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DateNumber of items: 2.
Journal article
Fanciulli, Alessandra; Leys, Fabian; Lehner, Fabienne; Sidoroff, Victoria; Ruf, Viktoria C.; Raccagni, Cecilia; Mahlknecht, Philipp; Kuipers, Demy J. S.; IJcken, Wilfred F. J. van; Stockner, Heike; Musacchio, Thomas; Volkmann, Jens; Monoranu, Camelia Maria; Stankovic, Iva; Breedveld, Guido; Ferraro, Federico; Fevga, Christina; Windl, Otto; Herms, Jochen; Kiechl, Stefan; Poewe, Werner; Seppi, Klaus; Stefanova, Nadia; Scholz, Sonja W.; Bonifati, Vincenzo und Wenning, Gregor K.
(2022):
A multiplex pedigree with pathologically confirmed multiple system atrophy and Parkinson's disease with dementia.
In: Brain Communications, Vol. 4, No. 4, fcac175
Amin, Najaf; Allebrandt, Karla V.; Spek, Ashley van der; Müller-Myhsok, Bertram; Hek, Karin; Teder-Laving, Maris; Hayward, Caroline; Esko, Tõnu; Mill, Josine G. van; Mbarek, Hamdi; Watson, Nathaniel F.; Melville, Scott A.; Del Greco, Fabiola M.; Byrne, Enda M.; Oole, Edwin; Kolcic, Ivana; Chen, Ting-hsu; Evans, Daniel S.; Coresh, Josef; Vogelzangs, Nicole; Karjalainen, Juha; Willemsen, Gonneke; Gharib, Sina A.; Zgaga, Lina; Mihailov, Evelin; Stone, Katie L.; Campbell, Harry; Brouwer, Rutger Ww; Demirkan, Ayse; Isaacs, Aaron; Dogas, Zoran; Marciante, Kristin D.; Campbell, Susan; Borovecki, Fran; Luik, Annemarie I.; Li, Man; Hottenga, Jouke Jan; Huffman, Jennifer E.; Hout, Mirjam C. G. N. van den; Cummings, Steven R.; Aulchenko, Yuru S.; Gehrman, Philip R.; Uitterlinden, Andre G.; Wichmann, Heinz-Erich; Müller-Nurasyid, Martina; Fehrmann, Rudolf S. N.; Montgomery, Grant W.; Hofman, Albert; Kao, Wen Hong Linda; Oostra, Ben A.; Wright, Alan F.; Vink, Jacqueline M.; Wilson, James F.; Pramstaller, Peter P.; Hicks, Andrew A.; Polasek, Ozren; Punjabi, Naresh M.; Redline, Susan; Psaty, Bruce M.; Heath, Andrew C.; Merrow, Martha; Tranah, Gregory J.; Gottlieb, Daniel J.; Boomsma, Dorret I.; Martin, Nicholas G.; Rudan, Igor; Tiemeier, Henning; IJcken, Wilfred F. J. van; Penninx, Brenda W.; Metspalu, Andres; Meitinger, Thomas; Franke, Lude; Roenneberg, Till ORCID: https://orcid.org/0000-0003-2939-0332 und Duijn, Cornelia M. van
(2016):
Genetic variants in RBFOX3 are associated with sleep latency.
In: European Journal of Human Genetics, Vol. 24, No. 10: pp. 1488-1495
This list was generated on Sun Sep 29 05:53:56 2024 CEST.