Pre-anesthetic assessment with three core questions for the detection of obstructive sleep apnea in childhood: An observational study

por Schnoor, Joerg, Busch, Thilo, Turemuratov, Nazar, Merkenschlager, Andreas
Publicado 2018

Harlequin Syndrome after Thoracoscopic Repair of a Child with Tracheoesophageal Fistula (TEF)

por Wagner, Richard, Lacher, Martin, Merkenschlager, Andreas, Markel, Moritz
Publicado 2019

Quantitative T1 mapping of the normal brain from early infancy to adulthood

por Gräfe, Daniel, Frahm, Jens, Merkenschlager, Andreas, Voit, Dirk, Hirsch, Franz Wolfgang
Publicado 2020

Lamotrigine Reduces Stress Symptoms of Chronic Anxiety in the Times of the Covid-19 Natural Catastrophe-A Case Report

por Pham, Thuylinh L., Chrousos, George P., Merkenschlager, Andreas, Petrowski, Katja, Ullmann, Enrico
Publicado 2021

Pronounced reversible hyperammonemic encephalopathy associated with combined valproate–topiramate therapy in a 7-year-old girl

por Weise, Sebastian, Syrbe, Steffen, Preuss, Matthias, Bertsche, Astrid, Merkenschlager, Andreas, Bernhard, Matthias K
Publicado 2015

STEAM-DWI as a robust alternative to EPI-DWI: Evaluation in pediatric brain MRI

por Gräfe, Daniel, Päts, Anne, Merkenschlager, Andreas, Roth, Christian, Hirsch, Franz Wolfgang, Frahm, Jens, Voit, Dirk
Publicado 2022

Brain deposition of gadobutrol in children—a cross-sectional and longitudinal MRI T1 mapping study

por Gräfe, Daniel, Simion, Stefan-Horia, Rosolowski, Maciej, Merkenschlager, Andreas, Frahm, Jens, Voit, Dirk, Hirsch, Franz Wolfgang
Publicado 2022

Opsoclonus-myoclonus syndrome after adenovirus infection

por Syrbe, Steffen, Merkenschlager, Andreas, Bernhard, Matthias K., Grosche, Jens, Liebert, Uwe Gerd, Hirsch, Wolfgang, Härtig, Wolfgang
Publicado 2015

Unusual mechanical failures of intrathecal baclofen pump systems: symptoms, signs, and trouble shooting

por Gburek-Augustat, Janina, Krause, Matthias, Bernhard, Matthias, Sorge, Ina, Gräfe, Daniel, Siekmeyer, Manuela, Nestler, Ulf, Merkenschlager, Andreas
Publicado 2021

Effects of theophylline on ADCY5 activation—From cellular studies to improved therapeutic options for ADCY5-related dyskinesia patients

por Tänzler, Dirk, Kipping, Marc, Lederer, Marcell, Günther, Wiebke F., Arlt, Christian, Hüttelmaier, Stefan, Merkenschlager, Andreas, Sinz, Andrea
Publicado 2023

Cerebrospinal Fluid Protein Concentrations in Hydrocephalus

por Wilhelmy, Florian, Krause, Matthias, Schob, Stefan, Merkenschlager, Andreas, Wachowiak, Robin, Härtig, Wolfgang, Meixensberger, Jürgen, Gburek-Augustat, Janina, Wende, Tim
Publicado 2023

Complementing the phenotypical spectrum of TUBA1A tubulinopathy and its role in early-onset epilepsies

por Schröter, Julian, Popp, Bernt, Brennenstuhl, Heiko, Döring, Jan H., Donze, Stephany H., Bijlsma, Emilia K., van Haeringen, Arie, Huhle, Dagmar, Jestaedt, Leonie, Merkenschlager, Andreas, Arelin, Maria, Gräfe, Daniel, Neuser, Sonja, Oates, Stephanie, Pal, Deb K., Parker, Michael J., Lemke, Johannes R., Hoffmann, Georg F., Kölker, Stefan, Harting, Inga, Syrbe, Steffen
Publicado 2022

Safety and efficacy of mTOR inhibitor treatment in patients with tuberous sclerosis complex under 2 years of age – a multicenter retrospective study

por Saffari, Afshin, Brösse, Ines, Wiemer-Kruel, Adelheid, Wilken, Bernd, Kreuzaler, Paula, Hahn, Andreas, Bernhard, Matthias K., van Tilburg, Cornelis M., Hoffmann, Georg F., Gorenflo, Matthias, Hethey, Sven, Kaiser, Olaf, Kölker, Stefan, Wagner, Robert, Witt, Olaf, Merkenschlager, Andreas, Möckel, Andreas, Roser, Timo, Schlump, Jan-Ulrich, Serfling, Antje, Spiegler, Juliane, Milde, Till, Ziegler, Andreas, Syrbe, Steffen
Publicado 2019

Immune dysregulation in patients with PTEN hamartoma tumor syndrome: Analysis of FOXP3 regulatory T cells

por Chen, Hannah H., Händel, Norman, Ngeow, Joanne, Muller, James, Hühn, Michael, Yang, Huei-Ting, Heindl, Mario, Berbers, Roos-Marijn, Hegazy, Ahmed N., Kionke, Janina, Yehia, Lamis, Sack, Ulrich, Bläser, Frank, Rensing-Ehl, Anne, Reifenberger, Julia, Keith, Julia, Travis, Simon, Merkenschlager, Andreas, Kiess, Wieland, Wittekind, Christian, Walker, Lisa, Ehl, Stephan, Aretz, Stefan, Dustin, Michael L., Eng, Charis, Powrie, Fiona, Uhlig, Holm H.
Publicado 2017

Cerebrospinal fluid findings in patients with myelin oligodendrocyte glycoprotein (MOG) antibodies. Part 2: Results from 108 lumbar punctures in 80 pediatric patients

por Jarius, Sven, Lechner, Christian, Wendel, Eva M., Baumann, Matthias, Breu, Markus, Schimmel, Mareike, Karenfort, Michael, Marina, Adela Della, Merkenschlager, Andreas, Thiels, Charlotte, Blaschek, Astrid, Salandin, Michela, Leiz, Steffen, Leypoldt, Frank, Pschibul, Alexander, Hackenberg, Annette, Hahn, Andreas, Syrbe, Steffen, Strautmanis, Jurgis, Häusler, Martin, Krieg, Peter, Eisenkölbl, Astrid, Stoffels, Johannes, Eckenweiler, Matthias, Ayzenberg, Ilya, Haas, Jürgen, Höftberger, Romana, Kleiter, Ingo, Korporal-Kuhnke, Mirjam, Ringelstein, Marius, Ruprecht, Klemens, Siebert, Nadja, Schanda, Kathrin, Aktas, Orhan, Paul, Friedemann, Reindl, Markus, Wildemann, Brigitte, Rostásy, Kevin
Publicado 2020

Defining and expanding the phenotype of QARS-associated developmental epileptic encephalopathy

por Johannesen, Katrine M., Mitter, Diana, Janowski, Robert, Roth, Christian, Toulouse, Joseph, Poulat, Anne-Lise, Ville, Dorothee M., Chatron, Nicolas, Brilstra, Eva, Geleijns, Karin, Born, Alfred Peter, McLean, Scott, Nugent, Kimberly, Baynam, Gareth, Poulton, Cathryn, Dreyer, Lauren, Gration, Dylan, Schulz, Solveig, Dieckmann, Andrea, Helbig, Katherine L., Merkenschlager, Andreas, Jamra, Rami, Finck, Anja, Gardella, Elena, Hjalgrim, Helle, Mirzaa, Ghayda, Brancati, Francesco, Bierhals, Tatjana, Denecke, Jonas, Hempel, Maja, Lemke, Johannes R., Rubboli, Guido, Muschke, Petra, Guerrini, Renzo, Vetro, Annalisa, Niessing, Dierk, Lesca, Gaetan, Møller, Rikke S.
Publicado 2019

The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood

por Döring, Jan Henje, Saffari, Afshin, Bast, Thomas, Brockmann, Knut, Ehrhardt, Laura, Fazeli, Walid, Janzarik, Wibke G., Kluger, Gerhard, Muhle, Hiltrud, Møller, Rikke S., Platzer, Konrad, Santos, Joana Larupa, Bache, Iben, Bertsche, Astrid, Bonfert, Michaela, Borggräfe, Ingo, Broser, Philip J., Datta, Alexandre N., Hammer, Trine Bjørg, Hartmann, Hans, Hasse-Wittmer, Anette, Henneke, Marco, Kühne, Hermann, Lemke, Johannes R., Maier, Oliver, Matzker, Eva, Merkenschlager, Andreas, Opp, Joachim, Patzer, Steffi, Rostasy, Kevin, Stark, Birgit, Strzelczyk, Adam, von Stülpnagel, Celina, Weber, Yvonne, Wolff, Markus, Zirn, Birgit, Hoffmann, Georg Friedrich, Kölker, Stefan, Syrbe, Steffen
Publicado 2020

Temporal Dynamics of MOG Antibodies in Children With Acquired Demyelinating Syndrome

por Wendel, Eva Maria, Thonke, Helen Sophie, Bertolini, Annikki, Baumann, Matthias, Blaschek, Astrid, Merkenschlager, Andreas, Karenfort, Michael, Kornek, Barbara, Lechner, Christian, Pohl, Daniela, Pritsch, Martin, Schanda, Kathrin, Schimmel, Mareike, Thiels, Charlotte, Waltz, Stephan, Wiegand, Gert, Anlar, Banu, Barisic, Nina, Blank, Christian, Breu, Markus, Broser, Philip, Della Marina, Adela, Diepold, Katharina, Eckenweiler, Matthias, Eisenkölbl, Astrid, Freilinger, Michael, Gruber-Sedlmayr, Ursula, Hackenberg, Annette, Iff, Tobias, Knierim, Ellen, Koch, Johannes, Kutschke, Georg, Leiz, Steffen, Lischetzki, Grischa, Nosadini, Margherita, Pschibul, Alexander, Reiter-Fink, Edith, Rohrbach, Doris, Salandin, Michela, Sartori, Stefano, Schlump, Jan-Ulrich, Stoffels, Johannes, Strautmanis, Jurgis, Tibussek, Daniel, Tüngler, Victoria, Utzig, Norbert, Reindl, Markus, Rostásy, Kevin
Publicado 2022

De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy

por Syrbe, Steffen, Hedrich, Ulrike B.S., Riesch, Erik, Djémié, Tania, Müller, Stephan, Møller, Rikke S., Maher, Bridget, Hernandez-Hernandez, Laura, Synofzik, Matthis, Caglayan, Hande S., Arslan, Mutluay, Serratosa, José M., Nothnagel, Michael, May, Patrick, Krause, Roland, Löffler, Heidrun, Detert, Katja, Dorn, Thomas, Vogt, Heinrich, Krämer, Günter, Schöls, Ludger, Mullis, Primus E., Linnankivi, Tarja, Lehesjoki, Anna-Elina, Sterbova, Katalin, Craiu, Dana C., Hoffman-Zacharska, Dorota, Korff, Christian M., Weber, Yvonne G., Steinlin, Maja, Gallati, Sabina, Bertsche, Astrid, Bernhard, Matthias K., Merkenschlager, Andreas, Kiess, Wieland, Gonzalez, Michael, Züchner, Stephan, Palotie, Aarno, Suls, Arvid, De Jonghe, Peter, Helbig, Ingo, Biskup, Saskia, Wolff, Markus, Maljevic, Snezana, Schüle, Rebecca, Sisodiya, Sanjay M., Weckhuysen, Sarah, Lerche, Holger, Lemke, Johannes R.
Publicado 2015

Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease

por Zagaglia, Sara, Selch, Christina, Nisevic, Jelena Radic, Mei, Davide, Michalak, Zuzanna, Hernandez-Hernandez, Laura, Krithika, S., Vezyroglou, Katharina, Varadkar, Sophia M., Pepler, Alexander, Biskup, Saskia, Leão, Miguel, Gärtner, Jutta, Merkenschlager, Andreas, Jaksch, Michaela, Møller, Rikke S., Gardella, Elena, Kristiansen, Britta Schlott, Hansen, Lars Kjærsgaard, Vari, Maria Stella, Helbig, Katherine L., Desai, Sonal, Smith-Hicks, Constance L., Hino-Fukuyo, Naomi, Talvik, Tiina, Laugesaar, Rael, Ilves, Pilvi, Õunap, Katrin, Körber, Ingrid, Hartlieb, Till, Kudernatsch, Manfred, Winkler, Peter, Schimmel, Mareike, Hasse, Anette, Knuf, Markus, Heinemeyer, Jan, Makowski, Christine, Ghedia, Sondhya, Subramanian, Gopinath M., Striano, Pasquale, Thomas, Rhys H., Micallef, Caroline, Thom, Maria, Werring, David J., Kluger, Gerhard Josef, Cross, J. Helen, Guerrini, Renzo, Balestrini, Simona, Sisodiya, Sanjay M.
Publicado 2018