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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 3
2020
Donald, Aimee; Tan, Chong Y.; Chakrapani, Anupam; Hughes, Derralyn A.; Sharma, Reena; Cole, Duncan; Bardins, Stanislav; Gorges, Martin; Jones, Simon A. und Schneider, Erich
(2020):
Eye movement biomarkers allow for the definition of phenotypes in Gaucher Disease.
In: Orphanet Journal of Rare Diseases, Bd. 15, Nr. 1, 349
2019
Heuvel, Martijn P. van den; Scholtens, Lianne H.; Burgh, Hannelore K. van der; Agosta, Federica; Alloza, Clara; Arango, Celso; Auyeung, Bonnie; Baron-Cohen, Simon; Basaia, Silvia; Benders, Manon J. N. L.; Beyer, Frauke; Booij, Linda; Braun, Kees P. J.; Busatto Filho, Geraldo; Cahn, Wiepke; Cannon, Dara M.; Chaim-Avancini, Tiffany M.; Chan, Sandra S. M.; Chen, Eric Y. H.; Crespo-Facorro, Benedicto; Crone, Eveline A.; Dannlowski, Udo; Zwarte, Sonja M. C. de; Dietsche, Bruno; Donohoe, Gary; Du Plessis, Stefan; Durston, Sarah; Diaz-Caneja, Covadonga M.; Diaz-Zuluaga, Ana M.; Emsley, Robin; Filippi, Massimo; Frodl, Thomas; Gorges, Martin; Graff, Beata; Grotegerd, Dominik; Gasecki, Dariusz; Hall, Julie M.; Holleran, Laurena; Holt, Rosemary; Hopman, Helene J.; Jansen, Andreas; Janssen, Joost; Jodzio, Krzysztof; Jancke, Lutz; Kaleda, Vasiliy G.; Kassubek, Jan; Masouleh, Shahrzad Kharabian; Kircher, Tilo; Koevoets, Martijn G. J. C.; Kostic, Vladimir S.; Krug, Axel; Lawrie, Stephen M.; Lebedeva, Irina S.; Lee, Edwin H. M.; Lett, Tristram A.; Lewis, Simon J. G.; Liem, Franziskus; Lombardo, Michael; Lopez-Jaramillo, Carlos; Margulies, Daniel S.; Markett, Sebastian; Marques, Paulo; Martinez-Zalacain, Ignacio; McDonald, Calm; McIntosh, Andrew M.; McPhilemy, Genevieve; Meinert, Susanne L.; Menchon, Jose M.; Montag, Christian; Moreira, Pedro S.; Morgado, Pedro; Mothersill, David O.; Merillat, Susan; Müller, Hans-Peter; Nabulsi, Leila; Najt, Pablo; Narkiewicz, Krzysztof; Naumczyk, Patrycja; Oranje, Bob; Ortiz-Garcia de la Foz, Victor; Peper, Jiska S.; Pineda, Julian A.; Rasser, Paul E.; Redlich, Ronny; Repple, Jonathan; Reuter, Martin; Rosa, Pedro G. P.; Ruigrok, Amber N.; Sabisz, Agnieszka; Schell, Ulrich; Seedat, Soraya; Serpa, Mauricio H.; Skouras, Stavros; Soriano-Mas, Cares; Sousa, Nuno; Szurowska, Edyta; Tomyshev, Alexander S.; Tordesillas-Gutierrez, Diana; Valk, Sofie L.; Berg, Leonard H. van den; Erp, Theo G. M. van; Haren, Neeltje E. M. van; Leeuwen, Judith M. C. van; Villringer, Arno; Vinkers, Christiaan C. H.; Vollmar, Christian; Waller, Lea; Walter, Henrik; Whalley, Heather C.; Witkowska, Marta; Witte, A. Veronica; Zanetti, Marcus; Zhang, Rui und Lange, Siemon C. de
(9. Mai 2019):
10Kin1day: A Bottom-Up Neuroimaging Initiative.
In: Frontiers in Neurology, Bd. 10, 425: S. 1-7
[PDF, 1MB]
Forouhideh, Yalda; Mueller, Kathrin; Ruf, Wolfgang; Assi, Muhannad; Seker, Tuncay; Tunca, Ceren; Knehr, Antje; Strom, Tim M.; Gorges, Martin; Schradt, Falk; Meitinger, Thomas; Ludolph, Albert C.; Pinkhardt, Elmar H.; Basak, A. Nazli; Kassubek, Jan; Uttner, Ingo und Weishaupt, Jochen H.
(2019):
A biallelic mutation links MYORG to autosomal-recessive primary familial brain calcification.
In: Brain, Bd. 142
[PDF, 446kB]