Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Mehmet E Kirlangic"'
Autor:
Svenja eCaspers, Susanne eMoebus, Silke eLux, Noreen ePundt, Holger eSchütz, Thomas W Mühleisen, Vincent eGras, Simon B Eickhoff, Sandro eRomanzetti, Tony eStöcker, Rüdiger eStirnberg, Mehmet E Kirlangic, Martina eMinnerop, Peter ePieperhoff, Ulrich eMödder, Samir eDas, Alan eEvans, Karl-Heinz eJöckel, Raimund eErbel, Sven eCichon, Markus M Nöthen, Dieter eSturma, Andreas eBauer, Jon eShah, Karl eZilles, Katrin eAmunts
Publikováno v:
Frontiers in Aging Neuroscience, Vol 6 (2014)
The ongoing 1000 brains study (1000BRAINS) is an epidemiological and neuroscientific investigation of structural and functional variability in the human brain during aging. The two recruitment sources are the 10-year follow-up cohort of the German He
Externí odkaz:
https://doaj.org/article/1bbd56c2e70d437c91a3d02590e38635
Autor:
Tanja Schmitz‐Hübsch, Silke Lux, Peter Bauer, Alexander U. Brandt, Elena Schlapakow, Susanne Greschus, Michael Scheel, Hanna Gärtner, Mehmet E. Kirlangic, Vincent Gras, Dagmar Timmann, Matthis Synofzik, Alejandro Giorgetti, Paolo Carloni, Jon N. Shah, Ludger Schöls, Ute Kopp, Lisa Bußenius, Timm Oberwahrenbrock, Hanna Zimmermann, Caspar Pfueller, Ella‐Maria Kadas, Maria Rönnefarth, Anne‐Sophie Grosch, Matthias Endres, Katrin Amunts, Friedemann Paul, Sarah Doss, Martina Minnerop
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 8, Iss 4, Pp 774-789 (2021)
Abstract Objectives Genetic variant classification is a challenge in rare adult‐onset disorders as in SCA‐PRKCG (prior spinocerebellar ataxia type 14) with mostly private conventional mutations and nonspecific phenotype. We here propose a refined
Externí odkaz:
https://doaj.org/article/01bebd976eac43a5bb41b90154ae31c0