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Gruppiert nach: Dokumententyp | Veröffentlichungsdatum
Anzahl der Publikationen: 5

Zeitschriftenartikel

Cruz, Pedro M. Rodriguez; Cossins, Judith; Estephan, Eduardo de Paula; Munell, Francina; Selby, Kathryn; Hirano, Michio; Maroofin, Reza; Mehrjardi, Mohammad Yahya Vahidi; Chow, Gabriel; Carr, Aisling; Manzur, Adnan; Robb, Stephanie; Munot, Pinki; Liu, Wei Wei; Banka, Siddharth; Fraser, Harry; De Goede, Christian; Zanoteli, Edmar; Reed, Umbertina Conti; Sage, Abigail; Gratacos, Margarida; Macaya, Alfons; Dusl, Marina; Senderek, Jan; Topf, Ana; Hofer, Monika; Knight, Ravi; Ramdas, Sithara; Jayawant, Sandeep; Lochmüller, Hans; Palace, Jacqueline und Beeson, David (2019): The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations. In: Brain, Bd. 142: S. 1547-1560

Dusl, Marina; Moreno, Teresa; Muneii, Francina; Macaya, Alfons; Gratacos, Margarida; Abicht, Angela; Strom, Tim M.; Lochmuller, Hanns und Senderek, Jan (2019): Congenital myasthenic syndrome caused by novel COL13A1 mutations. In: Journal of Neurology, Bd. 266, Nr. 5: S. 1107-1112

Kogelman, Lisette J. A.; Esserlind, Ann-Louise; Christensen, Anne Francke; Awasthi, Swapnil; Ripke, Stephan; Ingason, Andres; Davidsson, Olafur B.; Erikstrup, Christian; Hjalgrim, Henrik; Ullum, Henrik; Olesen, Jes; Hansen, Thomas Folkmann; Gudbjartsson, Daniel; Gastafsson, Omar; Stefansson, Kari; Stefansson, Hreinn; Porsteinsdottir, Unnur; Andersen, Steffen; Banasik, Karina; Brunak, Soren; Buil, Alfonso; Burgdorf, Kristoffer; Gregor, Jemec; Jennum, Poul; Nielsen, Kasper Rene; Nyegaard, Mette; Paarup, Helene Mariana; Pedersen, Ole Birger; Sorensen, Erik; Werge, Thomas; Anttila, Verneri; Artto, Ville; Belin, Andrea Carmine; de Boer, Irene; Boomsma, Dorret; Borte, Sigrid; Chasman, Daniel; Cherkas, Lynn; Cormand, Bru; Cuenca-Leon, Ester; Davey-Smith, George; Dichgans, Martin; van Duijn, Cornelia; Esko, Tonu; Ferrari, Michel; Frants, Rune R.; Freilinger, Tobias; Furlotte, Nick; Gormley, Padhraig; Griffiths, Lyn; Hamalainen, Eija; Hiekkala, Marjo; Ikram, M. Arfan; Jarvelin, Marjo-Riitta; Kajanne, Risto; Kallela, Mikko; Kaprio, Jaakko; Kaunisto, Mari; Kubisch, Christian; Kurki, Mitja; Kurth, Tobias; Launer, Lenore; Lehtimaki, Terho; Lessel, Davor; Ligthart, Lannie; Litterman, Nadia; van den Maagdenberg, Arn; Macaya, Alfons; Malik, Rainer; Mangino, Massimo; McMahon, George; Muller-Myhsok, Bertram; Neale, Benjamin M.; Northover, Carrie; Nyholt, Dale R.; Palotie, Aarno; Palta, Priit; Pedersen, Linda; Pedersen, Nancy; Posthuma, Danielle; Pozo-Rosich, Patricia; Pressman, Alice; Raitakari, Olli; Schurks, Markus; Sintas, Celia; Steinberg, Stacy; Strachan, David; Terwindt, Gisela; Vila-Pueyo, Marta; Wessman, Maija; Winsvold, Bendik S.; Zhao, Huiying und Zwart, John-Anker (2019): Migraine polygenic risk score associates with efficacy of migraine-specific drugs. In: Neurology-Genetics, Bd. 5, Nr. 6, e364

Kingswood, John C.; Bruzzi, Paolo; Curatolo, Paolo; de Vries, Petrus J.; Fladrowski, Carla; Hertzberg, Christoph; Jansen, Anna C.; Jozwiak, Sergiusz; Nabbout, Rima; Sauter, Matthias; Touraine, Renaud; O'Callaghan, Finbar; Zonnenberg, Bernard; Crippa, Stefania; Comis, Silvia; d'Augeres, Guillaume Beaure; Belousova, Elena; Carter, Tom; Cottin, Vincent; Dahlin, Maria; Ferreira, Jose Carlos; Macaya, Alfons; Benedik, Mirjana Perkovic; Sander, Valentin; Youroukos, Sotirios; Castellana, Ramon; Ulker, Bulent und Feucht, Martha (2014): TOSCA - first international registry to address knowledge gaps in the natural history and management of tuberous sclerosis complex. In: Orphanet Journal of Rare Diseases 9:182 [PDF, 1MB]

de Vries, Boukje; Freilinger, Tobias; Anttila, Verneri; Malik, Rainer; Kallela, Mikko; Terwindt, Gisela M.; Pozo-Rosich, Patricia; Winsvold, Bendik; Nyholt, Dale R.; van Oosterhout, Willebrordus P. J.; Artto, Ville; Todt, Unda; Hamalainen, Eija; Fernandez-Morales, Jessica; Louter, Mark A.; Kaunisto, Mari A.; Schoenen, Jean; Raitakari, Olli; Lehtimaki, Terho; Vila-Pueyo, Marta; Goebel, Hartmut; Wichmann, Erich; Sintas, Celia; Uitterlinden, Andre G.; Hofman, Albert; Rivadeneira, Fernando; Heinze, Axel; Tronvik, Erling; Van Duijn, Cornelia M.; Kaprio, Jaakko; Cormand, Bru; Wessman, Maija; Frants, Rune R.; Meitinger, Thomas; Mueller-Myhsok, Bertram; Zwart, John-Anker; Farkkila, Markus; Macaya, Alfons; Ferrari, Michel D.; Kubisch, Christian; Palotie, Aarno; Dichgans, Martin und van den Maagdenberg, Arn M. J. M. (2013): Migraine without aura: genome-wide association analysis identifies several novel susceptibility. In: The Journal of Headache and Pain, Bd. 14, P18 [PDF, 134kB]

Diese Liste wurde am Sat Mar 23 22:21:18 2024 CET erstellt.