar, Ludwig, Hans-Christoph, Gärtner, Jutta, Frahm, Jens, Dreha-Kulaczewski, Steffi

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Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease... von Lazarov, Elinor, Hillebrand, Merle, Schröder, Simone, Ternka, Katharina, Hofhuis, Julia, Ohlenbusch, Andreas, Barrantes-Freer, Alonso, Pardo, Luis A., Fruergaard, Marlene U., Nissen, Poul, Brockmann, Knut, Gärtner, Jutta, Rosewich, Hendrik

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Dysferlin mediates membrane tubulation and links T-tubule biogenesis to muscular dystrophy von Hofhuis, Julia, Bersch, Kristina, Büssenschütt, Ronja, Drzymalski, Marzena, Liebetanz, David, Nikolaev, Viacheslav O, Wagner, Stefan, Maier, Lars S, Gärtner, Jutta, Klinge, Lars, Thoms, Sven

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