A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathy von Jonckheere, A I, Hogeveen, M, Nijtmans, L G J, van den Brand, M A M, Janssen, A J M, Diepstra, J H S, van den Brandt, F C A, van den Heuvel, L P, Hol, F A, Hofste, T G J, Kapusta, L, Dillmann, U, Shamdeen, M G, Smeitink, J A M, Rodenburg, R J T

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ADULT MANIFESTATION OF L-2-HYDROXYGLUTARATE DEHYDROGENASE DEFICIENCY BY A NOVEL MUTATION von SÜHS, Kw, ERDMANN, P, SHAMDEEN, M. G, PAPANAGIOTOU, P, DILLMANN, U

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Effects of short‐term propofol administration on pancreatic enzymes and triglyceride levels in children von Gottschling, S., Meyer, S., Krenn, T., Kleinschmidt, S., Reinhard, H., Graf, N., Shamdeen, G. M.

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Effect of propofol on seizure‐like phenomena and electroencephalographic activity in children with epilepsy vs children with learning difficulties von Meyer, S., Shamdeen, M. G., Kegel, B., Mencke, T., Gottschling, S., Gortner, L., Grundmann, U.

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A floppy neonate with respiratory failure and burst suppression EEG (Case Presentation) von Meyer, S, Shamdeen, MG, Furtwängler, R, Gottschling, S, Gortner, L

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Laser Acupuncture in Children with Headache: A double-blind, randomized, bicenter, placebo-controlled trial von Gottschling, S., Meyer, S., Gribova, I., Distler, L., Berrang, J., Gortner, L., Graf, N., Shamdeen, MG, Pothmann, Raymund

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Benign epilepsy with centrotemporal spikes: Correlating spike frequency and neuropsychology von Tacke, Moritz, Rupp, Nina, Gerstl, Lucia, Heinen, Florian, Vill, Katharina, Bonfert, Michaela, Neubauer, Bernd Axel, Bast, Thomas, Borggraefe, Ingo, Baumeister, F A M, Baethmann, M, Schreiber‐Gollwitzer, B, Bentele, K, Blank, C, Held, J, Blank, H M, Liebrich, K, Bode, H, Braun, J, Bosch, F, Wagner, R, Brandl, U, Wetzel, K, Brockmann, K, Schlockwerder, C, Dahlem, P, Baudler, I, Ernst, J P, Mayer, H, Feldmann, E, Pattber‐Wolff, A, Fiedler, A, Sonnleitner, S, Gerigk, M, Heß, S, Feiereis, T, Hikel, C, Hoffmann, H G, Rickeshenrich, A, Kieslich, M, Dewitz, R, Baz Bartels, M, Klepper, J, Kleuker, S, Kluger, G, Kirsch, A, Koch, H, Meerpohl, U, Koch, W, Korinthenberg, R, Stehle‐Renner, B, Krois, I, Kühne, H, Weiß, C, Elkemann, U, Mandl, M, Friedl, A, Mause, U, Müller, M, Navratil, P, Iken, U, Opp, J, Walter, J, Penzien, J, Prietsch, V, Siegrist, B, Quattländer, A, Reuner, G, Schara, U, Shamdeen, M G, Struchholz, H, prinz, A, Wendker‐Magrabi, H, Stephani, U, Muhle, H, Carlsson, G, Straßburg, H M, Ottensmeier, H, Töpke, B, Tatsek, K, Trollmann, R, Poida‐Herzing, E, Tuschen‐Hofstätter, E, Menschig, M, Waltz, S, Pickartz, A, Weber, G, Gehnen, T, Wien, F U, Antemann, J, Wolff, M, Serra, E, Polster, T, Freitag, H, Sönmez, Ö, Rheinhardt, K, Traus, M, chröder, A, Hoovey, S, Navratil, C

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Levetiracetam vs. sulthiame in benign epilepsy with centrotemporal spikes in childhood: A double-blinded, randomized, controlled trial (German HEAD Study) von Borggraefe, Ingo, Bonfert, Michaela, Bast, Thomas, Neubauer, Bernd Axel, Schotten, Klaus Juergen, Maßmann, Kai, Noachtar, Soheyl, Tuxhorn, Ingrid, May, Theodor W, Heinen, Florian

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Effect of anticonvulsive treatment on neuropsychological performance in children with BECTS von Tacke, Moritz, MD, Gerstl, Lucia, MD, Heinen, Florian, MD, Heukaeufer, Isabel, Bonfert, Michaela, MD, Bast, Thomas, MD, Cornell, Sonia, PhD, Neubauer, Bernd Axel, MD, Borggraefe, Ingo, MD

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G.P.71 Myasthenia gravis in young children and adolescents: Clinical symptoms and treatment options von Della Marina, A, Trippe, H, Lutz, S, Shamdeen, G.M, Schara, U

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Congenital muscular dystrophies: muscle-eye-brain disease von Meyer, S, Struffert, T, Uyanik, G, Oehl-Jaschkowitz, B, Hehr, U, Shamdeen, M G

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A floppy neonate with respiratory failure and burst suppression EEG (Case Presentation). Discussion von MEYER, S, SHAMDEEN, M. G, FURTWÄNGLER, R, GOTTSCHLING, S, GORTNER, L

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A floppy neonate with respiratory failure and burst suppression EEG (Discussion and Diagnosis) von Meyer, S, Shamdeen, MG, Furtwängler, R, Gottschling, S, Gortner, L

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Rolandic epileptiform discharges in children with minimal cerebral disorders: is a therapy with sulthiame indicated? von Shamdeen, MG, Frohnhöfer, M, Jost, W, Weber, R, Rohrer, T

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Kongenitale Muskeldystrophie: Muscle-Eye-Brain disease von Meyer, S., Struffert, T., Uyanik, G., Oehl-Jaschkowitz, B., Hehr, U., Shamdeen, M. G.

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Broad phenotypic spectrum of FLNA-associated disorders resulting in brain malformation, epilepsy, mental retardation and stroke von Uyanik, G, Hehr, A, Schuierer, G, Bohring, A, Spranger, S, Neumann, L, Shamdeen, MG, Kasper, B, Stefan, H, Reardon, W, Bogdahn, U, Hehr, U, Winkler, J

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Effects of Levetiracetam and Sulthiame on EEG in benign epilepsy with centrotemporal spikes: A randomized controlled trial von Tacke, Moritz, Borggraefe, Ingo, Gerstl, Lucia, Heinen, Florian, Vill, Katharina, Bonfert, Michaela, Bast, Thomas, Neubauer, Bernd Axel, Baumeister, Friedrich, Baethmann, Martina, Bentele, Karl, Blank, Christian, Blank, Harald M., Bode, Harald, Bosch, Friedrich, Brandl, Ulrich, Brockmann, Knut, Dahlem, Peter, Ernst, Jan-Peter, Feldmann, Evemarie, Fiedler, Andreas, Gerigk, Michael, Heß, Soeren, Hikel, Christiane, Hoffmann, Hans-Georg, Kieslich, Matthias, Klepper, Joerg, Kluger, Gerhard, Koch, Hartmut, Koch, Walter, Korinthenberg, Rudolf, Krois, Ilona, Kühne, Hermann, Kurlemann, Gerhard, Mandl, Michaela, Mause, Ulrike, Navratil, Peter, Opp, Joachim, Penzien, Johann, Prietsch, Viola, Quattländer, Axel, Rating, Dietz, Schara, Ulrike, Shamdeen, Mohammed G., Sprinz, Andreas, Wendker-Magrabi, Hildegard, Stephani, Ulrich, Muhle, Hiltrud, Straßburg, Hans-Michael, Töpke, Bärbel, Trollmann, Regina, Tuschen-Hofstätter, Elisabeth, Waltz, Stephan, Weber, Gabriele, Wien, Frank U., Wolff, Markus, Polster, Tilman, Freitag, Hedwig, Sönmez, Ötzcam, Reinhardt, Klaus, Traus, Marion, Hoovey, Zeecam

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High burden of acute respiratory tract infections leading to hospitalization at German pediatric hospitals: fall/winter 2022–2023 von Doenhardt, Maren, Armann, Jakob P., Diffloth, Natalie, Gano, Christin, Schneider, Josephine, Schneider, Dominik T., Tenenbaum, Tobias, Trotter, Andreas, Berner, Reinhard

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Störungen der O-Glykosylierung führen zu Muskeldystrophie und Gehirnfehlbildungen von Uyanik, G, Gross, C, Haliloglu, G, Oehl-Jaschkowitz, B, Shamdeen, M, Bogdahn, U, Topaloglu, H, Hehr, U, Winkler, J

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