نتائج البحث - Pechmann, Astrid
- يعرض 1 - 11 نتائج من 11
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Experiences of caregivers of children with spinal muscular atrophy participating in the expanded access program for nusinersen: a longitudinal qualitative study حسب Kiefer, Petra, Kirschner, Janbernd, Pechmann, Astrid, Langer, Thorsten
منشور في 2020نص -
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Transcranial magnetic stimulation with a half-sine wave pulse elicits direction-specific effects in human motor cortex حسب Jung, Nikolai H, Delvendahl, Igor, Pechmann, Astrid, Gleich, Bernhard, Gattinger, Norbert, Siebner, Hartwig R, Mall, Volker
منشور في 2012نص -
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De-duplicating patient records from three independent data sources reveals the incidence of rare neuromuscular disorders in Germany حسب König, Kirsten, Pechmann, Astrid, Thiele, Simone, Walter, Maggie C., Schorling, David, Tassoni, Adrian, Lochmüller, Hanns, Müller-Reible, Clemens, Kirschner, Janbernd
منشور في 2019نص -
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Coagulation disorders in Duchenne muscular dystrophy? Results of a registry-based online survey حسب Schorling, David C., Müller, Cornelia K., Pechmann, Astrid, Borell, Sabine, Langer, Thorsten, Thiele, Simone, Walter, Maggie C., Zieger, Barbara, Kirschner, Janbernd
منشور في 2020نص -
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Safety and Treatment Effects of Nusinersen in Longstanding Adult 5q-SMA Type 3 – A Prospective Observational Study حسب Walter, Maggie C., Wenninger, Stephan, Thiele, Simone, Stauber, Julia, Hiebeler, Miriam, Greckl, Eva, Stahl, Kristina, Pechmann, Astrid, Lochmüller, Hanns, Kirschner, Janbernd, Schoser, Benedikt
منشور في 2019نص -
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SMArtCARE - A platform to collect real-life outcome data of patients with spinal muscular atrophy حسب Pechmann, Astrid, König, Kirsten, Bernert, Günther, Schachtrup, Kristina, Schara, Ulrike, Schorling, David, Schwersenz, Inge, Stein, Sabine, Tassoni, Adrian, Vogt, Sibylle, Walter, Maggie C., Lochmüller, Hanns, Kirschner, Janbernd
منشور في 2019نص -
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Evaluation of Children with SMA Type 1 Under Treatment with Nusinersen within the Expanded Access Program in Germany حسب Pechmann, Astrid, Langer, Thorsten, Schorling, David, Stein, Sabine, Vogt, Sibylle, Schara, Ulrike, Kölbel, Heike, Schwartz, Oliver, Hahn, Andreas, Giese, Kerstin, Johannsen, Jessika, Denecke, Jonas, Weiß, Claudia, Theophil, Manuela, Kirschner, Janbernd
منشور في 2018نص -
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Congenital myasthenic syndrome with mild intellectual disability caused by a recurrent SLC25A1 variant حسب Balaraju, Sunitha, Töpf, Ana, McMacken, Grace, Kumar, Veeramani Preethish, Pechmann, Astrid, Roper, Helen, Vengalil, Seena, Polavarapu, Kiran, Nashi, Saraswati, Mahajan, Niranjan Prakash, Barbosa, Ines A., Deshpande, Charu, Taylor, Robert W., Cossins, Judith, Beeson, David, Laurie, Steven, Kirschner, Janbernd, Horvath, Rita, McFarland, Robert, Nalini, Atchayaram, Lochmüller, Hanns
منشور في 2019نص