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Browsing by Author Münchau, Alexander
Showing results 1 to 5 of 5
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2013 | Genome-wide association study in musician's dystonia: A risk variant at the arylsulfatase G locus? | Lohmann, Katja; Schmidt, Alexander; Schillert, Arne; Winkler, Susen; Albanese, Alberto; Baas, Frank; Bentivoglio, Anna Rita; Borngräber, Friederike; Brüggemann, Norbert; Defazio, Giovanni;
Del, Sorbo Francesca; Deuschl, Günther; Edwards, Mark J.; Gasser, Thomas; Gómez-Garre, Pilar; Graf, Julia; Groen, Justus L.; Grünewald, Anne; Hagenah, Johann; Hemmelmann, Claudia; Jabusch, Hans-Christian; Kaji, Ryuji; Kasten, Meike; Kawakami, Hideshi; Kostić, Vladimir
 ; Liguori, Maria; Mir, Pablo; Münchau, Alexander; Ricchiuti, Felicia; Schreiber, Stefan; Siegesmund, Katharina; Svetel, Marina ; Tijssen, Marina A.J.; Valente, Enza Maria; Westenberger, Ana; Zeuner, Kirsten E.; Zittel, Simone; Altenmüller, Eckart; Ziegler, Andreas; Klein, Christine; | Article | 21aM21a |
| 2011 | Identification and functional analysis of novel THAP1 mutations | Lohmann, Katja; Uflacker, Nils; Erogullari, Alev; Lohnau, Thora; Winkler, Susen; Dendorfer, Andreas; Schneider, Susanne A; Osmanovic, Alma; Svetel, Marina ; Ferbert, Andreas;
Zittel, Simone; Kühn, Andrea A; Schmidt, Alexander; Altenmüller, Eckart; Münchau, Alexander; Kamm, Christoph; Wittstock, Matthias; Kupsch, Andreas; Moro, Elena; Volkmann, Jens; Kostić, Vladimir
; Kaiser, Frank J; Klein, Christine; Brüggemann, Norbert; | Article | 21M21 |
| 2014 | Mutations in GNAL: a novel cause of craniocervical dystonia | Kumar, Kishore R.; Lohmann, Katja; Masuho, Ikuo; Miyamoto, Ryosuke; Ferbert, Andreas; Lohnau, Thora; Kasten, Meike; Hagenah, Johann; Brüggemann, Norbert; Graf, Julia;
Münchau, Alexander; Kostić, Vladimir
; Sue, Carolyn M.; Domingo, Aloysius R.; Rosales, Raymond L.; Lee, Lilian V.; Freimann, Karen; Westenberger, Ana; Mukai, Youhei; Kawarai, Toshitaka; Kaji, Ryuji; Klein, Christine; Martemyanov, Kirill A.; Schmidt, Alexander; | Article | 21a+M21a+ |
| 2017 | Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans | Lohmann, Katja; Masuho, Ikuo; Patil, Dipak N.; Baumann, Hauke; Hebert, Eva; Steinrücke, Sofia; Trujillano, Daniel; Skamangas, Nickolas K.; Dobricic, Valerija; Hüning, Irina;
Gillessen-Kaesbach, Gabriele; Westenberger, Ana; Savić Pavićević, Dušanka
 ; Münchau, Alexander; Oprea, Gabriela; Klein, Christine; Rolfs, Arndt; Martemyanov, Kirill A.; | Article | 21aM21a |
| 2016 | The role of mutations in COL6A3 in isolated dystonia | Lohmann, Katja; Schlicht, Felix; Svetel, Marina ; Hinrichs, Frauke; Zittel, Simone; Graf, Julia; Lohnau, Thora; Schmidt, Alexander; Mir, Pablo; Krause, Patricia;
Lang, Antony E.; Jabusch, Hans-Christian; Wolters, Alexander; Kamm, Christoph; Zeuner, Kirsten E.; Altenmüller, Eckart; Naz, Sadaf; Chung, Sun Ju; Kostić, Vladimir
; Münchau, Alexander; Kühn, Andrea A.; Brüggemann, Norbert; Klein, Christine; | Article | 21M21 |