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Page 1
Brain atrophy measures in preclinical and manifest spinocerebellar ataxia type 2.
Reetz K, Rodríguez-Labrada R, Dogan I, Mirzazade S, Romanzetti S, Schulz JB, Cruz-Rivas EM, Alvarez-Cuesta JA, Aguilera Rodríguez R, Gonzalez Zaldivar Y, Auburger G, Velázquez-Pérez L. Reetz K, et al. Among authors: schulz jb. Ann Clin Transl Neurol. 2018 Jan 7;5(2):128-137. doi: 10.1002/acn3.504. eCollection 2018 Feb. Ann Clin Transl Neurol. 2018. PMID: 29468174 Free PMC article.
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. Among authors: schulz jb. Brain. 2013 Mar;136(Pt 3):905-17. doi: 10.1093/brain/aws369. Epub 2013 Feb 18. Brain. 2013. PMID: 23423669
Neural correlates of impaired emotion processing in manifest Huntington's disease.
Dogan I, Saß C, Mirzazade S, Kleiman A, Werner CJ, Pohl A, Schiefer J, Binkofski F, Schulz JB, Shah NJ, Reetz K. Dogan I, et al. Among authors: schulz jb. Soc Cogn Affect Neurosci. 2014 May;9(5):671-80. doi: 10.1093/scan/nst029. Epub 2013 Mar 11. Soc Cogn Affect Neurosci. 2014. PMID: 23482620 Free PMC article.
491 results