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Prominent White Matter Involvement in Multiple System Atrophy of Cerebellar Type.
Faber J, Giordano I, Jiang X, Kindler C, Spottke A, Acosta-Cabronero J, Nestor PJ, Machts J, Düzel E, Vielhaber S, Speck O, Dudesek A, Kamm C, Scheef L, Klockgether T. Faber J, et al. Mov Disord. 2020 May;35(5):816-824. doi: 10.1002/mds.27987. Epub 2020 Jan 29. Mov Disord. 2020. PMID: 31994808
A language-based sum score for the course and therapeutic intervention in primary progressive aphasia.
Semler E, Anderl-Straub S, Uttner I, Diehl-Schmid J, Danek A, Einsiedler B, Fassbender K, Fliessbach K, Huppertz HJ, Jahn H, Kornhuber J, Landwehrmeyer B, Lauer M, Muche R, Prudlo J, Schneider A, Schroeter ML, Ludolph AC, Otto M; FTLD consortium. Semler E, et al. Alzheimers Res Ther. 2018 Apr 25;10(1):41. doi: 10.1186/s13195-018-0345-3. Alzheimers Res Ther. 2018. PMID: 29695300 Free PMC article.
Characterization of Cerebellar Atrophy and Resting State Functional Connectivity Patterns in Sporadic Adult-Onset Ataxia of Unknown Etiology (SAOA).
Jiang X, Faber J, Giordano I, Machts J, Kindler C, Dudesek A, Speck O, Kamm C, Düzel E, Jessen F, Spottke A, Vielhaber S, Boecker H, Klockgether T, Scheef L. Jiang X, et al. Among authors: faber j. Cerebellum. 2019 Oct;18(5):873-881. doi: 10.1007/s12311-019-01072-y. Cerebellum. 2019. PMID: 31422550 Clinical Trial.
Minor neuropsychological deficits in patients with subjective cognitive decline.
Wolfsgruber S, Kleineidam L, Guski J, Polcher A, Frommann I, Roeske S, Spruth EJ, Franke C, Priller J, Kilimann I, Teipel S, Buerger K, Janowitz D, Laske C, Buchmann M, Peters O, Menne F, Fuentes Casan M, Wiltfang J, Bartels C, Düzel E, Metzger C, Glanz W, Thelen M, Spottke A, Ramirez A, Kofler B, Fließbach K, Schneider A, Heneka MT, Brosseron F, Meiberth D, Jessen F, Wagner M; DELCODE Study Group. Wolfsgruber S, et al. Neurology. 2020 Sep 1;95(9):e1134-e1143. doi: 10.1212/WNL.0000000000010142. Epub 2020 Jul 7. Neurology. 2020. PMID: 32636322
Validation of a German version of the Cerebellar Cognitive Affective/ Schmahmann Syndrome Scale: preliminary version and study protocol.
Thieme A, Roeske S, Faber J, Sulzer P, Minnerop M, Elben S, Jacobi H, Reetz K, Dogan I, Barkhoff M, Konczak J, Wondzinski E, Siebler M, Mueller O, Sure U, Schmahmann JD, Klockgether T, Synofzik M, Timmann D. Thieme A, et al. Among authors: faber j. Neurol Res Pract. 2020 Sep 29;2:39. doi: 10.1186/s42466-020-00071-3. eCollection 2020. Neurol Res Pract. 2020. PMID: 33324939 Free PMC article. Clinical Trial.
Natural History, Phenotypic Spectrum, and Discriminative Features of Multisystemic RFC1 Disease.
Traschütz A, Cortese A, Reich S, Dominik N, Faber J, Jacobi H, Hartmann AM, Rujescu D, Montaut S, Echaniz-Laguna A, Erer S, Schütz VC, Tarnutzer AA, Sturm M, Haack TB, Vaucamps-Diedhiou N, Puccio H, Schöls L, Klockgether T, van de Warrenburg BP, Paucar M, Timmann D, Hilgers RD, Gazulla J, Strupp M, Moris G, Filla A, Houlden H, Anheim M, Infante J, Basak AN, Synofzik M; RFC1 Study Group. Traschütz A, et al. Among authors: faber j. Neurology. 2021 Mar 2;96(9):e1369-e1382. doi: 10.1212/WNL.0000000000011528. Epub 2021 Jan 25. Neurology. 2021. PMID: 33495376 Free PMC article.
1,338 results