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Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6.
Reetz K, Costa AS, Mirzazade S, Lehmann A, Juzek A, Rakowicz M, Boguslawska R, Schöls L, Linnemann C, Mariotti C, Grisoli M, Dürr A, van de Warrenburg BP, Timmann D, Pandolfo M, Bauer P, Jacobi H, Hauser TK, Klockgether T, Schulz JB; axia Study Group Investigators. Reetz K, et al. Brain. 2013 Mar;136(Pt 3):905-17. doi: 10.1093/brain/aws369. Epub 2013 Feb 18. Brain. 2013. PMID: 23423669
Diminished activation of motor working-memory networks in Parkinson's disease.
Rottschy C, Kleiman A, Dogan I, Langner R, Mirzazade S, Kronenbuerger M, Werner C, Shah NJ, Schulz JB, Eickhoff SB, Reetz K. Rottschy C, et al. Among authors: reetz k. PLoS One. 2013 Apr 19;8(4):e61786. doi: 10.1371/journal.pone.0061786. Print 2013. PLoS One. 2013. PMID: 23620791 Free PMC article.
Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data.
Jacobi H, Reetz K, du Montcel ST, Bauer P, Mariotti C, Nanetti L, Rakowicz M, Sulek A, Durr A, Charles P, Filla A, Antenora A, Schöls L, Schicks J, Infante J, Kang JS, Timmann D, Di Fabio R, Masciullo M, Baliko L, Melegh B, Boesch S, Bürk K, Peltz A, Schulz JB, Dufaure-Garé I, Klockgether T. Jacobi H, et al. Among authors: reetz k. Lancet Neurol. 2013 Jul;12(7):650-8. doi: 10.1016/S1474-4422(13)70104-2. Epub 2013 May 22. Lancet Neurol. 2013. PMID: 23707147
Altered resting-state connectivity in Huntington's disease.
Werner CJ, Dogan I, Saß C, Mirzazade S, Schiefer J, Shah NJ, Schulz JB, Reetz K. Werner CJ, et al. Among authors: reetz k. Hum Brain Mapp. 2014 Jun;35(6):2582-93. doi: 10.1002/hbm.22351. Epub 2013 Aug 24. Hum Brain Mapp. 2014. PMID: 23982979 Free PMC article.
206 results