Search Results - Cirak, Sebahattin

Clinical effectiveness of newborn screening for spinal muscular atrophy: a nonrandomized controlled trial by Schwartz, Oliver (Author) , Vill, Katharina (Author) , Pfaffenlehner, Michelle (Author) , Behrens, Max (Author) , Weiß, Claudia (Author) , Johannsen, Jessika (Author) , Friese, Johannes (Author) , Hahn, Andreas (Author) , Ziegler, Andreas (Author) , Illsinger, Sabine (Author) , Smitka, Martin (Author) , Moers, Arpad von (Author) , Kölbel, Heike (Author) , Schreiber, Gudrun (Author) , Kaiser, Nadja (Author) , Wilichowski, Ekkehard (Author) , Flotats Bastardas, Marina (Author) , Husain, Ralf (Author) , Baumann, Matthias (Author) , Köhler, Cornelia (Author) , Trollmann, Regina (Author) , Schwerin-Nagel, Annette (Author) , Eisenkölbl, Astrid (Author) , Schimmel, Mareike (Author) , Fleger, Martin (Author) , Kauffmann, Birgit (Author) , Wiegand, Gert (Author) , Baumgartner, Manuela (Author) , Rauschert, Christian (Author) , Cirak, Sebahattin (Author) , Gläser, Dieter (Author) , Bernert, Günther (Author) , Hagenacker, Tim (Author) , Goldbach, Susanne (Author) , Probst-Schendzielorz, Kristina (Author) , Lochmüller, Hanns (Author) , Müller-Felber, Wolfgang (Author) , Schara, Ulrike (Author) , Walter, Maggie C. (Author) , Kirschner, Janbernd (Author) , Pechmann, Astrid (Author) ,

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Efficacy and safety of gene therapy with onasemnogene abeparvovec in children with spinal muscular atrophy in the D-A-CH-region: a population-based observational study by Weiß, Claudia (Author) , Becker, Lena-Luise (Author) , Friese, Johannes (Author) , Blaschek, Astrid (Author) , Hahn, Andreas (Author) , Illsinger, Sabine (Author) , Schwartz, Oliver (Author) , Bernert, Günther (Author) , Hagen, Maja von der (Author) , Husain, Ralf A. (Author) , Goldhahn, Klaus (Author) , Kirschner, Janbernd (Author) , Pechmann, Astrid (Author) , Flotats-Bastardas, Marina (Author) , Schreiber, Gudrun (Author) , Schara, Ulrike (Author) , Plecko, Barbara (Author) , Trollmann, Regina (Author) , Horber, Veronka (Author) , Wilichowski, Ekkehard (Author) , Baumann, Matthias (Author) , Klein, Andrea (Author) , Eisenkölbl, Astrid (Author) , Köhler, Cornelia (Author) , Stettner, Georg M. (Author) , Cirak, Sebahattin (Author) , Hasselmann, Oswald (Author) , Kaindl, Angela M. (Author) , Garbade, Sven (Author) , Johannsen, Jessika (Author) , Ziegler, Andreas (Author) ,

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• Verlag, kostenfrei, Volltext

Newbornscreening SMA: from pilot project to nationwide screening in Germany by Müller-Felber, Wolfgang (Author) , Blaschek, Astrid (Author) , Schwartz, Oliver (Author) , Gläser, Dieter (Author) , Nennstiel, Uta (Author) , Brockow, Inken (Author) , Wirth, Brunhilde (Author) , Burggraf, Siegfried (Author) , Röschinger, Wulf (Author) , Becker, Marc (Author) , Durner, Jürgen (Author) , Eggermann, Katja (Author) , Kölbel, Heike (Author) , Müller, Christine (Author) , Hannibal, Iris (Author) , Olgemöller, Bernd (Author) , Schara, Ulrike (Author) , von Moers, Arpad (Author) , Trollmann, Regina (Author) , Johannssen, Jessika (Author) , Ziegler, Andreas (Author) , Cirak, Sebahattin (Author) , Hahn, Andreas (Author) , von der Hagen, Maja (Author) , Weiss, Claudia (Author) , Schreiber, Gudrun (Author) , Flotats-Bastardas, Marina (Author) , Hartmann, Hans (Author) , Illsinger, Sabine (Author) , Pechmann, Astrid (Author) , Horber, Veronka (Author) , Kirschner, Janbernd (Author) , Köhler, Cornelia (Author) , Winter, Benedikt (Author) , Friese, Johannes (Author) , Vill, Katharina (Author) ,

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Correction to: Novel mutations in KMT2B offer pathophysiological insights on childhood-onset progressive dystonia by Dafsari, Hormos Salimi (Author) , Sprute, Rosanne (Author) , Wunderlich, Gilbert (Author) , Daimagüler, Hülya-Sevcan (Author) , Karaca, Ezgi (Author) , Contreras, Adriana (Author) , Becker, Kerstin (Author) , Schulze-Rhonhof, Mira (Author) , Kiening, Karl (Author) , Karakulak, Tülay (Author) , Kloss, Manja (Author) , Horn, Annette (Author) , Pauls, Amande (Author) , Nürnberg, Peter (Author) , Altmüller, Janine (Author) , Thiele, Holger (Author) , Assmann, Birgit (Author) , Koy, Anne (Author) , Cirak, Sebahattin (Author) ,

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Novel mutations in KMT2B offer pathophysiological insights into childhood-onset progressive dystonia by Dafsari, Hormos Salimi (Author) , Sprute, Rosanne (Author) , Wunderlich, Gilbert (Author) , Daimagüler, Hülya-Sevcan (Author) , Karaca, Ezgi (Author) , Contreras, Adriana (Author) , Becker, Kerstin (Author) , Schulze-Rhonhof, Mira (Author) , Kiening, Karl (Author) , Karakulak, Tülay (Author) , Kloss, Manja (Author) , Horn, Annette (Author) , Pauls, Amande (Author) , Nürnberg, Peter (Author) , Altmüller, Janine (Author) , Thiele, Holger (Author) , Assmann, Birgit (Author) , Koy, Anne (Author) , Cirak, Sebahattin (Author) ,

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Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis by Naumann, Marcel (Author) , Peikert, Kevin (Author) , Günther, Rene (Author) , van der Kooi, Anneke J. (Author) , Aronica, Eleonora (Author) , Hübers, Annemarie (Author) , Danel, Veronique (Author) , Corcia, Philippe (Author) , Pan‐Montojo, Francisco (Author) , Cirak, Sebahattin (Author) , Haliloglu, Göknur (Author) , Ludolph, Albert C. (Author) , Goswami, Anand (Author) , Andersen, Peter M. (Author) , Prudlo, Johannes (Author) , Wegner, Florian (Author) , Van Damme, Philip (Author) , Weishaupt, Jochen H. (Author) , Hermann, Andreas (Author) ,

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Fukutin mutations in non-Japanese patients with congenital muscular dystrophy: less severe mutations predominate in patients with a non-Walker-Warburg phenotype by Yiş, Uluç (Author) , Uyanik, Gökhan (Author) , Bambul Heck, Pinar (Author) , Smitka, Martin (Author) , Nobel, Hannes (Author) , Ebinger, Friedrich (Author) , Dirik, Eray (Author) , Feng, Lucy (Author) , Kurul, Semra H. (Author) , Brocke, Katja (Author) , Unalp, Aycan (Author) , Özer, Erdener (Author) , Cakmakci, Handan (Author) , Sewry, Caroline (Author) , Cirak, Sebahattin (Author) , Muntoni, Francesco (Author) , Hehr, Ute (Author) , Morris-Rosendahl, Deborah J. (Author) ,

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• Verlag, lizenzpflichtig, Volltext

Fukutin mutations in non-Japanese patients with congenital muscular dystrophy: less severe mutations predominate in patients with a non-Walker-Warburg phenotype

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